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1. Diagnosis Of Dengue Virus Serotypes In Effected Patients By Elisa In Lahore Pakistan

by Muhammad Khurram Shahzad | Dr. Muhammad Younus Rana | Dr. Muti-ur-Rehman Khan | Faculty of Veterinary Sciences.

Material type: book Book; Format: print ; Literary form: not fiction Publisher: 2010Dissertation note: Dengue haemorrhagic fever (DHF) is an acute febrile disease caused by any of the four serotypes of dengue virus (DENV I , DENV 2, DENV 3 and DENV 4), belonging to flaviviruses. It is a public health problem of growing importance in areas where the insect vector, Aedes aegypti mosquitoes are present. A total of I 50 clinically suspected dengue patients were recruited, mean age of the patients was 31 .86+1 .66. The maximum age of the patients was 81 years and minimum age of the patient was 5 years. Out of I 50 patients 24.0% (n=36) were tested negative for any of the four serotype of the Dengue virus. The analysis showed that 45.3% (n=68) patients had DENV2 serotype, 16.7% (n=25) had DENV 3 serotype and 14.0% (n=21) patients were diagnosed to have DENV 4 serotype; none of the 150 patients was reported to have DENV I serotype. The most prevalent serotype was Dengue virus serotype 2 and Dengue virus serotype 4 was observed as lowest, while Dengue virus serotype I was having zero prevalence. Out of 150 patients 58.7% (n=88) were male while 41.3% (n=62) were females. Among the male population 31 were affected by Dengue virus serotype 2, 18 males were Dengue virus serotype 3, and Dengue virus serotype 4 was observed in 18 males while 21 males were reported negative for any of the serotype. In contrast among female population Dengue virus serotype 2 was present in 37 females, Dengue virus serotype 3 was observed in 7 and Dengue virus serotype 4 was fixed in 3 females only; while 15 females were negative for any of the serotype of Dengue virus. The data showed that p-value (p< 0.005) depict the association between gender and serotypes of Dengue fever. Our Research point out the prevalence of three out of four serotypes among the Pakistani population, which is a shocked fact as per pathogenesis theory that second infection by a different serotype may prove fatal for previously recovered person. Therefore a strict mosquito control programme is direly needed to prevent these incoming events to occur, the only hope and solution is in our environment. Moreover masses education regarding dengue fever might prove helpful in preventing zoonoses. Availability: Items available for loan: UVAS Library [Call number: 1163,T] (1).

2. Toxico-Pathological And Hematological Study In Japanese ( Coturnix Coturnix Japonica ) Exposed To Ochratoxin A And Aflatoxin B

by Muhammad shahzad | Dr. Muti-ur-rehman khan | Dr. kamran | Dr. M. younus rana.

Material type: book Book; Format: print ; Literary form: not fiction Publisher: 2011Dissertation note: Mycotoxins are secondary metabolite toxins produced by fungi in or on grains, cereals and nuts used as feed in the poultry industry. Mycotoxicity in birds has been well documented and its severity increases in combination with other toxins. The study determined synergistic pathological responses in quail chicks when fed different level of Aflatoxin B1 (AFB1) and Ochratoxin A (OTA). A total of 245 quails chicks were divided into seven groups (G1-G7) having 35 quail chicks in each. OTA mixed feed was fed to quail chicks at a dose rate of 1 and 1.5 ppm in G1 and G2 respectively. G3 were fed 2 ppm OTA + 1 ppm AFB1. AFB1 was offered in the feed at a level of 1 and 1.5 ppm in G4 and G5 respectively. G6 birds were fed 2 ppm AFB1 + 1 ppm OTA while G7 acted as a control. All the birds offered toxin free basal diet for first 7 days. Day 7 was considered zero day of experiment. At this day chicks shifted to different groups of 35 each (G1-G7). Group G7 was control group and offered toxin free diet. Birds were monitored twice daily for clinical signs. Randomly selected six birds from each group were slaughtered at day 14, 21, and 28. Blood samples with and without anticoagulant were collected for hematological and biochemical studies respectively. Morbid tissue of liver, kidney, and intestine were collected for histopathological studies. The OTA groups developed anemia manifested by a significant decrease in the red blood cell count, packed cell volume percentage and hemoglobin concentration, while increase erythrocyte sedimentation rate at the end of the experiment all groups showed significant reduction in red blood cell count. This reduction was found to increase with time proportionally to the level of OTA and AFB1 alone or in combination exposure. Clinical signs in chicks administered AFB1 and OTA included depression, decreased feed intake and decreased body weight. Severity in clinical signs was dose related. Pathological lesions in liver of these chicks were hemorrhages, fatty change, centrilobular necrosis and periportal fibrosis. Microscopically, liver showed vacuolation, fatty change, congestion and individual cell necrosis. Kidney of these chicks included pyknotic changes in the epithelium of proximal and distal convoluted tubules. Severe necrotic changes in the collecting ducts and accumulation of pink homogenous material in the lumen of tubules. Intestine showed hemorrhages, edema, degeneration and infiltration of mononuclear cells were observed. OTA damaged intestinal mucosa more severely than AFB1. Serum biochemical study indicated a significant decrease in total serum proteins and increase in urea and creatinine. It is concluded that AFB1 and OTA are capable of inducing hematological and histopathological alterations in quail chicks at higher dietary concentrations, either individually or in combination. Availability: Items available for loan: UVAS Library [Call number: 1301,T] (1).

3. 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.

Material type: book Book; Format: print ; Literary form: not fiction 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).

4. 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.

Material type: book Book; Format: print 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).

5. 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: book Book; Format: print 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).

6. Etiological Study Of Pancytopenic Children

by Dr. Syed Maaz Nadeem | Dr. Muti-ur-Rehman Khan | Dr. Aftab Ahmed Anjum | Dr. Asim Aslam.

Material type: book Book; Format: print Publisher: 2011Dissertation note: Pancytopenia is a hematological condition in which there is a decrease in all three cell lines of peripheral blood i.e. erythrocytes, leucocytes and platelets leading to anemia, leucopenia and thrombocytopenia. Complications of anemia, repeated infections and bleeding tendencies are sometimes horrifying and may result in death of individual. The present study was designed to analyze the underlying pathology, different clinico-haematological features and importance of bone marrow study in one hundred children presenting with pancytopenia. Present study was carried out in pediatric laboratory of Mayo Hospital, Lahore, Pakistan.. Detailed history was taken in all cases. Complete blood counts were done on an automated blood analyzer (Sysmex Kx-21). For counter check of total leucocyte count, differential leucocyte count and platelets, smears were also prepared and stained by using Giemsa stain. Red cell morphology was done on blood smear for theconfirmation of red cell indices. A total volume of 3 ml venous blood was drawn into a syringe. Out of which 1.0 ml was delivered into EDTA containing vacutainer and remaining 2 ml blood was transferred to a plain glass tube. After clotting and centrifugation serum was obtained for screening of hepatitis B surface antigen and antibodies against hepatitis C virus. Bone marrow aspiration was also performed where indicated. Megaloblastic anaemia (42%) Aplastic anaemia (26%) and ALL (8%) were found to be the common causes of pancytopenia in our scenario. Less common causes of pancytopenia were infections (8%), mixed deficiency (4%), MDS (4%) and lymphoma (4%). In all above mentioned cases clinical manifestations and peripheral blood counts played an important role in their evaluation. Two cases of haemophagocytic syndrome (2%), a rare cause of pancytopenia were also diagnosed in this study. This study also explained the importance of physical examination, peripheral blood findings and bone marrow examinations in the management of pancytopenic patients. Peripheral blood film and bone marrow aspiration should be performed simultaneously in pancytopenia patients when the diagnosis is not confirmed. Bone marrow examination in most cases gives the specific diagnosis. However, in few cases, additional tests may be required. Serum vitamin B12 and folic acid levels may be needed for confirmation of megaloblastic anemia. Serum iron, TIBC and iron staining on bone marrow smears may be required in iron deficiency anemia. In cases of leukemia flow cytometry study may be more helpful in reaching a final diagnosis. Bone marrow biopsy is mandatory in aplastic anemia. Availability: Items available for loan: UVAS Library [Call number: 1539,T] (1).

7. 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: book Book; Format: print Publisher: 2011Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1546,T] (1).

8. 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: book Book; Format: print ; 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).

9. 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: book Book; Format: print ; 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).

10. Immunohistochemical Identification Of Adenovirus Type 4 In Liver, Heart, Kidney, And Pancreas Of Broiler Chicken

by Muhammad Tanzil-ur-Rehman | Dr. Muti-ur-Rehman Khan | Dr. Aftab Ahmad Anjum | Dr. Yasin Tipu.

Material type: book Book; Format: print ; Literary form: drama Publisher: 2013Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1736,T] (1).

11. Comparative Pathological Studies Of Brucellosis In Azikheli And Nili Ravi Buffaloes At Slaughter House I District Sawat

by Sayyed Irfanullah Khan | Dr. Muti-ur-Rehman Khan | Dr. Asim Aslam | Dr. Saima Masood.

Material type: book Book; Format: print ; Literary form: drama Publisher: 2013Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1741,T] (1).

12. Pathobiologeical Studies Of Infectious Bursal Disease Virus (Ibdv) In Experimentally Infected Birds

by Maria Ali | Dr. Muti-ur-Rehman Khan | Dr. Aftab | Dr. Ishtiaq Ahmed.

Material type: book Book; Format: print ; Literary form: drama Publisher: 2014Dissertation note: Poultry industry is rapidly growing under the shelter of livestock, with the contribution of 11.4% of value addition in GDP. However infectious and noninfectious diseases are major threat to the growth of poultry industry. Among the infectious diseases, infectious bursal disease (IBD) is one of the major malady which causes great economic losses to poultry in terms of both morbidity and mortality. IBD virus was first identified in 1962 in gumboro, since then the disease spread to all parts of world. Until 1980s IBD virus was efficiently controlled by use of vaccine however with the emergence of variant strains of virus it was become difficult to control the disease. Studies on molecular structure of IBDV revealed that it has a hyper variable region in VP2 gene. Mutations in this hyper variable region lead to emergence of different strain of virus and hence causing vaccine failure. In Pakistan there is an outbreak of disease each year despite of vaccination. So there was a need to characterize field isolate and vaccine isolate of IBDV to find any mutation in field isolate of virus. The current study was designed by keeping above factors in mind. Purpose of present study was to compare local field and vaccine isolate of virus. RNA was isolated by TRIzol method from both vaccine isolate and bursa collected from field. RNA was converted to cDNA by using oligoDT. In next step VP2 gene was amplified by using a set of primers P1 and P2. cDNA was digested by 2 enzymes BstN1 and MboI. Results of RFLP showed that there was a difference in genetic sequence of both strains. Howeverthe pattern of disease produced by both of the strains was same. Chicks were given experimental infection at age of 2 week and slaughtered after 3 days post infection. Gross and histopathological lesions were observed and compared to each other and also with negative control. Statistical analysis was done by using one way ANOVA followed by Duncan's multiple range test. Availability: Items available for loan: UVAS Library [Call number: 1770,T] (1).

13. Cytotoxic Efects Of Saw-Scaled Viper Snake Venom On Brain, Heart, Liver And Hematological Parameters Of Albino

by Amara Mushtaq | Dr. Asim Aslam | Dr. Muti-ur-Rehman Khan.

Material type: book Book; Format: print ; Literary form: drama Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1783,T] (1).

14. Pathological Findings Of Field Isolated Peste Des Petits Ruminants Virus (Pprv) In Experimentally Infected Goats

by Qamar Ullah | Dr. Muti-ur-Rehman Khan | Dr. Saima Masood | Dr. Yasin Tipu.

Material type: book Book; Format: print Publisher: 2013Dissertation note: The Peste des Petits Ruminants (PPR) is the influential disease of small ruminants chiefly goats and sheep. It is highly contagious viral disease of economic point of view. It produces hurdles in farming of small ruminants in areas where it is present such as Africa and Asia. Those areas where the disease is endemic and huge numbers of small ruminants are reared by needy farmers; it threats their subsistence. Epidemically the disease identified since 1991 in Punjab province of Pakistan. The aim of the present study was detection of PPR virus through Reverse Transcription-Polymerase Chain Reaction during period of incubation. The course of the disease was monitored through regular clinical examination and hematological profile. The nature of the disease was evaluated through gross and microscopic lesions. The comparative proteomic analysis of field and vaccinal PPR virus was done through SDS-PAGE. A total of twenty healthy teddy goats were purchased from local market of Lahore and were reared for 21 days. The goats were randomly divided into Group-A (experimental group) and Group-B (control group), with ten goats (n=10) in each group. Experimental infection of field isolated PPR virus was given intratracheally to the goats of group-A. The goats of group-B served as un-infected control group. For early detection of PPR virus through RT-PCR, ocular and nasal secretions were collected on day 1, 3, 5 and 10 from experimentally infected goats and on day 5 and 10 from goats of control group. Clinical examination of all goats of both groups was performed on daily basis. For hematological analysis, 2.5 mL blood was drawn from jugular vein on day 0, 1, 3, 5, 7, 9, 12, 15, 18 and 21st day post infection from all goats of both groups. Gross and microscopic lesions were recorded after slaughtering one goat from each group at day 7, 14 and slaughtering all the remaining goats of both groups on day 21 post infection. Two goats of the experimental group were died naturally, one goat at day 8 and one goat at day 13 post infection. Proteomic analysis of PPR virus harvested from experimentally infected goats was done through SDS-PAGE and was compared with PPR virus vaccinal strain Nigeria 75/1. The results showed that PPR virus was detected by RT-PCR in PPRV infected goats at day three post infection and before the occurrence of acute clinical signs. The PPR virus was not detected in uninfected goats throughout the studied period which showed that there was no natural circulation of virus in the area of experimental sheds. The clinical examination showed significant increase in rectal temperature, pulse and respiration rates in PPRV infected goats as compared to uninfected goats. From the comparison of hematological parameters in PPR infected and uninfected goats, it was observed that PPRV is linked with some obvious alterations in its hematological profile. PPR in experimentally infected goats led to obvious decrease in the number of leucocytes, erythrocytes, platelets, hemoglobin estimation and packed cell volume but marked increase in mean corpuscular hemoglobin, mean corpuscular hemoglobin concentration and mean corpuscular volume as compared to uninfected goats. The gross lesions were specific for PPR which were prominently observed in the digestive and respiratory systems and lymphoid organs. The microscopic lesions revealed that there was congestion in trachea, sloughing in mucosa of rumen, mitotic activity in cardiac myocytes and hemorrhagic & effaced mediastinal lymph nodes of infected goats. From the comparative proteomic analysis through SDS-PAGE, differences in bands of proteins were observed. Availability: Items available for loan: UVAS Library [Call number: 1802,T] (1).

15. 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: book Book; Format: print ; Literary form: not fiction Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2022,T] (1).

16. 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: book Book; Format: print ; Literary form: not fiction Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2050,T] (1).

17. Role Of Aqueous Extracts From Zingiber Officinalis (Ginger) And Allium Sativum (Garlic) On Pathogenicity Of Avian Influenza Virus H9N2 on Chicken Embryoes

by Amir Rasool | Dr. Muti ur Rehman Khan | Mr. Muhammad | Mr. Muhammad Asad Ali.

Material type: book Book; Format: print ; Literary form: not fiction Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2127,T] (1).

18. Pathologenesis Of Anaplasmosis In Balkhi Sheep And Their Confirmation With Polymerase Chain Reaction

by Ajab Khan | Dr. Muti ur Rehman Khan | Dr. Gulbeena Saleem | Dr. Saima.

Material type: book Book; Format: print Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2145,T] (1).

19. 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: book Book; 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).

20. Pathobiological Studies On Bovine Ephemeral Fever Infected Cattle In District Swabi

by Sahibzada Waheed Abdullah (2013-VA-560) | Dr. Muti Ur Rehman Khan | Prof. Dr. Asim Aslam | Dr. Ali Ahmad Shiekh.

Material type: book Book; Literary form: not fiction Publisher: 2015Dissertation note: Among the non-contagious diseases Bovine ephemeral fever is important disease of cattle the course of the disease is usually three days due to which it is called “three days sickness”. This is transfer to other cattle through insects Culicoides (biting midges a group that include many kinds of flies) and mosquitoes. Bovine ephemeral fever virus (BEFV) has been collected from Culicoides coarctatus, Culicoides brevitarsis, and Anopheles bancroftii (Walker et al. 2012). Cattle and buffaloes are the main species affected from Bovine ephemeral fever (BEF) which gives huge economic losses to the dairy sector. The etiologic agent, Bovine ephemeral fever virus belong to Rhabdoviridae family, enveloped (negative sense) ssRNA virus. It generally recur in Australia, Asia, and Africa also in the Middle East (Walker 2005). The theme of the present study was detection of BEF virus through Reverse Transcriptase-Polymerase Chain Reaction from the cattle suspected for bovine ephemeral fever virus on the basis of clinical signs. Hematological profile and serum calcium level were checked in the confirmed positive samples for BEFV. A total of 50 blood samples were collected from the suspected animals in aseptic condition using a sterilized disposable syringe and were preserved in vacutainers (Anticoagulant added n = 50, without anticoagulant n = 50). The 10 blood samples were collected from healthy animals in vacutainers (Anticoagulant added n = 10, without anticoagulant n = 10). Buffy coat were separated from blood samples and from this the RT-PCR was performed and successfully diagnosed the BEFV infected cattle. Hematology and serum calcium were performed for both confirm positive and healthy animals. Summary 31 The result showed that BEF virus was diagnosed with the help of RT-PCR in samples suspected for BEFV infection, and there was no virus detected in samples taken from healthy animals. Comparison of hematology between BEFV infected cattle and healthy animals were performed there was no changes in the RBC, Hemoglobin, Hematocrit, MCV, MCH, MCHC, and MID (it include monocyte, eosinophils, and basophils) except Neutrophils, which number was increases and lymphocytes which was decreased in BEFV infection, while in healthy animals there was no change in the whole hematology. Serum calcium was also determined there was decrease in serum calcium level of BEFV infected cattle, while in the healthy animal samples there was no change in the serum calcium level. Availability: Items available for loan: UVAS Library [Call number: 2284-T] (1).

21. Study On The Pathogenesis Of Co-Infection Of Infectious Bronchitis (Ibv) And Escherichia Coli (E. Coli) In Experimental Chickens

by Sohail Khan (2013-VA-606) | Prof. Dr. Asim Aslam | Dr. Muti Ur Rehman Khan | Prof. Dr. Tahir Yaqub.

Material type: book Book; Literary form: not fiction Publisher: 2015Dissertation note: Infectious bronchitis and colibacillosis are infectious diseases affecting chicken of all ages and breeds. They are of major economic importance in commercial chicken flocks, causing huge losses. As both in humans and animals it is well documented that preceding respiratory infection of virus predispose individual to bacterial infection. Moreover, mix infection in poultry which occur when different organisms simultaneously invade birds is a major threat to poultry industry causes highly epidemic debilitating disease with high mortality which eventually leads to economic catastrophe. In recent past prevalence studies of field, E. coli had been reported with high prevalence and exaggerated disease along with other respiratory pathogens, additionally IBV had also isolated from same flocks in same season. Although a plethora of pioneering work had been done on IBV and E. coli in the previous decades but still a window in time exist in revealing there co-infection. Looking to field scenario in our country, the present study was designed to study an ideal challenge model for IBV and E. coli, by reproducing the natural infection. 80 SPF day old broiler birds were arranged into four groups, (A, B, C and D). Each group was comprised of 20 birds. Group D served as uninoculated control while, Group A and B were challenged with IBV on 23rd day of trails, and Group B and C were inoculated with E. coli infection on day 26th. Birds, (n=3) from each group were slaughtered on various days post infection, gross and histopathological lesions were observed and serum samples for HI were taken, throughout experiment. Variable clinical signs were recorded in various groups. In IBV infected group, respiratory distress i.e., tracheal rales, coughing, sneezing and gasping were noted during early stages, later up to 10 days post infection watery diarrhea with ruffled feathers were observed. In mix infected group clinical signs manifested rapidly and were persistent with high severity. Gross lesions in mixed infection were more profound, Summary 56 including; airsacullitis, tracheitis with catarrhal exudation throughout respiratory tract; severe sepicemic lesions i.e. perihepaitis, pericarditis, pneumonia and polyserositis with swollen and pale kidneys distended by urates. 5 birds died in mix infected group revealed ascites with asphyxiation of trachea with caseous exudate. While in IBV infected group lesions were mild and confined to trachea, airsac and kidneys. Mortality was high in mix infected followed by IBV in which two birds died. While in E. coli and control group mortality were not noted. Histopathological lesions in mix infected group were aggravated markedly tracheal epithelium degeneration, deciliation and sloughing; congestion, interstitial nephritis, leukocytes infiltration, tubular degeneration and necrosis while were observed. In lungs, pneumonia of peribronchiolar area and interstitium with lymphocyte and macrophages infiltration, additionally degeneration and vacuolization of hepatocytes with focal necrotic areas were also noted. In IBV and E. coli group microscopic lesions were of mild degree. GMT of both IBV and mix infected birds were high but were not significant different (P>0.05). Among the groups, statistically significant increase in FCR of birds in mix infected group was observed followed by E. coli, with IBV infected came third in the row. On the bases of these findings we might conclude that mix infection of IBV and E. coli causes severe lesions with high morbidity and mortality. Availability: Items available for loan: UVAS Library [Call number: 2306-T] (1).

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