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猫II型冠状病毒毒株79-1683和79-1146源自猫I型冠状病毒和犬冠状病毒之间的双重重组。

Feline coronavirus type II strains 79-1683 and 79-1146 originate from a double recombination between feline coronavirus type I and canine coronavirus.

作者信息

Herrewegh A A, Smeenk I, Horzinek M C, Rottier P J, de Groot R J

机构信息

Department of Infectious Diseases and Immunology, Faculty of Veterinary Medicine, Utrecht University, The Netherlands.

出版信息

J Virol. 1998 May;72(5):4508-14. doi: 10.1128/JVI.72.5.4508-4514.1998.

Abstract

Recent evidence suggests that the type II feline coronavirus (FCoV) strains 79-1146 and 79-1683 have arisen from a homologous RNA recombination event between FCoV type I and canine coronavirus (CCV). In both cases, the template switch apparently took place between the S and M genes, giving rise to recombinant viruses which encode a CCV-like S protein and the M, N, 7a, and 7b proteins of FCoV type I (K. Motowaka, T. Hohdatsu, H. Hashimoto, and H. Koyama, Microbiol. Immunol. 40:425-433, 1996; H. Vennema, A. Poland, K. Floyd Hawkins, and N. C. Pedersen, Feline Pract. 23:40-44, 1995). In the present study, we have looked for additional FCoV-CCV recombination sites. Four regions in the pol gene were selected for comparative sequence analysis of the type II FCoV strains 79-1683 and 79-1146, the type I FCoV strains TN406 and UCD1, the CCV strain K378, and the TGEV strain Purdue. Our data show that the type II FCoVs have arisen from double recombination events: additional crossover sites were mapped in the ORF1ab frameshifting region of strain 79-1683 and in the 5' half of ORF1b of strain 79-1146.

摘要

最近的证据表明,II型猫冠状病毒(FCoV)毒株79 - 1146和79 - 1683源自I型FCoV与犬冠状病毒(CCV)之间的同源RNA重组事件。在这两种情况下,模板切换显然发生在S基因和M基因之间,产生了重组病毒,这些重组病毒编码类似CCV的S蛋白以及I型FCoV的M、N、7a和7b蛋白(K. Motowaka、T. Hohdatsu、H. Hashimoto和H. Koyama,《微生物与免疫学》40:425 - 433,1996;H. Vennema、A. Poland、K. Floyd Hawkins和N. C. Pedersen,《猫科动物医学》23:40 - 44,1995)。在本研究中,我们寻找了其他FCoV - CCV重组位点。选择了pol基因中的四个区域,对II型FCoV毒株79 - 1683和79 - 1146、I型FCoV毒株TN406和UCD1、CCV毒株K378以及猪传染性胃肠炎病毒(TGEV)普渡毒株进行比较序列分析。我们的数据表明,II型FCoV源自双重重组事件:在79 - 1683毒株的ORF1ab移码区域以及79 - 1146毒株的ORF1b的5'端一半区域发现了额外的交叉位点。

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