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一种用于单纯疱疹病毒分型的新型微孔板中和试验。

A new microplate neutralization test for typing of herpes simplex virus.

作者信息

Tada A, Yoshino K

出版信息

Microbiol Immunol. 1978;22(7):415-26. doi: 10.1111/j.1348-0421.1978.tb00387.x.

Abstract

A microplate serum neutralization test for estimation of complement-requiring neutralizing (CRN) antibody was established as the first step for simplification of typing of herpes simplex virus (HSV). When guinea pigs were immunized with type 2 HSV, the late sera could mostly differentiate the types of HSV better than hyperimmune rabbit sera, the CRN titer against the heterologous type 1 HSV being much lower than the homologous titer. Sera of guinea pigs immunized with type 1 HSV showed about the same level of cross reaction against type 2 HSV as did rabbit antisera. Guinea pig sera having minimal levels of cross reaction were selected, and their high dilution (1:160) and complement were added to serial 10-fold dilutions of virus in the microplate titration of virus infectivity. Selective reduction of virus titer by either antiserum could determine the type of HSV. No equivocal intermediate case was found among a number of stock strains including many fresh isolates. The typing result coincided with that determined by a modification of Yang et al's method based on virus titers obtained with Vero and primary chick embryo cells. The typing based on plaquing in chick embryo cells sometimes failed to identify type 1 HSV.

摘要

建立了一种用于估计补体依赖中和(CRN)抗体的微孔板血清中和试验,作为简化单纯疱疹病毒(HSV)分型的第一步。用2型HSV免疫豚鼠时,晚期血清大多比超免疫兔血清能更好地区分HSV的类型,其针对异源1型HSV的CRN滴度远低于同源滴度。用1型HSV免疫的豚鼠血清对2型HSV的交叉反应水平与兔抗血清大致相同。选择交叉反应水平最低的豚鼠血清,并在病毒感染性的微孔板滴定中,将其高稀释度(1:160)和补体加入病毒的系列10倍稀释液中。任何一种抗血清对病毒滴度的选择性降低都可以确定HSV的类型。在包括许多新鲜分离株在内的众多毒株中未发现模棱两可的中间情况。分型结果与基于用Vero细胞和原代鸡胚细胞获得的病毒滴度对Yang等人方法进行改进后所确定的结果一致。基于在鸡胚细胞中形成蚀斑的分型有时无法鉴定1型HSV。

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