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Govind Ballabh Pant University of Agriculture and Technology, Pantnagar

After independence, development of the rural sector was considered the primary concern of the Government of India. In 1949, with the appointment of the Radhakrishnan University Education Commission, imparting of agricultural education through the setting up of rural universities became the focal point. Later, in 1954 an Indo-American team led by Dr. K.R. Damle, the Vice-President of ICAR, was constituted that arrived at the idea of establishing a Rural University on the land-grant pattern of USA. As a consequence a contract between the Government of India, the Technical Cooperation Mission and some land-grant universities of USA, was signed to promote agricultural education in the country. The US universities included the universities of Tennessee, the Ohio State University, the Kansas State University, The University of Illinois, the Pennsylvania State University and the University of Missouri. The task of assisting Uttar Pradesh in establishing an agricultural university was assigned to the University of Illinois which signed a contract in 1959 to establish an agricultural University in the State. Dean, H.W. Hannah, of the University of Illinois prepared a blueprint for a Rural University to be set up at the Tarai State Farm in the district Nainital, UP. In the initial stage the University of Illinois also offered the services of its scientists and teachers. Thus, in 1960, the first agricultural university of India, UP Agricultural University, came into being by an Act of legislation, UP Act XI-V of 1958. The Act was later amended under UP Universities Re-enactment and Amendment Act 1972 and the University was rechristened as Govind Ballabh Pant University of Agriculture and Technology keeping in view the contributions of Pt. Govind Ballabh Pant, the then Chief Minister of UP. The University was dedicated to the Nation by the first Prime Minister of India Pt Jawaharlal Nehru on 17 November 1960. The G.B. Pant University is a symbol of successful partnership between India and the United States. The establishment of this university brought about a revolution in agricultural education, research and extension. It paved the way for setting up of 31 other agricultural universities in the country.

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  • ThesisItemOpen Access
    Immunogenicity induced by the soluble antigens derived form cefotaxime treatment of Brucella abortus S99 and Brucella melitensis B115 cells
    (G.B. Pant University of Agriculture and Technology, Pantnagar (Uttarakhand), 2005) Maansi; Thapliyal, D.C.
  • ThesisItemOpen Access
    Biochemical activity and phytochemical analysis of butea frondosa embelia ribes and varnonia anthelmintica
    (Govind Ballabh Pant University of Agriculture and Technology;Pantnagar, 2006) Mittal, Vaishali; Mahesh Kumar
  • ThesisItemOpen Access
    Molecular epidemiology and serodiagnosis of foot and mouth disease in bovines
    (G.B. Pant University of Agriculture and Technology, Pantnagar - 263145 (Uttarakhand), 2010-08) Singh, Arbind; Mahesh Kumar
    The present study was conducted to know the distribution pattern of virus types, validation of quality diagnostics for precise serotyping of FMD virus, antigenic and genetic analysis and to understand the molecular epidemiology of the disease in part of Uttar Pradesh state. For this purpose, 400 serum and 25 tongue epithelium samples were collected from different districts of Uttar Pradesh adjacent to Uttarakhand state. Serological diagnosis of FMD virus was based on the NSP-ELISA which revealed non-significant difference of positivity percentage of NSP antibodies in cattle (29.00%) and buffaloes (26.50%). Positivity percentage was highest in Bareilly district (47.50%) whereas it was lowest in the district Rampur (6.25%). Isolation of virus from 25 tongue epithelium was done using BHK-21 cell line. Out of these 25 samples, virus could be recovered from 8 samples (3 serotype O and 5 serotype A) and the overall recovery was 32.00%. However on serotyping of virus of these 25 tongue epithelium by sandwich ELISA, 17 were characterized (10 serotype O and 7 serotype A) and the overall typeability was 68.00%. Of the 25 tongue epithelium analyzed with RT-PCR, the amplicons (1301 bp and 865 bp) could be amplified from 20 specimens (12 serotype O and 8 serotype A). Sensitivity and specificity of RT-PCR considering virus isolation as golden standard test was calculated to be 100% and 66.67%, respectively. The 1D gene of 2 isolates of FMD virus serotype A was sequenced revealing a coding region of 865 bp. On phylogenetic analysis sequence obtained from UPl isolate was more homologous (29%) to FJ755013 and FJ755012 and Brl sequence proved to be more homologous (about 28%) to EF494504 and EF494506. Such continuous monitoring of the field strains can assist in selection of vaccine strains and evolving a proper control strategy for the disease in future.