Stewart H, Jarrett O, Hosie M J, Willett B J
Medical Research Council, University of Glasgow Centre for Virus Research, Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Genome Announc. 2013 Jan;1(1). doi: 10.1128/genomeA.00036-12. Epub 2013 Jan 15.
It is generally accepted that all primary isolates of feline leukemia virus (FeLV) contain a subgroup A virus (FeLV-A) that is essential for transmission. In contrast, FeLV-B is thought to arise de novo in the infected animal through RNA recombination events with endogenous FeLV transcripts, presumably through copackaging of RNA from endogenous FeLV and exogenous FeLV-A. Here, we report the complete genome sequences of two novel strains of FeLV-B (FeLV-2518 and FeLV-4314) that were isolated in the absence of FeLV-A. The env genes of these isolates have been characterized previously, and the 3' recombination sites have been identified. We describe herein the 5' recombination breakpoints of each virus. These breakpoints were found to be within the signal peptide of the env gene and the reverse transcriptase-coding region, respectively. This is the first report of a recombination site within the pol gene of an FeLV-B genome and the first genetic characterization of multiple independently arising FeLV-B isolates that have been identified without a functional FeLV-A ancestral virus.
一般认为,所有猫白血病病毒(FeLV)的原始分离株都包含一种对传播至关重要的A亚群病毒(FeLV-A)。相比之下,FeLV-B被认为是在受感染动物体内通过与内源性FeLV转录本发生RNA重组事件而重新产生的,推测是通过内源性FeLV和外源性FeLV-A的RNA共包装。在此,我们报告了在没有FeLV-A的情况下分离出的两种新型FeLV-B毒株(FeLV-2518和FeLV-4314)的完整基因组序列。这些分离株的env基因先前已被表征,并且已确定了3'重组位点。我们在此描述了每种病毒的5'重组断点。这些断点分别位于env基因的信号肽和逆转录酶编码区域内。这是关于FeLV-B基因组pol基因内重组位点的首次报道,也是对多个独立产生且未鉴定出功能性FeLV-A祖先病毒的FeLV-B分离株的首次遗传表征。