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Chaudhary Sarwan Kumar Himachal Pradesh Agriculture University, Palampur

Himachal Pradesh Krishi Vishvavidyalaya (renamed as Chaudhary Sarwan Kumar Himachal Pradesh Krishi Vishvavidyalaya in June, 2001) was established on 1st November, 1978.The College of Agriculture (established in May, 1966) formed the nucleus of the new farm University. It is ICAR accredited and ISO 9001:2015 certified institution. The Indian Council of Agricultural Research has ranked this University at eleventh place among all farm universities of the country. The University has been given the mandate for making provision for imparting education in agriculture and other allied branches of learning, furthering the advancement of learning and prosecution of research and undertaking extension of such sciences, especially to the rural people of Himachal Pradesh. Over the years, this University has contributed significantly in transforming the farm scenario of Himachal Pradesh. It has developed human resources, varieties and technologies and transferred these to farming community enabling the State to receive the “Krishikarman award” of Govt. of India four times in row for food grain production among small states of the country. Today, the State has earned its name for hill agricultural diversification and the farming community has imposed its faith in the University.

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  • ThesisItemOpen Access
    STUDY ON PATHOLOGY OF TERMINAL ILEUM IN SHEEP WITH PARTICULAR EMPHASIS ON PARATUBERCULOSIS
    (CSKHPKV, Palampur, 2014-07-19) Maity, Madhulina; Gupta, Vipin K.
    The present research work was planned to study the pathology of terminal ileum and associated lymph nodes in sheep with particular emphasis on paratuberculosis and to detect the antibody against M. avium subsp. paratuberculosis (MAP) using suitable serological method(s). Out of the 45 sheep samples collected, 39 were used to study paratuberculosis as the remaining six samples showed incidental lesions in lymph nodes. On gross examination, the lesions were scored from mild to moderate on the basis of thickening and corrugation in terminal ileum and enlargement and presence of greyish-white patches on cut surface of lymph nodes (LNs). A total of 34 (87.18%), 3 (7.70%) and 1 (2.56%) samples were found to be showing lesions suggestive of paratuberculosis and scored as mild, moderate and severe, respectively. Ziehl-Neelsen (ZN) stained tissue impression smears made from ileo-caecal lymph node (ICLN), mesenteric lymph node (MLN) and terminal ileum, demonstrated acid-fast bacilli (AFB) in nine (23.08%) cases. On histological examination, the tissue samples were graded from 0 to IV on the basis of type and amount of the cellular infiltrates (macrophages and epitheloid cells) and the nature and extent of granulomatous reaction. The only (2.56%) Grade I case revealed infiltration of a few macrophages and epitheloid cells with formation of focally distinct microgranuloma in the lamina propria of the villi as well as in the LNs. Twenty-one (53.84%) cases with Grade II lesion characterized by moderate infiltration of macrophages and epitheloid cells in the lamina propria of the villi as well as in the LNs were observed. Thirteen (33.33%) Grade III cases showed granulomatous enteritis composed of groups of macrophages and epitheloid cells distributed in a diffuse manner throughout the ileal mucosa and lymph nodes. Grade IV cases revealed the same lesions as described in Grade III but with presence of giant cell(s). The focal areas of caseous necrosis, with or without mineralization, were observed in one (Grade II), four (Grade III), three (Grade IV) sheep. Only one case of Grade III showed AFB on ZN stained ileum and ICLN tissue sections (paucibacillary type). A varying degree of fibrosis in lymph node sections (ICLN & MLN) from majority of the cases suggesting replacement of granulomatous reaction was observed as unique finding. ELISA revealed a total of twenty cases (51.28%) positive, while none of the case was detected by AGID. In conclusion, histopathological examination was found to be the most effective method for detection of JD in sheep.