1.
Comparative Efficacy Of Casoni Skin Test, Indirect Haemagglutination And Double Diffusion Tests For The Detection Of Hydatidosis In Goats
by Azam Mahmood | Prof. Dr. Tufail Muhammad Khan | Dr. Manzoor Ahmad Basraa | Dr. Muhammad | Faculty of Veterinary Sciences.
Material type: ; Format:
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Publisher: 1991Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 0149,T] (1).
2.
Comparative Study On The Incidence And Pathology Of Morbid Conditions Of Uterus And Cervix Of Teddy And Local Non Descriptive Goats
by Yousaf Hassan Khera | Dr. Shakil Akhtar Khan | Dr. Ahmad Raza | Prof. Dr. Rashid Ahmed Ch | Faculty of Veterinary Sciences.
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Publisher: 1996Dissertation note: The project was designed to study incidence and pathology of uterine and cervical maladies in two breeds (Teddy and Local non- descriptive) of goats. Three hundred uteri and cervices (150 from each breed) of goats of three age groups, 1-2 years, 2-3 years and above three years (50 in each group) were collected from Lahore slaughter house and then thoroughly examined for any gross pathological change. The organs exhibiting macropathological lesions were subjected to morphometric, histopathological and histochemical examinations.
Of the 300 uteri and cervices, 35 (11.66%) showed morbid conditions. In 150 Teddy goats, pathological conditions were observed in, 1-2 years age group 4 (8%), 2-3 years age group 7 (14%) and in above 3 years age group 8 (16%). In 150 local non-descriptive goats, gross pathological conditions were present in, 1-2 years age group 3 (6%), 2-3 years age group 6 (12%) and in above 3 years age group 7 (14%). These results showed that incidence of pathological conditions increased with the age of the goats in both the breeds and incidence was slightly higher in Teddy goats than Local non descriptive goats in the same age groups. The following eight pathological conditions namely metritis, pyometra, pigmentation, endometrial cysts, adhesions, fibrosis, hemorrhages and aplasia of uterus were found. The morphometric, gross and histopathological changes of each disease condition of uterine horns, uterine body and cervices were studied. The histochemical evidence of tissue exhibited PAS and alcian blue reactions revealing presence of carbohydrates were also studied.
Availability: Items available for loan: UVAS Library [Call number: 0440,T] (1).
3.
Study On Various Mineral Levels And Pathology Of Visceral Organs Of Broiler Chickens Affected With Leg Deformities
by Asim Aslam | Dr. Shakil Akhtar Khan | Dr. Ahmad Raza | Prof. Dr. Rashid Ahmad | Faculty of Veterinary Sciences.
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Publisher: 1996Dissertation note: This project was designed to determine the incidence of various leg disorders in commercial broiler chickens and to elucidate the effects of leg deformity on the metabolism of broiler chickens in terms of serum levels of calcium, phosphorus, sodium, potassium, chloride and also on the morphology of liver, kidneys and pancreas. Fifty leg deformed broiler chickens were collected from 38 different commercial poultry farms in and around Lahore, kasur, Sialkot and Gujranwala Districts.
Out of the observed cases of leg deformity, 18 cases of valgus, 13 cases of slipped gastrocnemius tendon, 9 cases of curly toe, 5 cases of femoral head necrosis, 3 cases of varus and only 2 cases of synovitis were reported. This data of incidence of various leg deformaties were analysed on the basis of age, sex, strain of bird and also on the basis of location of deformity. It was noted that the most frequently encountered leg deformity was valgus. The maximum incidence of valgus occurred at 5th week of age. The males have greater incidence of valgus as compared to females. Hubbard strain had greater incidence of valgus in comparison to other strains of birds.
Unilateral cases of valgus were more common than bilateral. The levels of all minerals were decreased in experimental birds as compared to control ones. The mineral levels of birds affected with valgus deformity showed that there was a highly significant difference in the levels of calcium phosphorus and sodium between the experimental and control groups. But there was a non-significant difference in the levels of potassium and chloride in both the groups. The slipped gastrocnemius tendon was noted frequently at 7th week of age, slightly more in females and all the reported cases were unilateral. Hubbard strain was found to be most liable to slipped tendon. The mineral levels of birds affected with slipped tendon showed a highly significant difference in the levels of calcium, phosphorus and potassium between the experimental and control groups. A significant difference was also noted between the experimental and control groups in terms of levels of chloride, but a non-significant difference was recorded between the experimental and control groups in case of serum sodium level. Curly toe was again recorded to its peak in birds of 7 week age, more in males and mostly bilateral. Hubbard strain was found to be the most affected one. The mineral levels of birds affected with curly toe showed a highly significant difference in the levels of calcium and phosphorus between the experimental and control groups. But a non-significant difference was noted between the two groups in cases of serum levels of sodium, chloride, and potassium. Femoral head necrosis was recorded at its highest incidence at 9th week of age, more in males, and all the recorded cases were unilateral. The strain most liable to femoral head necrosis was Indian river. The mineral levels of birds affected with femoral head necrosis showed a highly significant difference in the levels of phosphorus and potassium between experimental and control groups. A significant difference was also recorded between the experimental and control groups in terms of levels of calcium. But in the serum levels of sodium and chloride a non-significant difference was obtained between the two groups. Varus was recorded more frequently at 6 and 7 week of age, more in females, and mostly unilaterally although bilateral cases were also noted. Hubbard, Arboracres, and Lohmann strains showed more susceptible behaviour. The mineral levels of birds affected with varus showed a highly significant difference in the level of calcium. A significant difference was also recorded between the experimental and control groups in terms of levels of phosphorus and potassium, but a non-significant difference was noted in the sodium level between the two groups. Synovitis was noted mostly between 3 and 6 week of age, more or less equally between males and females. Both unilateral and bilateral cases were seen, and Hubbard and Arboracres strains were found to be more prone to synovitis. The mineral levels of birds affected with synovitis showed a significant difference in the levels of calcium and sodium in the experimental and control groups. But a non-significant difference lies between the two groups.
In all these various types of leg deformities, the macroscopic lesions like, slight enlargement of liver along with discolorization and necrotic areas and in some cases congested livers showing the lesions of perihepatitis were also noticed. The kidneys showed inflammatory signs alongwith urates deposits. A pale fibrosed pancreas showed atrophic changes. The pancreas was the most severely affected organ. In majority of the birds it was severely atrophied presenting a shrunken fibrous band like structure in the convoluted duodenal loop. The colour of these pancreases was white or off-white to pink and were firm in consistency. Microscopically cloudy swellings and severe necrosis were seen in the affected livers. Mononuclear and plasma cell infiltration were also quite evident. Leukocytic infiltration in the interstitial spaces and glomerular region were quite evident. The dilated blood vessels and haemorrhages in tissue spaces were observed. In some of the severely affected cases the glomeruli were enlarged and were less in number as compared to that of normal birds.Lesions of necrosis were also noted in some of the affected kidneys. Pancreas was observed that the acinar cells were atrophied and underwent vacuolation, degeneration and necrosis. The Zymogen granules were almost absent from acinar cells. Heterophil, leukocytic and lymphocytic infiltration were frequently encountered in affected cases. A characteristic change was an inflammatory reaction in one or more pancreatic ducts where the epithelium and fibrous tissues occluded the lumen of the ducts and led to obstruction in pancreatic drainage.
Availability: Items available for loan: UVAS Library [Call number: 0513,T] (1).
4.
Comparative Studies On The Sensitivity Of Polymerase Chain Reaction (Pcr) And Microscopic Examination For The Detection of Trypanosoma Evansi in Horses
by Muhammad Asif Muieed | Prof. Dr. Zafar Iqbal Chaudhary | Dr. Azhar Maqbool | Mr. Asim Aslam | Faculty of Veterinary Sciences.
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Publisher: 2005Dissertation note: The polymerase chain reaction (PCR) was standardized and its efficacy was evaluated against microscopic examination i.e. Giemsa stained smear method ['or the diagnosis of Trypanosoma evansi infection (Surra) in horses. l3lood samples were collected from 100 suspected horses from different localities in Lahore.
Under aseptic precautions blood smears were prepared, after drying and fixing with methanol, slides were stained by Giemsa stain method of staining. By stained blood smear method 5 out of 100 horses were found positive For T. evansi infection. The polymerase chain reaction (PCR) was carried out on the blood of' the same suspected horses to evaluate its efficacy in the diagnosis of' T. evansi infection and to compare its diagnostic value against the microscopic examination method currently in use. For this purpose total genomic DNA was extracted from suspected blood samples. The PCR reaction was performed in a 50tl reaction mixture containing I X Taq BuFfer, 0.2 mM dNTP Mixture. I .5 mM MgCIl2 2.5 U/1i1 Taq Polymerase. 4uM of' each primer, 2 ul of DNA extracted and 31.5 p1 of DNase - free deionised water. The tubes containing the mixture were subjected to 30 cycles of amplification in a thermocycler. During each cycle the sample of' DNA was denatured at 93° C' For 30 seconds, annealed at 45° C For 30 seconds and extended at 720 C For I minute. Prior to the cycling and at the end of' cycling the mixture was subjected to incubation at 93° C for a period of 3 minutes and final extension at 72° C for a period of 5 minutes, respectively. PCR product was then characterized by 2.5% of agarose gel electrophoresis. To confirm the presence of DNA and to estimate its size it was compared with a DNA ladder and was photographed with a Polaroid camera. The polymerase chain reaction (PCR) revealed 16 positive cases out of 100 above mentioned suspected cases. These 16 positive cases diagnosed by polymerase chain reaction (PCR) also included animals, which were diagnosed by stained blood smear method.
It can be concluded that polymerase chain reaction (PCR) is a superior and sensitive (16%) in comparison with the microscopic examination i.e. Giemsa stained smear method (5%). Polymerase chain reaction (PCR) is more effective in cases where the parasitemia is low and this test could be used in other species of animals especially camels where the disease is more chronic and difficult to confirm by. other routine methods. PCR would not only ensure early diagnosis and treatment in individual animals but can detect animal reservoirs of infection and would help to eliminate threat to equine and camel herds which are grazed and housed together and where blood sucking mechanical fly vectors are ever present.
Availability: Items available for loan: UVAS Library [Call number: 0860,T] (1).
5.
Detection Of Toxoplasma Gondii Infectionin Butchers And Buffaloes By Polymerase Chain Reaction (PCR) and Latex Agglutination Test
by Rana Sajjad Ahmed | Prof. Dr. Zafar Iqbal Chaudhary | Prof. Dr. Muhammad Naeem Khan | Faculty of Veterinary Sciences.
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Publisher: 2005Dissertation note: Toxoplasmosis, a common parasitic zoonotic infection is usually aymptomatic in immunocompetent persons although it may be present as lymphadenopathy, febrility, etc. but it is a life threatening opportunistic infection in congenitally infected patients and in immunocompromised individuals (those with AIDS, malignancy, organ transplantation, etc). Human beings become infected with T. gondii usually by ingesting oocysts in food and water contaminated with cat feces or by consuming tissue cysts in undercooked meat.
The diagnosis of toxoplasmosis is mainly based on serological tests latex agglutination test (LAT). Detection of specific DNA seems to be of clinical value in the ingestion of patients infected with toxoplasmosis.
In this study, latex agglutination test was used for the detection of the antibodies against Toxoplasma gondii and Polymerase Chain Reaction (PCR) based on the amplification of repetitive B1 gene of T. gondii. The study was based on a total of 200 samples involving 50 butchers, 50 buffalo's sera and whole blood respectively.
LAT established an overall infection of T. gondii in butchers and buffaloes as 20 % and 22 % respectively. The PCR analysis confirmed this T. gondii prevalence in butchers and buffaloes.
LAT proved to be an efficacious method for routine serological screening for antibodies to T. gondii. The costly and sophisticated PCR results in our investigation showed good correlation with the serological data of these patients showing that LAT can be used as an alternation to PCR. The results demonstrated that PCR analysis of clinical samples of patients suspective for acute toxoplasmosis including those with an acquired infection presented by lymphadenopathy can be a promising diagnostic method that enables direct detection of parasitic DNA.
Availability: Items available for loan: UVAS Library [Call number: 0861,T] (1).
6.
Diagnosis And Prevalence Of Trypanosoma Evansi In Camels Through Polymerase Chain Reaction (PCR) And Haematocrit Centrifugation Thechnique (HCT) in Punjab (Pakistan)
by Jahanzaib | Prof. Dr. Zafar Iqbal Chaudhary | Prof. Dr | Prof. Dr. H.A. Hashmi | Faculty of Veterinary Sciences.
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Publisher: 2005Dissertation note: The most important protozoan disease of camels is trypanosomiasis caused by Trypanosoma evansi. There was little epidemiological information on the prevalence of infection. The present study was conducted to find out the prevalence of Trypanosorna evansi in camels through haematocrit centrifugation technique (HCT) and polymerase chain reaction (PCR). A total number of 100 camels of different age and sex groups were selected from different localities including Bahawalpur, Lahore, Gujranwala and faisalabad to find out the prevalence of Trypanosomiasis in Punjab (Pakistan) and to evaluate the sensitivity of PCR assay and HCT for the diagnosis Trypanosoma evansi. Blood samples were collected and examined by haematocrit centrifugation technique (HCT) and polymerase chain reaction (PCR). The prevalence was recorded as 4% and 13% by haematocrit centrifugation technique (HCT) and polymerase chain reaction. The positive samples by the polymerase chain reaction also included the positive animals by the haermatocrit centrifugation technique.
The results showed that PCR was more sensitive method for the detection of trypanosomiasis as compared to the haematocrit centrifugation technique. Thus PCR can be used for the diagnosis of camel trypanosornosis during both acute and chronic phases of infection, and for use in the evaluation of treatment. Application of PCR to field diagnosis is therefore clearly indicated.
Availability: Items available for loan: UVAS Library [Call number: 0862,T] (1).
7.
Effect Of Potassium Chloride And Sodium Bicarbonate Suplementation On Thermotolerance Of Broileers Exposed to Heat Stress
by Muhammad Tahir Naseem | Prof. Dr. Zafar Iqbal Chaudhry | Dr. Kamran | Prof. Dr. Haji Ahmad Hashmi | Faculty of Veterinary Sciences.
Material type: ; Format:
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Publisher: 2005Dissertation note: A total of 100-day-old broiler chicken were randomly divided into five groups and kept under elevated temperature (95-98.6ºF) to observe the effect of potassium chloride and sodium bicarbonate on the weight gain, feed conversion ratio (FCR), serum potassium and serum bicarbonate level. Thermostress lead to significant in decrease (P<0.05) weight gain, serum potassium and serum bicarbonate level, while FCR was increased. During heat stress, KCl and NaHCO3 at levels of 1.5% and 0.5% respectively, improved weight gain, and FCR and significantly increased (P<0.05) serum potassium and bicarbonate level. The results showed that combination of KCl and NaHCO3 supplementation alleviated the negative effects of heat stress in broilers.
Availability: Items available for loan: UVAS Library [Call number: 0863,T] (1).
8.
Toxicological Effects Of Feeding First Cut Sorghum Vegeation And Stalks To Rabbits
by Shahzad Bhatti | Prof. Dr. Zafar Iqbal Chaudhry | Dr. Azhar | Prof. Dr. Naeem Khan | Faculty of Veterinary Sciences.
Material type: ; Format:
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Publisher: 2005Dissertation note: The present project was designed to study the hematological and biochemical changes due to toxicity caused by sorghum (stalks, leaves) in rabbits and compared with grass feeding. For this purpose 18 rabbits of almost same body weight and age were randomly divided into three groups (6 animals per group) designated as A, B and C. Animals of each group were caged separately.
Group A was fed on grass; group B was fed on sorghum stalks; group C was fed on sorghum leaves. Sorghum samples were collected from different fields A, B, C and D, near Bund road Lahore. From each field four samples were collected and analyzed for nitrate. Nitrate analysis in sorghum stalks and leaves showed that in all the four fields there was high level of nitrate in stalks as compared to leaves and nitrate content both in stalks and leaves was high in field A as compared to field B, C and D. This high level of nitrate in sorghum was due to excessive use of nitrogen containing fertilizers by farmers. Therefore group B and C was fed on sorghum stalks and leaves of field A for 30 days in experimental room of Pathology, UVAS, Lahore.
Blood samples were taken from marginal ear veins of all rabbits aseptically with the help of syringe at the start of the experiment and then at the interval of 10 days till the expiry of the experiment. Hematological studies revealed erythrocytopenia, leukocytopenia, decreased hemoglobin and lowered erythrocyte sedimentation rate (ESR) in group B as compared to group A and C from day 10 to 30.
Biochemical analysis reveled methemoglobinemia and high level of liver enzymes alanine aminotransferase (ALT) and aspartate aminotransferase (AST) of group B as compared to group A and C from day 10 to 30.
Availability: Items available for loan: UVAS Library [Call number: 0864,T] (1).
9.
Molecular Diagnosis Of Bovine Tuberculosis In Humans
by Muhammad Bilal | Prof. Dr. Zafar Iqbal Chaudhary | Dr. Asim Aslam | Dr. Mnsur-uddin | Faculty of Veterinary Sciences.
Material type: ; Format:
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Publisher: 2005Dissertation note: Tuberculosis is a highly infectious disease. In humans it is mainly caused by Mycobacterium tuberculosis and occasionally by Mycobacterium bovis and Mycobacterium africanum. Bovine tuberculosis caused by M bovis is the main cause of enteric TB in humans. it is transmitted through milk, meat and dairy products. It is also recorded that it can also cause pulmonary tuberculosis in humans.
A study was conducted to detect the M bovis in human pulmonary sputum samples through PCR based techniques. A PCR assay was described which could differentiate M bovis from M. tuberculosis in clinical samples. Sputum of 400 patients was randomly analyzed with PCR assay. Two (0.5%) out of 400 sputum samples were positive for M bovis while remaining were positive for M tuberculosis. Over all 0.5% cases were positive for M bovis causing pulmonary tuberculosis in humans.
The two positive cases were analyzed in the background of their history. History revealed that both of them belong to different families and areas were in close contact with animals for a long time. It suggested that they caught infection from animals. It was an evidence of pulmonary tuberculosis of M bovis in humans.
Availability: Items available for loan: UVAS Library [Call number: 0865,T] (1).
10.
Effect Of High Dietary Fat On Serum Cholesterol And Fatty Liver Syndrome In Broiler
by Imran Ahmed Qureshi | Dr. Zafar Iqbal Chaudhry | Dr. H. A. Hashmi | Prof. Dr. Nisar | Faculty of Veterinary Sciences.
Material type: ; Format:
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; Literary form:
not fiction
Publisher: 2003Dissertation note: The present study was designed to evaluate the effects of high dietary fat on serum cholesterol and fatty liver syndrome in broiler. For this purpose 90 (day-old) chicks were procured from local hatchery. They were divided into three groups A, B and C having 30 chicks each. The birds of group B were fed on diet containing plant and animal fat while birds of group C were fed on diet containing animal fat. Group A acted as control. Experimental parameters included serum cholesterol values and pathological changes in liver. The serum cholesterol values in chicks of groups B and C were higher than that of control group. Furthermore, the serum cholesterol value was greater in birds fed on animal fat that on plant fat. Grossly the livers of group B and C were enlarged in size, paler in colour, soft in consistency, having petechial haemorrhages, deposition of fat and fibrin. The livers of group A were grossly normal. Histopathologically, livers of group B and C showed fatty infiltration, haemorrhages and mass of eosinophilic materials. The vacuoles coalesced to create clear space that displaced the nuclei to the periphery of the cell. Addition of dietary fat from animal and plant sources in the diet of broiler chicks not only resulted in increase in serum cholesterol but also in marked macroscopic and microscopic changes in liver.
Availability: Items available for loan: UVAS Library [Call number: 0866,T] (1).
11.
Molecular Detection Of Babesia Bigemina And Babesia Bovis In Carrier Cattle By Duplex Polymerase Chain Reaction
by Muhammad Suleman | Prof. Dr. Zafar Iqbal Ch | Dr.Asim Aslam | Prof. Dr Abdul Rauf Shakoori | Faculty of Veterinary Sciences.
Material type: ; Format:
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Publisher: 2006Dissertation note: Babesiosis is a highly important disease in the world, caused by the intraerythrocytic protozoan parasites of the genus Babesia. A wide range of domestic and wild animals and occasionally man are affected by this disease, which is transmitted by ticks and has a worldwide epidemiological distribution. While the major economic impact of babesiosis is on the cattle industry, infections also occurs in other domestic animals , including horses, sheep, goats, pigs and dogs.
The present study targeted the carrier cattle infected with Babesia bigemina and Babesia bovis, as they are difficult to detect because of the low numbers of parasites that occur in peripheral blood. However, diagnosis of low-level infections with the parasite is important for studying the transmission and standardizing epidemiological studies. Using the Polymerase Chain Reaction (PCR) to amplify a portion of the gene from the parasite, and tested the ability of this method to detect carrier cattle.
A study was conducted to detect the. Babesia in blood samples through PCR based techniques. A PCR assay was described which could differentiate Babesia bigemina and Babesia bovis by using specific primer in carrier cattle. Blood samples of 100 cattle were randomly analyzed with PCR assay 29 (29.0%) out of 100 blood samples were positive for babesiosis in which 18% were positive for Babesia bigemina and 11% were positive for Babesia bovis, While the Light Microscopy detected only 18 (18%) out of the same samples. The samples found positive by LM were reconfirmed during the PCR assay but no sample was found to be having both Babesia bigemina and Babesia bovis infections simultaneously.
Thus it is concluded that PCR is a reliable molecular diagnostic technique to detect low level of infections in carrier animals in a population and thus could be used as an effective screening tool for the control and eradication of disease.
Availability: Items available for loan: UVAS Library [Call number: 0929,T] (1).
12.
Pathogenesis Of Salmonellosis With Respect To Carrier States In Poultry And Its Public Health Impact
by Younus, M | Prof. Dr. Zafar Iqbal Chaudhry | Prof.Dr.Abdul Rauf Shakoori | Prof.Dr.Muham | Faculty of Veterinary Sciences.
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Publisher: 2006Dissertation note: The present research endevour was made to study and investigate the prevalence of Salmonella enteritidis and Salmonella typhimurium from poultry feed, poultry meat and poultry eggs and their role in the chain of transmission of salmonellae to human beings. The objective was to generate data to improve the quality of poultry products and human health awareness.
Salmonellosis is one of the most wide spread food borne zoonoses. The etiological agents Salmonella enteritidis and Salmonella typhimurium not only' produce the disease but during the convalescent phase (after the recovery of disease) remain carriers for indefinite period of time. In this study 400 samples were collected and were distributed and detailed as; poultry feed (n=100), poultry intestines (n100 Small and n=100 Large intestines) and eggs (n=100) were collected for the identification of the organism through polymerase chain reaction (PCR). The Positivity percentage as tested through PCR for Salmonella enteritidis in the poultry feed was 20,15,10,15 and 10 for layer starter, layer grower, layer finisher, broiler starter and broiler finisher respectively (P>0.05). The positivity percentage as tested through PCR for Salmonella typhimurium for layer starter, layer grower, layer finisher, broiler starter and broiler finisher feed was 15,10,10, 10, and 10 respectively (P>0.05). There was no significant difference between layers feed and broilers feed as far as identification of salmonella enteritidis and salmonella typhimurium was concerned (P>0.05) but the prevalence range of salmonella enteritidis and salmonella typhimuilum from poultry feed was 10-20% which was biologically significant. The positivity percentage rate of Salmonella enteritidis for small and large intestine in Desi birds (local breed) was 2 and 16 % respectively. Where as for broilers in small and large intestine it was 4 and 18% respectively. The positivity of Salmonella typhimurium in small and large intestine of Desi birds was 2 and 14% where as in broilers it was 4 and 16% in the small and large intestine respectively. There was a significant difference (P <0.05) between the positivity of percentage of salmonella enteritidis and salmonella typhimurium as far as identification of Salmonellae from Desi and broiler meat was concerned.
It was found that 16%, 8%, 16'Y0 and 16% egg albumin was found positive for Salmonella enteritidis in layer egg albumin, Desi (local breed) eggj albumin, double yolk albumin and broken egg albumin respectively. In each case 25 egg albumin were collected and tested for the detection of Salmonellae. Similarly the egg yolk from layers, Desi (local breed) double yolk and broken eggs was taken and positivity rate for Salmonella enteritidis was found 12%, 4%, 12% and 12% respectively. It was found that 12%, 4%, 12% and 12% egg albumin was found positive for Salmonella lyphimurium in layer egg albumin, Desi egg albumin, double yolk albumin and broken egg albumin respectively. In each case 25 egg albumin were collected and tested for the' detection of Salmonella. Similarly the egg yolk from layers, desi double yolk and broken eggs was taken and positivity rate for Salmonella enteritidis was found 8%, 4%, 8% and 4% respectively. The positively rate for Salmonella typhimurium in both albumin and yolk was relatively less in both albumin and yolk of layers, desi double yolk and broken eggs. Statistically there was no significant difference (P> 0.05) but the prevalence of Salmonella enteritidis and Salmonella typhimurium from different eggs ranged between 4-16% and 4-12% respectively which was biologically significant.
The Salmonella enteritidis and Salmonella typhimurium were isolated, identified and grown on the artificial and selective media. The virulence of the organisms of Salmonella enteritidis and Salmonella typhimurium were estimated through calculation of LD50. It was found as 10358/mI and 103/ml for Salmonella enteritidis and Salmonella typhimurium respectively, having significant difference (P< 0.05). In order to understand the pathogenesis and carrier states of salmonella organisms in poultry, a group of 300 broiler birds were procured and divided into three groups were studied upto the age of 3 months. The infection was orally given on the 7th day of their age. As an average 86.74% of the birds were maintaining the organism of the Salmonella enteritidis in the large intestine during the entire experimental period in contrast to the small intestine in which 0% were found positive (P< 0.05). Similarly an average 94.94% of the birds were maintaining the organism of the Salmonella typhimurium in the large intestine during the entire experimental period in contrast to the small intestine in which 0% were found positive (P< 0.05) but non of the samples of Small and Large intestine of control group (Group-C) were found positive for Salmonella enleritidis and Salmonella typhimurium. There was a significant difference between Salmonella enteritidis and Salmonella typhimurium in large intestine of poultry (P< 0.05). The histopathology of different organs of broiler chickens i.e liver, lung, spleen, kidney, small intestine, large intestine, bursa of fabracious and lean muscles at different phases of disease was also conducted for the better understanding of pathogenesis due to salmonellosis. The principal lesions in the liver at the age of 14 to 28 days in groups A and B were leukocytic infiltration, necrosis and haemmorrhage. No lesions were recorded in liver after 28 days of age in groups A and B. No lesions were recorded in group C. The principal lesions of the lungs at the age of 14 to 28 days in groups A and B were leukocytic infiltration,' mild necrosis, vascular congestion and haemrnorrhages. No lesions were recorded in lungs after 28 days of age in groups A and B. No lesions were recorded in group C. The principal lesions of the spleen were mild leukocytic infiltration, necrosis and congestion at the age of 14 to 28 days in groups A and B. No lesions were recorded in spleen after 28 days of age in groups A and B. No lesions were found in group C. The principal lesions of the kidneys were marked tubutar necrosis with glomerular degeneration and Ieukocytic infiltration and haemmorrhages at the age of 14 to 28 in groups A and B. No lesions were1 recorded in kidneys after 28 days of age in groups A and B. No lesions were found in group C. The principal lesions of the small intestine were degeneration of mucosa with inflammatory cells, necrosis, inflammation, superficial ulceration on mucosal lining of intestine at the age of 14 to 21 days. No lesions were recorded in small intestine after 21 days of age in group A and B. No lesions were recorded in control group C. The principal lesions of the large intestine were leukocytic infiltration with necrosis and inflammation at the age of 14 to 91 days. The lesions were recorded up to 91 days of age in group A and B. No lesions were recorded in control group C. The principal lesions of Bursa of1, fabricious were atrophy & necrosis of bursal follicles and leukocytic infiltration at the age of 14 to 21 in groups A and B. No lesions were recorded in Bursa of fabricious after 21 days of age in groups A and B. No lesions were found in group C. The principal lesions of lean muscle were muscular degeneration and necrotic areas at the age of 14 to 21 days in groups A and B. No lesions were recorded in lean muscles after 21 days of age in groups A and B. No lesions were found in group C.
The carrier state was not only the source of spread of disease with in the poultry but also caused typhoid fever and food poisoning in humans. The chain of transmission started fron poultry feed to poultry meat and ultimately to humans as dead end host. Finally, the 400 samples of stool and blood from 200 human patients (100 suspected of typhoid fever and 100 suspected of food poisoning) were also collected from four different hospitals from urban area of Lahore for the identification of Salmonella enteritidis and Salmonella typhimurium through PCR method in order to see the public health impact of Salmonellosis through consuming the meat and eggs of the carrier birds. A total of 14% and 10% stool samples were found positive for Salmonella enteritidis and Salmonella Typhimurium in case of suspected typhoid fever patients respectively. Similarly 6% and 2% blood samples were found positive for Salmonella enteritidis and Salmonella Typhimurium. There was a significant difference (P< 0.05) in the sero positivity of stool and blood samples of suspected typhoid fever patients and also as for as Salmonella enteritidis and Salmonella typhimurium was concerned. However there was no significant difference (P> 0.05) between the hospitals On the average 14 and 10 stool samples were found positive against Salmonella enteritidis and Salmonella typhimurium from each of the 25 patients of each hospital respectively in case of suspected food poisoning patients. Similarly on an average 5% and 6% blood samples were found positive from 25 patients of each hospital respectively. There was a significant difference (P< 0.05) in the sero positivity of stool and blood samples of suspected food poisoning patients as far as Salmonella enteritidis and Salmonella typhimurium was concerned. However there was no significant difference (P> 0.05) between the hospitals.
CONCLUSION
A series of five experiments were conducted and carried out to study and explore the project Pathogenesis of Salmonellosis with respect to carrier states in poultry and its public health impact."
For this purpose, in the 1st phase, identification, isolation and characterization of Salmonella enteritidis and Salmonella typhimurium was attempted. It was followed by the estimation of LD 50 and carrier states and histopathological study at different phases of disease in broiler chickens experimentally infected with Salmonella enteritidis and Salmonella typhimurium to ascertain the nature of carrier states in terms of maintenance of the Salmonellae by different organs leading to histopathological changes and finally to the stage of shedding of the organism through the feces in the environment. Dissemination to human beings and the Public health impact of Salmonellosis was studied in the human subjects who consumed the meat and eggs of the carrier birds which were followed by testing their stool and blood samples through polymerase chain reaction (PCR). In this way the pathogenesis and chain of Salmonellas enteritidis and Salmonella typhimurium infection through poultry feed, meat, eggs and humans beings was transmissible. However, the humans were considered as dead end host. It was concluded that Salmonella enteritidis and Salmonella typhimurium was maintained in the large intestine of the poultry and has transmitted from poultry feed, poultry meat and poultry eggs to human beings and thus, causing typhoid fever and food poisoning.
RECOMMENDATIONS /SUGGESTIONS
Major aim of this research endeavour was to help in understanding the basic principles involved in the chain of infectious cycle of SalmoneUosis. In addition to that the application of the quality control of poultry products with respect to Salmonella infection to broiler chicks and broiler meat available in the market for human consumption is the ultimate goal of this project. The objective was to reduce the risk of Salmonellosis in poultry and humans. The following measures are suggested.
1. PREVENTION AND CONTROL OF SALMONELLOSIS IN POULTRY! ANIMALS
A. Monitoring
o The poultry and their environment should be monitored by frequente testing of Salmonellae.
o Bacteriological profile of poultry house environment.
o Serological testing of flock and removal of infected birds.
o Culturing of tissues from selected birds.
o Egg sheils, egg albumin & egg yolk culturing.
B. Hygiene and Sanitation
o Eggs from infected layer flocks should be pasteurized before consumption.
o Salmonella positive breeder flocks should be given pellet feed.
o Hatching sanitation
o Proper disinfection of hatching eggs.
o Proper sanitation and disinfection of farm premises.
o The provision of salmonella-free feed i.e pellet feed is of prime importance for the prevention of salmonella infections of poultry flocks and parent flocks.
o Control of rodent, insects and wild birds
C. Managemental
o For routine treatment of eggs and progeny, only those antibiotics should be used that do not cause microbial resistance against drugs widely used in humans
o Resistance of Campylobacter spp, and Salmonella spp. to fluoroquinolones has become a public health risk. This does not exclude well targeted and transient use of antibiotics as essential measures in salmonellosis control programmes.
o Vaccination of breeder flock is recommended for decrease of the salmonella infection pressure.
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1. MEASURES FOR THE PREVENTION AND CONTROL OF SALMONELLOSIS IN HUMANS
A. Meat and Eggs
o Wrap fresh meat in plastic bags at the market to prevent blood from1 dripping on other foods.
o Cook poultry products at temperature of 170°F for breast meat and at 180°F for thigh meat.
o Avoid eating raw or under cooked meat and egg.
o Cook poultry meat and egg thoroughly.
o Purchase only inspected grade AA eggs and animal food products.
o Handle raw eggs carefully:
o Keep eggs refrigerated
o Throw away cracked or dirty eggs.
o Do not eat half fried and half boiled eggs.
o Wash hands immediately after handling raw poultry or raw eggs.
o Full fried and full boiled eggs should be used for eating to prevent food borne Salmonellosis problem.
b. PERSONNEL HYGIENE MEASURES
o Washing of hands with soap and warm water before and after handling foods, after using the bath rooms.
o Refrigerate foods properly.
- Use bleach to wash cutting boards and counters used for preparation immediately after use to avoid cross contamination of other foods.
o People who have Salmonellosis should not prepare food for others.
o Educate the food handlers and persons who prepare food. Educational programmes covering pre- and post harvest food safety procedures, especially salmonella control, should be initiated in the animal and food production sectors for the public awareness.
Availability: Items available for loan: UVAS Library [Call number: 0938,T] (1).
13.
Standardization Of Avian Leukosis Diagnostic Techniques Through Polymerase Chain Reaction (Pcr) And Confirmation With Enzyme Linked Immunosorbant Assay (Elisa)
by Abdul Razzaq (M.Phil) | Prof. Dr. Zafar Iqbal Ch | Mr. Asim Aslam | Prof. Dr.Abdul Rauf Shakoori | Faculty of Veterinary Sciences.
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Publisher: 2006Dissertation note: Avian Leukosis Virus type J infection of chickens is a neoplastic disease affecting chickens. ALV-J is of great economic significance not only because of tumor mortality, but also because of decreased egg production in meat breeding stocks, increased rate of infections, poor response to vaccination and weight suppression in broilers. There is wide spread prevalence of ALV-A and ALV-J in commercial chicken flocks. For control of ALV's eradication programmes based solely on dam testing may be less effective than those where dam testing is combined with procedures to mitigate early horizontal transmission in progeny chicks. For this purpose PCR along with antigen capture ELISA was used in combination for detection of ALV-J proviral DNA, and ALV group specific antigen i.e. p 27 antigen of ALV-J. Polymerase chain reaction technique was standardized by using improved version of H7 primers specific for ALV sub group J targeting env gene encoding gp85 for the detection of avian leucosis virus type J and its confirmation was carried out by comparing it with antigen capture immunosorbant assay which measures group-specific antigen (GSA) i.e. p27 antigen. Feather pulp and serum samples from 50 broiler birds of up to 7 weeks of age were randomly selected from 10 different broiler poultry farms of district Lahore Pakistan. The prevalence of ALV-J was 22 % for antigen capture immunosorbant ELISA and 34 % for polymerase chain reaction (PCR).
Availability: Items available for loan: UVAS Library [Call number: 0943,T] (1).
14.
Standardization Of Tuberculin Test In Buffaloes And Detection Of Mycobacterium Bovis In Blood Through PCR
by Asad Ullah Khan | Prof. Dr. Zafar Iqbal Chaudhary | Dr. Asim Aslam | Prof. Dr. Abdul Rauf Shakoori | Faculty of Veterinary Sciences.
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Publisher: 2007Dissertation note: Tuberculosis is a highly infectious disease. In bovine it is mainly caused by Mycobacterium bovis. Bovine tuberculosis caused by M bovis is the main cause of enteric TB in humans. It is transmitted through milk, meat and dairy products. Bovine TB is still a significant zoonosis in many parts of the world and it accounts for 25.8% of TB in man.
A study was conducted to standardize the tuberculin test in buffaloes and to detect the M bovis in buffalo blood samples through PCR based techniques. A total of 100 buffaloes were tested by Single Comparative Cervical Intradermal Tuberculin Test (SCCIDTT) for this research and 100 blood samples were also collected from the same under aseptic condition. Data was also collected from owners & milkers of buffalo before and after SCCIDTT. A PCR (is a nucleic acid-based technique that enables the rapid and sensitive detection of micro-organism) assay was described which could detect M bovis in blood samples. Blood of 100 buffaloes was randomly analyzed with PCR assay. Over all two (2.0%) out of 100 buffaloes were found positive to tuberculin test while fifty four (54 %) out of 100 blood samples of the same buffaloes were found positive for M bovis in PCR.
The positive cases were analyzed in the background of their history. History revealed that the animals herd was crowded and were reared much closed to each other for a long time. It suggested that they got infection from other animals. It was an evidence of bovine tuberculosis of M bovis in buffaloes.
Availability: Items available for loan: UVAS Library [Call number: 0951,T] (1).
15.
Comparison Of Multiplex Pcr & Conventional Methods For The Diagnosis Of Tuber Culosis (TB) in Human, Buffalo & Cattle in Lahore District
by Naima Mumtaz | Prof. Dr. Zafar Iqbal Chaudhary | Dr. Asim Aslam | Prof. Dr. Abdul Rarf Shakoori | Faculty of Veterinary Sciences.
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Publisher: 2007Dissertation note: Tuberculosis, one of the most widespread infectious diseases, is the leading cause of death due to single infectious agent among humans and animals in the world. It is endemic in Pakistan with about 1.5 million people infected, and Pakistan ranks seventh among the 22 high-burden tuberculosis countries worldwide (WHO, 2006). Mycobacterium tuberculosis is the most common cause of human TB, but an unknown proportion of cases are due to Mycobacterium. bovis.
The study was conducted in Lahore to compare the multiplex PCR and conventional methods for the diagnosis of tuberculosis caused by M tuberculosis and M bovis in 300 humans' sputum and 1000 bovines' milk samples. Conventional methods included Ziehi Neelsen staining, culture and biochemical tests. For M tuberculosis and M bovis the pncA gene and specie -specific 500 bp fragments were targeted respectively. The sensitivity and specificity of multiplex PCR was found statistically significant in comparison to Ziehl Neelsen staining and culture for the differential diagnosis of TB. Pyrazinamide resistance was found in 15 (34.8%) out of 43 isolates recovered from media inoculated by sputum and milk.
Availability: Items available for loan: UVAS Library [Call number: 0954,T] (1).
16.
Comparative Studies On The Sensitivity Of Polymerase Chain Reaction (Pcr) And Conventional Serological Methods For the Diagnosis of Bovine Brucellqsis
by Raheela Akhtar | Prof. Dr. Zafar Iqbal Chaudhary | Prof. Dr. Abdul Rauf Shakoori | Prof. Dr. Asim | Faculty of Veterinary Sciences.
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Publisher: 2007Dissertation note: The polymerase chain reaction was standardized and its efficacy was evaluated against Rose Bengal Plate Test (RBPT) and Milk Ring test (MRT) for the diagnosis of brucellosis in 200 cows and buffaloes from Lahore and Okara districts of Punjab. Under aseptic measures 200 serum and 200 milk samples were tested by RBPT, MRT and PCR on both milk and serum samples in both cows and buffaloes as described in materials and methods. RBPT showed high sensitivity values (27.7% in cows and 45.2% in buffaloes) than serum PCR (25% in cows and 3 9.6% in buffaloes) but on other hands MRT showed low sensitivity (11.1% in cows, 25.4% in buffaloes) and high specificity (98.4% in cows and 93.6% in buffaloes) than milk PCR with sensitivity of 13.8% in cows, 29.4% in buffaloes and specificities of 95.2% in cows and 89.3% in buffaloes respectively. The comparison of PCR assays conducted on both types of samples showed high sensitivity of serum PCR against milk PCR. The comparison of RBPT and MRT in both species showed high sensitivity of RBPT than MRT. But due to low positive predictive value of RBPT and instability in its results in both species it is concluded that there is no significant difference in PCR and serological methods so no single test can be used for the exact diagnosis of bovine brucellosis.
Availability: Items available for loan: UVAS Library [Call number: 0957,T] (1).
17.
Diagnosis Of Bovine Tuber Culosis In Deers Kept In Captivity By Pcr And Tuberculin Test
by Zeeshan Nayyer | Prof. Dr. Zafar Iqbal Chaudhary | Dr. Asim Aslam | Dr. Azhar Maqbool | Faculty of Veterinary Sciences.
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Publisher: 2007Dissertation note: Tuberculosis is an infectious, chronic, granalomatous, highly communicable, zoonotic and debilitating disease. The etiological agents of tuberculosis belong to the bacteria Mycobacterium bovis. A total of 50 blood samples from emaciated deers were collected from deer’s kept in captivity suspected from TB. These samples were subjected to DNA extraction for polymerase chain reaction and tuberculin test for the sensitivity and specificity of these tests.The results obtained were analyzed by standardization of PCR for M. bovis.
PCR is a nucleic acid based technique that enables the rapid and sensitive detection of microorganism. Results indicated that 4% and 20% of deers were positive for M. bovis infection with the tuberculin test and polymerase chain reaction (PCR) respectively. From the results it is evident that polymerase chain reaction (PCR) technique is more sensitive than the tuberculin test for the diagnosis of tuberculosis and gives much higher percentage of positive cases.
Availability: Items available for loan: UVAS Library [Call number: 0970,T] (1).
18.
Differntial Diagnosis Of Malaria And Dengue Fever On The Basis Of Clinical Findings And Laboratory Investigations
by Aqeel Ahmad | Prof. Dr. M. Younus Rana | Dr. Muti ur Rehman | Prof. Dr. Azhar.
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Publisher: 2010Dissertation note: I took two hundred (200) patients in total for purpose of my study. I included all cases with pyrexia of unknown origin with chills and rigors with 6-7 days history. These cases were first evaluated for Malaria by making their thin and thick films for malarial parasites.
There were thirty patients out of two hundred who were positive for malarial parasites. There complete blood picture was done that is RBC count, Heamogolobin percentage, platelet count, WBC count and ESR. The cases who were negative from malaria were further evaluated for dengue viral infection by doing capture ELISA 1gM. Before doing ELISA 1gM dengue strip method test was done and the cases who were positive on strip (Paper Chromatography) were included in 1gM ELISA study. The cases that were positive for 1gM ELISA were studied for same blood investigation which was mentioned earlier. It was also found that there had been some incidence of dual dengue infection and malaria and the incidence rate was 2%.
Now after collecting the data it was analyzed by SPSS. It was inferred afterwards from the data that all the patients +ve for dengue 1gM had been facing with low platelet count increased reticulocyte count, increased hemoglobin, decreased WBC and no significant effect on ESR had been seen. About 83% of dengue 1gM patients were having decrease platelet count. This thrombocytopenia varies from person to person and an inverse relationship has been found between dengue 1gM and platelet of the patients.
The intensity of thromobocytopenia was more in old age patients or in patients with poor health status or in those patients in which tire of anti dengue 1gM was very high. This thromobocytopenia can be used as a diagnostic tool in addition to clinical history in patients who live in periphery where the facility of ELISA is not available. The rise in platelet number indicates recovery of the patients and it should be monitored daily till the complete recovery of patients is achieved.
The rise in hemoglobin concentration has also been noticed due to hemo concentration about 76% of patients with anti dengue 1gM positive were having elevated level of hemoglobin that is ranging from 17-19 gram/dl. The increase in RBC count has also been noticed in association with increased hemoglobin concentration a mild fall in WBC count has also been noticed i-e upto 4000 in 76% of the patients. In those patients who were +ve for malarial parasites and negative for dengue 1gM, such changes in blood pictures were not appreciated although the vector of both diseases is same but AD's mosquitoes which is the carrier of dengue virus (an ARBO virus) causes more severe form of disease.
Availability: Items available for loan: UVAS Library [Call number: 1198,T] (1).
19.
Study Of Hepatic Dysfunction In Patients Infected With Dengue Virus
by Aiysha Ejaz | Prof. Dr. Younus Rana | Dr. Muti ur Rehman | Prof. Dr. Azhar.
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Publisher: 2010Dissertation note: Dengue is the mosquito born viral illness which causes a broad spectrum of disease ranging from in apparent infection, flu like mild undifferentiated fever and classical DF to the most severe form DHF and DSS in which rate of morbidity and mortality is very high. Dengue infection also causes liver damage and this liver impairment is more marked in case of DHF. My study was also aimed at depicting the fact that dengue infection also causes hepatic impairment which is directly related.to the level of dengue 1gM in the body. The serum liver enzyme level rises as the infection progress.
I conducted my study over 200 patients of different age groups including both sexes. All of the patients were having history of pyrexia of unknown origin for the last 7-lO days not subsiding inspite of taking treatment. Some of them presented with mild to moderate petechiae rashes on their body. I categorized the patients into two categorize according to the WHO criteria that is the patients having high grade fever with rash and thrombocytopenia were designated as dengue hemorrhagic fever while those without rash and hemorrhagic manifestations were said to be dengue fever group. Firstly I screened all patients for anti dengue 1gM by rapid strip testing method which shows dark pink line in addition to control line in positive cases within few minutes. The strip +ve cases were further confirmed by using capture ELISA, The Dengue 1gM Capture ELISA (MACELISA) is the immunoenzymatic system recommended by the Pan American Health Organization and the World Health Organization for the serological diagnosis of dengue virus infection due to its high sensitivity, ease of performance, and use of a single acute- phase serum sample. Then all the ELISA +ve cases were estimated for hepatic dysfunction by performing their liver function test. For performing liver function test the serum was obtained by centrifuge machine and enzyme including AST, ALT and Alkaline phosphatase were done by using Merck biochemistry Analyzer which calculated the enzyme itself and displayed the reading in U/L. The analysis established that DF is more common in 21-30 years of age group, more prevalent in males and the level of serum liver enzyme rises as the serum level of dengue 1gM raises that is with the increase of severity of infection.
Availability: Items available for loan: UVAS Library [Call number: 1199,T] (1).
20.
Clinicopathological Changes Induced By Heat Stress, Their Resolution By Minerals And Vitamin C Supplementation In Quails
by Khurshid Anwar | Dr. Asim Aslam | Prof. Dr. Muhammad Younus Rana.
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Publisher: 2011Dissertation note: The present study was designed to overcome heat stress in Japanese quails through potassium chloride, sodium bicarbonate and vitamin C solution in calculated amount in water on thermo tolerance, histopathology and hematology of quails exposed to heat stress: This experimental trial was carried out at Avian Research and Training Centre (ARTC), UVAS Lahore and tests were performed at Department of Pathology UVAS, Lahore. There were three replicates in each treatment group and each replicate was of twenty quails, each group was comprised of 60 birds. The body weight of each the bird was. recorded on weekly basis. Blood samples were collected on the 21, 22, 23, 24, 29, 30 and 31 days of treatment from each group to evaluate the serum potassium and bicarbonate level in the blood. For hematological parameters the blood samples were collected on 22, 28 and 31 day of treatment and the vital organs for histopathology were collected after slaughtering 3 birds from each group. The hematological parameters were studied and the data was analyzed by two ways ANOVA. Group A quails revealed significantly higher weight gain than those of group B, but no significant difference was observed, when all groups were compared. Significantly less weight gain was revealed by the quails of group B, when compared to all other groups. Comparison between groups A, C, D, E, F and G was non significant. The highest FCR was exhibited by the birds of group A while the group B showed the poorest FCR. Better FCR was exhibited by group C, D, E, F and G. Serum samples were obtained from each group, for bicarbonate and potassium determination by spectrophotometric method. Group A, C, E, F and G exhibited a significantly higher serum potassium level than those of groups B and D. A significantly higher bicarbonate level was revealed in the serum of group A, D, E, F and G as compared to group B and C, on day 23 and onwards. But no significant difference was observed in serum of groups A, D, E, F and G. Blood hematology revealed no significant difference in red blood cells of groups A, C, D, E, F and G. Group B exhibited a significant lower values of red blood cells, packed cell volume, basophils, monocytes and showed a significant increase H/L ratio and eosinophils when compared to all other groups. Histopathological studied showed infiltration of heterophils, hyperemia, congestion of liver, heart and adrenal gland. It is concluded that, quails of group B (kept in high environmental temperature) revealed a decreased weight gain, poorest FCR, decreased serum potassium and bicarbonate level, decrease in hematocrit, monocytes and basophils and increased in eosinophils and H/L ratio. Supplementation of electrolytes and vitamin C (125 mg/L KC1, 75 mg/L NaHCO3 and vitamin C 62.5 mg/L) in water effect on heat stressed quails exhibited the better results in term of weight gain, serum electrolytes, blood profile and histology than those quails kept in heat stressed condition with no supplementation. From the present results it is concluded that 125 mg/L of KCI, 75 mg/L of NaHCO3 and 62.5 mg/L of vitamin C solution in water, alone or in combination may be used in quails to combat the effect of high ambient temperature and heat stress.
Availability: Items available for loan: UVAS Library [Call number: 1226,T] (1).
21.
Immuo-Pathological Response Of Pigeons To Challenge Infection Of Newcastle Disease Virus (Ndv)
by Yasir Amin | Dr. Asim Aslam | Prof. Dr. Muhammad Younus Rana.
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Publisher: 2011Dissertation note: This study trial was designed to evaluate and compare the efficacy of two locally available live Newcastle disease vaccines (Medivac ND LaSota and VRI, Mukteshwar ND vaccine), also to compare two routes (Oral and Ocular) of vaccine administration in term of antibody titre and assessment of protection against field (chicken) isolated virulent Newcastle virus challenge (NDV) in pigeons. Study of clinical signs, gross and histopathological lesion in different organ of non-vaccinated and challenged birds was also the part of our present study. For this purpose one hundred and twenty pigeons were purchased from the local market and screened for Newcastle disease antibodies using Hemagglutination inhibition test. Healthy pigeons were randomly divided into six groups i.e. A, B, C, D, E and F, comprising 20 birds each. Group E and F were kept as positive and negative Control respectively. Group A and C were vaccinated with Medivac ND LaSota vaccine at day 7th and 21st of experiment through oral and ocular route. Similarly Group B and D were immunized with VRI (Mukteshwar) ND vaccine through oral and ocular route respectively. At 28th day of experiment all the groups except group F were challenged with velogenic field isolate of NDV at a dose rate of 0.1 ml through ocular route. Serum samples were collected at day 14, 21, 28, 35 and 42 of experiment for the determination of antibody titre. Post-infection clinical signs in control positive group were i.e. anorexia, dullness, depression, decreased feed intake, discharge from mouth, greenish diarrhea, nervous manifestations, leg and wing paralysis. Gross lesions on different organs were hemorrhages in trachea, proventriculus, spleenomegaly and greenish intestinal contents. Medivac ND LaSota vaccine produced higher immune response in term of antibody titre as compared to VRI (Mukteshwar) ND vaccine. It was also observed that ocular route irrespective to vaccine type produced significantly (P<0.05) higher immune response than oral route. Vaccine strains used in this study efficiently induced immune response through ocular route, suggesting that implementation of this vaccination programs in future may prevent ND outbreaks in pigeons, especially in racing pigeons, and may prevent NDV spread to other avian species, mainly poultry.
Availability: Items available for loan: UVAS Library [Call number: 1228,T] (1).
22.
Haematologial And Immunological Effects Of Naturally Occurring Probiotic (Yogurt) And Garlic Supplementation On Broiler Chicks Vaccinated Against Newcastle Disease
by Muhammad Ishaq | Dr. Asim Aslam | Prof. Dr. Muhammad Younus Rana.
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Publisher: 2011Dissertation note: The present project was undertaken to study the various hematological. immunological and gross/histopathological parameters in ND vaccinated chicks with different supplementation of yogurt and garlic. For this purpose one hundred twenty-six day old broiler chicks were divided into three experimental groups A, B and C. each having 42 chicks per group. The group B and C \\ere Further subdivided into 3 groups yl, y2, y3 and gi, g2. g3 respectively comprising of 14 chicks per group having different supplementation of yogurt and garlic respectively, while group A was kept as a control and fed basal diet having no supplementation. Our result showed that yogurt augmented serological response and help in increasing HI antibody titer in which 200 gm yogurt showed immense potential in increasing HI titer until last day of experiment. All levels of Garlic group augmented serological response in term of antibody titer hut remain statistically insigni flcant in increasing HI titer.The heterophil population and I I/L ratio was also improved in both yogurt and garlic groups however 40 grn garlic fed group showed a better response in increasing hctcrophil population. TLC remains insignificant both at treatment and levels throughout the experiment. Body weight gain and FCR was also improved with yogurt and garlic supplementation however 200 gm yogurt showed a curvilinear response over the range of yogurt bd levels. Yogurt and garlic supplementation also showed improvement in the development of immune organ such as spleen, thymus and liver, their I listological examination revealed that an increase in supplementation of yogurt and garlic have no lethal effect upon morphological structure of these organs. In conclusion, yogurt as a probiotic and garlic as a growth promoter agent displayed a greater efficacy in increasing HI titer, heterophils population and improving productive performqnce of broilers in which 200 gm yougurt/kg diet group and 40gm garlic/kg diet showed an immense potential in improving above traits, so their use in broiler diet should be considered instead of using costly commercial probiotics and antibiotics.
Availability: Items available for loan: UVAS Library [Call number: 1229,T] (1).
23.
Detection Of Mycoplasma Synoviae By Pcr And Its Histopatholohical Studies In Poutry Breeder In District Abbottabad
by Sajjad Ahmad | Dr. Muti- ur- Rehman Khan | Prof. Dr. Muhammad Younus Rana.
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Publisher: 2011Dissertation note: Poultry, an important sub-sector of livestock, has emerged a cheaper source of protein for human consumption. Mycoplasmas are the smallest known bacteria, 300-800 nm in diameter and are capable of replicating outside the cell. Mycoplasma synoviae is a member of the class Mollicutes, order Mycoplasmatales, family Mycoplasmataceae. Mycoplasma synoviae (MS) is considered economically to be most important pathogen. Mycoplasma synoviae infections occur in poultry worldwide, affecting poultry and causes diseases like respiratory distress, synovitis and arthritis. Mycoplasma is transmitted from infected to healthy birds both by horizontal and vertical routes. Horizontally disease is transmitted via infected and healthy carrier birds, hatchery, housing, equipments, feeding and during transportation.
To have an insight on pathogenesis and reliable diagnostic techniques, the present project was designed to know comparative sensitivity of rapid agglutination test and polymerase chain reaction for MS diagnosis and to study the gross lesion and histopathological changes in chicken joints produced by MS.
The birds showing clinical signs that included respiratory i.e. tracheal rales, conjunctivitis, coughing, sneezing, ocular and nasal discharge and infectious synovitis were selected for sample collection. Initially the collected sera samples were examined by Rapid Serum Agglutination test. RSA and PCR tests were used in order to confirm the pathogenic agent. RSA and PCR positive samples were further processed for histopathological study in order to identify the lesions in tissues produced by causative organism. In field visits it was observed that the suspected birds were with pale comb, mild to severe lameness, dull, depressed, ruffled feather, conjunctivitis, oculo-nasal discharge, tracheal rales and greenish or sulfur faeces. Birds hock joints, toe joints and paws pad were swelled. The infected birds were occasionally found with generalized infection. The infected birds complicated with other diseases of poultry such as Newcastle and infectious bronchitis causes infection airsacculitis.
Rapid serum agglutination test was conducted at 14 broiler breeder farms. The birds at a farm were showing respiratory and infectious synovitis signs and symptoms, suspected to Mycoplasma synoviae. The tests were performed at the spot. A total of 239 sera samples were examined out of which 63 (26.35%) sera samples were positive for MS. The clinical samples were identified and confirmed as Mycoplasma synoviae infection by PCR. The amplified PCR product was given about 211 bp size while PCR buffer was used as negative control. A total of 213 samples were subjected to PCR and 65 (30.52%) revealed PCR positive results for tracheal swabs, 28.16% (20 samples out 71) showed positive results. For tracheal and lung 33.38 % (24 out of 71) and 29.57% (21 out of 71 samples) were positive, respectively. The PCR test successfully amplified the DNA of MS clinical positive samples. Sixty five out of 213 Mycoplasma synoviae isolates were positive in MS specific PCR while the other 148 samples were negative. The sensitivity and specificity of molecular method Polymerase chain reaction was 100 percent.
For histopathological studies the samples of different organs including trachea, lungs, liver, hock joints (articular cartilage, piece of synovial membrane) and foot pad were further processed. The trachea was examined. There was epithelial degeneration, desquamation. congestion, haemorrhages and inflammatory cell infiltration. The lungs were examined and it was revealed that there was marked congestion, haemorrhages, necrosis and mononuclear cells infiltration. Liver showed infiltration of lymphocytes, plasma cells and macrophages. Articular cartilage showing chondrocytes degenration. Synovial membrane was thickened due to infiltration of lymphocytes and plasma cell. Foot pad showed hyperkaratosis and thickning of epidermis, acanthosis, degeneration of cartilage, infiltration of both mononuclear and plasma cell.
It is concluded from findings of present study that PCR is more appropriate technique than RSA for timely diagnosis of Mycoplasma synoviae. However combination of findings of both techniques may be utilized for accurate detection of Mycoplasma synoviae from broiler breeder in district Abbottabad.
Availability: Items available for loan: UVAS Library [Call number: 1316,T] (1).
24.
Surveillance Of Tuberculosis In Buffaloes, Cattle And Derectton Of Mycobacterium Bovis And Mycobacterium Tuberculosis in Food of Animal Origin
by Muhammad Yasin Tipu | Prof. Dr. Zafar Iqbal Chaudhry | Dr. Muhammad Younus | Prof. Dr.
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Publisher: 2010Dissertation note: The main objectives of this study were: to survey the prevalence of TB infection in livestock and their products in Pakistan; to standardize PCR based techniques for the detection of TB in buffaloes, cattle and animal products (milk and meat) as presently no such system has been developed for the detection of TB in animals and their products in Pakistan; to evaluate improved tests for the differentiation of Mycobacterium complex isolates in cattle, buffaloes and animal food products and to compare modern and conventional methods for rapid diagnosis of the Mycobacterial spp. The study was performed in different experiments to have surveillance of tuberculosis in Buffaloes and Cattle; and to detect the presence of different Mycobacteria in animal food products. One thousand animals from different areas of Lahore District were screened with the tuberculin test. The milk and blood of tuberculin tested animals were further studied for the presence of Mycobacterial spp. by conventional methods as well as Polymerase Chain Reaction (PCR). In other experiments one hundred market milk samples and ten thousand five hundred tissue samples from twenty-one hundred carcasses at Lahore slaughter house were screened with conventional microbiological tests and multiplex PCR for differentiation of Mycobacterium species. The results indicated that PCR had more sensitivity and required less time to detect and differentiate different Mycobacterial species as compared to conventional methods. It was also noted that M. bovis were found in milk and blood of milking animals as well as tissue sample collected from Lahore slaughter house. On the basis of findings, regular monitoring of the milking animals, animals to be slaughtered, and workers handling these animals is suggested. It is also recommended to review the current slaughter act to prevent the slaughtering of TB affected animals.
Availability: Items available for loan: UVAS Library [Call number: 1321,T] (1).
25.
Clinico- Pathological Studies Of Ascites In Broiler Chickens
by Hafiz Muhammad Anwar- ul- Haq | Dr. Asim Aslam | Prof. Dr | Prof. Dr. M. Younus Rana.
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Publisher: 2011Dissertation note: This study was carried out on total of 310 samples. Out of these samples, 200 were the blood samples (100 from the diseased birds and 100 from the apparently healthy birds), second were the tissue samples of liver which were 80 in number (50 from the ascitic birds and 30 from the apparently healthy birds). Then 20 were the water samples (10 from the source of water production and remaining 10 were from the drinking levels of the birds) and 10 feed samples. Samples were collected from randomly selected ten (10) broiler poultry farms in the district Gujranwala having the problem of ascites. The study was completed in four parts. In first part, serum biochemical parameters of liver were studied. The included parameters were total serum proteins, albumins, globulins, A/G ratio and SGPT. In second part of project, mineral profiles of serum concentrations were studied. Then in third part of the study, the collected, feed and water samples were analyzed for their dietary mineral levels. Sodium, potassium and chloride were the minerals, selected for study. Studies of the mineral profiles of feed and water samples were conducted at the Department of Nutrition, U.V.A.S. Lahore. Then the correlation was studied between the dietary mineral levels present in the feed and water, to the mineral levels exhibiting in the serum samples. On the basis of mineral levels present in the feed, water and serum samples, it was concluded that the Na and chloride may contribute to the development of ascities as the results were significant (P>0.05) but the role of K in this regard was not seemed to be significant (P<0.05) thus it may not has any significant contribution in the development of ascites syndrome. In fourth and last part of study, histopathology of the tissue samples was conducted. In this part of study, the tissue samples, collected from liver of ascitic birds and apparently healthy birds were subjected to histopathology and microscopic examination for significant changes. Histopathological studies showed that the hepatic degeneration, hepatic necrosis and fibrosis of the hepatic capsule were the common findings in the diseased group. The study elucidated the marked decrease of serum proteins including the total serum proteins and albumin while it was observed that the ascites syndrome has no significant effect on the enzyme assays of the liver.
Availability: Items available for loan: UVAS Library [Call number: 1326,T] (1).
26.
Histopathological Investigation Of Pleuropneumonia In Buffaloes Caused By Mycoplasma Bovis
by Ayesha Rabail | Dr. Muti-Ur-Rehman Khan | Dr. Kamran | Prof. Dr. M Younus Rana.
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Publisher: 2009-2011Dissertation note: This study was conducted by keeping in view the worldwide importance of Mycoplasma bovis to cause pneumonia and many other diseases, as it causes great economic losses to bovine industry. In the current project the incidence of Mycoplasma bovis to cause pleuropneumonia was studied, and its respective histopathological changes in lungs of the pneumonic adult buffaloes and buffalo calves were examined. 100 lung samples for this purpose (50 lung samples from adult buffaloes and 50 lung samples from buffalo calves) were collected from the Lahore Bakar Mandi Abbatoir. Samples were collected on the basis of following criteria: Red hepatization, grey hepatization, multifocal abscess, necrotic lung tissue. These samples were then divided into two portions, one half placed in 10% buffered formalin in the bottles and other half kept in sterile polythene bag. The portion of lungs for bacteriological study was kept in ice box. Histopathological procedure was performed in the pathology department of University Of Veterinary And Animal Sciences Lahore. The samples were subjected to histopathological procedures and then slides were observed microscopically for the changes. Microscopically pulmonary odema, consolidation, caseous necrosis, abscess infiltration of mononuclear cells, plasma cells, macrophages, neutrophils infiltration were observed. For culturing of Mycoplasma bovis PPLO broth was prepared and samples were inoculated in the broth medium. At 7th day of inoculation the yellow color of the broth medium appeared which was indicative of positive samples. 30% positive samples in adult buffaloes and 36% in buffalo calves were obtained. These samples were then inoculated on the PPLO agar plates for further precision of results. On agar plates typical colonies of the Mycoplasma were observed under bright field compound microscope and 60% positive samples in adult buffaloes and 66% in buffalo calves were obtained. Next step towards the confirmation of Mycoplasma bovis was specific acridine staining, in which positive of Mycoplasma bovis samples gave dull yellow to colorless appearance of yellow broth medium and gave egg fried colony on agar. 78% adult buffalo and 67% buffalo calves showed positive results. These samples were then subjected to final confirmatory test which was growth inhibition disk test, in which hyper immune sera was raised in rabbits and filter paper disks soaked in this sera were used to check the zone of inhibition on cultured agar plates. 70% positive samples in adult buffaloes and 75% in buffalo calves were obtained which confirmed the presence of Mycoplasma bovis. CFU/ml of the positive samples calculated between 105-108. So the incidence of Mycoplasma bovis to cause pneumonia in adult buffaloes and buffalo calves calculated was (10% and 12%) respectively.
Availability: Items available for loan: UVAS Library [Call number: 1335,T] (1).
27.
Effect Of Zinc Supplementation On Cadmium (Cd) Toxicity In Japanese Quail (Coturnix Coturnix Japonica)
by Umair Ishtiaq | Prof. Dr. Muhannad Younus Rana | Dr. Muti - Ur- Rehman Khan | Prof. Dr.
Material type: ; Format:
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Publisher: 2010Dissertation note: Cadmium (Cd) has been recognized as an environmental pollutant especially due to its anthropogenic activity. Exposure to Cd is known to cause harmful effects of different levels of the trophic chain, because of bioaccumulation. Toxic effects of Cd are observed in the kidneys, lungs, testes, prostate, and the erythropoietic system in chicken and rat. These effects are associated with teratogenesis and carcinogenesis. Zinc posseses protective and antagonistic action in the uptake and toxic effects of cadmium, probably because of Zn-induced synthesis of metallothionein that detoxifies Cd by firmly binding this metal. The objectives of present study are:
1) To understand the effect of zinc on cadmium toxicity in Japanese quails
2) To study the effect of zinc and cadmium on liver and kidney function along with histopathological changes.
This experimental trial was carried out at Avian Research and Training Centre (ARTC), UVAS Lahore and tests were performed at Pathology Deptt UVAS Lahore. Day old Japanese quails (C. coturnix japonica) (n = 560) were used in this experiment. For this purpose, a total number of 560, day old chicks of Japanese quail were procured from the hatchery of ART Centre. They were assigned to seven dietary treatments. There were four replicates in each treatment group and each replicate was of twenty chicks.
A =Control diet group will receive only basal diet without any supplementation. B= Basal diet + 50 mg/kg Cd, C = Basal diet + 75 mg/kg Cd, D =Basal diet +100 mg/kg Cd E=Basal diet+50 mg/kg Cd+40 mg/kg Zn, F=Basal diet+75 mg/kg Cd + 40mg/kg Zn and G =. Basal diet+100 mg/kg Cd + 40mg/kg Zn. Each group consisted of 80 birds. The body weight of each the birds was carried out weekly. Blood samples were collected on the 21st (3rd week), 28th (4th week), 35th (5th week) and 42nd (6th week) days of treatment from each group to evaluate the liver and kidney functions and vital organs were collected after slaughtering from each group and then histo-pathological analysis was done. The data was analyzed by two way ANOVA.
Availability: Items available for loan: UVAS Library [Call number: 1339,T] (1).
28.
Isolation, Characterization And Pathogenesis Of Capripox Virus
by Abdul Sajid | Prof. Dr. Zafar Iqbal Chaudhry | Dr. Aftab | Prof. Dr. Azhar Maqbool.
Material type: ; Format:
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; Nature of contents: ; Literary form: Publisher: 2010Dissertation note: Goat pox is the most important pox diseases of livestock and it usually
causes huge economic losses. The economic losses occur in terms of mortality,
reduced productivity and lower quality of wool and leather. The clinical
manifestations of the disease include high temperature, lesions skin in the form of
macules, papules, vesicles, pustule and scabs on hairless areas of the body. The
disease is highly contagious having high morbidity and mortality in the infected
herds. The present study was conducted to document the prevalence of goat pox
disease in the different regions of Punjab. The study was based on clinical
manifestation of the disease in various collecting spots including slaughter houses,
cattle and hide markets and tanneries. The prevalence of goat pox at slaughter
houses in different regions was 9.93% in arid region followed by 8.69% and 7% in
southern and northern irrigated regions respectively. The prevalence of pox disease
in sheep was highest (8.54%) in the northern irrigated region, 7.69% and 6.62% in
arid and southern irrigated regions respectively.
The prevalence of pox recorded in the hide markets shows a trend of high
presence 7.29% in arid region followed by 6.22% and 3.84% in southern and
northern irrigated regions. Whereas in sheep the overall prevalence was 0.51 %,
4.44% and 1.66% in northern irrigated, arid and southern irrigated regions.
In tanneries the pox lesions were identified on the basis of method as
adopted in hide markets. The overall prevalence of pox in goat was 3.96%, 4.06%
and 4.09% while in sheep 9.58%, 2.41 % and 10% in northern irrigated, arid and
southern irrigated regions.
The overall prevalence of pox disease in goat was 5%, 5.79% and 5.34% in
Northern irrigated, arid and southern irrigated regions respectively. Where as in
sheep, pox was 3.133%, 4.11 % and 2.67% in Northern irrigated, arid and southern
irrigated regions respectively. The highest trend of incidence of disease was present
in the arid regions followed by southern and northern regions. The slaughter houses
shows high incidence of disease as compared to cattle and hide market and
tanneries. The result was significant (P<0.05) among the regions and samples
collecting spots.
A total of 100 samples consisting of 55 scabs and 45 skin tissues were
randomly selected from the different collecting spots of the three regions. The scabs
and skin tissue samples were processed on dehydrated minimum essential media
tor virus isolation. The virus was isolated on Vero cell line culture and its
characteristics were observed on the basis of specific cytopathic effects. All 55 scab
samples consisting 20 from cattle markets, 20 from slaughter house and 15 from
hide market and tannery were tested through cell culture. The cell culture positive
result for scabs was 60% cattle markets, 20% hide market and tannery and 40%
slaughter house.
All 45 skin tissue samples including 5 from cattle markets and tannery, 20
from hide market and 20 from slaughter house were subjected to virus isolation on
Vero cell line. The cell culture positive result for skin tissue samples was 100% cattle
markets, 30% hide market and tannery and 60% slaughter house. In this way the
total cell culture result for scabs and skin tissue samples from all areas become
41.82% and 51.11 % respectively.
The isolated virus was confirmed through peR. All the collected samples
were also analyzed through peR in order to compare the two techniques for disease
diagnosis. Out of 40 samples from slaughter houses 18 scabs and 15 tissues
sample were positive through peR with 82.5%. Out of 25 samples collected from
cattle markets consisting of 20 scabs and 5 skin tissues, 17 of scabs and 5 skin
tissues were positive with 92%.
Similarly a total of 35 samples out of which 15 were scabs and 20 were skin
tissues collected from hide markets and tanneries. The peR of 7 scabs and 14 skin
tissues was positive with 60%. In this way the total peR result for scabs and skin
tissue from all areas was 42% and 34% respectively.
In the 3rd study of the present project the isolated virus was inoculated in to
experimental animal to study the detail pathogenesis. The disease followed the
same pattern as in the natural outbreak. But however the routes of inoculation affect
the severity of the disease. During the study the diseased animals were periodically
slaughter at weekly interval after the appearance of 1 st clinical signs. The detailed
lesions were observed in different visceral organs and the tissues were collected
and preserved in 10% formalin. The tissues were processed for histopathology and
immunohistochemical examination. The IHC was successfully optimized for the
detection of viral antigen in the tissues of skin, lung and lymph nodes.
Availability: Items available for loan: UVAS Library [Call number: 1372,T] (1).
29.
Detection Of Soulfonamide Residues With Associated Histopathological Findings In The Tissues Of Cattle An Buffalo
by Mujahid Iqbal | r. Muhammad Yasin Tipu | Dr. Asim Aslam | Prof. Dr. Tahir Yaqub.
Material type: ; Format:
print
Publisher: 2012Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1483,T] (1).
30.
Study On The Pathogenesis Of Clostridium Perferingens (Necrotic Enteritis) In Experimentally Infected
by Arif Mehmood | Dr. Muti-ur-Rehman Khan | Prof. Dr | Prof. Dr. M. Younus Rana.
Material type: ; Format:
print
Publisher: 2011Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1546,T] (1).
31.
Comparative Study Of Lipid Profile In Obese And Diabetic Patients Of Rural And Urban Areas Of Lahore.
by Hamad Ahmed | Dr. Raheela Akhtar | Dr. Qamar-un-Nisa | Prof. Dr.
Material type: ; Format:
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; Literary form:
drama
Publisher: 2013Dissertation note: Diabetes mellitus is dangerous condition predisposing to number of complications and deaths every year. Obesity and diabetes mellitus type-2 are interconnected conditions which share a number of pathophysiological mechanisms which leads to cardiovascular complications. Reliable estimate shows a elevated prevalence of CVD risk in Pakistan. Each fourth middle-aged adult in Pakistan is at risk of CAD. Present study was conducted with hypothesis diabetes and obesity is risk factor for dyslipidosis and coronary artery disease in humans. Patient were included on the basis of body mass index (BMI) Fasting Blood Glucose (FBS) and further confirmation was done on the basis of Glycosylated hemoglobin (HbA1c) According to BMI and diabetes status, study subjects were cassified in four groups: (Group A; obese and diabetic, Group B; non-obese and diabetic, Group C; obese and non-diabetic and Group D; non-obese and non-diabetic) and HbA1c, FBS, Lipid profile and ETT were performed. Analysis of results shows obesity and diabetes was the major cause of dyslipidemia, group A was the worst group dyslipidemia, group C with obesity was the second and group B was the least with dyslipidemia. While obesity and diabetes mellitus was the leading cause of cardiovascular risk 27.5%, 15%, 22.5% and 2.5% in all groups respectively as above.
Availability: Items available for loan: UVAS Library [Call number: 1559,T] (1).
32.
Pathology Of Experimental Enterotoxemia In Sheep And Goats
by Azam Ali Nasir | Prof. Dr. M. Yonus Rana | Dr. Muhammad | Dr. Muti-ur Rehman Khan.
Material type: ; Format:
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; Literary form:
drama
Publisher: 2012Dissertation note: During the present study intestinal scrapings were collected from sheep suspected for enterotoxaemia. Samples were subjected for the isolation by repeated culturing in Reinforced Clostridium medium. Growth on blood agar revealed characteristic colonies of Clostridium perfringens after 18-24 hours. Biochemical and mice inoculation tests were performed. Isolated organism was identified by indirect ELISA. The pure growth was subcultured in RCM in bulk quantity and calculated the dose for experimental infection.
In the second part of the study, sheep and goats were procured, dewormed and kept in the experimental house of UVAS, Lahore. The experimental infection comprised of the whole culture of C. perfringens type D was inoculated intraduodenally via para-mid line between animals of group A and B while in animals of group C and D inoculated only starch solution to achieve the objectives. Accumulative clinical score in sheep was found to be 9 to 16, 13 to 22 and 15 to 23 at 10, 20 and 30 hours PI respectively while in goats the accumulative scores varied from 5 to 15, 9 to 16 and 14 to 21 at above mentioned time intervals. The highest mean score for clinical findings in sheep was anorexia, frothing followed by dehydration while in goats, the highest mean score was recorded for diarrhea dehydration, and anorexia. No significant clinical findings were noted in control groups.
There was a significant increase in blood glucose, urea and serum creatinine in infected group of sheep and mean values reached up to 141 mg/dl, 92 mg/dl and 7.5 mg/dl respectively at 30 hours PI while in goats a similar pattern was observed with the mean values raised to 142 mg/dl, 111 mg/dl and 10.2 mg/dl for blood glucose, urea and serum creatinine respectively. There was no significant change found in RBC and platelet count of both species but there was an early increase in the mean WBC count of sheep 19.7x103/µl at 10 hours but then decreased to 14.7x103/µl at 30 hours PI while in goats it was 23.6x103/µl and then decreased to 15.3x103/µl. The mean PCV % age increased in animals of both infected groups but more in goats and reached to 52% in 30 hours.
During the third part of the present study, the animals were slaughtered and PME performed. The accumulative score for gross lesions were recorded and it was found between 14 to 24 in animals of group A with the highest score for congestion and edema of different organs whereas in goats it was between 12 to 22 with congestion and hemorrhages of intestine having highest scores. The samples were kept in formalin for histopathological examination and accumulative lesions score was noted in different organs. The highest mean score in sheep was recorded in kidneys and lungs and in goat intestine, lung and kidneys were the major organs affected.
A polymerase chain reaction was optimized under our own laboratory condition for the detection of alpha and epsilon toxins of Clostridium perfringens type D from different tissues. Alpha gene was amplified at annealing temperature 52.2oC with amplicon size 247bp and ETX gene at the annealing temperature.
50.2oC with amplicon size 665bp.
The erythrocytes of different species were used to know the sensitivity against culture supernatants of C. perfringens type D. It was observed maximum hemolysis occurred in human erythrocytes (68%) followed by mice (57%) at 37oC. It was also recorded that a significant increase was found at 37oC as compared to25oC except for dog and rabbits where no significant difference was observed.
Availability: Items available for loan: UVAS Library [Call number: 1596,T] (1).
33.
Clinicopathological Study Of Theileriosis In Naturally Infected Sheep
by Muhammad Waseem Akhter | Dr. Asim Aslam | Dr. Muti ur Rehman Khan | Prof. Dr. Habib.
Material type: ; Format:
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; Literary form:
drama
Publisher: 2013Dissertation note: Theleiriosis in sheep is an important infectious disease of small ruminants characterized by General weakness, weight loss, anorexia, elevated body temperature, petechial hemorrhages on conjunctival mucosa, swollen lymph nodes, anemia and cough. Changes in hematological, serum biochemical and histopathological parameters are good indicators for diagnosis of theileriosis. For this purpose a total of 100 blood samples from infected sheep as well as 50 blood samples from healthy sheep were collected on the basis of clinical examination and peripheral blood smears from different farms in and around Lahore. The collected samples were processed at Clinical Pathology Laboratory, Department of Pathology, University of Veterinary & Animal Sciences, Lahore. Hematological parameters were measured by automatic hematology analyzer & serum biochemical parameters were measured by using commercial kits by colorimetric methods using spectrophotometer. Histopathological changes were observed by making slides of tissue samples, and observed under microscope. Molecular confirmation of Theleria sp. was done by using Polymerase Chain Reaction. Finally the data obtained for hematological and serum biochemical parameters were analyzed by using Student's t test.
Previous studies on serum biochemical parameters and hematological parameters were mostly done in large ruminants. But there is little investigation available on the biochemical and hematological alterations of theileriosis in small ruminants. In this study blood samples taken from sheep were examined under microscope by making thin blood smears using Giemsa stain. Theileria piroplasms were seen in RBCs at 100x. Blood samples were also processed for PCR test. In all Theileria ovis positive samples 520-bp fragment was generated on gel by using primers TSsr 170F and TSsr 670R for sheep. All samples positive on microscopy were also positive by PCR. This study provides the base line data for molecular diagnosis of Theileria ovis in sheep in Pakistan. Hematological and biochemical parameters were evaluated in the sheep naturally infected with theileriosis while healthy sheep were selected as control. Hematological findings revealed a significant decrease (P<0.05) in RBC count, WBC count, Hb Conc. and PCV in infected animals as compared with healthy animals. Serum biochemical findings also revealed alterations in activities of enzymes and plasma proteins. A significant decrease in total proteins, albumin, glucose and creatinin and triglycerides was observed while significant increase (P<0.05) in ALT, AST, bilirubin was observed in affected animals as compared with healthy animals. A non significant increase in urea and cholesterol concentration was also observed in infected animals as compared to healthy animals. Different tissues were examined to study gross and histopathological changes. Liver was large, pale and friable. Prescapular lymph nodes were swollen and spleenomegaly was also seen. Kidney showed hemorrhagic spots and some were mottled. Histological examination of the lymph nodes revealed edema, widened intercellular spaces, parenchyma degeneration, massive lympholysis, widened sinuses at some areas and macrophages. Splenic nodules were sparse, diminished in size and lymphocyte depletion in follicles was prominent.In liver, mild infiltration of leukocytes around blood vessels, vacuolation in hepatocytes, increase in sinusoidal space and atrophy of hepatic cord was seen and hepatic cord was broken. In kidney, degeneration of tubular epithelium cells was seen. This study concluded that theileriosis in sheep was associated with some alterations in blood parameters and histopathological changes which could be useful in the diagnosis of ovine theileriosis.
Availability: Items available for loan: UVAS Library [Call number: 1642,T] (1).
34.
Prevalence, Identification And Pathogenesis Of Clostridium Chauvoei In Cattle And Buffaloes In Punjab
by Muhammad Asif Idress | Prof. Dr. Zafar Iqbal Chaudhary | Prof. Dr. Muhammad Younus.
Material type: ; Format:
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; Literary form:
drama
Publisher: 2012Dissertation note: In the first phase of the project, the sampling of diseased animals presumably affected by Black quarter was carried out from six districts of Punjab belonging to three different zones. Around two hundred and fifty samples from each zone were collected and were subjected to bacterial culturing and isolation procedures followed by biochemical identification mechanism. The prevalence of Black quarter in Cattle and buffaloes were thus calculated for each district and zone. Highest prevalence of BQ in Zone II was observed (27.2%) for cattle while in case of Buffaloes highest prevalence (3.2%) was noted in Zone I. similarly higher Prevalence of BQ was noted in 1st quarter of year for Zone I followed by zone II and III while 2nd quarter of season was showing higher prevalence of BQ in zone II and III.
During 2nd phase of experiment tissue samples were inoculated in RCM and blood agar for the re-isolation of C. chauvoei, identified on the basis of colony characteristics and later on subjected to biochemical tests for the confirmation of the isolated organism. Then it was further confirmed through Polymerase chain Reaction for the identification of the causative agent i.e. C. Chauvoei on the basis of 16S rRNA gene sequence. Another set of primers corresponding to alpha toxin gene sequence of C. chauvoeui was also used which strengthened the belief that this strain of C. chauvoei possessed alpha toxin producing ability.
During third phase of project blood samples collected were subjected to hematological estimation for buffaloes and cattle having confirmed as BQ This study revealed significant effect on RBC's count and white blood cells count (P<0.05), while Differential leukocyte count were also showing significant different as compared to Non-infected (P< 0.05). Serum samples were tested for the change in levels of different enzymes. It was found that blood-glucose level and ALT levels were not significantly higher (P>0.05) when compared with control values, Values of AST, CPK and LDH were found significantly higher (P< 0.05) in all infected animals.
Histopathology of affected muscle tissues of both cattle and buffaloes was done to study microscopic changes in the muscle fibers and surrounding tissues. Lesions were somehow disappointing as compared to the magnitude of gross lesions. There were segmental degeneration, Zenker necrosis, discrete edema, occasional neutrophils and emphysema in affected muscle.
Finally, alpha toxin (hemolysin) in culture supernatant of RCM broth was titrated against 2% washed RBC's of cattle, buffalo, sheep, goat, chicken, rabbit and mice to study the hemolytic activity of the toxin. It was found that highest percentage of hemolysis was observed in mice followed by cattle, sheep, buffalo, chicken and rabbit respectively at 25°C. Higher the dilution of toxin, lower the extent of hemolysis. At 37°C variable results were obtained. It showed the biological activity of alpha toxin is also temperature dependant.
Availability: Items available for loan: UVAS Library [Call number: 1664,T] (1).
35.
Immunohistochemical Detection Of Infectious Bronchitis Virus In Different Organs Of Experimentally Infected
by Mudassar Iqbal | Dr. Asim Aslam | Dr. Ishtiaq ahmed | Prof. Dr. Tahir.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2013Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1671,T] (1).
36.
Immuno Pathological Effects Of Neem (Azadirachta Indica) In Commercial Broiler Chickens
by Zahid Jawad | Prof. Dr. Muhammad Younus | Dr. Muti-ur-Rehman | Prof. Dr. Azhar.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2012Dissertation note: These experiments were conducted to study the effects of Azadirachta indica admixed in poultry feed on weight gain performance, haemtological values,immune modulations, and toxic effects in broiler chickens. A total number of 144 commercial broiler 1-day old chicks were reared in the experimental sheds of the Department of Pathology, University of Veterinary & Animal Sciences, Lahore, The birds were fed with balanced commercial feed and water ad libitum. The birds were divided into 3 groups; A, B and C having fourty eight chicks each. Birds of all groups were sub divided into four groups of each i.e. A1, A2, A3 and A4; B1, B2, B3 & B4 and C1, C2, C3 and C4, respectively. Each of the sub groups containd 12 birds. Sub groups A4, B4 and C4 were control group with no medication. The birds of groups A, B and C were fed with poultry feed containing dry powder of neem leaves @ 2 gm, 4 gm and 6gm per kg of feed respectively. The birds of groups A1, B1 and C1 were treated with the herb from day 0 to 42 of their life. The birds of groups A2, B2 and C2 were given the neem from day 14 to 42 of their life, whereas the birds of groups A3, B3 and C3 were treated with the herb from day 28 to 42 of their life. Difference between weekly weight gain in the birds of groups A1, B1 and C1 was non significant (P>0.05) however the difference between weight gain in the treated and control groups was significant (P<0.05). The birds treated with the herb from day 0 of their life showed more weight gain. There was no difference in the haematological indices between all of the treated groups and the control groups. The neem treated birds showed increased antibody titers against ND and IBD viruses as compared to control groups. The values of ALP and ASTshowed decreasing trend when the level of neem leaf meal was increased in the ration. Serum creatinine and serum uric acid values posed a slight declining trend in the neem fed birds. There was a decrease in serum cholesterol level in the neem treated bird groups, the higher the concentreation of the herb, the lower the cholesterol value. The organ body weight indices showed that there was no significant difference in liver, spleen and thymus weights among treated groups as well between treated and control groups. There was absence of prominent gross pathological lesions in liver, spleen, kidneys and thymus, however some treated groups showed mild hypertrophied liver and kidneys as did the organs of the birds in control groups. No histopathological changes except a few mild changes were observed in liver, spleen, kidneys and thymus in the birds of experimental groups.
Availability: Items available for loan: UVAS Library [Call number: 1774,T] (1).
37.
Tissue Tropism Of Velogenic-Viscerotropic Newcastle Disease Virus In Broiler Chickens
by Tasra Bibi | Prof. Dr. Asim Aslam | Dr. Raheela Akhtar | Prof. Dr. Tahir.
Material type: ; Format:
print
; Literary form:
drama
Publisher: 2014Dissertation note: ND is an infectious, highly contagious and widespread disease of avian species and has a considerable economic impact on poultry industry. This study is a preliminary work to understand the mode of action of the recent VVNDV isolate of the UVAS, towards the tissue tropisms of both lymphatic and non lymphatic organs. One hundred chicks purchased from the local hatchery and reared for the trial including control, however, the VVNDV strain was received from the QOL, UVAS, Lahore, Pakistan. Three trials were conducted using the challenge dose 100,000 ELD50 (Group C) and 10,000 ELD 50 as (Group B) and 1000 ELD 50 as (Group A). Five chickens were selected randomly from each group and slaughtered on daily basis, including two chicks from control. These samples were used for histopathology and immunohistochemistry (IHC) test. Conclusively, the study indicates that NDV induces early necrosis in the lymphoid tissues of infected chickens which is correlated with the severity of the disease caused by each dilution. Necrosis does not seem only to be the direct viral replication and indirect effects may lead to death of the animals, due to depletion of lymphoid organs. However, the peak hours were recorded 72 hours to 96 hours post infection in all lymphoid and non lymphoid organs irrespective of the dilution factor of the VVNDV. Immunohistochemistry is not a routine practice in diagnostic test, however, this study may lead to a roadmap in understanding the interpretation of the clinical/pathological picture and the tropism may be helpful in future to study some other aspects like failure of commercial vaccines and to control the outbreaks of NDV in the country an endemic as well as a devastating disease of the poultry industry.
Availability: Items available for loan: UVAS Library [Call number: 1824,T] (1).
38.
Study Of Carrier Potential Of Newcastledisease Virus In Common Wild Bird Species
by Tahir Munir | Prof. Dr. Asim Aslam | Dr. Muhammad | Dr.Ishtiaq Ahmed.
Material type: ; Format:
print
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1892,T] (1).
39.
Optimization Of Multiplex Pcr For The Simultaneous Detection Of Babesia Caballi Theileria Equi And Trypanosoma
by Muhammad Zeeshan Khalid | Prof. Dr. Asim aslam | Dr. Yasin tipu | Prof. Dr.Habib ur rehman.
Material type: ; Format:
print
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2006,T] (1).
40.
Comparison Of Ameliorative Potential Of Sacccharomyces Cerevisiae And Bentonite Clay On Pathological Effects Induced By Aflatoxin in Broilers
by Muhammad Saqlain | Dr. Ishtiaq ahmad | Dr. Gulbeena saleem | Prof. dr. Aftab.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2014,T] (1).
41.
A Study On Immunomodulatory Effect Of Nigella Sativa And Allium Sativum Against Escherichia Coli Infection In Broiler Birds
by Fiza Ahmad | Dr Muhammad yasin tipu | Dr. Muti-ur- rehman khan | Prof. Dr.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2022,T] (1).
42.
Esponse Of Lymphatic Tissues To Dietary Supplementation Of Nigella Sativa And Curcuma Longa In Broilers Challenged With Pasteurella Multocida (strain A)
by Muhammad Akmal raheem | DR. Muhammad Yasin tipu | Dr. Muti ur rehman khan | Prof. Dr.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2050,T] (1).
43.
Pathological Studies On Contagious Edthyma In Naturally Infected Small Ruminants
by Muhammad Usman ghani | Dr. Mati ur rehman khan | Dr. Muhammad | Prof. Dr. Asim aslam.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2070,T] (1).
44.
Comparisons Of Histopathological Effects Of Live Vector Immune Complax And Intermediate Plus Vaccines Of Infectiors Bursal Disease on the Bursa of Fabricius of Commercial Broiler
by Rana Waqas Arshad | Prof. Dr. Asim Aslam | Dr, Muhammad Saeed Imran.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2086,T] (1).
45.
Haematological And Serum Biochemical Responses Of Nili- Ravi Buffalo Fed On Aflatoxin B1 Contaminated Feed With And Without Toxin Binders
by Muqaddas Sardar | Dr. Raheela Akhtar | Dr. Ishtiaq Ahmad | Prof. Dr. Tahir.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2108,T] (1).
46.
Study Of Carrier Potential Of Salmonella Infections In Common Wild Birds Species
by Mutahir Ali Mir | Prof. Dr. Asim Aslam | Dr. Ishtiaq Ahmad | Dr. Muhammad.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2148,T] (1).
47.
Molecular Characterization Of Brucella Abortus Strains In Bovines
by Muhammad Ramzan | Dr. Raheela Akhtar | Prof. Dr. Aneela | Prof. Dr. Asim Aslam.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2169,T] (1).
48.
Pathological Investigations Of Theileriosis (T.Annulata) In Cattle In Disteict Lahore Punjab
by Syed Sadeed ud din Shah | Dr. Muti-ur- Rehman Khan | Dr. Raheela Akhtar | Prof. Dr. Aneela Zameer Durrani.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Theileriosis is very important protozoal disease in crossbred cattle. According to an
assessment, about 250 million cattle are endangered by this disease and millions of high milk
yielding cattle are at risk of exposure to disease. It acts as a bigger restraint on livestock
improvement and production in many developing countries (Nagore et al. 2004). Theileria
annulata is the main specie that causes high morbidity and mortality. It causes heavy economic
and production losses in cattle in tropical and sub-tropical regions. The recorded mortality rates
in cattle reached to 70% (Moor house et al. 2001).
Theileria species are intracellular obligate hemoprotozoan parasites. All Theileria species
are dangerous and cause disease but two of them are important for livestock. Theileria parva and
T. annulata produces diseases named as East Coast fever and tropical theileriosis in cattle
respectively. Genus Theileria has many other species like T. buffeli, T. taurotragi, T. velifera, T.
sergenti and T. mutans. These species cause infections in wild and domesticated ruminants.
Theileria species present in large and small animals show signs like fever, anorexia,
swelling of the superficial lymph nodes, dyspnoea, lethargy, progressive anemia, constipation,
diarrhea, lacrimation and nervous symptoms (Saeed et al. 2010; Irvin and Mawmachi 1983). A
pronounced rise in body temperature, reaching 40-41.5 °C is pursued by lacrimation, depression,
swelling of the superficial lymph node and nasal discharge. The characteristic sign of tropical
theileriosis is anemia and finally haemoglobinuria occur with heavy weight losses. The clinical
course of the disease alter from per acute to acute or sub-acute to chronic (Oliveira- Sequeira et
al. 2005). The disease is lymphoproliferative in its early phases resulting enlargement of lymph
nodes, later on enters lymph destructive phase which is associated with a pronounced
Introduction
2
leukopenia. In the piroplasms phase in erythrocytes, the parasite becomes infective for the tick
(El-Deeb and Younis 2009).
Trans placental Bovine Tropical Theileriosis causing a deadly disease in a 3 day old
neonate cross bred calf and cerebral form of the disease (turning sickness) in a cow were
incriminated to T.annulata infection. It mainly depends upon the harmful effects of the T.
annulata on lymphoid tissues and susceptibility of the host (Sudan et al. 2012).
Theileriosis is prevalent in various regions of the world including Pakistan. It is transmitted by
Hyalomma species ticks. These ticks spread T. annulata which causes tropical theileriosis
(Durrani et al. 2009). The developmental stages of Theileria inside the Hyalomma ticks varies in
different shapes and forms (Hamed et al. 2011). Therefore to increase the milk and meat
production of cattle we can prevent the spread of the disease by controlling ticks
(Hekmatimoghaddam et al. 2012). The sufficient amount of Hyalomma ticks are found in warm,
commonly hard marshland and in central and Southern Europe, south west Asia and Southern
Africa having very long dry season. A toxin is produced in the adult ticks. This toxin produce
clinical signs of mucus membrane hyperemic and moist profuse eczema (Adam et al. 2000).
The sporozoites of Theileria enter into cattle host during tick feeding and they
immediately infect mononuclear leukocytes, these sporozoites develop into macroschizonts and
induce proliferation of the host cells. Macroschizonts constantly mature into microschizonts and
finally into merozoites, which are discharged from leukocytes. These merozoites attack
erythrocytes and mature into piroplasms, become available to ticks. Infective sporozoites,
injected during tick feeding, rapidly enter target cells, escape from the surrounding host-cell
membrane and differentiate to schizonts that interact with different host-cell components
(Dobbelaereand Rottenberg 2003). This interaction includes host cell signaling pathways that
Introduction
3
regulate proliferation and cell survival (Chaussepied and Langsley 2011) and thus cause
blastogenesis and clonal expansion of predominantly T and B cells (Fawcett et al. 1982; Baldwin
et al. 1988; Spooner et al. 1989). Merozoites released from these schizonts subsequently infect
red blood cells and become trophozoites. Lymphocytic stage of Theileria (schizonts) is the cause
of many of the severe disease manifestations like lymphadenopathy, pyrexia, thrombocytopenia,
and panleukopenia (Homer et al. 2000). Marked anemia, anisocytosis, pikilocytosis, and
leucopenia were commonly observed in bovine theileriosis (Ceci et al. 1997). Cattle may survive
the disease, but recovery and convalescence may be protracted and incomplete, this leads to
permanent debilitation, loss of productivity and prolonged carrier state. (Shahnawaz et al. 2011).
Cattle with subclinical infection in endemic regions become carrier of piroplasms and act as a
source of infection for the vectors (Brown 1997; Brown 1990; Uilenberg 1995).
The diagnosis of theileriosis in acute cases is majorly done on clinical signs and Giemsa
stained blood smears of cattle but the detection of agent is not reliable and is almost impossible
in carrier stage. Advances in molecular biological techniques have resulted in the improved
detection, identification, and genetic characterization of many hemoparasites. Species specific
polymerase chain reaction (PCR) has been developed for the detection and identification of
various Theileria species and has been shown to have higher sensitivity and specificity compared
with serological assays and examination of Giemsa-stained blood smears (Bhoora et al. 2009).
Primers were derived from the gene encoding the 30-kDa major merozoite surface antigen for T.
annulata (Aktas et al. 2006).
Most of the previous studies on haematological parameters in T. annulata infection were
carried out on experimentally infected cattle (Sandhu et al. 1998; Singh et al. 2001). The present
investigation was conducted to study haematological parameters in cattle naturally infected with
Introduction
4
T. annulata. Hematology has been broadly used in attempts to give information about disease
condition, performance problems and health in cattle (Rezaei and Naghadeh. 2006).
Hematological and sero-biochemical alterations are the indicators of severity of disease and are
considered to be good tools for the diagnosis, prognosis for effective therapy (Col and Uslu
2007; Nazifi et al. 2010b).
Lahore is one of the larger district in the Punjab province of Pakistan. Different cattle
breeds are reared by the people of the area for meat and milk production. The exact current
situation about the prevalence and pathogenesis of Theileriosis in the selected area is unknown.
The present study was conducted to screen cattle by finding schizonts or piroplasms in Giemsa
stained thin blood smears at slaughter house of district Lahore (Aktas et al. 2006) and later to
confirm through Polymerase Chain Reaction (PCR) (Chaisi et al. 2013) in order to implement
efforts and regulation to eradicate the spread of disease in the selected area. Data generated from
this study provided the latest status of Theileriosis, sex wise prevalence and its pathogenesis in
cattle population of Lahore. The study has also provided the necessary information to formulate
strategies for control of disease in the area. An investigation was also undertaken to ascertain the
changes in haematology as a result of Theileria annulata infection. These studies will help better
understanding of the pathogenesis and supportive therapy of this disease. Availability: Items available for loan: UVAS Library [Call number: 2186,T] (1).
49.
Detection Of Influenza A Virus Contamination In Newcastle Disease Live Virus Vaccines And Their Pathological Effects On Visceral Organs
by Munir Hussain (2004-VA-64) | Mr. Muhammad Saeed Imran | Prof. Dr. Asim Aslam | Dr. Shafqat Fatima Rehmani.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: Poultry is one of the most vibrant commercial sector which is playing a vital role to
bridge the gap between supply and demand of animal protein foods to cater for its ever
increasing human population 2.1 per cent annually in Pakistan (Sahota et al. 2003).
Vaccination is one of the most effective way to prevent the poultry birds from the
specific diseases. Disease producing microorganisms can be classified smallest to largest as
viruses, bacteria, fungi, protozoa and parasites. All, except the viruses are sensitive to drugs
when outbreaks occur. Vaccination is basically the introduction of a specific biological substance
(antigen) into the bird to stimulate the antibodies formation or immunity to a particular disease.
Usually the biological substance is avirulent the live disease organisms, which are capable to
protect the bird against the particular disease by producing an immune response. Presence of
these organisms (antigen) in the blood stimulates the body's defense mechanism to produce
antibodies that neutralize the disease causing organisms when the bird is exposed to them
(Kamboh et al. 2009).
A danger of such type of live vaccines is that the live microbes can back mutate to a
virulent form. While, dead vaccines that contain whole killed (usually by formalin or phenol)
microbes are safe. They may contain little or no extraneous material and therefore tend to
produce fewer adverse effects (Palombo and Semple 2001). The vaccines that contain dead
organisms are safe with respect to residual virulence and are easy to store, since organisms are
already dead. While live vaccines may possess residual virulence for the animal by reversion of
avirulent organisms to fully virulent type or spread to nonvaccinated animals. Dead vaccines
have very little risk of ‘alive’ contamination, while live vaccines always run the risk of
contamination with unwanted organisms; for instance, outbreaks of reticuloendotheliosis in
Introduction
______________________________________________________________________________
2
chickens in Japan and Australia have been traced to contaminated Marek’s disease vaccine
(Tizard 1995).
Avian Influenza viruses typically produce Syndromes ranging from asymptomatic
infection to respiratory disease and drops in egg production to severe, systemic disease with near
100% mortality (Olsen et al. 2002). Avian influenza initially was recognized as a highly lethal,
systemic disease (i.e., highly pathogenic). HPAI was known by various name including fowl
plague, fowl pest etc. Avian Influenza viruses are classified in the family orthomyxoviridae,
genus influenza virus A (Garten et al. 2009). Avian influenza viruses can be categorized into
four clinical groups:1) highly virulent, 2) moderately virulent, 3) mildly virulent, and 4)
Avirulent (Swayne and Suarez 2000). Avian Influenza further sub type based on serologic
reaction of HA and NA surface glycoproteins. Fifteen sub types of HA and nine sub types of
NA are recognized (Swayne and Suarez 2000). MP AI viruses in domestic poultry produce
clinical sign reflect abnormalities in the respiratory, digestive, urinary and reproductive organs
(Allwright et al. 1993). To date, naturally occurring highly virulent influenza A viruses that
produce acute clinical disease in chickens, turkeys and other birds of economic importance have
been associated only with the H5, H7 and H9 subtypes. Influenza A viruses of subtype H9 are
now considered to be wide spread in poultry and have demonstrated the ability to infect humans
(Fedorko et al. 2006).
To date, all outbreaks of the highly pathogenic form have been caused by influenza A viruses
of the subtypes H5 and H7. The disease is transmitted horizontally by direct contact through
contamination. There is little or no evidence of vertical transmission (egg-borne infection).
However, eggshell surfaces can be contaminated with the virus (Potima 2007). Wild and
domesticated water fowl is the major natural reservoir of influenza A viruses. Representatives of
Introduction
______________________________________________________________________________
3
all of the different subtypes of avian influenza A virus have been isolated from birds, particularly
from aquatic species such as ducks, geese, and gulls (Karasin et al. 2000). Wild birds such as
geese, ducks and game birds; they can be carriers of even highly pathogenic strain H5N1
shedding the virus in their feces without clinical signs of disease.
Thus, the present study was carried out to examine the viral contamination (Influenza A
virus) in poultry vaccines manufactured locally and imported from different countries of the
world in Pakistan. The findings of the study have helped us to see the Avian Influenza A virus
contamination in vaccines which are used in field conditions and also help to evaluate the purity
of vaccines. The RT-PCR based technology has been described for the detection of different
RNA viruses such as Newcastle disease virus etc. (Payne et al. 1981) revealed contamination of
vaccines with ALVs, specifically in two Marek´s vaccines, which confirms that these agents are
potential contaminants of viral vaccines applied in poultry. This assay has meant a considerable
advance due to a higher sensitivity and specificity upon differentiating the subgroups compared
with ELISA. It is quicker test for detection of RNA viruses than the viral isolation, which
requires until 10 days and it needs detection by ELISA for the identification result. Availability: Items available for loan: UVAS Library [Call number: 2212,T] (1).
50.
Toxicopathological Alterations And Tissue Residue Of Colistinsulphate (Polymixin E) In Broilers
by Muhammad Aslam (2012-VA-809) | Dr. Muhammad Raza Hameed | Prof. Dr. Muhammad Younus | Dr. Syed Ehtisham ul Haque.
Material type: ; Literary form:
not fiction
Publisher: 2014Dissertation note: Poultry industry is the 2nd largest industry in Pakistan playing important role to meet daily protein requirement with an investment of more than 200 billion rupees. It is contributing 6.1% and 10.8% share in total contribution of agriculture and livestock the national GDP, respectively. Total poultry meat production in the last year was 987 thousand tones (Economic survey of Pakistan 2013-2014). Because of high density and lack of biosecurity measures, outbreaks of infectious disease are more common and often occurs. Different antibiotics are used rational and irrational to treat and control these outbreaks. Colistin is among the most widely used antibiotic in intensive poultry farming, it is used to combat gram negative bacterial infections particularly for collibacillosis and gastrointestinal tract infections (Hussain and Khalil 2013).
Colistin belongs to the polymixins group of antibiotics. It is also known as Polymixin E. Polymixins are structurally related substances consisting of a cyclic peptide with a hydrophobic tail, mainly produced from gram positive nitrogen fixing bacteria Bacillus polymyxa. Polymixins are classified into six subtypes namely polymixin A to F and among these polymixin B and E are commonly used for the treatment of gram negative infections in animal and human beings. Colistin is mixture of two subtype’s colistin A (polymixin E1) and colistin B (polymixin E2). Commercially, it is available in two forms colistin sulfate and colistimethate sodium but colistin sulfate is more stable cationic water soluble salt (Landman et al. 2000) and is easily available in markets.
colistin sulphate has lipophilic and lipophobic(hydrophilic) properties, that makes it easier to interact on bacterial cell membrane by displacing counter ions in lipopolysaccharides, influencing Mg efflux that’s why it is effective against gram negative bacteria (Poole and Sheffield 2013). Polymixins also presents antipyretic activity by binding endotoxins, especially lipid A, (the active compound of lipopolysaccharide). Owing to this property it is extensively used to treat gram negative infections in livestock and poultry industries (Hanasawa et al. 1990).
The use of colistin was restricted in the past due to its toxic properties mainly in nephrotoxicity. There are reports available in the literature indicating that the parental use of colistin leads to the alterations of biochemical parameters in chicken i.e. increase in glutamic oxaloacetic transaminase, catalase activity, creatinine while, adversely affect total plasma proteins (Ibrahin et al. 2011). In ostriches it leads to the development of neurotoxic signs along with histologically odema formation in pericardium, intestinal serosa and heart was observed (Landman et al. 2000).
Toxic effects of colistin were also reported in humans including nephrotoxicity, increased serum creatinine during the treatment (Falagas et al. 2005). As bioavailability for oral route is minimal and it is used parentally to treat systemic infections. Parenteral route may cause toxopathological effects in birds. Other effects includes change in aspartate aminotransferase and alanine aminotransferase which indicate liver damage. Red blood cells, white blood cells, packed cell volume and hemoglobin estimation were also decreased (Saleemi et al. 2013). The incidence of nephrotoxicity is severe but less common in oral administration as polymixins absorption through gastrointestinal tract is very slow and limited, and cannot be detected in plasma concentrations at ordinary doses (Falagas and Kasiakou 2006). Instead of all these toxic effects, now a days it is frequently used for the treatment against gram negative bacterial infections (Vaara 2010).
The emergence of bacterial resistance has become an important public health hazard throughout the world). Due to irrational use of antimicrobial drugs against different diseases (Naqvi et al.2013. Colistin is one of the most widely used antibiotic in poultry industry against diseases like collibacillosis, salmonellosis and clostridial infections through drinking water, feed additives and parenteral route in developing countries like Pakistan (Tanweer et al.2013). Parenteral use of colistin sulphate may leads to the deposition of residues in different tissues. The presence of its residues in edible parts may lead to the toxicity as well as development of antibacterial resistance in human.
Keeping in view the potential toxic effects and other hazards relating to the extensive use of colistin in poultry birds, present study has been designed to investigate dose dependent patho-morphological alterations and tissue residue in broiler chickens.
Objective
1. To study the toxicopathological effects of parenteral administration of colistin in broilers.
2.Investigation of the tissue deposition of colistin as residues and its withdrawal period.
Availability: Items available for loan: UVAS Library [Call number: 2221-T] (1).
