Watanabe T, Morikawa S, Suzuki K, Miyamura T, Tamaki K, Ueda Y
Department of Virology II, National Institute of Infectious Diseases, University of Tokyo, Japan.
J Infect Dis. 1998 Feb;177(2):284-92. doi: 10.1086/514197.
A library of molluscum contagiosum virus (MCV) transferred into the cowpox vector expression system was screened with 12 sera from molluscum patients. Two recombinant proteins of 70 and 34 kDa were detected by immunoblotting and mapped to the open-reading frames MC133L and MC084L, respectively. Consensus sites were found between the C-terminus of the 70-kDa MCV protein and the 14-kDa fusion protein of vaccinia and variola virus, and between the 34-kDa MCV protein and the 37.5-kDa viral membrane-associated protein of vaccinia and variola virus. Rabbit antisera against these two proteins were prepared. An immunofluorescence study demonstrated that the 70- and 34-kDa proteins were predominantly expressed on the surface of recombinant virus-infected HeLa cells, indicating the potential to be inserted into the membrane. On immunoelectron microscopy, antiserum against 70-kDa protein showed significant labeling of the MCV membrane, while the antiserum against 34-kDa protein failed to do so.
用来自传染性软疣患者的12份血清对转入牛痘载体表达系统的传染性软疣病毒(MCV)文库进行筛选。通过免疫印迹检测到两种分别为70 kDa和34 kDa的重组蛋白,它们分别定位到开放阅读框MC133L和MC084L。在70 kDa的MCV蛋白C末端与痘苗病毒和天花病毒的14 kDa融合蛋白之间,以及在34 kDa的MCV蛋白与痘苗病毒和天花病毒的37.5 kDa病毒膜相关蛋白之间发现了共有位点。制备了针对这两种蛋白的兔抗血清。免疫荧光研究表明,70 kDa和34 kDa蛋白主要在重组病毒感染的HeLa细胞表面表达,表明其具有插入膜中的潜力。在免疫电子显微镜下,针对70 kDa蛋白的抗血清显示出对MCV膜的显著标记,而针对34 kDa蛋白的抗血清则未显示出这种标记。