Hoelzer Karin, Shackelton Laura A, Holmes Edward C, Parrish Colin R
Baker Institute for Animal Health, Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.
J Virol. 2008 Nov;82(22):11096-105. doi: 10.1128/JVI.01003-08. Epub 2008 Sep 3.
Viral emergence can result from the adaptation of endemic pathogens to new or altered host environments, a process that is strongly influenced by the underlying sequence diversity. To determine the extent and structure of intrahost genetic diversity in a recently emerged single-stranded DNA virus, we analyzed viral population structures during natural infections of animals with canine parvovirus (CPV) or its ancestor, feline panleukopenia virus (FPV). We compared infections that occurred shortly after CPV emerged with more recent infections and examined the population structure of CPV after experimental cross-species transmission to cats. Infections with CPV and FPV showed limited genetic diversity regardless of the analyzed host tissue or year of isolation. Coinfections with genetically distinct viral strains were detected in some cases, and rearranged genomes were seen in both FPV and CPV. The sporadic presence of some sequences with multiple mutations suggested the occurrence of either particularly error-prone viral replication or coinfection by more distantly related strains. Finally, some potentially organ-specific host effects were seen during experimental cross-species transmission, with many of the mutations located in the nonstructural protein NS2. These included residues with evidence of positive selection at the population level, which is compatible with a role of this protein in host adaptation.
病毒的出现可能源于地方性病原体适应新的或改变的宿主环境,这一过程受到潜在序列多样性的强烈影响。为了确定一种新出现的单链DNA病毒在宿主体内的遗传多样性程度和结构,我们分析了犬细小病毒(CPV)或其祖先猫泛白细胞减少症病毒(FPV)自然感染动物期间的病毒群体结构。我们比较了CPV出现后不久发生的感染与最近的感染,并研究了CPV在实验性跨物种传播给猫后的群体结构。无论分析的宿主组织或分离年份如何,CPV和FPV感染均显示出有限的遗传多样性。在某些情况下检测到与基因不同的病毒株的共感染,并且在FPV和CPV中均观察到重排的基因组。一些具有多个突变的序列的零星存在表明要么发生了特别容易出错的病毒复制,要么发生了与关系更远的菌株的共感染。最后,在实验性跨物种传播期间观察到一些潜在的器官特异性宿主效应,许多突变位于非结构蛋白NS2中。这些包括在群体水平上有正选择证据的残基,这与该蛋白在宿主适应中的作用相符。