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马立克氏病病毒CVI988/Rispens株H19表位点突变体的构建与鉴定

Construction and characterization of a H19 epitope point mutant of MDV CVI988/Rispens strain.

作者信息

Cui Z, Qin A, Lee L F, Wu P, Kung H J

机构信息

Department of Veterinary Medicine, Yangzhou University, P.R. China.

出版信息

Acta Virol. 1999 Apr-Jun;43(2-3):169-73.

Abstract

A recombinant virus, CVI/rpp38, was developed from the Marek's disease virus (MDV) CVI988/Rispens vaccine strain. This recombinant was obtained by transfection of CVI988/Rispens-infected chick embryo fibroblasts (CEFs) with plasmid pHA25 DNA containing pp38 gene from GA strain of MDV. Monoclonal antibody (MAb) H19 which reacts with pp38 from GA but not with that from CVI988 was used to screen for recombinant viruses in transfected cell culture plates by immunofluorescent assay (IFA). A positive plaque was isolated, propagated, and purified from cell-free virus particles after sonication of infected CEFs. The mutant CVI/rpp38 was not only reactive with MAb H19 in IFA but also in immunoprecipitation. A 38 kDa protein was immunoprecipitated from the CVI/rpp38 mutant virus but not from parental CVI988 virus. DNA sequence of the mutant virus showed a substitution of G at position 320 by a resulting in a change of an amino acid residue from arginine to glutamine. Comparison of nucleotide sequence of pp38 from strains GA, Md5 and Md11/75c/R2 and CVI988 revealed change to glutamine in this position. The result of this study provides a direct evidence for the location of the identified H19 epitope in pp38. This mutant is potentially useful to further explore the biological function of pp38 and its H19 epitope.

摘要

一种重组病毒CVI/rpp38是由马立克氏病病毒(MDV)CVI988/Rispens疫苗株培育而成。该重组病毒是通过用含有来自MDV GA株的pp38基因的质粒pHA25 DNA转染感染了CVI988/Rispens的鸡胚成纤维细胞(CEF)而获得的。用与GA株的pp38反应但不与CVI988株的pp38反应的单克隆抗体(MAb)H19,通过免疫荧光测定法(IFA)在转染细胞培养板中筛选重组病毒。从感染的CEF经超声处理后的无细胞病毒颗粒中分离、增殖并纯化出一个阳性噬斑。突变体CVI/rpp38不仅在IFA中与MAb H19反应,在免疫沉淀中也有反应。从CVI/rpp38突变病毒中免疫沉淀出一种38 kDa的蛋白质,而亲本CVI988病毒中则没有。突变病毒的DNA序列显示在第320位的G被替换,导致一个氨基酸残基从精氨酸变为谷氨酰胺。对GA、Md5和Md11/75c/R2以及CVI988株的pp38核苷酸序列比较显示,该位置都变为了谷氨酰胺。本研究结果为已鉴定的pp38中H19表位的定位提供了直接证据。该突变体对于进一步探索pp38及其H19表位的生物学功能可能具有重要作用。

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