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G10血清型10型轮状病毒(B223)VP4在犊牛异源免疫反应诱导中的作用研究。

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

作者信息

Xu Z, Woode G N

机构信息

Department of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M University, College Station 77843-4467.

出版信息

Virology. 1993 Sep;196(1):294-7. doi: 10.1006/viro.1993.1478.

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.

摘要

在先前的一项研究中,发现感染了G10血清型牛轮状病毒(B223)的无菌小牛(GC)的恢复期抗血清能中和一些代表G1 - G6和G8 - G10血清型的轮状病毒,但G8血清型69M除外(Z. Xu等人,《兽医微生物学》,1993年)。为了确定免疫显性抗原,构建了一组B223和69M之间的重配病毒,并使用B223 GC抗血清进行检测。结果发现,该抗血清以与亲代病毒B223相似的效价中和了含有B223 VP7的重配病毒的感染性,而含有B223的VP4但不含VP7的重配病毒的中和效价则显著较低。这些效价接近用B641(一种G6血清型轮状病毒)获得的异源效价,B223能诱导针对B641的保护性免疫。相反,含有69M的VP4和VP7的重配病毒不能被B223 GC抗血清中和。这表明,小牛初次免疫反应期间的免疫显性中和抗原是VP7,而异源反应可能针对VP4。通过一种交叉反应性的B223 VP4单克隆抗体(MAB)B223 - N6获得的证据表明,B223、B641和各种G血清型轮状病毒之间存在一个共同表位。这些数据支持了VP4是G10以及G6轮状病毒免疫的重要抗原这一结论。还用两种交叉反应性VP4 MABs B223 - N6和2G4对B223/69M重配病毒进行了检测。发现B223 VP7能提高MABs对含有同源(B223)VP4或异源(69M)VP4的轮状病毒的中和效价。

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