Literature DB >> 8395118

Studies on the role of VP4 of G serotype 10 rotavirus (B223) in the induction of the heterologous immune response in calves.

Z Xu1, G N Woode.   

Abstract

In a previous study, convalescent antisera from gnotobiotic calves (GC) infected with the G10 serotype bovine rotavirus (B223) were found to neutralize a number of rotaviruses representing G1-G6 and G8-G10 serotypes, except for a G8 serotype 69M (Z. Xu et al., Vet. Microbiol., 1993). In order to determine the immunodominant antigen, a panel of reassortants between B223 and 69M was generated and tested with the B223 GC antisera. It was found that the antisera neutralized the infectivities of the reassortants containing VP7 of B223 at titers similar to those with the parental virus B223, whereas the neutralization titers with the reassortants containing VP4 but not VP7 from B223 were significantly lower. These titers were close to the heterologous titers obtained with B641 (a G6 serotype rotavirus) against which B223 induced protective immunity. In contrast, the reassortants with both VP4 and VP7 from 69M were not neutralized by the B223 GC antisera. This indicates that the immunodominant neutralizing antigen during the primary immune response in calves is VP7 and the heterologous response is probably directed at VP4. Evidence was obtained through a cross-reactive B223 VP4 monoclonal antibody (MAB), B223-N6, that a shared epitope exists among B223, B641, and various G serotype rotaviruses. These data support the conclusion that VP4 is an important antigen for G10 as well as G6 rotavirus immunity. The B223/69M reassortants were also assayed with two cross-reactive VP4 MABs B223-N6 and 2G4. B223 VP7 was found to enhance the neutralization titers of the MABs with rotaviruses containing either homologous (B223) VP4 or the heterologous (69M) VP4.

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Year:  1993        PMID: 8395118     DOI: 10.1006/viro.1993.1478

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  5 in total

1.  Production of reassortant viruses containing human rotavirus VP4 and SA11 VP7 for measuring neutralizing antibody following natural infection.

Authors:  R J Gorrell; R F Bishop
Journal:  Clin Diagn Lab Immunol       Date:  1997-09

2.  G (VP7) serotype-dependent preferential VP7 gene selection detected in the genetic background of simian rotavirus SA11.

Authors:  N Kobayashi; K Taniguchi; K Kojima; T Urasawa; S Urasawa
Journal:  Arch Virol       Date:  1996       Impact factor: 2.574

3.  Preferential selection of VP7 gene from a parent rotavirus strain (SA11) in sequential passages after mixed infection with SA11 and SA11-human rotavirus single-VP7 gene-substitution reassortants.

Authors:  N Kobayashi; K Taniguchi; K Kojima; T Urasawa; S Urasawa
Journal:  Arch Virol       Date:  1995       Impact factor: 2.574

4.  Interactions between the two surface proteins of rotavirus may alter the receptor-binding specificity of the virus.

Authors:  E Méndez; C F Arias; S López
Journal:  J Virol       Date:  1996-02       Impact factor: 5.103

5.  In vitro studies on the use of clay, clay minerals and charcoal to adsorb bovine rotavirus and bovine coronavirus.

Authors:  K J Clark; A B Sarr; P G Grant; T D Phillips; G N Woode
Journal:  Vet Microbiol       Date:  1998-10       Impact factor: 3.293

  5 in total

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