نتایج جستجو برای: infectious bursal disease virus

تعداد نتایج: 1845680  

D. Shahbazzadeh H. Goudarzi M. Azizy M.R. Seyfi Abad Shapoori R. Toroghi S.A. Pourbakhsh,

Infectious bursal disease virus (IBDV) is the causative agent of Gumboro disease, an infectious disease of global economic importance in poultry. The expression of heterologous proteins in P.pastoris is fast, simple and inexpensive. In this study, VP2 encoding gene of classical D78 IBDV was amplified using reverse transcription (RT) polymerase chain reaction (PCR) and cloned into pPICZαA vector...

Journal: :Journal of virology 2005
Dolores González Jose Francisco Rodríguez Fernando Abaitua

A search for dominant-negative mutant polypeptides hampering infectious bursal disease virus (IBDV) replication has been undertaken. We have found that expression of a mutant version of the VP3 structural polypeptide known as VP3/M3, partially lacking the domain responsible for the interaction with the virus-encoded RNA polymerase, efficiently interferes with the IBDV replication cycle. Transfo...

Journal: :World's Poultry Science Journal 1986

M. Habib M. S. D. Shah R. S. A. Khan, S. Kiran W. Ali Z. A. Tahir

Infectious bursal disease (IBD) is an immunosuppressive, acute and highly contagious illness of growing-poultry stock infected with infectious bursal disease virus (IBDV). It is common in Pakistan, causing potential economic losses throughout the year. The objective of the study is to propose a rapid, sensitive and specific diagnostic tool, and compare it with existing commonly used reverse tra...

2017
Hyun-Jeong Lee Il Jang Sun-Hwa Shin Hee-Soo Lee Kang-Seuk Choi

Here, we report the complete coding genome sequence of a novel reassortant and very virulent infectious bursal disease virus (IBDV), designated JBN2011. Characterization of the JBN2011 genome suggests that it is a rare recombinant virus having a very virulent IBDV segment A and a Bursine-2-like attenuated IBDV segment B.

Jamshid Razmyar Seyed Mostafa Peighambari,

Abstract: This study was conducted to characterize infectious bursal disease virus (IBDV) isolates collected from different parts of Iran during 2005-2006. Pooled bursal samples from 49 broiler and layer pullet flocks suspected to IBD infection were collected and processed. A reverse transcriptase-polymerase chain reaction (RT PCR) procedure was used to amplify a VP2 gene fragment (743 bp) from...

Journal: :Proceedings of the National Academy of Sciences 2009

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