马立克病病毒血清2型和CVI-988株感染培养细胞中病毒特异性抗原的鉴定。

M Horiuchi, H Kodama, T Mikami
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引用次数: 4

摘要

为了鉴定马立克病病毒(Marek’s disease virus, MDV)血清1型(MDV1)或血清2型(MDV2)的血清型特异性抗原,共建立了24个杂交瘤克隆,分泌CVI-988 (MDV1)或hrs -24 (MDV2)株的单克隆抗体(mab),并通过免疫荧光法、病毒中和和免疫沉淀分析对其进行了鉴定。根据免疫沉淀多肽的分子量(mol. wt.),将单克隆抗体细分为7组。其中,鉴定出两组单克隆抗体与未报道的抗原发生反应。第一组单克隆抗体与CVI-988-和mdv2特异性抗原反应,分子量范围为29 K ~ 34 K (29/34 K),在MDV1的Md/5和JM株感染的细胞中未发现该抗原,抗原表达动力学分析结果表明该抗原可能与晚期膜抗原有关。第二组单克隆抗体免疫沉淀MDV2特异性抗原,分子量分别为hprs -24感染细胞的37 K、33 K和31 K,或SB-1(MDV2)感染细胞的37 K、34 K和31 K,这些抗原似乎与早期抗原有关。其他5组单克隆抗体包括识别先前报道的相似抗原或本研究未充分表征的抗原。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of virus-specific antigens in cultured cells infected with Marek's disease virus serotype 2 and CVI-988 strain.

For the identification of serotype-specific antigens of Marek's disease virus (MDV) serotype 1 (MDV1) or serotype 2 (MDV2), a total of 24 hybridoma clones, secreting monoclonal antibodies (MAbs) against CVI-988 (MDV1) or HPRS-24 (MDV2) strain, were established and characterized by immunofluorescence assay, virus neutralization and immunoprecipitation analysis. Based upon the molecular weights (mol. wt.) of the immunoprecipitated polypeptides, the MAbs were subdivided into 7 groups. Among them, two groups of MAbs reacted with antigens that have not been reported, were identified. MAbs belonging to the first group reacted with CVI-988- and MDV2-specific antigens with mol. wt. ranging from 29 K to 34 K (29/34 K). This antigen was not found in cells infected with Md/5 and JM strains of MDV1, and the results of kinetic analysis of antigen expression showed this antigen appeared to be related to late membrane antigens. MAbs belonging to the second group immunoprecipitated MDV2-specific antigens with mol. wt. of 37 K, 33 K and 31 K from HPRS-24-infected cells or with those of 37 K, 34 K and 31 K from SB-1(MDV2)-infected cells, and these antigens appeared to be related to early antigens. MAbs belonging to the other 5 groups included those which recognized similar antigens reported previously or the antigens characterized insufficiently in this study.

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