Matthijnssens Jelle, Ciarlet Max, Heiman Erica, Arijs Ingrid, Delbeke Thomas, McDonald Sarah M, Palombo Enzo A, Iturriza-Gómara Miren, Maes Piet, Patton John T, Rahman Mustafizur, Van Ranst Marc
Laboratory of Clinical and Epidemiological Virology, Department of Microbiology and Immunology, Rega Institute for Medical Research, Minderbroedersstraat 10, B-3000 Leuven, Belgium.
J Virol. 2008 Apr;82(7):3204-19. doi: 10.1128/JVI.02257-07. Epub 2008 Jan 23.
Group A rotavirus classification is currently based on the molecular properties of the two outer layer proteins, VP7 and VP4, and the middle layer protein, VP6. As reassortment of all the 11 rotavirus gene segments plays a key role in generating rotavirus diversity in nature, a classification system that is based on all the rotavirus gene segments is desirable for determining which genes influence rotavirus host range restriction, replication, and virulence, as well as for studying rotavirus epidemiology and evolution. Toward establishing such a classification system, gene sequences encoding VP1 to VP3, VP6, and NSP1 to NSP5 were determined for human and animal rotavirus strains belonging to different G and P genotypes in addition to those available in databases, and they were used to define phylogenetic relationships among all rotavirus genes. Based on these phylogenetic analyses, appropriate identity cutoff values were determined for each gene. For the VP4 gene, a nucleotide identity cutoff value of 80% completely correlated with the 27 established P genotypes. For the VP7 gene, a nucleotide identity cutoff value of 80% largely coincided with the established G genotypes but identified four additional distinct genotypes comprised of murine or avian rotavirus strains. Phylogenetic analyses of the VP1 to VP3, VP6, and NSP1 to NSP5 genes showed the existence of 4, 5, 6, 11, 14, 5, 7, 11, and 6 genotypes, respectively, based on nucleotide identity cutoff values of 83%, 84%, 81%, 85%, 79%, 85%, 85%, 85%, and 91%, respectively. In accordance with these data, a revised nomenclature of rotavirus strains is proposed. The novel classification system allows the identification of (i) distinct genotypes, which probably followed separate evolutionary paths; (ii) interspecies transmissions and a plethora of reassortment events; and (iii) certain gene constellations that revealed (a) a common origin between human Wa-like rotavirus strains and porcine rotavirus strains and (b) a common origin between human DS-1-like rotavirus strains and bovine rotaviruses. These close evolutionary links between human and animal rotaviruses emphasize the need for close simultaneous monitoring of rotaviruses in animals and humans.
A组轮状病毒的分类目前基于两种外层蛋白VP7和VP4以及中层蛋白VP6的分子特性。由于所有11个轮状病毒基因片段的重配在自然界轮状病毒多样性的产生中起着关键作用,因此基于所有轮状病毒基因片段的分类系统对于确定哪些基因影响轮状病毒宿主范围限制、复制和毒力,以及研究轮状病毒流行病学和进化是很有必要的。为了建立这样一个分类系统,除了数据库中已有的序列外,还测定了属于不同G和P基因型的人及动物轮状病毒株编码VP1至VP3、VP6以及NSP1至NSP5的基因序列,并用于确定所有轮状病毒基因之间的系统发育关系。基于这些系统发育分析,为每个基因确定了合适的同一性截止值。对于VP4基因,80%的核苷酸同一性截止值与已确定的27种P基因型完全相关。对于VP7基因,80%的核苷酸同一性截止值与已确定的G基因型基本一致,但确定了另外四种由鼠或禽轮状病毒株组成的不同基因型。对VP1至VP3、VP6以及NSP1至NSP5基因的系统发育分析表明,基于分别为83%、84%、81%、85%、79%、85%、85%、85%和91%的核苷酸同一性截止值,分别存在4、5、6、11、14、5、7、11和6种基因型。根据这些数据,提出了轮状病毒株的修订命名法。新的分类系统能够识别:(i) 可能遵循不同进化路径的不同基因型;(ii) 种间传播和大量重配事件;以及(iii) 某些基因组合,这些组合揭示了(a) 人Wa样轮状病毒株与猪轮状病毒株之间的共同起源,以及(b) 人DS-1样轮状病毒株与牛轮状病毒之间的共同起源。人轮状病毒和动物轮状病毒之间这些紧密的进化联系强调了同时密切监测动物和人类轮状病毒的必要性。