51.
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: ; Format:
print
; Literary form:
drama
Publisher: 2013Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1736,T] (1).
52.
The Development Of Tea Whitener By Partial Replacement Of Palm Oil With Canola Oil
by Junaid Kabir | Dr. Muhammad Nasir | Dr. Aftab Ahmad anjum | Dr. Saima.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2013Dissertation note: Tea whitener is now become a popular trend in Pakistan with 01 billion tons consumption annually according to my personal information and its consumption is increasing day by day. The replacement of hydrogenated palm oil used traditionally is necessary as they contains 49.3% saturated fatty acids, the majority of which are palmitic acid, myristic acid and lauric acid which are proved to be most injurious for human health, raises the total and LDL cholesterol (Bonanome et. Al, 1998). Canola oil is known for its low level of saturated fatty acids, a relatively high level of monounsaturated fatty acids, and a very good amount of the n-3 fatty acid a-linolenic acid. Canola oil consists of an appreciable amount of a-linolenic acid which amounts for almost 10 percent which is a fairly good quantity. In addition, 1:2 is the ratio balance between linolenicacid and linoleic acid which is favorable and well balanced. Canola oil is a relatively rich source of tocopherols,60-70 mg/100g, contains high level of phytosterols (892 mg/100 g. Keeping in mind the above mentioned nutritional aspects, canola oil based tea whitener is developed.
The research was conducted in two phases. During 1stphase the HLB requirement of the canola oil and partially hydrogenated palm oil was determined which are determined as 08 and 06 respectively. Then the emulsifier's percentages are calculated according to their standard HLB values and the doses of the emulsifiers "DATEM" and "GMS" are adjusted according to the ratios of hydrogenated palm oil and canola oil in all the formulations. During second phase the proximate, chemical, physical and sensory analysis are done for all the emulsions so as to determine their resemblance with the control formulation S1.
Different graph analysis regarding proximate analysis of canola oil based tea whitener showed that the results for moisture percentage are (85.69 ± 0.089), for crude protein the values are (1.66±0.22), for dry matter its (14.32±0.04) for crude fat the result shows (7.01±0.03). The variation in all the emulsions were negligible, as the ingredients except fat source is almost the same in all the formulations.
The results for acidity of tea whitener emulsions on the 2nd day which is 0.09± 0.02 which shows the acceptable range, while on the 6th day the mean value of the acidity is also in the acceptable range which is 0.14± 0.01 which means acidity increases to some extent on the 6th day of storage. The mean of the acidity on the 8th day is 0.16± 0.01. The trend shows the acidity increases from 0.09±0.02 to 0.16±0.01 in 08 days. The variation was observed in all the emulsions with the passage of time, but there is not a very significant difference among all the emulsions as compared to control S1.
Mean values for pH on the 2nd day is 6.79±0.03 while the control sample S1 has the pH value of 6.82 on the 2nd day and the treatment which has the lowest pH values on day 2nd is S6 with pH 6.75. The observations on 6th days are shown in pH chart which shows slight decrease in pH in the 6th day with the mean value 6.71±0.02. The mean value of pH on the 8th day is 6.61±0.02. The results showed that pH of tea whitener emulsionsdecreases as storage progressed. A very interesting point raised during study that the pH values of the standard emulsion S1 is higher among all the emulsions on the 2nd day, but as the days proceeds, the pH of the emulsions with different rations of canola oil retains their pH and the pH becomes almost the same as standard on the 8th day. This may concludes that the emulsions containing canola oil retains their ph more as compared to palm oil based emulsion.
The mean value of density of the tea whitener emulsions 1.12±0.02. So overall the results variation is not significant. The little difference may be due to the fact that palm oil has density of 0.89 L/kg at 25 C while the density if canola oil is 0.91 L/kg on the same temperature. The density of all the formulations are comparable with the control emulsion S1.
The results depicted that 'L" value was decreaseswith increase in the ratio of canola oil. Mean comparison for color "L" parameter showed that highest value for S1 which is 90.45 and least value for S8 which is 89.29. The variation is very slight but the palm oil based emulsions are slight whiter in the appearance.The mean value of a* is -0.285 ± 0.095 which shows a very little variation. The level of greenness decreases slightly as the ratio of the canola oil increases from S1 to S8. The degree of yellowness in the emulsion increases as the ratio of canola oil in increases in the emulsions. The mean value of b* is 2.94±0.27 which shows a slight variation as we go from S1 to S8.
The sensory attributes scores obtained from sensory evaluation by trained panelists varies a lot. Addition of canola oil in place of palm oil significantly alters the flavor, After taste and over all acceptability of the tea made with tea whitener emulsions from S1 to S8, the scores are almost the same up to S4 as compared to control formulation S1 for all the attributes mentioned above. Score decreases from S5 to S8 which is definitely due to the addition of canola oil in the formulations. The sensory attributes like fat separation and color get the same scored almost for all the formulations.
Flavor scores are almost the same up to S5 but the scores decreases significantly from S6 to S8, for the sensory attribute of "after taste" the formulations from S1 (standard) to S4 get good scores means the after taste if the S2, S3 and S4 are comparable to the control emulsion S1 while S5 to S8 get lower scores, For "overall acceptability" S2, S3 and S4 are nearly equivalent and good scores as compared to control formulation with 100 percent palm oil formulation with the mean value of 90±02 which gives a green signal that we can partially replace hydrogenated palm oil with canola oil. The formulation S5 get a little lower score as compared to control one. The formulations from S6 to S8 get lower scores in overall acceptability.
Finally it is concluded that the formulation S4 is the one which can be replaced with the control emulsion S1 for making of tea which means 42.5 percent of the total fat in tea whitener can be replaced successfully with canola oil without compromising the physical, chemical and sensory properties of the tea.
Recommendations
The main aim of this project was to make a tea whitener which is based on healthier and heart friendly oil (canola oil) instead of palm oil. Canola oil has been used as a cooking oil and also in nutritional products like "Ensure Plus" and "Glucerna" due to its health friendly composition. The idea is drawn from the nutritional products compositions whose fat part is mostly consists of canola oil.
In Pakistan, keeping in mind a very huge consumption of tea whitener of 01 billion annually according to my personal information. The production may be much higher as my information may be limited. Keeping in mind the annual production or consumption of liquid tea whitener in Pakistan, the delivery of more healthy oil to the consumers by incorporating it in the liquid tea whitener product seems to be a pretty good idea. It is not only the matter of incorporation of healthy canola oil but also the matter of replacement of saturated fatty acids rich palm oil. Keeping in mind the chemical, physical and sensory properties of tea whitener emulsions S4 with 42 percent canola oil of the oil phase gives similar physical, chemical and sensory properties when compared to control formulation tea whitener S1 with 100 percent palm oil as oil phase. Keeping in mind the composition of the canola oil, if tea whitener is made with 07 percent fat level, in case of S4 (The formulation with resemblance to control up to maximum canola oil extent) canola oil percentage if the total fat is 42.5 percent of the total fat, it will give 0.7 grams of omega-3 as ALA per 250 ml of the tea whitener which means that it will provide 2.8 grams of omega-3 per liter of tea whiteners which can help us to meet up to some extent the ADA recommendations which is 1.3 to 2.9 grams based on 2000 Kcal diet (ADA, 2007)
The real challenge in the making of tea whitener formulations with different ratios of canola oil and palm oil is to make a successful emulsions without fat separation, thanks to HLB system for successful making of emulsions. Another challenge is to mask the after taste of the canola oil which can be prominent in the tea whitener, the after taste of canola oil is masked by milk flavor due to which the successful replacement of palm oil with canola oil up to 42 percent becomes possible. The purpose of the product development of making it a source of omega-3 was successfully met as the results shows the partial replacement of palm oil with canola oil is possible.
From the present study it can be concluded that canola oil can be incorporated in liquid tea whitener up to the percentage of 42.5 percent of the total fat without any persistent change in chemical, physical and sensory properties of the tea whitener. The concluded value of omega-3 which it gives per 250 ml is 0.7 grams according to fatty acid profile given by ADA reports (ADA, 2007). They do not affect the taste or texture of the product. My study showed that the replacement of palm oil with canola oil up to 42.5 percent in tea whitener formulation was acceptable among consumers and also the tea whitener retained its quality and sensory properties after storage for 08 days at 04 C. The tea prepared from S4 has the same sensory properties as the tea made with the control formulation. It is recommended that canola oil based tea whitener should be a introduced in the market for creating awareness among the general population about the role of omega-3 n human health and threats of consuming saturated fatty acids. There are need of studies forefficacy of developed tea whitener whether it beneficially transmit the omega-3 to human body or not and what are the health benefits among the subjects. More research work is required to testify the product under UHT treatment to find out what are the changes in physical and chemical properties of the product up to 03 months, it's emulsion stability and it's sensory properties during and after 03 months of shelf life in tetra packaging.
Availability: Items available for loan: UVAS Library [Call number: 1756,T] (1).
53.
Immunobiological And Molecular Characterization Of Pasteurella Multocida From Buffaloes
by Muhammad Kamran | Prof. Dr. Mansur-ud-Din Ahmad | Dr. Aftab Ahmad Anjum | Prof. Dr. Azhar.
Material type: ; Format:
print
; Literary form:
drama
Publisher: 2012Dissertation note: Hemorrhagic septicemia is an acute bacterial disease of buffaloes and cattle caused by Pasteurella multocida. In the present study, 400 samples (200 from carriers and 200 from sick animals) from Sargodha division were collected. Among four districts of the division, 15 samples were positive by API Kit, 13 by conventional biochemical tests and eleven were found positive for P. multocida through serological and molecular characterization. Biochemical profile index obtained with API kits had lesser accuracy than conventional and serological profiles for the identification of P. multocida. Passive mouse protection test and AGPT were used for serological confirmation. Different molecular techniques like SDS-PAGE, PCR and RFLP were used to investigate variation at the molecular level in field and vaccinal strains. There were no significant variation between field isolates and vaccinal strain in sick animals and carriers, or in isolates of different districts. Five major and three minor polypeptide bands were observed by SDS-PAGE. Genetic relatedness among the isolates was assessed by cluster analysis using Fingerprint Analysis of Missing Data (FAMD) of 12 isolates. The12 isolates clustered into 5 groups namely I, II, III, IV and V. Group I and II consisted of only one isolate in each (8.33%) of the total designated BKC-01 (S5) and KBO-01 (S1), respectively. Group III composed of 2 isolates (16.67%) namely KBC-02 (S4) and MNO-01 (S2). Group IV had the highest numbers of isolates (50%) designated as KBC-02 (S3), MNO-01 (S6), BKO-02 (S7), MNC-02 (S8), SGO-02 (S9) and V. Only two isolates were typed in group V (16.67%) named as SGO-01 (S10) and BKO-01 (S11).
The size of amplified gene was 460 bp. HindIII I endonuclease cleaved bacterial genome at four sites as compared to other four enzymes (DNase1, PstlI, EcorI and BamHI) change the writing of these enzymes which cleaved at two sites. The isolates were also subjected to ten routinely used antibiotics for sensitivity testing and found enrofloxacin as drug of choice with 90.91% sensitivity, followed by gentamycine, chloramphenicol, ciprofloxacine and norfloxacine (72.73%), ampicillin and amoxycillin (45.45%), amikacin (36.36%) and lowest to sulfadiazine and erythromycine (18.18%).
Availability: Items available for loan: UVAS Library [Call number: 1767,T] (1).
54.
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: ; 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).
55.
Chemical Characterizaton And Toxicological Screening Of Auto-Rickshaw Emissions Particulate
by Khaleeq Anwar | Prof. Dr. Muhammad Ashraf | Dr. Aftab | Dr. Aqeel Javeed.
Material type: ; Format:
print
; Literary form:
drama
Publisher: 2013Dissertation note: Vehicular air pollution is a mounting health issue of the modern age, particularly in urban populations of the developing nations. Auto rickshaws are not considered eco-friendly as to their inefficient engines producing large amount of particulate matter (PM), which poses a significant environmental threat.
Major transformations in the environmental composition are principally attributable to the combustion of fuels by automobiles. Motorized gasoline powered two-stroke auto-rickshaws (TSA) and CNG powered four-stroke auto-rickshaws (FSA)are major sources of air pollution in south Asia and produce toxic amount of PM to the environment. In this study, during the first phase, the PM of TSA and FSA was characterized by using proton induced x-ray emission (PIXE) analysis. The observations of the existing investigation recognized significant increase in Al (P < 0.05), P (P < 0.01), and Zn (P < 0.01) from the PM samples of FSA. In addition, the concentrations of Cu, Fe, K, Mn, Mg, Na, S and Si were also observed exceeding the recommended NIES limits. On the contrary, increased concentration of Sr and V were observed in the PM samples from TSA. It is generally believed that FSA generates smaller amount of PM but the data obtained from this study clearly shows that emissions from FSA are comprised of potentially more toxic substances than TSA. The current research is specific to the metropolitan population and has evidently revealed an inconsistent burden of exposure to air pollutants engendered by FSA in urban communities, which could lead to disruption of several biological activities and may cause severe damage to entire ecological system.
The second phase of this study was conducted to ascertain toxic effects on angiogenesis, embryo development, embryonic movement and phytotoxicity of the PM from TSA and CNG powered FSA. Based on high amounts of aluminum quantified during PIXE analysis of PM from TSA and FSA, different concentrations of aluminum sulfate were also tested to determine its eco-toxicological potential. The PM solution from FSA, TSA and Aluminum sulfate exhibited anti-angiogenic potential with reduction in total area of CAM. Morphological evaluation of embryos exhibited varying degrees of hemorrhages in different groups. In case of phytotoxicity screening using Zea mays, the results demonstrated that all three tested materials were equally phytotoxic at higher concentrations in seed germination(p<0.001). Aluminum sulfate proved to be a highly phytotoxic agent even at the lowest concentration examined.
During the last phase, of the study, the MTT assay demonstrated a significant (p<0.001) dose dependent cytotoxic effect for TSA, FSA and aluminum sulfate on the BHK-21 cell line, establishing that the PM from FSA is a highly cytotoxic material. Mutagenicity was assessed by fluctuation Salmonella reverse mutation assay adopting TA100 and TA98 mutant strains with (+S9) and without (-S9) metabolic activation. Despite the fact that different concentrations of PM from both sources i.e. TSA and FSA were highly mutagenic (p<0.001) even at lower concentrations, the mutagenic index was higher in TSA. The chronic toxicity study revealed that chronic exposure to PM emitted from FSA and TSA resulted in peribrochiolitis, emphesema and infilteration of leukocytes in lung tissues. On the other hand liver, cardiac and kidney tissues exhibited degeneration and necrosis. The data shows that all tested materials are equally ecotoxicand if the existing trend of atmospheric pollution by auto-rickshaws is continued, air-borne metals/heavy metals will seriously affect the normal growth of local inhabitants and increased contamination of agricultural products, which will amplify the dietary intake of toxic element and could result in genetic mutation or long-term health implications.
Availability: Items available for loan: UVAS Library [Call number: 1795,T] (1).
56.
Molecular Charaterization Of Ampk Gene Of Pakistan Buffalo
by Waqas Ahmed Khan | Prof. Dr. Masroor Ellahi Babar | Dr. Aftab | Dr. Ali Raza Awan.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2011Dissertation note: Pakistan is an agriculture country and its economy is mainly dependent on agriculture, agriculture products. Livestock has been playing an important role in the economy of the country. Livestock sector contributed approximately 51.8 percent of the agriculture value added and 11.3 percent to national GDP. Buffalo which is known as black gold of Pakistan is famous for its largest milk production in the world. A better understanding of the genetic control of energy metabolism in farm animals can have far-reaching implications for molecular breeding programs. It can allow the implementation of knowledge-based breeding to increase feed efficiency and to improve meat quality. In addition, because of the high degree of evolutionary conservation of these genes, the information gained about the genetic control of animal nutrition can be extrapolated back to questions about human nutritional genomics and disease. This study was performed to discover the single nucleotide polymorphism at AMP-activated protein kinase (AMPK) gene in Nilli Ravi and Kundi Buffalo and their possible association with milk production. As AMPK is a sensor of energy metabolism so genetic variations in AMPK gene may also have effect the feed utilizing efficiency of animals. Buffalo is popular for utilizing low quality roughages in a better way. Buffaloes are popular in the world for high fat content and low cholesterol content as compare to cattle. A total of 128 single nucleotide polymorphisms were discovered at AMPK gene in Nilli-Ravi and Kundi Buffalo. Out of which 10 are in exonic region and 118 are in Intronic region. Most of the SNPs are Intronic it also shows that AMPK is highly conserved as it has been shown by many studies. The Intronic SNPs may have role in regulation of AMPK gene. Forty-six SNPs were discovered in Intronic region of A1 subunit of AMPK gene. Out of these 46 SNPs. Forty-four SNPs are same in both Nilli-Ravi&Kundi buffalo.
Two SNPs found at position 11908 and 12217 was present only in Kundi buffalo. These two SNPs can be used for breed characterization of Nilli-Ravi&Kundi buffalo. The numbers of SNPs discovered in exonic region are 6. These all SNPs are non-synonymous mutations and changes amino acids at position 23333 from Histidine>Tyrosine, at 23387 from Glutamic acid>Lysine, at 23402 from Valine>Isoleucine, at 23426 from Ser>Pro, at 23489 from Stop codon>Arg and at 23612 from Ala>Thr. Forty SNPs were discovered in Intronic region of A2 subunit of AMPK gene. Out of these 43 SNPs 28 are same in both Nilli-Ravi & Kundi buffalo. SNPs at positions 71371, 71382, 71383, 71396, 71558, 42736, 42766, 42881, 41661, 41900 and 42021 are only present in Kundi buffalo while SNPs at position 70900, 71613, 42935 and 42944 are present only in Nilli-Ravi buffalo. These SNPs can also be used for breed characterization of Nilli-Ravi and Kundi buffalo. The B1 subunit of AMPK gene has 21 SNPs in Intronic region, which is common, both in Nilli-Ravi and Kundi buffalo. These polymorphisms may have role in regulation of AMPK gene. The SNPs found in exonic region are 3 which are all non-synonymous mutations and changes amino acids at position 4362 from Histidine>Tyrosine and at positions 8193, 8195 from Glycine>Serine. All exonic SNPs are non-synonymous mutations, which show that it will change the function of protein and might be associated with milk production and feeding efficiency in Nilli-Ravi & Kundi buffalo. This study is an example of candidate gene approach to find some novel variations at population level. It is the first study conducted for Molecular Characterization of AMPK gene in Buffalo. The only way to associate these polymorphisms to the trait under consideration (energy metabolism) by back tracing the sampling groups. This study is first in finding some molecular markers for energy metabolism in Nilli-Ravi and Kundi buffalo that can be used for future selection and breeding programs. More the population will be diversified for the trait and showing trends of heterozygosity, better will be the chances of selection of animals with suitable genetic makeup.
Availability: Items available for loan: UVAS Library [Call number: 1796,T] (1).
57.
Comparative Efficacy Of Different Diagnostic Techniques For Ovine Haemonchosis Through Faecal
by Sadaf Anwar | Dr. Muhammad Lateef | Dr. Aftab | Prof. Dr. Azhar Maqbool.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2013Dissertation note: Livestock plays pivotal role in the economy of country and small ruminants are the major source of food products for human. Haemonchus contortus is the most significant parasite of small ruminants and cause heavy production losses by causing reduction in meat and wool production. The parasite directly affects the health of an animal and causes anemia, hemorrhages, anorexia, weight loss and death of affected animal.
This study was designed to diagnose the Haemonchosis in sheep in and around Lahore. The accurate diagnoses of the parasite are important for its control and treatment. Direct smear, floatation technique and Polymerase Chain Reaction (PCR) were applied to check the sensitivity and specificity in diagnosing Haemonchosis in sheep. For this purpose 100 faecal samples were collected randomly from different areas of Lahore. Each faecal sample was examined by direct smear method and floatation technique. Out of 100 faecal samples 44 were microscopically positive. 30 by direct smear method and 44 by floatation technique.
Specific primers were designed to diagnose Haemonchosis in sheep by using ITS-2 Region. 44 microscopically positive samples were confirmed by PCR. 29 (66%) samples were found to be PCR-positive and 15 (34%) were found to be PCR-negative.
Several other species of parasites were also found during microscopic examination of faecal samples. Two samples wetre found positive for coccidial oocyst and seven samples were also positive for other nematodes along with Haemonchus spp.
Flotation technique was found to be superior in diagnosis of Haemonchosis as compared to direct smear.
Conclusion:
From current study it is concluded that Haemonchosis is widely prevalent in ovines. Its accurate diagnosis is essential for the treatment of infectious diseases and control of this parasite. Molecular technique has the advantage over conventional diagnostic techniques because PCR is more specific than conventional methods of diagnosis. According to the present study by conventional method there is 34% error chances to diagnose other Trichstrongylid eggs as Haemochus spp. The main advantage of using PCR as diagnostic test, are an increased speed of diagnosting the disease and its capability to notice low worm burden in small volume of faeces from individual animals.
Availability: Items available for loan: UVAS Library [Call number: 1809,T] (1).
58.
Vectorial Role Of Anopheles Subpictus By Using Poymerase Chain Reaction
by Shumaila Kausar | Prof. Dr. Kamran Ashraf | Dr. Aftab | Dr. Haroon Akber.
Material type: ; Format:
print
; Literary form:
drama
Publisher: 2014Dissertation note: Vector-borne diseases are among the major causes of illness, death and economic losses particularly in tropical and subtropical areas of the world. Mosquitoes are most important single group of insects, transmitting wide range of human diseases like malaria, Japanese encephalitis, dengue fever, yellow fever, filariasis and several other infectious diseases. Malaria is a major global public health problem. Several Anopheline species are prevalent in Pakistan among which Anopheles stephensi and Anopheles culicifacies are confirmed vector of Plasmodium. An. subpictus is a confirmed secondary vector of malaria in many countries. A wide range of this species is also distributed in Pakistan. The aim of the present study was to determine the vectorial role of An. subpictus in the transmission of malaria in Pakistan through microscopy and polymerase chain reaction (PCR).
After species identification, the mosquitoes were examined microscopically and were found negative for the presence of human Plasmodium sporozoites. The DNA extracted from An. subpictus was subjected to PCR but no Plasmodium specific amplification was observed. Keeping in view the sample size, it was concluded that further study is required with even large sample size before declaring that An. subpictus is not a vector of Plasmodium in Pakistan.
Availability: Items available for loan: UVAS Library [Call number: 1811,T] (1).
59.
Bioconversion Of Agricultural Wastes To Polyhydroxybutyrate By Azotobacter Vinelandii
by Tehmina Aslam | Ms. Shagufta Saeed | Dr. Aftab | Ms. Huma Mujahid.
Material type: ; Format:
print
; Literary form:
drama
Publisher: 2014Dissertation note: Background
Polyhydroxybutyrate (PHB) is a biopolymer. It can be used as a biodegradable thermoplastic material for waste management strategies. It can be produced by various microorganisms. A bacterium, Azotobacter vinelandii accumulates PHB as intracellular granules inside their cells in response to physiological stress such as excess of carbon sources and limitation of nutrients e.g. nitrogen and phosphorus etc. During this research work PHB was produced from agricultural wastes like wheat bran and rice polishing through fermentation and by the optimization of different parameters like water substrate ratio, incubation time, volume of inoculum, pH and nitrogen concentration.
Methodology
A parent strain of Azotobacter vinelandii was maintained on Jerman agar plate. Fermentation media containing wheat bran and rice polishing as substrates was used to check the production of PHB for the selected bacteria. 0.5 ml of inoculum media was added into sterilized fermentation media and incubated for 24-72 hours. After that, culture media was centrifuged. Further extraction, determination and identification of PHB were carried out by using the pellet.
It was found that Azotobacter vinelandii gave maximum PHB yield (192mg/100mL) at 4% of wheat bran after 48 hours of incubation and at 5% of rice polishing after 36 hours (158mg/100mL). Wheat bran gave maximum PHB production (236mg/100mL) at 1.0mL volume of inoculum and rice polishing gave maximum yield (216mg/100mL) at 2.5mL. For wheat bran optimum pH was observed to be 7 to give higher PHB yield (256mg/100mL) and for rice polishing at pH 8.0 maximum PHB was observed (236mg/100mL). From wheat bran maximum quantity of PHB was produced at 0.2% of peptone (268mg/100mL) and at 0.3% of yeast extract (256mg/100mL) while in rice polishing based media higher PHB yield was studied at 0.25% of peptone (258mg/100mL) and at 0.2% of yeast extract (250mg/100mL). In this study Azotobacter vinelandii produced higher yield of PHB using wheat bran as compared to rice polishing.
Outcomes
So it is concluded that PHB produced in this work can be used in various industries like pharmaceutics, food industry and also in medical fields. It will also be helpful to reduce the pollution caused by other synthetic plastics.
Availability: Items available for loan: UVAS Library [Call number: 1818,T] (1).
60.
Reversal Of Antibiotics Resistance In Methicillin-Resistant Staphylococcus Aureus By Non-Antimicrobial Agents
by Sohaib Danyaal | Prof. Dr. Muhammad Ashraf | Dr. Aftab | Dr. Muhammad Adil Rasheed.
Material type: ; Format:
print
; Literary form:
drama
Publisher: 2014Dissertation note: Antibiotic resistance is increasing along with the increasing use of antibiotic for the treatment of infectious diseases. The in-vitro study was designed to observe the reversal of
antibiotics resistance in Methicillin-resistant Staphylococcus aureus by non-antimicrobial
agents.
One hundred pus samples were processed for isolation and identification of MRSA.
Out of 100, 37 (37%) islotes were Gram +ve cocci, from these 37 isolates 34 (92%) turn red
colour of mannitol salt media to yellow and 23 (62%) gave +ve catalase and coagulase. In
this study Antibiotic Sensitivity Test was performed on pure culture of MRSA strain by
applying disc diffusion method. Out of 23 pure MRSA isolate, 100% isolates were
methacillin resistant, 79% isolates were co-amoxiclav resistant, 30% isolates were
meropenum resistant, 8% isolates were vancomycin resistant, 26% isoltes were moxifloxacin
resistant and 39% isolates were linezolid resistant. Reversal of antibiotics resistance was
observed by MIC or serial dilution method, using non antibiotic agents like Amiloride,
Lansoprazole and Promethazine, Concentrations of non-antibiotic agents 1024ìg, 512ìg,
256ìg, 128ug, 64ìg and 32ìg were used in combination of antibiotics to reverse the
antibiotics resistance in MRSA. These non antibiotic agents may cause the alteration in
mechanisms by which microorganism develop resistance. The collected data analyzed by
applying analysis of variance (ANOVA) through SPSS 16.0 computer software. Now we would be
able to treat some lethal infection caused by MRSA, and help to increase patient compliance
and decrease the cost of therapy.
Availability: Items available for loan: UVAS Library [Call number: 1828,T] (1).
61.
Role Of Non-Antimicrobial Agents In Reversal Of Antibiotic Resistance In Escherichia Coli
by Kalim Ullah | Prof. Dr. Muhammad Ashraf | Dr. Muhammad Adil Rasheed | Prof. Dr. Aftab.
Material type: ; Format:
print
; Literary form:
drama
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1839,T] (1).
62.
Identification Of Multiple Drug Resistant (Mrd) Mastitis Causing Bacteria In Dairy Goats
by Muhammad Faisal najees | Dr. Aftab ahmad anjum | Prof. Dr. mansur-ud-Din ahmad.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2013Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1852,T] (1).
63.
Isolation And Molecular Characteracterization Of Staphylococcus Aureus From Raw Milk
by Ibrar hussain | Prof. Dr. Muhammad ayaz | Dr. Imran javed | Prof. Dr. Aftab ahmad anjum.
Material type: ; Format:
print
; Literary form:
drama
Publisher: 2013Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1853,T] (1).
64.
Genetic And Evolutionary Characterization Of Pakistani Pigeons And Parrots Through Mitochondrial D-
by Sehrish firyal | Dr. Ali raza awan | Prof, Dr. Aftab | Prof, Dr. Tahir yaqub.
Material type: ; Format:
print
Publisher: 2013Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1873,T] (1).
65.
Isolation Characterization And Growth Optimization Of Starch Hydrolyzing Fungi From Soil Of Livestock Farms
by Saba Sana | Prof. Dr. Aftab ahmad anjum | Dr. Muhammad Nawaz | Prof. Dr.
Material type: ; Format:
print
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1898,T] (1).
66.
Plasmid Mediated Analyses And Plasmid Curing Of Previously Isolatedmulti-Drug Resistant Eschetichia Coli From Retail
by Mawra gohar | Dr. Ali ahmad sheikh | Dr.Tanveer | Prof, Dr. Aftab ahmad anjum.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1923,T] (1).
67.
Genotoxic Mutagenic And Cytotoxic Potential Of Metformin And Celecoxib Alone And In Combination
by Asad ullah | Prof/ Dr. Muhammad Ashraf | Dr. Aqeel javeed | Prof. Dr. Aftab.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1989,T] (1).
68.
Isolation Characterization And Optimization Of Potential Probiotic Bacteria From Poultry Droopings
by Muhammad Hashim khan | Prof. Dr. Aftab ahmad anjum | Dr. Jawad nazir | Prof. Dr. Mansur-ud-din.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 1991,T] (1).
69.
Isolation And Characterization Of Antibiotic Resistant Lactobacilli From Fermented Food Products
by Shahgull | Dr. Muhammad Nawaz | Prof. Dr | Prof. Dr. Aftab anjum.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2002,T] (1).
70.
Cytotoxicity Mutagenicity And Genotoxicity Potential Of Carvedilol And Celecoxib Alone And In Combination
by Ali attiq | Prof.Dr. Muhammad Ashraf | DR. Aqeel Javeed | Prof. DR. Aftab.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2004,T] (1).
71.
Comparative Efficiency Of Coprological Identificatiocn With Sensitive Detection Of Cryptosporidium By PCR In Domestic and Commercial Chickens
by Hafiz fahad nazir | Dr. Nisar ahmad | Prof DR. Azhar maqbool | Prof. DR. Aftab.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2010,T] (1).
72.
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).
73.
Evaluation Of Antibacterial Activity Of Macrolides In Combination With Levamisole Hc1 Against Different Pathogenic Bacteria
by Sheeza javaid | Prof. Dr. Muhammad Ashraf | Dr. Muhammad Adil rasheed | Proff. Dr. Aftab.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2026,T] (1).
74.
In Vitro Antibacterial Activity Of Star Anise (Illicium Verum) Oil Against Common Food Borne Pathogens And Its Utilization in Cookies Preparation
by Shamim khalid | Dr. Naureen naeem | Dr. Sanaullah iqbal | Prof. Dr. Aftab.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2033,T] (1).
75.
Mutation Of Aspergillus Niger And It,S Application In Bioconversion Of Whey To Beta-Galactosidase
by Zulfiqar ali khaki | Ms.Huma mujahid | Dr. Aftab ahmed anjum | Ms. Asma waris.
Material type: ; Format:
print
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2064,T] (1).
76.
Phylogenetic Analysis Of Plasmodium Species In Sparrows And Domestic Chicken
by Ghanwa ahmad | Dr. Haroon Akbar | Dr. Muhammad lateef | Prof Dr. Aftab.
Material type: ; Format:
print
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2075,T] (1).
77.
Detection Of Bacterial Load In Quail Meat Available In Lahore Market
by Muhammad Rameez akram | Dr. Naureen naeem | Ms. farasat rizwan | Prof. Dr. Aftab.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2078,T] (1).
78.
Assessment Of Microbial Load In Vegetables Grown In Sewage Polluted Water In Lahore Surroundings
by Asifa | Dr. Sanaullah Iqbal | Dr. Naureen Naeem | Prof. Dr. Aftab.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2119,T] (1).
79.
Synergistic Effect Of Antimicrobial Agents In Combination With Colistin Against Bacterial Isolates From Patients
by Sahar Safdar | Prof. Dr. Muhammad Ashraf | Dr. Muhammad Adil Rasheed | Prof. Dr. Aftab.
Material type: ; Format:
print
; Literary form:
not fiction
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2123,T] (1).
80.
Determination Of Microbial Contaminants Of Canned Fruit Products Available In Local Markets Of Lahore Pakistan
by Muhammad Waseem Akram | Dr. Muhammad Nasir | Dr. Zubair Farooq | Prof. Dr. Aftab.
Material type: ; Format:
print
Publisher: 2014Dissertation note: Abstract Availability: Items available for loan: UVAS Library [Call number: 2143,T] (1).
81.
Prevelance Of Brucellosis In Aborted Women Visiting Tertiary Care Hospitals Of Lahore City
by Saba Yasmin (2009-VA-211) | Prof. Dr. Aftab Ahmad Anjum | Dr. Tayyaba Ijaz (Co Supervisor) | Prof. Dr. Khushi Muhammad | Dr. Muhammad Tayyab.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: Pakistan is an agriculture based country whose rural population depends upon livestock for livelihood. Contribution of livestock to agriculture sector is 55.9 percent while 11.8 percent to the national GDP during 2013-14 (GOP 2013-2014). A number of infectious diseases hamper the growth of livestock sector. Some of the livestock diseases are zoonotic in nature and threat to human health. Brucellosis is considered among major zoonotic diseases throughout the world. The Mediterranean Basin, south and Central America, Eastern Europe, Asia, Africa, the Caribbean and the Middle East are considered as high-risk countries (Memish 2001).
Brucellosis in human beings is a major concern of community health. It causes acute and chronic illness, physical incapacity and loss of health. Bacterial species involved include Brucella abortus, Brucella melitensis or Brucella suis. Brucellosis is acquired by human beings from infected animals by close contact with vaginal secretions, urine, feces, blood, aborted fetus, or consumption of unpasteurized milk or other raw milk products. Shepherds, milkmen, butchers, knackers, veterinary assistants and abattoir workers are at high risk (Agasthya et al. 2007). Prevalence of brucellosis recorded by Mukhtar and Kokab (2008) in abattoir workers of Lahore Pakistan was 21.7 percent. Higher prevalence of brucellosis was observed in females (37.06%) than males (24.2%) in patients admitted at Peshawar, Pakistan (Shahid et al. 2014).
Symptoms of disease vary among human patients, ranging from non–specific, flu-like symptoms (acute form) to undulant fever (chronic form). Some of the serious complications of skeletal system, cardiovascular and central nervous systems may develop. Other important signs observed include arthritis, orchitis, epididymitis, abortion, retained placenta and stillbirth (Baba et al. 2001; Grilló et al. 2006). In animals, brucellosis in most of the cases results in abortion, birth of weak calves, death of young stock, infertility in males and reduced milk yield in females (Maadi et al. 2011; Abubakar et al. 2012).
There is actual need for teamwork between public health officials and veterinary officers to reduce communication of brucellosis between animals and human in endemic areas (Jelastopulu et al. 2008; Makis et al. 2008). Clinical picture of brucellosis is nonspecific and may vary from patient to patient. Therefore, laboratory diagnosis by isolation and culture or recognition of specific anti–Brucella antibodies is essential for confirmation of brucellosis (Al-Attas et al. 2000).
Diagnosis of brucellosis by culture and phenotypic description is time-consuming. Furthermore, risk of infection to worker is always there. Serological tests are commonly preferred for brucellosis in cattle and small ruminants, especially at farm level screening. Chance of cross-reactions with other gram negative bacteria is a major problem. Rose Bengal Plate Agglutination Test (RBPT) and Slow Agglutination Test (SAT) are extensively used for detection of anti-Brucella antibodies (Halling et al. 2005). Enzyme Linked Immunosorbent Assays (ELISA) have been developed to resolve suspected samples by RBPT. ELISA is more sensitive, so it can detect Brucella carriers which are negative by RBT, SAT and CFT (Aert et al. 1984). Molecular techniques are more reliable and specific than serological tests. Final confirmation of brucellosis is carried out using polymerase chain reaction (PCR), a molecular technique. Real-time PCR offers enhanced sensitivity, specificity and rapidity of performance when compared to conventional PCR (Gwida et al. 2012). Availability: Items available for loan: UVAS Library [Call number: 2225-T] (1).
82.
Status Of Awareness Among Zoo Workers About Zoonotic Diseases
by Tahir Khan (2012-VA-806) | Prof. Dr. Mansur Ud Din Ahmed | Shelly Saima Yaqub | Dr. Shakera Sadiq Gill | Prof. Dr. Aftab Ahmad Anjum.
Material type: ; Literary form:
not fiction
Publisher: 2014Dissertation note: A zoo is a place where wild animals are kept for exhibition purposes to the public.It includes: aquaria, sanctuaries, bird gardens and safari/wildlife parks. These are centers for wild animal’sconservation and for public recreation and education (Cuaron2005). Epidemiologists, wildlife biologists, veterinarians and conservationists used these for research purpose.According to an estimate Pakistan is maintainingapproximately 27 zoos, deer parks, etc.(Walker 2014).
Zoonotic diseases are those which are naturally transmitted from animals to human beings and vice versa. The word Zoonosis is derived from the Greek word zoon (animal) and nosos (disease). The diseases which are transferred from human beings to animals are known as Zooanthroponotic (Greek “Zoon” = animal, “anthrópos” = man, “nosos” = disease) diseases e.g. tuberculosis, measles, giardiasis and amoebiasis. On the other hand the diseases which are transmitted from animals to human beings are known as anthropozoonotic diseases e.g. anthrax, AIDS, psittacosis and rabies (Epstein and Price 2009).
Zoonosis can be classified according to their circulation in the ecosystem. These are either classified as synanthropic zoonosis, with an urban (domestic) cycle in which the source of infection are domestic and synanthropic animals (e.g. cat scratch disease, urban rabies and zoonotic ringworm) or exoanthropic zoonosis, with a sylvatic (feral and wild) cycle in natural foci outside human habitats (e.g. wildlife rabies, arbovirus, lyme disease and tularemia). Some zoonotic diseases can circulate in both urban and natural cycles (e.g. chagas disease and yellow fever).
A review study identified that 1415 species of infectious organism are pathogenic to human beings. This includes 217 viruses and prions, 538 bacteria and rickettsia, 307 fungi, 66 protozoa and 287 helminthes. Out of these, 868 (61%) are zoonotic in nature (Taylor et al. 2001). More than 60% of the emerging human infectious diseases are zoonotic in nature and 70% of their reservoirs are wild animals (Cutler et al. 2010).
The reservoirs of several zoonotic diseases are wild animals whose causative agents are viral, rickettsial, chlamydial, bacterial, parasitic and mycotic(Bengis et al. 2004). Zoonotic diseases like tuberculosis, plague and rabies have badly affected the mankind since ancient times and the reservoirs of all of these are wild animals (Stone et al. 2009). Some zoonotic diseases in human beings are self-limiting whose signs range from few days to a long term illness e.g. gastroenteritis caused byGiardia, Cryptosporidium, and Salmonella species.Some zoonotic diseases may cause abortions (Toxoplasmosis) and fatal encephalitis (Japanese encephalitis). Whereas some zoonotic diseases may causes high mortality e.g. Marburg hemorrhagic fever(MacNeil and Rollin 2012). Zoonotic diseases cause death not only in their natural hosts but also in endangered wild animal species near to extinctione.g. Ebola virus cause high mortality in monkeys (Nunn et al. 2008). It is clear from various studies in different zoos that both anthropozoonotic and zooanthroponotic transmission can occur (Adejinmi and Ayinmode 2008).
Zoonotic agents have potential to be used for bioterrorism. The bioterrorism attack is aimed to cause fear, destabilization, stress, illness and death in people, animals and plants. (Lin 2014). Air, water and food may be the warfare biological vehicles for its spread. During World War 1, anthrax was used as a biological warfare in animal populations. Glanders and typhoid were also used for bioterrorism attack in 1910 and 1970, respectively. Several cases of bioterrorism also occurred in the United States due to anthrax in September and October 2001 (Spencer 2007).
A Zoo worker should haveknowledge of the transmission of the disease to avoid its transmission. The common ways of the transmission are direct mode (ingestion, animal bites, inhalation, needle prick injuries and skin contact) and indirect mode (vector borne, fomite, long distanceand airborne transmission). In zoo management, the role of veterinarians is extremely useful. Their job exposes them to several health-related threats during routine operations. e.g. animal bites, needle prick injuries, back injuries, exposure to anesthetic gases and even mortality in certain cases (Hill et al. 1998; Kabuusu et al. 2010).
The personal protective equipment’s are not used during restraining, treatment, necropsy and cleaning the animal enclosures. It may increases the chances of zoonotic diseases to zoo workers and veterinarians. The disposal of wild animal carcasses, organs, unused food, feces and urine by unscientific methodsenhances the process of pathogens transmission(McLaughlin 2002). Laboratory personnel can also be infected with zoonotic diseases due to lack of good laboratory practices in wildlife disease diagnostic laboratories(Rietschel 1998).
Therefore, prevention and control of zoonosis must be an important part of zoo occupational health and safety measures. Preventive measures can be either general or specifically designed for a particular disease. It is possible to prevent many of the zoonotic diseases by following basic hygiene and sanitation procedures.The present study was conducted to determine knowledge, attitude, practice and experience levels about zoonosis among zoo workers of district Lahore(Lahore Zoo, Jallo Wildlife Park and Lahore Safari Zoo).
Availability: Items available for loan: UVAS Library [Call number: 2229-T] (1).
83.
Modulation Of Antibiotics Resistance Pattern In Escherichia Coli By Different Plant
by Bushra Chaudary (2009-VA-232) | Dr.Muhammad Nawaz | Prof. Dr. Aftab Ahmed | Dr. Naureen Naeem.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: Escherichia coli (E. coli) is Gram negative microorganism belonging to family
Enterobacteriaceae. It is part of normal micro flora of gastrointestinal tract of human and all
warm blooded animals (Kaper et al. 2004). Escherichia coli is source of many infectious diseases
in human as well as in animals. Common E. coli infections are enteritis, urinary tract infection,
septicemia and neonatal meningitis. In pets and farm animals, E. coli is associated with diarrhea
(Allocati et al. 2013). Poultry industry is facing huge annual losses due to infection of avian
Pathogenic E. coli (APEC) in broilers (Oosterik et al. 2014). E. coli causes a variety of
syndromes in poultry including yolk sac infection, respiratory tract infection, swollen head
syndrome, septicemia and cellulitis (Buys et al. 1989)
Antibiotics are chemical agents which inhibit the microbial growth and used to eradicate
infections. Mechanisms of action of antibiotics provide a base to categorize antimicrobial agents.
Most important classes of antibiotics act as inhibitors of cell wall synthesis, protein synthesis
(tetracyclines and macrolides), nucleic acid synthesis (fluoroquinolones), metabolic pathway
(trimethoprim-sulfamethoxazole) and cell membrane (polymyxins). Bacteria may have intrinsic
or acquired resistance to antimicrobials (Tenover 2006).
Urinary tract infections are mostly caused by E.coli. Antibiotics generally used for the treatment
of E. coli infections include ampicillin, nitrofurntion, cephalosporin, sulphonamides
(trimethoprim-sulfamethoxazole) and quonolones (neladixic acid, ofloxacine, ciprofloxacin and
levofloxacine) (Lin and Lin 2010).
Extended use and misuse of antibiotics lead to the development of resistant bacteria. Resistant
E. coli strains are common source of hospital born and community acquired infections. Ease of
Introduction
2
international travelling is one of the major spreading factor for antibiotic resistance. Resistant
bacteria got opportunity to move from one geographical area to another (van der Bij and Pitout
2012). New strains of E. coli resistant to carbapenems (New Delhi metallo-β-lactamase 1 (NDM-
1) are major global health issue (Kumarasamy et al. 2010). Antibiotic resistance has become a
serious public health problem. Currently, world is facing great difficulty in treatment of many
infectious disease of human and animals. One of the reasons of treatment failure is emergence of
resistant bacteria (Levy 2002).
To develop new strategies for treatment of infectious diseases, it is necessary to understand the
mechanisms of resistance. Efflux pump inhibitors, enzymatic degradations and alteration of
target sites are major strategies by which bacteria acquire or develop resistance to antibiotics
(Sibanda and Okoh 2007).
Scientists are looking for alternatives of antibiotics such as bacteriopheges, naturally
antimicrobial compounds and some non antimicrobial agents (Worthington and Melander 2013).
Probiotics (Lactobacillus and bifidobacterium) can be a prophylactic measures against E. coli
and may be used to treat intestinal tract infections of E. coli and other bacteria (de Vrese and
Schrezenmeir 2008).
Phytochemicals, secondary metabolites of plants, have antibacterial activity against many
pathogenic organisms. These phytochemicals in combination with antibiotics may show
synergistic effect. Phytochemicals and plant extracts can be a source of antibiotic resistancemodifying
agents (RMAs) (Abreu et al. 2012). Plant extracts shown antibacterial activity
because of phytochemicals like alkaloids, tannins, flavonoids, phenolic compounds and steroids
(Gobalakrishnan et al. 2013). Plant extracts are used as traditional medicine for the treatment of
many diseases. Plant extracts like Zingiber officinalis (Ginger) Gymnema sylvestre (Gurmar buti), Astragalus (goat’s thorn), Calotropis procera (apple of Sodom) and oputia dillenii (cactus)
have antimicrobial activity (indu et al. 2006 and Kumaar et al. 2013). Plant extracts also have
antibiotic resistance modulation potential (Mako et al. 2012).
Availability: Items available for loan: UVAS Library [Call number: 2247-T] (1).
84.
Occurrence Of Bacterial Contaminants In Poultry Meals And Their Antibiotic Resistance Pattern
by Nayyab Tariq (2009-VA-207) | Prof. Dr. Aftab Ahmad Anjum | Dr. Muhammad Nawaz | Dr. Muhammad Nasir.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: Poultry is the second largest industry after textile industry in Pakistan. Its consumption
rate is very high as compared to other animal protein sources, as it is cheaper as compared to red
meat. To fulfill increasing demand of poultry, poultry production quality must be improved.
Many factors affect poultry production. One factor is feeding process. Efficiency of poultry
production depends mainly on feeding process which influences both the quality and quantity of
the poultry production (Grepay 2009). The rearing of poultry birds on commercial level requires
use of bulk quantities of poultry feed. Poultry feed costs 60-70% of total cost for production
(Sahraei et al. 2012). The main purpose to increase poultry production is to fulfill nutritional
requirements of human population that largely rely on poultry and poultry by products as a
source of protein(Obi and Ozugbo 2007).
Poultry feeds are food materials designed to contain all necessary feed ingredients for
proper growth, meat and egg production in birds (Obi and Ozugbo 2007). It is a mixture of
various components including plant proteins (cereals and by products, grains etc), animal byproducts,
fats, vitamins and minerals (Ravindran 2013). The major component of poultry feed is
protein which is the key component of eggs and meat. Protein sources in poultry feed are of
plant, marine and animal origin. Plant proteins may lack some of the essential amino acids, thus
are incomplete protein. Proteins of animal origin are better growth promoter than protein of plant
origin, but their safety is a concern. Among plant based proteins, soybean and canola meal are
produced in higher amounts worldwide (Alali et al. 2011). The animal protein sources include
poultry, fish, meat bone and poultry by products meal. Poultry meal is derived from clean tissues
Introduction
2
of slaughtered poultry including bone after the moisture and fat have been extracted in the
rendering process. It may contain whole birds excluding feathers (Anonymus 2014). Among all
protein based meals, poultry meals and poultry by products meal are of superior quality and
provide higher protein content than plant, marine and meat based meals (Samli et al. 2006).
Quality of animal feed has gained importance worldwide. The feeds are found to be
associated with infectious or non-infectious hazards, thus influence human health (Sherazi et al.
2015). Poultry feed can act as carrier of animal and human pathogens (Aliyu et al. 2012). Poultry
feed can get contaminated at any point of harvesting, processing, storage or dispersal of feed.
Primary mode of poultry feed contamination is by dust, soil, water and insects. Poultry meals can
be another source of feed contamination. Poultry meals are added in feed as a source of protein.
Feeds of animal origin like poultry meals are richer in nutrients and water as compared to feed of
plant origin thus are found to have higher microbial load, facilitating the multiplication of
bacteria (Kukier and Kwiatek 2011). Inclusion of contaminated meals in feed increases microbial
load of poultry feed. The contamination of poultry feed not only influences appearance and
nutritional value of feed, but also affects animals and human who consumes it (Maciorowski et
al. 2007). The profitability of poultry production can be greatly affected due to the frequency of
feed contamination and the detrimental effects of the aflatoxins on performance of chickens
(Anjum et al. 2011). Poultry feeds have been implicated in several poultry diseases of viral
(Avian Influenza, Newcastle disease), bacterial (Salmonellosis, Infectious Coryza) and fungal
origin. Many human diseases like Traveler’s Diarrhea and Salmonella Paratyphoid fever have
been associated with consumption of poultry birds that contracted infections from poultry feed
(Obi and Ozugbo 2007).
Introduction
3
The poultry industry relies on ready to use poultry feed prepared by feed mills (Arotupin
et al. 2007). Both bacteria and fungi including mycotoxins usually contaminate feed at different
stages of pre or post processing, depending upon the conditions under which it is handled or
stored (D’Mello 2006). Poultry meals mostly get contaminated post rendering process. The
cooking step in rendering process inactivates bacteria, viruses, protozoa, and parasites(Meeker
and Hamilton 2006) . Still presence of contaminants in meals is attributed to post processing
contamination. Many bacterial pathogens reported in feed are Escherichia coli, Erwinia
herbicola, Salmonella spp., Listeria spp., Enterococcus fecalis, Cl. perferingens and Cl.
botulinum (Aliyu et al. 2012; Lateef and Gueguim-Kana 2014) . The contaminated feed results
in excessive activation of immune system and ultimately decreases poultry production and its
profitability (Kukier et al. 2012). In addition to bacterial contaminants, toxigenic fungi have
threatened quality and safety of feed and have caused severe losses to poultry industry in recent
times. Cereals and grains based poultry feed mostly get contaminated with fungi (Kwiatek and
Kukier 2008). Mycotoxin producing fungal genera that are reported in poultry feed are
Aspergillus, Penicillium and Fusarium (Greco et al. 2014).
As Poultry feed is the first step of the food safety chain in "farm-to-fork" model. Contaminated
feed can also serve as a source of antimicrobial resistant bacteria in poultry meat(da Costa et al.
2007). There are many evidences that pathogens in feed are transmitted to humans through
animals and food of animal origin. It can also become source of some human pathogens in
environment. Feed contamination by fungi is responsible for animal mycotoxicoses and through
consumption of contaminated animal food, results in human intoxications (Kukier et al. 2012).
Birds utilizing toxins containing feed are economical loss for farmers and also affects consumer
Introduction
4
health through its residues (Alam et al. 2012). Poultry feeds containing antibiotic resistant
bacteria results in loss of poultry productivity, making treatment of poultry diseases difficult.
Thus quality of animal food directly depends on usage of nutritionally balanced and safe feed.
Among many feed sources used, poultry meals are gaining importance for their higher nutritional
value, but very less work has been done in world particularly in Pakistan to determine
microbiological safety of poultry meals produced. There is the need to determine various quality
parameters which should be followed to ensure production of safe meal. Availability: Items available for loan: UVAS Library [Call number: 2252-T] (1).
85.
Antimicrobial Potential Of Bovine Lactoferrin Against Foodborne Pathogens
by Ammarah Khatoon (2012-VA-631) | Prof. Dr. Muhammad Ayaz | Mr. Ishtiaque Ahmed | Prof. Dr. Aftab Ahmed Anjum.
Material type: ; Literary form:
not fiction
Publisher: 2014Dissertation note: Health is recourse of everyday life, but not the object to live. It is positive to give special importance to personal and social resources. However, in Pakistan and other developing countries conditions are different, most people have low income and they live in un-sanitized environment. They eat un-hygienic food and also lack safe drinking water. People do not adopt any preventive measure to minimize the risk of contamination. Food storage is also un-hygienic. These conditions lead towards contamination and result in foodborne infections and gastro-enteritis. Foodborne illnesses are always a serious health issue in the Pakistan and throughout the world. Individual’s record for foodborne illnesses is impossible but it is reported that 7 out of 10 people suffer from foodborne illness caused by different microbes each year worldwide (WHO survey 2012).
Foodborne illness is caused by eating contaminated food with pathogenic bacteria. Some common pathogens are Escherichia coli, Campylobacter jejuni, Clostridium botulinum, Clostridium perfringens, Listeria monocytogens, Bacillus cereus, Staphylococcus aureus and Salmonellaspecies. Incubation period for onset of symptoms of food poisoning ranges from hours to days. Nausea, vomiting, abdominal cramps, fever and diarrhea are symptoms which appear commonly in most of food poisoning. However, foodborne illnesses if left untreated can lead severe dehydration, imbalance of intestinal micro flora, digestive disorders and even death in some cases. It was recorded that 2.2 million people killed from foodborne illness globally every year and the burden arising from foodborne diseases is larger (Kuchenmuller et al. 2009).
Antibioticsare massively used to overcome food poisoning; however, from health point of view they badly affect thenormal micro flora of gut but also microbes become antibiotic
resistance. The problem needs to be dealt with some other way like adding bio preservatives or antimicrobial agents in food.
To control microbes in foods, numerous methods have been adopted including the use of synthetic and natural antimicrobial agents. Scope of natural antimicrobial agents are increasing day by day and different natural sources are being utilized to get these agents. Among these natural sources milk is best and widely utilized source from long times. Milk contains many biologically active compounds among which lactoferrin is one of them.
Lactoferrin is a multifunctional globular glycoprotein from transferrin family, an iron-binding protein. It is part of innate immune system and has antibacterial activity known as far back as 1930. It was first isolated in 1939 from cow milk (Charrondiere et al. 2011). Lactoferrin belongs to the transferrin family having ability to bind iron two times higher than other transferrin proteins. Its molecular weight is 80 kDa and has about 700 amino acids depending upon species e.g. cow, buffalo, goat and sheep (Adlerova et al. 2008). Lactoferrin molecule consists of simple polypeptide chain folded into two symmetrical and highly homologous lobes (N and C) connected by a hinge region. Both lobes bind two metal ions in synergy with carbonate (CO32-). Not only Fe2+ and Fe3+ ions but Cu2+, Zn2+ and Mn2+ ions can also bind. Lactoferrin can bind Fe3+ reversibly so it can exist as free of Fe3+ (Apo-Lf) or in association with Fe3+ (Holo-Lf) and exhibits different three dimensional structure depending upon binding to Fe3+. Apo-Lf has an open structure and holo-Lf has closed which provide resistance to proteolysis. At iron-binding site Aspirin, two Tyrosine, and Histidine amino acids are directly involved in each lobe and Arginine is bound to CO32- ions. Number and position of Cystine-residues allows intermolecular disulfide bridges and Asparagine-residues in both lobes provide several sites for N-glycosylation (Farnaud and Evans 2003).
Lactoferrin is produced by mucosal epithelial mammary cells of human, cows, buffaloes, goat, horses, many other mammals and fish. It is widely distributed in body tissues and present in mucosal surfaces, specific granules of leukocytes and in biological fluids like tears, saliva, digestive fluids, seminal fluids and most abundant in milk comprising the second highest protein in human milk after casein. Concentration of lactoferrin in different species is for cow milk (80-500 mg/L), buffalo milk (50-320 mg/L), camel milk (200-728 mg/L), goat milk (98-150 mg/L) and sheep milk (20-140 mg/L) (Krol et al. 2011).
Many physiological functions of lactoferrin have been attributed. It plays an important role in iron regulation, non-specific immune response, regulation of cells growth and differentiation, protection from cancer, anti-inflammatory, anti-oxidant and strong antimicrobial activity against bacteria, fungi, yeast, viruses and parasites (Conneely et al. 2005). Another dominant role of lactoferrin is during involution of mammary gland. Concentration of lactoferrin increased dramatically from 0.1-0.3mg/ml in normal milk to 20-30mg/ml by 30 days in dry period. It is particularly important for bacteriostatic properties and non-specific defense against invading bacteria. Lactoferrin also affects phagocyte function and limit oxidative degeneration of cell components during inflammation and involution (Welty et al. 1976).
Lactoferrin exhibits strong antimicrobial activity against different bacteria, virus, protozoa, fungi and yeast (Hancock and Janssen 2009). The antibacterial activity of lactoferrin is due to two mechanisms; by binding the iron at infection sites, making it unavailable to bacteria and direct interaction of N-terminal of lactoferrin with micro-organism (Cruz et al. 2009, Orsi 2004). Lactoferrin acts differently with Gram-positive and Gram-negative bacteria (Sharma et al. 2013). It damages Gram-positive cell wall through interaction with negatively charged lipoteichoic acid causing reduction in negative charge on cell wall and favor contact between lysozyme and inner peptidoglycan (Fayad 2012). Gram-negative bacteria are destroyed by interaction of lactoferrin with external lipopolysaccharides by preventing contact with Ca2+ and Mg2+ ions which cause release of lipopolysaccharides, increase permeability and ensures damage (Ochoa and Cleary 2009, Ekins et al. 2004).
Milk and milk products are one of main diet in Pakistan and all over the world. During manufacturing different milk products, a number of by-products are obtained. Among them, cheese whey is produced in high volumes. It is commonly dumped off into sewerage which cause serious environmental problem as it contain high organic matter as well as loss of valuable nutrients it contain. Whey has Biological Oxygen Demand (BOD) ranges from 40,000 to 60,000 ppm (Sayadi et al. 2006) while permitted limit for BOD of domestic sewerage is 200 to 300 ppm. In order to overcome this problem there is need of effective and permanent way for treatment of whey. However, conversion of whey into non-food items like biogas is unreasonable as it is rich in unique nutrients.
Now-a-days there is an interest growing on to find new ways of whey utilization throughout the world. One option is to use the whey in processes in which saleable food or pharmaceutical products can be obtained. Whey could be subjected to different techniques to isolate different components like lactose, lysozyme and immunoglobulin. Likewise, lactoferrin can be isolated from cheese whey by cation exchange chromatography without loss of its biological properties in single step method and about 90% purity (Wu et al. 2011, Moradian et al. 2014).
In this study, we anticipated to use lactoferrin from bovine milk as natural antimicrobial agent. It has been shown that lactoferrin hasstrong antimicrobial activity against different bacteria, fungi, yeast, viruses and parasites (Conneely et al. 2005). In our country, very little work has been carried out onlactoferrin as natural anti-microbial agent. In fact, all over the world, the research scenario is now changing and concentrating toward the extraction of natural agents for product safety and health improvement. The lactoferrin has a potent anti-microbial activity against common foodborne pathogens. Due to the negative health effects of synthetic anti-microbial agents, the uses of natural sources are being encouraged all over the world. Our main focus of this study is to check the anti-microbial activity of lactoferrin against three pathogenic bacteria Escherichia coli, Staphylococcus aureus and Salmonella enteritidis isolatedduring our previous study.
Availability: Items available for loan: UVAS Library [Call number: 2265-T] (1).
86.
In Process Quality Control Factors Affecting The Quality Of Locally Prepared Salmonella Gallinarum Antigen
by Zahra Malik (2009-VA-245) | Dr. Arfan Ahmad | Prof. Dr. Aftab Ahmad Anjum | Prof. Dr. Asim Aslam.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: Fowl typhoid is a septicaemic disease caused by S. gallinarum biovar gallinarum has major economic significance in many parts of the world. It is an acute or chronic septicaemic disease that usually affects the birds (mostly adult birds). Eradication of disease is normally done by identifying the infected flocks and eliminating the reactor birds by using serological tests, but diagnosis of the disease is much expensive because antigen used for this purpose is imported. The study, therefore, has been proposed to prepare and evaluate the stained antigen of S. gallinarum using local isolates.
A total of 15 isolates were procured from Poultry Research Institute (PRI) Rawalpindi, University Diagnostic Lab (UDL) and Department of Microbiology, UVAS Lahore, which were identified by Biochemical testing and further confirmed by Polymerase Chain Reaction. Among all 15 isolates two isolates were confirmed as S. gallinarum and proceeded to prepare local antigen of S. gallinarum. Locally prepared antigen was checked with known positive and negative sera, Effect of different preservatives (Sodium azide and Thiomersal sodium) and different storage temperatures (4°C, 25°C and -20°C) was also studied after every fifteen days post storage upto 6 months to observe the stability and shelf life of local antigen. On the end of study both preservatives i.e. Sodium azide and Thiomersal sodium was found equally effective for antigen activity, whereas 4°C proved best storage temperature to be used for the antigen preservation.
Activity of locally prepared antigens was also compared with the imported antigen (Charles, River, USA) stored at different temperatures regularly throughout the six months, which showed that local antigens was almost as good as the imported antigen.
Summary
51
CONCLUSION
Locally prepared S. gallinarum antigen was found as effective as imported antigen. Both the test preservatives (Sodium azide and Thiomersal Sodium) had the same effect on antigen preservation. Among all three test temperatures, 4°C was accepted as best storage temperature for the long term preservation of local antigen with either of the preservative. Availability: Items available for loan: UVAS Library [Call number: 2278-T] (1).
87.
Antibacterial And Cytotoxic Evaluation Of Different Extracts Of Opuntia Dillenii (Ker-Gawl) Haw. Leaves Against Common Poultry Pathogens
by Sadaf Raana | Dr. Muhammad Ovais Omer | Dr. Muhammad Adil Rasheed | Prof. Dr. Aftab Ahmad Anjum.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: This project was designed to evaluate the antibacterial efficacy of hexane, chloroform, ethanol and aqueous extracts of Opuntia dillenii Haw. stems against common poultry pathogens. Pathogens used were Staphylococcus aureus, Escherichia coli, Salmonella, Clostridium perfringens type A and Haemophilus species.
This study was conducted to assess antibacterial and cytotoxic activity of O. dillenii Hexane, chloroform, ethanol and water extracts were prepared and antibacterial activity was evaluated by agar well diffusion method in which zones of inhibition were measured. Minimum inhibitory concentration (MIC) of plant extracts was evaluated by micro broth dilution method. The extracts which showed the antimicrobial activity were evaluated for cytotoxicity by using MTT assay on Vero cell line. Cell culture media was prepared and cell lines were propagated, monolayer was formed. Monolayer was exposed to plant extract dilutions. After 24-48 hours, MTT dye was introduced and cell survival percentage was calculated.
O. dillenii stems extracts inhibited the growth of both Gram negative and Gram positive bacteria. Chloroform and ethanol extracts of O. dillenii showed significant antibacterial activity against all the pathogens studied as compared to hexane and aqueous extracts. Hexane extract showed maximum zone of inhibition against Haemophilus species (13mm), for chloroform extract maximum zone of inhibition was obtained for C. perfringens (25.6mm), for ethanol extract maximum zone of inhibition was obtained for C. perfringens (23.0mm) and for aqueous extract maximum zone of inhibition was obtained for C. perfringens (23.0mm). Minimum inhibitory concentration for chloroform extract was lowest for all the tested strains. For S. aureus, C. perfringens type A and S. enterica MIC was 1250μg/mL. For E. coli and
CHAPTER 6
SUMMARY
Summary
88
Haemophilus species MIC was 2083.3 and 2916μg/mL, respectively. The extracts were further investigated to test cytotoxic effect on Vero cell line using MTT assay. Only ethanol extract was observed to be cytotoxic.
Statistical analysis was conducted with Statistic Package for Social Sciences (SPSS for windows version 16, SPSS inc, Chicago, IL, USA). The results of antibacterial activity and MTT assay were evaluated for significance of difference using analysis of variance (ANOV). The homogeneity of groups was verified by Duncan’s test at an alpha level equal to 5%.
Chloroform extract of O. dillenii stems possess antibacterial activity and can be used to design traditional medicines for the development of therapeutic agent which will be more safe, effective and economical. Availability: Items available for loan: UVAS Library [Call number: 2281-T] (1).
88.
Effect Of Oiling And Packaging On Shelf Life Of Eggs Stored At Two Different Temperatures
by Marium Munir (2008-VA-388) | Dr. Muhammad Nasir | Dr. Sanaullah Iqbal | Dr. Aftab Ahmad Anjum.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: In Pakistan, poultry industry is playing a vital role in the economy of the country. As eggs are perishable so it must be handled with safety. It is imperative to handle and store the eggs at appropriate conditions. But improper storage of eggs is a problem in our country which affects its quality and there is chance of microbial contamination in eggs. Oiling and packaging has variable impact on shelf life of eggs at different storage temperatures (Matt et al. 2009).Raw eggs have many benefits, they contain essential nutrients for the brain, nerves, glands and hormones, they are nutritionally balanced. raw eggs also contain an abundance of other vital substances including protein, essential fatty acids along with niacin, riboflavin, biotin, choline, vitamins A, D and E, magnesium, potassium, phosphorous, manganese, iron, iodine, copper, zinc and Sulphur. Egg yolks are one of the few foods that contain vitamin D(Watkins, 2002). As eggs are perishable food stuff,so the purposes of present research work are to analyze the effect of oiling and packaging on shelf life of eggs at two different temperatures. For this a total of 864 eggs were collected. The four different treatments were applied along with two different temperatures. Each category was further divided into four treatment strategies (108 eggs in each strategy) i.e. eggs without any treatment, oil coated eggs, eggs packed (air-tight) in white polythene bags, oil coated eggs packed (air-tight) in white polythene bags.Eggs undergone each treatment strategy were analyzed for six parameter i.e. sensory evaluation, microbial load, Physical parameters (weight, pH, egg shell percentage and haugh unit) using 18 eggs for each further divided into three replicates (6 eggs for each replicate). All the eggs were stored for 1, 7, 14, 21, 28 and 35 days.
Summary
76
Data was analyzed statistically by the 2- way ANOVA (Analysis of Variance) with 5% probability. Means was compared by DMR test.At the end of this study we were able to assess the shelf life of eggs with respect to their oiling, packaging and storage conditions. Availability: Items available for loan: UVAS Library [Call number: 2289-T] (1).
89.
Genetic Diversity Among Different Isolates Of Pasteurella Multocida From Poultry
by Arslan Sardar (2013-VA-282) | Dr. Imran Altaf | Prof. Dr. Aftab Ahmad Anjum | Dr. Sehrish Firyal.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: Fowl cholera is an acute bacterial disease of broiler breeders and layer breeders caused by Pasteurella multocida. In the present study, 10 isolates from different areas of Punjab were purified. These samples were confirmed by API Kit. Different molecular techniques like PCR and RFLP were used to investigate variation at the molecular level among 10 isolates collected from different areas of Punjab. Different mutations were observed among 10 field isolates at different mutation sites by sequencing. Phylogentic tree was also made using MEGA6 software that supported the sequencing results. ‘Msp1’ endonuclease cleaved bacterial whole genome at different cutting sites, all 10 isolates collected from different districts of Punjab cleaved into 3 to 5 fragments ranging from 600 to 10000 base pairs which showed the genetic variation among 10 isolates of P.mulocida. Availability: Items available for loan: UVAS Library [Call number: 2315-T] (1).
90.
Antibacterial And Cytotoxic Evaluation Of Different Extracts Of Zingiber Officinale Rhizome Against Common Poultry Pathogens
by Ghalia Qayyum (2013-VA-779) | Dr. Aqeel Javeed | Dr. Qamar Niaz | Prof. Dr. Aftab Ahmad Anjum.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: Antimicrobial compounds having plant origin inhibit bacteria through different mechanisms and can be used for the treatment of infections against resistant microbes. Majority of antibacterial drugs in clinical use are derived from natural origin. Hence, the present study is designed for antibacterial and cytotoxic evaluation of different extracts of Zingiber officinale rhizome against common poultry pathogens.
The four sequential i.e. hexane, chloroform, ethanol and aqueous extracts of Zingiber officinale were prepared by soxhlet extraction. Antibacterial activity of these extracts was determined by agar well diffusion method against Staphylococcus aureus, Clostridium perfringens type A, Escherichia coli, Salmonella enterica and Haemophilus paragallinarum. Zone of inhibitions were determined by well diffusion method. MICs of plant extracts were determined by micro broth dilution method. Cytotoxic activity was evaluated by applying MTT assay on Vero cell lines
The zone of inhibitions showed by hexane, chloroform, ethanol and aqueous extracts of Zingiber officinale against Staphylococcus. aureus were 12.33mm, 13.67mm, 16.33mm and 14mm; against Clostridium perfringens type A were 12mm, 16.33mm, 14mm and 8.33mm; against Escherichia coli were 14.33mm, 13.33mm, 14.33mm and 12mm; against Salmonella enterica were 17mm, 17.33mm and 12mm; against Haemophillus paragallinarum were 12.67mm, 13mm and 14mm respectively. Hexane extract showed no zone of inhibition against Salmonella enterica and aqueous extract was ineffective against Haemophillus paragallinarum.
MICs values of hexane, chloroform, ethanol and aqueous extracts of Zingiber officinale rhizome against Staphylococcus. aureus were 2500µg/ml, 625µg/ml, 2500µg/ml and 2083.33µg/ml; against Clostridium perfringens type A were 2500µg/ml, 312.5µg/ml, 1250µg/ml and 5000µg/ml; against Escherichia coli were 5000µg/ml, 1250µg/ml, 5000µg/ml and 5000µg/ml; against Salmonella enterica were 312.5µg/ml, 5000µg/ml, 5000µg/ml; against Haemophillus paragallinarum were 2500µg/ml, 1458.33µg/ml and 2500µg/ml respectively. MIC was not performed against hexane extract of Salmonella enterica and aqueous extract of Haemophillus paragallinarum as no zone of inhibition observed against them. Hexane extract of Zingiber officinale rhizome was cytotoxic at concentration ≥ 750µg/ml, chloroform extract at concentration ≥ 1500µg/ml and aqueous extract at concentration ≥5000µg/ml. Ethanol extract at concentration ranging from 1500µg/ml to 2.92µg/ml was not cytotoxic to cell.
The indigenous plant Zingiber officinale have antibacterial activity against common poultry pathogens and helpful to develop new drug from plant origin.
Availability: Items available for loan: UVAS Library [Call number: 2324-T] (2).
91.
Antibacterial And Cytotoxic Evaluation Of Different Extracts Of Zingiber Officinale Rhizome Against Common Poultry Pathogens
by Shumaila Nawaz (2013-VA-442) | Dr. Muhammad Adil Rasheed | Dr. Aqeel Javeed | Dr. Aftab Ahmad Anjum.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: Plants produce a diverse range of bioactive molecules, making them rich source of
different types of medicines. Calotropis procera, a giant milk weed, is known for its
pharmacological importance for centuries. This shrub has been known to possess analgesic,
antitumor,
antihelmintic,
antioxidant,
hepatoprotective,
anti-diarrhoeal,
anticonvulsant,
antimicrobial, oestrogenic, anti-nociceptive and anti-malarial activity. A very little information is
available regarding the antibacterial and cytotoxic activity of Calotropis procera so the present
study is designed to evaluate the antibacterial and cytotoxic activity of this plant. This study was
conducted to access antibacterial and cytotoxic activity of Calotropis procera.
Hexane, chloroform and ethanol, aqueous extracts were prepared by sequential extraction
method and antibacterial activity was evaluated against Staphylococcus aureus, Escherichia coli,
Salmonella enterica, Clostridium perfringens type A and Haemophilus paragallinarum by agar
well diffusion method in which inhibitory zones were measured. The extracts which showed the
antimicrobial activity were evaluated for cytotoxicity by using MTT assay on Vero cell line. Cell
culture media was prepared and cell lines were propagated, monolayer formed. Monolayer was
exposed to plant extract dilutions. After 24-48 hours, MTT dye was introduced and cell survival
percentage was calculated.
Statistical analysis was conducted with Statistic Package for Social Sciences (SPSS for
windows version 16, SPSS inc, Chicago, IL, USA). Results will be compared using one way
ANOVA analysis.
102
SUMMARY
Chloroform and ethanol extracts of Calotropis procera leaves have antibacterial activity.
It may help to design traditional medicines for the development of therapeutic agent which will
be more safe, effective and economical.
Availability: Items available for loan: UVAS Library [Call number: 2330-T] (1).
92.
Production Of Single Cell Protein By Using Banana Peels As Substrate And Its Biological Evaluation In Broiler Chicks
by Muhammad Sheraz Yasin (2012-VA-603) | Miss Shagufta Saeed | Dr. Muhammad Tayyab | Prof. Dr. Aftab Ahmed Anjum.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: The term single cell protein (SCP) refers to dead, dry microbial cells or total proteins extracted from pure microbial cell culture and is produced using a number of different microorganisms including bacterium, fungus and algae. It can also be called biomass, bioprotein or microbial protein.
Besides high protein content (about 60-82% of dry cell weight), SCP also contains fats, carbohydrates, nucleic acids, vitamins and minerals.
Fermentation media containing grinded banana peel as substrate was used to check the production of single cell protein for the selected Arachniotus sp. Different parameters were optimized for higher production of SCP e.g: Incubation period, pH, volume of inoculum, carbohydrate source, concentration of corn steep liquor and ionic salts concentration.
The biomass yield was estimated for total protein content by Lowrymethod. Biomass produced from fermentation was used for biological evaluation in feed trials of broiler chicks.
It is found that Arachniotus sp gave maximum single cell protein 7.49 g/L using 10 g banana peels at 72 hours incubation period. And protein concentration increased 7.58 g/L by optimizing volume of inoculum 2ml. It is observed in present study carbohydrate source also increases the protein concentration 8.41 g/L when carbohydrate source was optimized (glucose 3%).
Later on it was found that nitrogen source also enhance the protein production upto 12.61 g/L by using 2% corn steep liquor. Results also revealed that ionic salt concentration also play important role in the production of biomass protein, addition of 0.075% CaCl2.H2O produced 14.45 g/L single cell protein using above mentioned optimized conditions. 0.050 %
K2HPO4 produced 15.06 g/L. Addition of 0.050% MgSO4.7H2O produced maximum protein 15.86 g/L.
Biological evaluation in broiler chicks of this biomass protein shown there is no deleterious effects on weight gain, feed conversion ratio, protein efficiency ratio and net protein utilization. Maximum weight gain observed 215.6 grams in the group (C) in which 50% sunflower meal was replaced with biomass protein.
Feed conversion ratio in group (C) was 2.64 in which 50% sunflower meal was replaced by biomass protein and in group (B) was 2.51 in which 25% sunflower meal was replaced. And in control group (A) feed conversion ratio was 2.41.
Protein efficiency ratio was observed with non-significant value. And same results were shown by Chaves et al (1988) who reported non-significant differences among the standard and test diet when Chaetominumcellulolyticum biomass was fed to chicks. Net protein utilization observed in present study gave significant P value among the groups.
So it is concluded that single cell protein produced by this method is cheap and can be used in the food industry as food supplements and can also be included in poultry feed. The study findings suggested that microbial biomass produced by Arachniotus sp using banana peels as substrate can be replaced upto 50% of the protein supply by sunflower meal without any deleterious effects on growing broiler chicks. Moreover, it will also help in the reduction of pollution by using waste i.e. banana peel for useful purpose.
Availability: Items available for loan: UVAS Library [Call number: 2347-T] (1).
93.
Status Of Brucellosis And Its Effect On Hemogram And Serum Biochemistry In Indigenous, Cross-Bred And Exotic Dairy Cattle Herds
by Muhammad Hareem Afzal (2008-VA-250) | Dr. Muhammad Avais | Dr. Jawaria Ali Khan | Prof. Dr. Aftab Ahmad Anjum.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: Brucellosis mainly infects food animals such as cattle, buffalo, goats and sheep. Brucella abortus is the principal cause of brucellosis in cattle and is shed from the infected animal at or around the time of calving or abortion. The present study was conducted on 450 animals on three different strains/breeds of cattle i.e. Exotic (150), Cross-bred (150) and local cattle (150) from 10 different privately owned livestock farms of varying holdings of district Lahore. An epidemiological questionnaire focusing on herd traits as well as husbandry and sanitary practices that could be associated with the risk of Brucellosis infection was completed. Serum samples were collected and analyzed using Rose Bengal Plate Test (RBPT). The serum samples positive for Brucellosis through RBPT further subjected to Serum Agglutination Test (SAT). To check the effect of Brucellosis on hemogram, blood samples from 18 cattle (n=6 indigenous; n=6 cross-bred; n=6 exotic) positive for Brucellosis and 18 animals (n=6 indigenous; n=6 cross-bred; n=6 exotic) negative for brucellosis were collected and processed for TLC, DLC, RBC, Hb, MCV, MCHC MCH and platelets using automated haematology analysed at UDL, UVAS, Lahore. Similarly, to see the effect of Brucellosis on Serum biochemistry, serum samples from 18 cattle (n=6 indigenous; n=6 cross-bred; n=6 exotic) positive for Brucellosis and 18 animals (n=6 indigenous; n=6 cross-bred; n=6 exotic) negative for brucellosis collected and analysed for glucose, total protein, albumin, Creatinine, Alanine Aminotransferase (ALT), Aspartate Aminotranferase (AST) and Sorbitol Dehydrogenase (SD) using commercially available kits.
Summary
62
RBPT revealed overall prevalence 17.7% higher than SAT 10.6%. Prevalence of brucellosis is higher in Cross-Bred (22.7%) followed by local cattle (18.9%) and exotic (12%).
Hemato-boichemical results showed that increase in TLC, MCV While slight changes in Hb, MCHC, RBC and values of MCV stays within normal range. On the other hand serum biochemistry increase in AST while decrease in ALT and SD found. Availability: Items available for loan: UVAS Library [Call number: 2348-T] (1).
94.
Mutational Screening Of The RB1 Gene In Pakistani Patients With Retinoblastoma
by Saeeda Kalsoom (2007-VA-555) | Dr. Muhammad Wasim) | Dr. Khushnooda Ramzan | Dr. Ali Raza Awan | Dr. Aftab Ahmad Anjum.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: Retinoblastoma is a neonatal intraocular tumor caused by biallelic inactivation of RB1 gene. Rb
patients and asymptomatic carriers undergo a series of clinical tests for diagnosis and tumor
treatment. These clinical examinations prove to be expensive and time consuming. On the other
hand if the proband’s RB1 gene mutation status is determined by genetic testing, it can prove as
more significant and cost effective diagnostic methods. Secondly, only those asymptomatic or at
risk carriers with the mutation, require clinical surveillance while those proven to be unaffected
do not require additional clinical examinations. Furthermore early diagnosis of Rb by molecular
testing can enable and enhance clinical management, earlier treatment, follow-up care, carrier
screening, genetic counseling, prenatal diagnosis and reproductive planning in predisposed
families. Irrespective of the importance of molecular testing of Rb patients, in Pakistan only a
few clinical reports on Rb are available so, there was a dire need to find RB1 mutations in
Pakistani Rb patients and to set a molecular based diagnosis for poor affected families. Keeping
in view the importance of molecular diagnosis, in this study a reliable genetic test has been
developed to detect the RB1 germline mutations in Pakistani Rb patients.
During this study, 70 Rb patients including 38 unilateral and 32 bilateral cases were enrolled,
from different regions of Pakistan. By using direct sequencing method, seven novel and twelve
reported RBI mutations were found. The novel mutations included three frameshift mutations
(c.1116_1119delCACT in exon 11, c.1436_1437delAC in exon 16 and c.2060_2061insTCATT
in exon 20) and four substitutions (c.148G>T in exon 2, c.610G>T in exon 2, g.94G>C in exon
7, c.947A>T in exon 10 and g.1991G>C in promoter region) while twelve reported mutations in
146
22 patients included, 9 substitutions (c.160G>T in exon 2, c.289G>T in exon 3, c.751C>T in
exon 8, c.920C>T in exon 9, c.967G>T in exon 10, c.1072C>T in exon 11, c.1654C>T in exon
17, c.2063T>C in exon 20 and c.2359C>T in exon 23), one frameshift mutation (c.772_776del in
exon 8) and two splice site mutations (c.380+1G>T and c.1215+1G>A in intron 3 and 12
respectively). Mutation detection rate was found to be 77.8% in (7/9) bilateral familial, 50% in
(2/4) unilateral familial, 56.5% in (13/23) bilateral sporadic and 14.7% in (5/34) unilateral
sporadic patients while overall rate of mutations in bilateral and unilateral patients was detected
as 62.5% (20/32) and 18.4% (7/38) respectively. Beside mutations one novel c.940-64C>T
(intron 9) and nine reported intronic variants c.380+45 C>T (intron 3), c.501-77G>A (intron 4),
c.1128-72T>G (intron 11), c.1695+99A>T (intron 17), c.1695-1696delAA (intron 17), c.1815-
104A>G (intron 18), c.1961-10T>C (intron 19), c.2663+33T>C (intron 25) and c.2664-10T>A
(intron 25) were also found. Carrier screening facility was also provided to six asymptomatic
siblings (as possible carriers) of familial proband but none of them was found to be diseased.
Hopefully, in future the findings and developed protocol of this study will help to reveal the
molecular basis of Rb in Pakistani Rb patients which additionally help to secure vision and life
of Rb patients. Further, in Pakistan there is dire need to develop “National Rb Registry Centre”,
to register all new Rb cases for finding incidence rate and prevalence of Rb in Pakistan. Beside
this other related issues like financial constraints, health education, planning and awareness
about Rb, occupational training for health providers, capacity building for neonatal
ophthalmologic screening and cosmetic rehabilitation for surviving Rb patients are important and
should consider. Availability: Items available for loan: UVAS Library [Call number: 2370-T] (1).
95.
Proteomic And Genomic Analysis Of Methicillin-Resistant Staphylococcus Aureus And Efficacy Of Indigenous Medicinal Plants Essential Oils
by Sarwat Ali Raja | Prof. Dr. Muhammad Ashraf | Dr. Tayyaba Ijaz | Dr. Aqeel Javeed | Prof. Dr. Aftab Ahmed Anjum.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: A Cohort study (prospective and observational) was performed to study the prevalence of Methicillin resistant Staphylococcus aureus from the healthy individuals of community, hospitalized patients and associated health-care workers and indigenous plants essential oils were screened as new, improved & potent antibacterial/s against resistant strains of MRSA.
The method involved isolation and identification of MRSA from surgical wounds of hospitalized patients & associated health care workers in a tertiary care hospital in Lahore and healthy volunteers from the community. Plant essentials oils & extracts were evaluated for their antibacterial activity against selected MRSA isolates. Oils were recovered by steam distillation using an all-glass distillation assembly. Then in vitro sensitivity and MICs of plant essential oils were determined using vancomycin and linezolid as commercial standards. The essential oils were screened further for the active constituents by column chromatography using various solvents and identification of compounds were performed by GC/MS analysis and the fractions which showed prompt results were evaluated for antimicrobial activity against the MRSA isolates in quest to find new therapeutic options. Finally effective essential oils and their active fractions were studied for their toxicity using in vitro Genotoxic assays such as Ames and Comet assays. To further ensure their beneficial effects antimutagenic effect of the essential oils were also studied.
Prevalence of S. aureus among patients was 52.9%, in HCWs 86.5% and in community 74% with an overall percentage of 72.6%. Among S. aureus those declared as MRSA were 91.8% from patients, 50.6% from HCWs and 59.5% from community with an overall percentage of 62.2% MRSA. Among the isolated MRSA overall 90.6% were Coagulase positive and 75.2% were biofilm positive.
SUMMARY
211
The pattern of MRSA resistance against current antibiotics have shown an overall increase in the resistance with maximum shown for lincomycin followed by tetracycline, ampicillin, fusidic acid, amoxicillin and piperacillin with tazobactam. The most effective options among current regime were tigecyclin, amikacin and meropenem showing an overall least resistance. Resistance against linezolid was observed with an overall percentage of 25.6 % and vancomycin 33.3% by disc diffusion method.
The MRSA isolates resistant to one or more groups of antibiotics were declared as MDRs. Among patients and health-care workers all were declared as MDRs where as in community 93.1% isolates were MDRs.
Upon Protein profiling using whole cell proteins 44 bands of the polypeptides were produced with molecular size 10-200kDa from the three sampling groups and were categorized into 5 clusters showing an overall significance correlation with each other explaining an interesting fact that all these strains were interlinked establishing the fact of flow of hospital acquired MRSA in the community and vice versa. This analysis also gave an insight in explaining the fact of horizontal transmission of infection within the hospital.
Keeping in view the raise in resistance among current available antibiotics indigenous medicinal plants essential oils were screened for active constituents exhibiting anti-bacterial effects against MRSA isolates.
Maximum yield was obtained from Carum copticum followed by Cuminum cyminum and minimum yield was obtained in case of Zingiber officinale. Upon qualitative analysis of all five essential oils Carum copticum essential oil showed zones of inhibition greater than the standards vancomycin and linezolid followed Cuminum cyminum and Zingiber officinale in all three
SUMMARY
212
sampling groups. Anethum sowa and Myristica fragrans essential oils showed no activity against MRSA.
Minimum inhibitory concentration of the three essential oils determined by micro broth dilution method indicated that Carum copticum showed least value in all three types of MRSA isolates followed by Zingiber officinale and Cuminum cyminum.
Effective essential oils were further fractioned using silica gel gravity columns. All the fractions obtained were screened for the anti-bacterial activity against all three types of MRSA isolates. Only fraction F1 of Carum copticum showed activity greater than pure essential oil and the two commercial standards of vancomycin and linezolid.
For the identification of active constituents GC/MS analysis was performed on all three essential oils and their respective fractions. In case of fraction F1 the most dominant constituents were Carvacrol, p-Cymene, Ʈ-Terpinene and Apiol. In other two plants none of the fractions were effective. Therefore it was concluded to use pure essential oils in case of Zingiber officinale and Cuminum cyminum rather than their individual fractions and incase of Carum copticum Fraction F1 has shown superior activity.
Finally these essential oils were tested for possible mutagenic effect using bacterial reversion mutation assay and Comet assay. No mutagenic effects were observed at MIC and above doses. These effective essential oils were also evaluated for possible antimutagenic effect. Both Carum copticum and Zingiber officinale essential oils showed strong antimutagenic effects and weak antimutagenic effect by Cuminum cyminum. Upon analysis of nuclear damage none of the plants essential oils and fraction F1 of Carum copticum showed genotoxic effects and indicated to be safe. Thus from the study it was concluded that Carum copticum essential oil and its fraction F1 were the most effective to be further investigated as an alternative treatment for MRSA infections. Availability: Items available for loan: UVAS Library [Call number: 2410-T] (1).
96.
Sero-Screening Of Camels For Different Infectious Diseases
by Mazia Khalid (2008-VA-358) | Dr. Aamir Ghafoor | Prof. Dr. Aftab Ahmed Anjum | Dr. Wasim Shehzad.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: Camel is the precious and important animal in Pakistan. Camel is the most well adapted livestock species, survives and produces in climatic extremes and is well appreciated for its significance in the pastoral economy of the province. The camel being an important livestock species uniquely adapted to hot and arid environments and therefore contributes significantly to the food security of the nomadic pastoral households. Although camel being hardiest animal is less susceptible to diseases as compared to other livestock animals but literature shows that some diseases are still prevalent in camels. In view of the significance of camel as livestock animal as well as the symbol of cultural heritage of the nomadic pastoralists, there is a need to combat different diseases to which camels are susceptible and then appropriate control strategies should be applied.
Present study was designed to check the percentage positivity of different major diseases in camels that may pose serious issue relating to camel health and its importance as an important livestock animal. The diseases included in this study are Q fever, Brucellosis, FMD, CBPP and Neosporosis. ELISA is used to detect antibody prevalence by using specific kit based protocol for each disease whereas in case of Brucellosis RBPT is also used as basic screening test.
And it was found that Q fever has highest percentage seropositivity in both districts as compared to other diseases whose presence in camels was found to be almost seronegative.
So it was concluded that camel is still resistant to many diseases though some diseases are still prevalent in camels and these diseases should be controlled through public awareness and routine screening. Availability: Items available for loan: UVAS Library [Call number: 2401-T] (1).
97.
Antibacterial And Cytotoxic Evaluation Of Sequential Extracts Of Eucalyptus Globulus Leaves Against Common Poultry Pathogens
by Asma Iqbal (2013-VA-563) | Dr. Muhammad Adil Rasheed | Dr. Qamar Niaz | Prof. Dr. Aftab Ahmad Anjum.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: Phytomedicines mark the major component of health care as natural medicines have always provided the strong foothold for the discovery and manufacturing of synthetic drugs. So plants are a rich source of bioactive compounds having many therapeutic activities and majority of them are still untapped. Eucalyptus globulus is a medicinal plant known for its value to cure asthma, respiratory infections, cough and allergic reactions. The antimicrobial activity, insecticidal and hypoglycemic activity have also been credited to the plant. Most of the studies have been conducted on the essential oils of Eucalyptus globulus and little work has been reported on extracts. Whereas, sequential extracts has not been employed yet.
Hexane, chloroform and ethanol, aqueous extracts were prepared by the sequential extraction on Soxhlet apparatus and antibacterial activity was evaluated against Staphylococcus aureus, Escherichia coli, Salmonella enterica, Clostridium perfringens type A and Haemophilus paragallinarum by agar well diffusion and micro broth dilution method. The zones of inhibition and minimum inhibitory concentration were determined. The extracts showing antimicrobial activity were further evaluated for cytotoxicity by using MTT assay on Vero cell line. The cell culture media was prepared and cell lines were propagated to form monolayer then monolayer was exposed to plant extract dilutions. After 24-48 hours, MTT dye was introduced and cell survival percentage was calculated.
The statistical analysis was conducted with help of Statistic Package for Social Sciences (SPSS for windows version 16, SPSS inc, Chicago, IL, USA) and results were compared using one way ANOVA.
Summary
89
The zones of inhibitions showed by hexane, chloroform, ethanol and aqueous leaf extracts of Eucalyptus globulus against Staphylococcus aureus were 0.0, 19.3, 20.3 and 23.3mm; against Clostridium perfringens type A were 14, 22.3, 14.0 and 15.3mm; against Escherichia coli were 0.0, 12.6, 13.3 and 15.6mm; against Salmonella enterica were 10, 12.3, 18.6 and 21mm; against Haemophilus paragallinarum were 0.0, 8.6, 14 and 18mm respectively. Hexane extract showed no zone of inhibition against Staphylococcus aureus, Escherichia coli and Haemophilus paragallinarum.
The MICs values of hexane, chloroform, ethanol and aqueous leaf extracts of Eucalyptus globulus against Staphylococcus aureus were 0.00, 104.1, 32.55 and 312.5 μg/ml; against Clostridium perfringens type A were 52.08, 39.06, 16.27 and 312.5 μg/ml; against Escherichia coli were 0.00, 78.12, 260.4 and 625.0 μg/ml; against Salmonella enterica were 13.02, 104.1, 130.2 and 416.6 μg/ml; against Haemophillus paragallinarum were 0.00, 104.1, 260.4 and 416.6 μg/ml respectively. MIC was not performed against Staphylococcus aureus, Escherichia coli and Haemophilus paragallinarum for hexane extract as no zone of inhibition was observed against them.
Hexane extract of Eucalyptus globulus was cytotoxic at concentration ≥ 312.5μg/ml, chloroform extract at concentration ≥ 375μg/ml, ethanol extract at concentration ≥ 625μg/ml and aqueous extract was cytotoxic at concentration ≥312.5 μg/ml.
The indigenous plant Eucalyptus globulus has antibacterial activity against common poultry pathogens and can be helpful for development of new drugs of plant origin. Availability: Items available for loan: UVAS Library [Call number: 2429-T] (1).
98.
Effect Of Bio-Stimulation On Estrus Expression And Pregnancy Rate In Cidr Based Synchronization Protocol In Nili-Ravi Buffalo
by Abdul Waheed (2009-VA-133) | Dr. Aijaz ali Channa | Dr. Syed Murtaza Hassan Andrabi | Prof. Dr. Mian Abdul Sattar | Prof. Dr. Aftab Ahmad Anjum.
Material type: ; Literary form:
not fiction
Publisher: 2016Dissertation note: Our water buffalo (Bubalus bubalis) has much potential for production of milk. But this
animal has some problems regarding reproduction including delayed puberty, poor estrus behavior,
silent heat, long postpartum period and low conception rate by artificial insemination. This leads
to poor reproduction and hence great economic loss. Therefore, the requirement is to address these
problems efficiently and formulate more effective techniques for improvements. Researchers have
devised many estrus synchronization protocols (PGF2α, P4, GnRH, eCG, hCG etc.) that help
bringing many animals in heat and hence improve the reproductive performance when fixed time
artificial insemination is combined with them. But these protocols give inconsistent results when
they are applied on buffaloes making it necessary to improve the techniques.
This study was planned on the hypothesis that presence of bull (bio-stimulation), at the
time of synchronization, may play an important role in enhancement of estrus intensity and fertility
rate in Nili-Ravi buffaloes. Seventy one adult buffaloes were randomly selected from different
areas of field conditions and LRS (NARC) and subjected to CIDR based heat synchronization in
combination of either bio-stimulation or non-stimulation. The animals were observed for
behavioral estrus signs twice a day starting after 12 hours of CIDR removal till 96 hours.
Pregnancy diagnosis was done by rectal palpation 60 days post CIDR removal. Estrus response
and pregnancy rate were analyzed by Chi-square test using MINITAB version 15. Estrus signs and
total estrus intensity were compared by Mann Whitney U test. Difference was considered
significant at probability level of (P < 0.05).
In peri-urban areas, more animals from bio-stimulated group showed better behavioral
estrus signs, more total intensity score and significantly higher pregnancy rate as compared to nonSUMMARY
63
stimulated group of animals. At LRS (NARC), more animals from non-stimulated group were
found in behavioral estrus but intensity of heat signs was high in bio-stimulated animals.
Pregnancy rate was also higher in non-stimulated animals but the difference was not significant.
Overall, in this study, we got higher pregnancy rate in bio-stimulated animals than non-stimulated
group which indicates a positive response of bull stimulation on reproductive performance of Nili-
Ravi buffaloes who were synchronized with CIDR based estrus synchronization protocol. Availability: Items available for loan: UVAS Library [Call number: 2469-T] (1).
99.
Antibacterial And Cytotoxic Evaluation Of Sequential Extracts Of Astragalus Membranaceus Roots
by Sadia Alvi (2013-VA-595) | Dr. Aqeel Javeed | Dr. Muhammad Ovais Omer | Prof. Dr. Aftab Ahmad Anjum.
Material type: ; Literary form:
not fiction
Publisher: 2015Dissertation note: The present study was designed to evaluate antibacterial and cytotoxic evaluation of different extracts of Astragalus membranaceus root against common poultry pathogens. Sequential extraction with hexane, ethanol, chloroform and aqueous solvents was prepared and antibacterial activity was evaluated by using agar well diffusion. Minimum inhibitory concentration (MIC) of plant extracts was evaluated by micro broth dilution test. The extracts exhibiting antimicrobial activity were further evaluated for cytotoxicity by using MTT assay on Vero cell line. Cell culture media was prepared and cell lines were propagated, monolayer was formed. This monolayer was exposed to plant extract dilutions. After 24-48 hours, MTT dye was introduced and cell survival percentage was calculated. Statistical analysis was conducted with Statistic Package for Social Sciences (SPSS for windows version 16, SPSS inc, Chicago, IL, USA). Results of antibacterial activity and MTT assay were compared using DMR posthoc test. Growth of Clostridium perfringens, Escherichia coli, Haemophilus species, Salmonella enterica and Staphylococcus aureus inhibited by all extracts of Astragalus except aqueous extract which shows no zones of inhibition against C. perfringes. MIC values were higher for aqueous extract against all selected bacteria and lowest for chloroform against E. coli, S. enterica and Staph. aureus (208.3ug/ml, 156.25ug/ml, 78.125ug/ml respectively) for hexane against Haemophilus species (833.3ug/ml) and for all three extracts against C.perfringes (1250ug/ml). Hexane, chloroform and ethanol extracts were appeared to be safe at all concentrations except ≥ 2000μg/ml, ≥1000μg/ml and ≥3000μg/ml respectively while aqueous extracts showed cytotoxicity at concentrations ≥625μg/ml. Astragalus membranaceus
SUMMARY
104
showed antibacterial activity against all selected pathogens. Chloroform and hexane extracts showed greater antibacterial activity than ethanol and aqueous. Cytotoxicity values for chloroform extract are safer than rest of three extracts. Astragalus membranaceus may be used to design traditional medicines for the development of therapeutic agent which will be more safe, effective and economical. Availability: Items available for loan: UVAS Library [Call number: 2444-T] (1).
100.
Antibacterial And Cytotoxic Evaluation Of Sequential Extracts Of Ocimum Basilicum Leaves Against Common Poultry Pathogens
by Shomaila Naz (2013-VA-1001) | Dr. Muhammad Ovais Omer | Dr. Muhammad Adil Rasheed | Prof. Dr. Aftab Ahmad Anjum.
Material type: ; Literary form:
not fiction
Publisher: 2016Dissertation note: Antimicrobial compounds having plant origin inhibit bacteria through different mechanisms and can be used for the treatment of infections against resistant microbes. Majority of antibacterial drugs in clinical use are derived from natural origin. Hence, the present study is designed for antibacterial and cytotoxic evaluation of different extracts of Ocimum basilicum seeds against common poultry pathogens.
The four sequential i.e. hexane, chloroform, ethanol and aqueous extracts of Ocimum basilicum leaves and seeds were prepared by soxhlet extraction. Antibacterial activity of these extracts was determined by agar well diffusion method against Staphylococcus aureus, Clostridium perfringens type A, Escherichia coli, Salmonella enterica and Haemophilus paragallinarum. Zone of inhibitions were determined by well diffusion method. MICs of plant extracts were determined by micro broth dilution method. Cytotoxic activity was evaluated by applying MTT assay on Vero cell lines. All the results were statistically analyzed by one way ANOVA and compared means by Duncan’s multiple range of posthoc test at significance level of P≤0.05.
The results of zone of inhibitions showed by Ocimum basilicum leaves and seeds extracts ranging from 11.33-20.0 mm values of MIC results ranging from 4.889 μg/ml-2500 μg/ml of hexane, chloroform and ethanol. The aqueous extract of Ocimum basilicum have no activity against any bacterial pathogen. Ethanol extract of Ocimum basilicum leaves was cytotoxic at 500 μg/ml. Hexane extract of Ocimum basilicum seeds was cytotoxic at concentration ≥625 μg/ml, chloroform at concentration ≥19.53 μg/ml and ethanol extract at concentration ≥750 μg/ml.
The indigenous plant Ocimum basilicum have antibacterial activity against common poultry pathogens and helpful to develop new drug from plant origin. Availability: Items available for loan: UVAS Library [Call number: 2443-T] (1).
