Ramachandran M, Kirkwood C D, Unicomb L, Cunliffe N A, Ward R L, Bhan M K, Clark H F, Glass R I, Gentsch J R
Viral Gastroenteritis Section, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.
Virology. 2000 Dec 20;278(2):436-44. doi: 10.1006/viro.2000.0682.
Between 1992 and 1998, serotype G9 human rotavirus (RV) strains have been detected in 10 countries, including Thailand, India, Brazil, Bangladesh, Malawi, Italy, France, the United States, the United Kingdom, and Australia, suggesting the possible emergence of the fifth common serotype worldwide. Unlike the previously characterized reference G9 strains (i.e., WI61 and F45), the recent G9 isolates had a variety of gene combinations, raising questions concerning their origin and evolution. To identify the progenitor strain and examine the on-going evolution of the recent G9 strains, we characterized by genetic and antigenic analyses 16 isolates obtained from children with diarrhea in India, Bangladesh, the United States, and Malawi. Specifically, we sequenced their VP7 and NSP4 genes and compared the nucleotide (nt) and deduced amino acid sequences with the reference G9 strains. To identify reassortment, we examined the products of five gene segments; VP4, VP7, and NSP4 genotypes (genes 4, 9, and 10); subgroups (gene 6); electropherotypes (gene 11); and the genogroup profiles of all of the recent G9 isolates. Sequence analysis of the VP7 gene indicated that the recent U.S. P[6],G9 strains were closely related to the Malawian G9 strains (>99% nt identity) but distinct from G9 strains of India ( approximately 97% nt identity), Bangladesh ( approximately 98% nt identity), and the reference strains ( approximately 97% nt identity). Phylogenetic analysis identified a single cluster for the U.S. P[6],G9 strains that may have common progenitors with Malawian P[6],G9 strains whereas separate lineages were defined for the Indian, Bangladeshi, and reference G9 strains. Northern hybridization results indicated that all 11 gene segments of the Malawian P[6],G9 strains hybridized with a probe derived from a U.S. strain of the same genotype and may have the same progenitor, different from the Indian G9 strains, whereas the Bangladesh strains may have evolved from the U.S. G9 progenitors. Overall, our findings suggest that much greater diversity among the newly identified G9 strains has been generated by reassortment between gene segments than through the accumulation of mutations in a single gene.
1992年至1998年间,在泰国、印度、巴西、孟加拉国、马拉维、意大利、法国、美国、英国和澳大利亚这10个国家检测到了血清型G9人轮状病毒(RV)毒株,这表明全球可能出现了第五种常见血清型。与先前鉴定的参考G9毒株(即WI61和F45)不同,最近的G9分离株具有多种基因组合,这引发了关于其起源和进化的问题。为了鉴定祖代毒株并研究最近G9毒株的持续进化,我们通过遗传和抗原分析对从印度、孟加拉国、美国和马拉维腹泻儿童中获得的16株分离株进行了特征分析。具体而言,我们对它们的VP7和NSP4基因进行了测序,并将核苷酸(nt)和推导的氨基酸序列与参考G9毒株进行了比较。为了鉴定重配,我们检查了五个基因片段的产物;VP4、VP7和NSP4基因型(基因4、9和10);亚组(基因6);电泳型(基因11);以及所有最近G9分离株的基因组图谱。VP7基因的序列分析表明,最近美国的P[6],G9毒株与马拉维的G9毒株密切相关(核苷酸同一性>99%),但与印度的G9毒株(约97%核苷酸同一性)、孟加拉国的G9毒株(约98%核苷酸同一性)和参考毒株(约97%核苷酸同一性)不同。系统发育分析确定美国的P[6],G9毒株有一个单一的聚类,可能与马拉维的P[6],G9毒株有共同的祖代,而印度、孟加拉国和参考G9毒株则定义为不同的谱系。Northern杂交结果表明,马拉维P[6],G9毒株的所有11个基因片段都与来自同一基因型美国毒株的探针杂交,可能有相同的祖代,与印度G9毒株不同,而孟加拉国毒株可能是从美国G9祖代进化而来的。总体而言,我们的研究结果表明,新鉴定的G9毒株之间更大的多样性是由基因片段之间的重配产生的,而不是通过单个基因中突变的积累产生的。