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1. Genotyping Of Echinococcus Granulosus And Its Comparative Prevalance In Camels And Human Beings

by Azam Ali | Prf.Dr. Azhar Maqbool | Dr.Kamran Ashraf | Faculty of Veterinary Sciences.

Material type: book Book; Format: print Publisher: 2008Dissertation note: Hydaiidosis is caused by metacestode of the dog worm Echinococcus granulosus. It is a serious problem br both Public health and livestock economy. Echinococcus granaiiosu.s has number of genetically distinct strains which are known to differ morphologically and epidemiologically. Out of 100 camels examined only 25 Samples of hydatid cysts were collected from different organs i.e. livers, kidneys, lungs and hearts from Lahore abattoirs. Fertility and viability of the cysts was observed microscopically. Genotyp ing of Echinococcus granulosus was performed through Polymerase Chain Reaction Restriction Fragment Length Polymorphism (PCR-RFLP). Seroprevalence of hydatidosis in 25 butchers working in abattoir was also determined by the use of Latex agglutination test (LAT) kit for detection ob hydatidosis. Considerable information is available about genetic variants of E. granulosus around the world. Ten genotypes of E. granulosus have been described, which exhibit a diversity of morphology, development, and host range, as contrmed by various studies. In the Mediterranean area, the CI or common sheep strain, G2, Camel strain G6, and the equine strain G4 have been found in Spain, Italy, Lebanon, and Syria To date, molecular studies using mainly DNA sequences have identitied G-6 strain of E. granulosus. This categorization follows very closely the patterns of strain variation emerging from biological and epiderniological traits. In this study we perform serum analysis of butchers to detect antibodies against Echinococcus so that the prevalence of Echinococcus can be checked; the data available indicated that 14% of butcher's population is infected with Echinococcus. In order to confirm the strain of Echinococcus in camels the PCR-RFLP analysis were performed. The data obtained was analysed and it was concluded that the G6 strain of Echinococciis is prevalent in camels in Pakistan. The results demonstrated that PCRRFLP analysis of samples of patients suspected for Echinococcus is a promising diagnostic method and also confirms the type of Echinococcus prevalent in that area and also enables an early direct detection of parasite DNA. This will help to curtail this drastic malady at an early stage and will help to devise the strategy to minimize the losses due to this disease. It is hoped that the findings of the present study will be helpful for further planning about the control of the disease and correlating the prevalence in camels and butchers from the zoonotic point of view. Availability: Items available for loan: UVAS Library [Call number: 1010,T] (1).

2. Molecular Detection And Speciation Of The Canme Piropiasm

by Isma Nazli Bashir | Prof. Dr.Zrafar Iqbal Ch | Dr.Peter J.Irwin | Prof. Dr. Azhar Maqbool | Faculty of Veterinary Sciences.

Material type: book Book; Format: print Publisher: 2008Dissertation note: An epidemiological study of babesiosis in dogs was conducted at Pet center, University of Veterinary and Animal Sciences, Lahore, for one year and information on age, sex and breed was gathered. It was found that from a total number of 6204, dogs up to two years of age were more susceptible than other age groups (2-4, 4-6 and above 6 years).The data regarding genders revealed that males were more prone to the disease than female dogs. As far as the breeds were concerned, crossbred dogs were more susceptible followed by Pointers, Alsatians, German shepherds and Bull terriors.Hot and humid months (June to September) have greater impact on the occurrence of disease. The study regarding identification of ticks revealed that Rhiphicephalus sanguinus is the predominant vector of the disease in Pakistan. Molecular studies were conducted to characterize and identify the species responsible for canine babesiosis in Pakistan. In this regard, a nested polymerase chain reaction-Restriction fragment length polymorphism (PCR-RFLP) technique was employed on different specimens (Blood, Body tissues and Ticks). For this purpose blood samples were collected from twenty four chronically infected dogs and applied on the Flinders Technologies Associates (FTA) cards for transportation to Australia. Different body tissues (Liver, Spleen, Kidney, Intestine, Bone marrow and Pancreas) were procured after euthanizing the two dogs and DNA was extracted, for further studies. Similarly, the eighty eight ticks were also collected from the infested dogs in the 70% ethanol for transportation to Australia. A nested PCR-RFLP assay was used for the detection and differentiation of Piroplasm species on the basis of the 1 8S ribosomal RNA gene. The assay potentially amplified and identified Babesia gibsoni as the main canine piroplasm. Similar assays on the DNA extracted from body tissues and ticks revealed Babesia gibsoni as the main piroplasm. The PCR was found to have a high detection limit (equivalent to i0 dilution), when using the DNA extracted from blood applied to FTA cards, body tissues and ticks. A new technique was developed for extraction of DNA from FTA cards and tick, in this technique, instead of using the FTA specified punching machine, we used scalpel blades, and so the rest of the chemicals used are'generally and easily available. The same protocol was used for extraction of DNA from ticks, only chemicals used in different quantities with different spinning times. Both of which, resulted in cost reduction, less effort and speedy DNA extraction. The technique reported here has the potential to be standardized for routine DNA extractions from FTA cards and ticks. Availability: Items available for loan: UVAS Library [Call number: 1061,T] (1).

3. 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: book Book; 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).

4. Clinico-Epidemiological And Therapeutic Study On Babesiosis In Different Breeds Of Cattle In Balochistan

by Muhammad Essa Kakar (2005-va-229) | Prof. Dr. Muhammad Arif Khan | Prof. Dr. Kamran Ashraf | Prof. Dr. Muhammad Sarwar Khan | Prof. Dr. Muhammad Azam Kakar.

Material type: book Book; Literary form: not fiction Publisher: 2015Dissertation note: Babesiosis which is also called as piroplasmosisis, Texas fever, redwater or tick fever, is an emerging, tick-transmitted (by a vector ixodidea) disease caused by intraerythrocytic parasites of the genus babesia having considerable worldwide economic, medical, and veterinary impact. Keeping in view the importance of babesiosis under local conditions, the present study was designed to evaluate the status babesiosis in Balochistan. For this purpose field and experimental studies were carried in two districts Quetta and Sibi of Balochistan Province to find out the status of babesiosis in Bhag Nari, Holstein Friesian and Crossbred cattle. During field study epidemiological status of babesiosis was highlighted by selecting 600 cattle randomly from each district. The animals were distributed into 2 major groups i.e. Young animals less than 12 months and adult over 12 months of age. These groups were further sub-divided into Young animals (less than 6 months, up to 9 months and up to 12 months) while Adults animals (up to 2 years, 3 years and over 3 years). The vector of babesia was also kept under keen observation for the prevalence/infestation rate, identification and economic losses caused during the course of study. Blood samples were collected from each animal and processed for blood smears examination and PCR for further confirmation of babesia infection. The blood samples were also processed for hematological study to evaluate the effect of babesiosis on different blood parameters. For experimental study 148 animals were selected through clinical signs of babesiosis, blood smear examination and PCR. Out of theses 40 animals were maintained for therapeutic trail to find out the cheapest and easily available drug against bovine babesiosis. For this purpose Neem leaves were used in decoction form while Imidocarb dipopionate was kept as standard control. The Summary 177 results of epidemiological study revealed higher prevalence of babesiosis (20.5%) in district Quetta while 15.16% was recorded in District Sibi. Similarly higher prevalence was recorded in Holstein Friesian than in Crossbred and Bhag Nari cattle respectively in both districts Quetta and Sibi. Furthermore higher prevalence of babesiosis was recorded in adult groups of Holstein Friesian than in Crossbred and Bhag Nari cattle. Similarly season wise higher prevalence of babesia infection was noticed in summer followed by spring, autumn and winter respectively while higher prevalence was noted in female group of animals than male animals. Blood smears examination and PCR confirmed two babesia species i.e. babesia bigemina and babesia bovis. Similarly Boophilus tick species were identified as the vector of babesia parasites. During present study mixed hemoprotozaon infection of babesia mixed with theileria was recorded in both districts. The results of conventional method and modern diagnostic technique (PCR) revealed that PCR identified higher babesia infection during the entire 4 seasons as well as in all age groups whereas blood smears examination was capable to diagnose babesiosis in adult groups during the months of summer and spring season. Breed wise prevalence was also higher in samples treated with PCR than blood smears examination and even samples that were declared negative by blood smears examination were also found positive. The results of complete blood cell count from blood samples of infected experimental animal showed regenerative, macrocytic hypochromic anemia. Blood smear examination showed presence of many babesia with reticulocytes. Abnormalities in erythrocyte structure were seen. The result of blood parameters of total erythrocyte count, total leukocyte count, packed cell volume and hemoglobin showed significant decrease in all three affected Bhag Nari, Holstein Friesian and Cross bred cattle. The values of MCV and MCH were increased and MCHC was slightly less than normal value. No efficacy of neem decoction was noted against bovine babesiosis. Availability: Items available for loan: UVAS Library [Call number: 2367-T] (1).

5. 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: book Book; 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).

6. Effects And Remedial Measures Of Aflatoxin B1 On Bovine Calves In Punjab

by Omer Naseer (2002-VA-65) | Dr. Jawairia Ali Khan | Prof. Dr. Muhammad Sarwar Khan | Dr. Muhammad Ovais Omer.

Material type: book Book; Literary form: not fiction Publisher: 2016Dissertation note: Aflatoxins B1 are most toxic metabolites produced by Aspergillus fungi in/on foods and feeds, probably best known and most intensively researched aflatoxins globally. AFB1 have been associated with several diseases, e.g. aflatoxicosis in livestock, pets including humans throughout the world. Occurrence of AFB1 is influenced by certain environmental factors like geographic location, agro-economic practices and susceptibility of feed commodities to fungal invasion during pre-harvest, storage, and processing periods. AFB1 has grabbed greater attention than any other mycotoxins due to their demonstrated potent carcinogenic effect in susceptible animals and their acute toxicological effects in humans. As the absolute safety will be never achieved, most of the world struggled to limit aflatoxin exposure by imposing regulations on feed commodities. So, in this study, we had collected 67 concentrated samples, thirty six samples from Gujranwala and thirty one from Kasur to examine the occurrence of aflatoxin B1. The aims of this study were to investigate the aflatoxin B1 in calf feed, effect of different concentrations of aflatoxin B1 on productive performance of calves and determine the comparative efficacy of commercially available mycotoxin binders and liver tonics against AFB1 in bovine calves. Feed samples were obtained from different livestock farms and cattle feed mills, toxin levels in each feed sample were determined by HPLC. AFB1 level was higher at feed mills (40.33±2.21 ppb and 49.0±1.95 ppb) than farms (34.96±2.65 ppb and 44.95±2.41 ppb) both in Gujranwala and Kasur respectively. Fungus was isolated and grown on Sabouraud’s dextrose agar on the basis of microscopic characters and species within genus characterized by colony characters/macroscopic characters, mostly Aspergillus species was present in the feed samples which produce mycotoxins. The second most prevalent species were the Fusarium. Mucor and the Pencillium were respectively third and fourth in number. Our results have shown that Alternaria was not present in Gujranwala and Rhizopus was absent in the feed samples collected from the Kasur. Out of mycotoxin contaminated concentrate feed samples, the highest frequency of Aspergillus (43.3%) was observed, followed by Fusaram (38.8%), Mucor (8.9%), Penicillium(5.9%), Rhizopus (1.5%) and Alternaria species (1.5%). Our results also indicated that growth of Aspergillus spp. can be minimized by controlling the different factors like pH, temperature, light and humidity, which are essential for the proper growth and development. The antifungal activity of methanolic extract of clove, neem and garlic was also determined in which maximum MIC showed by garlic. Thirty six bovine calves of 6 to 12 months of age were kept in UVAS, Pattoki campus (Ravi Campus) .in four different replicates having 9 animals each. Different concentrations, i.e. 0.6 mg/kg, 0.8 mg/kg and 1.0 mg/kg was administered along with concentrated feed and check out productive performance along with physiological profile. The most pathological concentration of aflatoxin B1 in experiment number 3 was given to the two groups of bovine calves along with two different commercially available mycotoxin binders i.e. Yeast based and second one was clay based HSCAS mycotoxin binder at recommended doses. Efficacy of mycotoxin binders on feed samples was analyzed by using HPLC and also evaluates the productive performance of the animals.Efficacy of two liver tonics i.e.silymarin and choline chloride was observed on CBC, LFT and RFT of bovine calves. Present study has clearly displayed the adverse effect of aflatoxin B1 on feed consumption, hematological and serum biochemical parameters related to liver and kidney in bovine calf. Results indicated that HSCAS mycotoxin adsorbent was able to fully detoxify aflatoxin B1. Silymarin had great impact on the liver to cope the adverse effects of the AFB1 as compared to the choline chloride, which was proved with the help of CBC, LFT and RFT. Availability: Items available for loan: UVAS Library [Call number: 2630-T] (1).

7. Pathogenesis Of Aflatoxin B1 In Quails Under Experimental Conditions And Detoxification By Biological And Chemical Means

by Sakhra Mahmood (2005-VA-251) | Prof. Dr. Muhammad Younus Rana | Prof. Dr. Asim Aslam | Prof. Dr. Aftab Ahmed Anjum.

Material type: book Book; Literary form: not fiction Publisher: 2016Dissertation note: Secondary metabolites of certain fungi produce toxins under favorable conditions especially while growing on different food grains. Mycotoxins are among major threats to growing poultry industry and human beings. Aflatoxins are closely related, biologically active fungal metabolites and commonly produced by Aspergillus species. A research was carried out to evaluate the ability of Aspergillus flavus for Aflatoxin B1 production using rice, wheat and maize as substrates. Lethal effects on growth performance parameters, hematological and histopathological of graded doses of aflatoxin B1 in quails under experimental conditions were observed. Effect of Aflatoxin B1 on humoral immune response to Newcastle Disease virus vaccine in quails were determined. Biological detoxification of Aflatoxin B1 by Saccharomyces servisiae was evaluated in quails. Comparative evaluations of different commercially available toxin binders were checked. All these experiments were carried out till the six weeks (42 days). Aspergillus flavus was identified on the basis of macroscopic and microscopic characteristics. Rice, wheat and maize grains was used as substrate to check the level of Aflatoxin B1 produced by inoculating an aqueous suspension of 106 spores/ml. Aflatoxin B1 checked by Thin Layer Chromatography (TLC) and quantified by High Performance Liquid Chromatography (HPLC). Quails were reared under standard management conditions in five groups (A, B, C, D and E) having sixty each. Each group was further divided in two independent units. Diets offered to groups were control (without toxins), 0.25, 0.50, 1 and 2 mg Aflatoxin B1/kg feed. One unit of SUMMARY 187 each group was vaccinated with Newcastle Disease Virus (NDV) vaccine while other was not and studied the lethal effects on growth performance, blood parameters, immune response and histopathology of vital organs. At the end of the experiment, it was found that the deleterious effects of Aflatoxin B1 were dose and duration dependent. As the level of the toxin was increased, the lethal effects were prominent. The growth performance parameters including gain in body weight, feed intake and feed conversion ratio was adversely affected at high doses. The body weight gain was significantly reduced in Aflatoxin B1 treated groups as compared to control group. Similarly feed intake and feed conversion ratio were significantly different from the control group. The hematological studies exhibited that aflatoxin B1 significantly reduced the hemoglobin, packed cell volume and total leukocyte count whereas the erythrocyte sedimentation rate was significantly increased as compared to control group. The immune response against NDV vaccine was adversely effected in Aflatoxin B1 treated groups and values of Antibody titer in AFB1 were significantly low as compared to group A( control) In the second experiment, Saccharomyces cervisae (SC) dried powder was mixed in basal quail diet having 0.5mg Aflatoxin B1 for all experimental groups and control was without toxins. SC was added at levels of 0.5 gm, 1.0 gm and 2.0 gm /kg of feed. It was recorded that Saccharomyces cervisae (yeast) have the potential to remove the deleterious effects of Aflatoxin B1. Yeast effectively detoxified the Aflatoxin B1. The results recorded of growth performance and other parameters were non-significantly different from the control group. Chemical detoxification of Aflatoxin B1 was evaluated in quails using commercially available toxin binders. Toxin binders used were activated charcoal, kaoline, Myco AD and selenium plus vitamin E and mixed in basal quail diet having 0.5mg Aflatoxin B1 for all experimental groups and control was without toxins. The Myco AD and selenium plus vitamin E showed the highest detoxification potential as compared SUMMARY 188 to other chemical toxin binders. Groups E and F showed the results of growth performance, hematological, immune response and histopathological were non-significantly different from the control group (A). Kaolin was moderately detoxifying the toxin. Presence of aflatoxin B1 in soft tissues was checked by TLC and quantified using HPLC. The liver exhibited the residues of Aflatoxin B1 at high doses of toxin. Group D and E rearing on feeds having 1mg AFB1 /Kg feed and 2mg AFB1 /Kg feed of toxin showed the residues of AFB1 in liver and kidney. Statistical means for growth performance parameters, hematological, immune response and histopathological scores in each subunit of quails were analyzed by applying one way ANOVA and Duncans‟s Multiple Range (DMR) test at 95% probability. Aflatoxin B1 is lethal and lowers the performance of birds. The lethal effects can be detoxified by biological and chemical means to lower the economic losses to poultry industry. It can be concluded that biological detoxification is preferably better as compared to chemical detoxification. Availability: Items available for loan: UVAS Library [Call number: 2670-T] (1).



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