Results 191 to 200 of about 9,619 (201)
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Identification of three novel linear B-cell epitopes on the VP5 protein of BTV16
Veterinary Microbiology, 2013Bluetongue virus (BTV) VP5 protein is an important antigenic protein which is centrally involved in serotype determination and the virus entry process. Very little is known about the B-cell epitopes on the BTV VP5 protein recognized by humoral immune responses.
Wen-Shi, Wang +11 more
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TRIM103 activates the RLRs pathway to enhance antiviral response by targeting VP5 and VP7
Developmental & Comparative ImmunologyGrass carp (Ctenopharyngodon idella), crucial to global inland aquaculture with a production of 5.8 million tones in 2020, faces significant challenges from hemorrhagic disease caused by grass carp reovirus (GCRV). Rapid mutations compromise current vaccines, underscoring the need for a deeper understanding of antiviral mechanisms to enhance molecular ...
Beibei Qin +4 more
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Molecular cloning and prokaryotic expression of vp5 gene of grass carp reovirus strain GCRV096
Virus Genes, 2013VP5 is an outer capsid protein of grass carp reovirus (GCRV). It is predicted to involve in helping GCRV enter the host cells. In this study, the full-length vp5 gene (accession number in GenBank: JN206664.1) was cloned from GCRV strain GCRV096, which was isolated from diseased grass carp (Ctenopharyngodon idella) in southern China by RT-PCR technique ...
Ji-chang, Jian +5 more
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Virus Genes, 2010
The infectious bursal disease virus (IBDV; Birnaviridae family) constitutes one of the main threats to the poultry industry worldwide. Most of the progress in the molecular epidemiology of this virus has been achieved through the study of the coding region of the capsid protein VP2.
Martín, Hernández +7 more
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The infectious bursal disease virus (IBDV; Birnaviridae family) constitutes one of the main threats to the poultry industry worldwide. Most of the progress in the molecular epidemiology of this virus has been achieved through the study of the coding region of the capsid protein VP2.
Martín, Hernández +7 more
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In silico prediction and in vitro identification of bluetongue virus 4 VP5 protein B-cell epitopes
Applied Microbiology and Biotechnology, 2013VP5, the outer capsid protein of bluetongue virus (BTV), plays an important role in viral penetration and antibody-mediated viral neutralization. Therefore, VP5 represents an important target for development of vaccines and diagnostic tests. In this study, we use bioinformatic tools to predict nine antigenic B cell epitopes in the VP5 protein of a BTV ...
L, Sun +9 more
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The Veterinary Journal
Infectious bursal disease (IBD) is an important immunosuppressive disease affecting chickens and is caused by infectious bursal disease virus (IBDV) infection. VP5 is a non-essential protein for IBDV replication but plays a critical role in IBDV pathogenesis. A deeper understanding of the biological functions of VP5 is lacking.
Jinze, Han +20 more
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Infectious bursal disease (IBD) is an important immunosuppressive disease affecting chickens and is caused by infectious bursal disease virus (IBDV) infection. VP5 is a non-essential protein for IBDV replication but plays a critical role in IBDV pathogenesis. A deeper understanding of the biological functions of VP5 is lacking.
Jinze, Han +20 more
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Characteristics and functional roles of VP5 protein of herpesviruses
Reviews in Medical Microbiology, 2013Bihong Dai, Anchun Cheng, Mingshu Wang
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[Cloning of infectious bursal disease virus (Gt strain) lack of VP5 gene].
Wei sheng wu xue bao = Acta microbiologica Sinica, 2009Infectious bursal disease virus (IBDV) belongs to genus Avibirnavirus of the family Birnaviridae. The genome of IBDV consists of two segments of double-strand RNA, which encode four structural protein VP1-VP4 and one non-structural protein VP5.To study the function of VP5 of IBDV, the recombinant virus, lack of VP5 gene, was constructed and rescused by
Liting, Qin +5 more
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Gene Cloning and Sequence Analysis of VP5 for Chicken Infectious Bursal Disease Virus
2010Chicken infectious bursal disease viruses (IBDV) were isolated and purified from infected bursa and then the viruses were used to extract genomic RNA.The cDNA first strand was synthesized by reverse transcription using IBDV genomic RNA as the template.A DNA fragment coding for the viral protein 5(VP5) of IBDV was amplified by PCR,which was ligated with
Leung, FCC, Liu, CR, Yu, SQ
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Use of a Ds Chromosome-Breaking Element to Examine Maize Vp5 Expression
Journal of Heredity, 1992openaire +1 more source

