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用猫免疫缺陷病毒的分子克隆和生物学分离株对猫进行实验性感染后,包膜糖蛋白和OrfA序列在宿主体内的进化

Intrahost evolution of envelope glycoprotein and OrfA sequences after experimental infection of cats with a molecular clone and a biological isolate of feline immunodeficiency virus.

作者信息

Huisman Willem, Schrauwen Eefje J A, Rimmelzwaan Guus F, Osterhaus Albert D M E

机构信息

Erasmus MC, Institute of Virology, Rotterdam, The Netherlands.

出版信息

Virus Res. 2008 Oct;137(1):24-32. doi: 10.1016/j.virusres.2008.05.009. Epub 2008 Jun 11.

Abstract

Feline immunodeficiency virus (FIV) is a member of the genus Lentivirus and causes AIDS-like disease in its natural host, the cat. Like other lentiviruses, FIV displays a high degree of nucleotide sequence variability that is reflected in both the geographic distribution of the viruses and the different cat species that are infected. Although a lot of data on sequence variation at the population level is available, relatively little is known about the intrahost variation of FIV sequences. In the present study, cats were infected with either a biological isolate of FIV or a molecular clone that was derived from the same isolate, AM19. After infection, the cats were monitored for up to 3 years and at various time points sequences were obtained of virus circulating in the plasma. Regions of the env gene and the orfA gene were amplified, cloned and their nucleotide sequence analyzed. Furthermore, the extent of sequence variation in the original inocula was also determined. It was found that FIV is displaying relative little sequence variation during infection of its host, both in the env and the orfA gene, especially after infection with molecular clone 19k1. Although the extent of variation was higher after infection with biological isolate AM19, a large portion of these variant sequences was already present in the inoculum.

摘要

猫免疫缺陷病毒(FIV)是慢病毒属的成员,可在其天然宿主猫中引发类似艾滋病的疾病。与其他慢病毒一样,FIV表现出高度的核苷酸序列变异性,这在病毒的地理分布以及受感染的不同猫科动物物种中都有所体现。尽管有大量关于群体水平序列变异的数据,但对于FIV序列的宿主内变异了解相对较少。在本研究中,猫被感染了FIV的生物分离株或源自同一分离株AM19的分子克隆。感染后,对猫进行长达3年的监测,并在不同时间点获取血浆中循环病毒的序列。对env基因和orfA基因的区域进行扩增、克隆并分析其核苷酸序列。此外,还确定了原始接种物中的序列变异程度。结果发现,FIV在感染宿主期间,env基因和orfA基因的序列变异相对较小,尤其是在感染分子克隆19k1后。尽管感染生物分离株AM19后的变异程度较高,但这些变异序列中的很大一部分在接种物中就已经存在。

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