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风疹病毒疫苗TO-336株的突变发生在野生祖病毒的减毒过程中。

Mutations of rubella virus vaccine TO-336 strain occurred in the attenuation process of wild progenitor virus.

作者信息

Kakizawa J, Nitta Y, Yamashita T, Ushijima H, Katow S

机构信息

Department of Viral Disease and Vaccine Control, National Institute of Infectious Diseases, 4-7-1 Gakuen, Musashi-Murayama, Tokyo 208-0011, Japan.

出版信息

Vaccine. 2001 Apr 6;19(20-22):2793-802. doi: 10.1016/s0264-410x(01)00018-4.

Abstract

The sequences of the genomes in the TO-336 vaccine strain (TO-336vac) of rubella virus and its wild progenitor virus (TO-336wt) have been determined and compared with each other. There were 21 differences in the nucleotide sequences between the TO-336vac and the TO-336wt: 13 in the nonstructural protein open reading frame (NSP-ORF), five in the structural protein open reading frame (SP-ORF) and three in the untranslated regions (UTRs) (one in each three UTRs). These mutations resulted in amino acid substitutions at ten residues. Of the ten substitutions, eight were in NSP-ORF and two were in the SP-ORF. Of the eight substitutions in NSP-ORF, four (amino acids (aa) 320, 501, 573 and 704) were in the regions of unknown function, two (aa 1154 and 1159) were within the protease motif, and two (aa 1351 and 1559) were within the helicase motif. Both of the two residues (aa 890 and 954) in the SP-ORF were within the E1 gene. The predicted second structure of the 5'UTR of the TO-336vac was identical to that of TO-336wt. Comparing the TO-336 sequences with other four strains, Therien and M33 (wild viruses), and RA27/3 and Cendehill (vaccine viruses), the mutations responsible for attenuation are thought to differ with each vaccine strain. This is the first report of sequencing in a pair of live attenuated rubella vaccines and their wild-type parent.

摘要

风疹病毒TO - 336疫苗株(TO - 336vac)及其野生祖代病毒(TO - 336wt)的基因组序列已被测定并相互比较。TO - 336vac与TO - 336wt的核苷酸序列存在21处差异:非结构蛋白开放阅读框(NSP - ORF)中有13处,结构蛋白开放阅读框(SP - ORF)中有5处,非翻译区(UTR)中有3处(每个UTR各有1处)。这些突变导致10个残基处的氨基酸替换。在这10处替换中,8处位于NSP - ORF,2处位于SP - ORF。在NSP - ORF中的8处替换中,4处(氨基酸(aa)320、501、573和704)位于功能未知区域,2处(aa 1154和1159)位于蛋白酶基序内,2处(aa 1351和1559)位于解旋酶基序内。SP - ORF中的两个残基(aa 890和954)均位于E1基因内。TO - 336vac的5'UTR预测二级结构与TO - 336wt相同。将TO - 336序列与其他四个毒株,即Therien和M33(野生病毒)以及RA27/3和Cendehill(疫苗病毒)进行比较,认为导致减毒的突变因每个疫苗株而异。这是关于一对减毒风疹活疫苗及其野生型亲本进行测序的首次报告。

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