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

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

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

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Histopathological Investigation Of Pleuropneumonia In Buffaloes Caused By Mycoplasma Bovis

by Ayesha Rabail | Dr. Muti-Ur-Rehman Khan | Dr. Kamran | Prof. Dr. M Younus Rana.

Material type: book Book; Format: print Publisher: 2009-2011Dissertation note: This study was conducted by keeping in view the worldwide importance of Mycoplasma bovis to cause pneumonia and many other diseases, as it causes great economic losses to bovine industry. In the current project the incidence of Mycoplasma bovis to cause pleuropneumonia was studied, and its respective histopathological changes in lungs of the pneumonic adult buffaloes and buffalo calves were examined. 100 lung samples for this purpose (50 lung samples from adult buffaloes and 50 lung samples from buffalo calves) were collected from the Lahore Bakar Mandi Abbatoir. Samples were collected on the basis of following criteria: Red hepatization, grey hepatization, multifocal abscess, necrotic lung tissue. These samples were then divided into two portions, one half placed in 10% buffered formalin in the bottles and other half kept in sterile polythene bag. The portion of lungs for bacteriological study was kept in ice box. Histopathological procedure was performed in the pathology department of University Of Veterinary And Animal Sciences Lahore. The samples were subjected to histopathological procedures and then slides were observed microscopically for the changes. Microscopically pulmonary odema, consolidation, caseous necrosis, abscess infiltration of mononuclear cells, plasma cells, macrophages, neutrophils infiltration were observed. For culturing of Mycoplasma bovis PPLO broth was prepared and samples were inoculated in the broth medium. At 7th day of inoculation the yellow color of the broth medium appeared which was indicative of positive samples. 30% positive samples in adult buffaloes and 36% in buffalo calves were obtained. These samples were then inoculated on the PPLO agar plates for further precision of results. On agar plates typical colonies of the Mycoplasma were observed under bright field compound microscope and 60% positive samples in adult buffaloes and 66% in buffalo calves were obtained. Next step towards the confirmation of Mycoplasma bovis was specific acridine staining, in which positive of Mycoplasma bovis samples gave dull yellow to colorless appearance of yellow broth medium and gave egg fried colony on agar. 78% adult buffalo and 67% buffalo calves showed positive results. These samples were then subjected to final confirmatory test which was growth inhibition disk test, in which hyper immune sera was raised in rabbits and filter paper disks soaked in this sera were used to check the zone of inhibition on cultured agar plates. 70% positive samples in adult buffaloes and 75% in buffalo calves were obtained which confirmed the presence of Mycoplasma bovis. CFU/ml of the positive samples calculated between 105-108. So the incidence of Mycoplasma bovis to cause pneumonia in adult buffaloes and buffalo calves calculated was (10% and 12%) respectively. Availability: Items available for loan: UVAS Library [Call number: 1335,T] (1).

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