Ianiro Giovanni, Delogu Roberto, Fiore Lucia, Ruggeri Franco M
Dept of Veterinary Public Health and Food Safety.
National Center for Immunobiologicals Research and Evaluation, Istituto Superiore di Sanità, Viale Regina Elena, 299, 00161 Rome, Italy.
Virus Res. 2015 Jun 2;204:68-73. doi: 10.1016/j.virusres.2015.04.007. Epub 2015 Apr 16.
Group A rotaviruses (RVA) are the leading cause of acute gastroenteritis in young (<5 years of age) children, causing up to 450.000 deaths worldwide, mostly in developing countries. VP7 (G-type) and VP4 (P-type) genotypes are the basis for the binary RVA classification. Although at least 27 G-types and 37 P-types of rotavirus are presently known, most RVA infections in humans worldwide are associated with the five major G/P combinations G1P[8], G2P[4], G3P[8], G4P[8] and G9P[8]. During RVA gastroenteritis surveillance in Italy, a total of 1112 samples collected from children hospitalized with acute gastroenteritis in 2013 were RVA positive and were genotyped following standardized protocols from the EuroRotaNet. Most strains analyzed belonged to the five major human genotypes. Among these common strains, 22 G4P[8] RVA strains from different Italian regions were subjected to nucleotide sequencing of their VP4, VP6, VP7 and NSP4 genes to investigate their evolution. The phylogenetic analysis showed that the Italian strains belonged to lineage G4-I for VP7 and to lineage P[8]-III for VP4, in line with the modern G4P[8] RVA strains detected in children worldwide. The phylogenetic trees revealed high degrees of nucleotide identity between the RVA strains involved in this study and G4P[8] strains detected previously in Europe, Asia and Africa, but also demonstrated at least three separate evolution clusters within the same lineage. Based on the amino acid sequences deduced for their hypervariable regions, both the VP7 and VP8* proteins of the Italian G4P[8] RVA strains presented amino acid substitutions near known neutralizing epitopes.
A组轮状病毒(RVA)是5岁以下幼儿急性胃肠炎的主要病因,在全球范围内导致多达45万例死亡,其中大部分发生在发展中国家。VP7(G型)和VP4(P型)基因型是RVA二元分类的基础。虽然目前已知至少27种G型和37种P型轮状病毒,但全球大多数人类RVA感染与五种主要的G/P组合G1P[8]、G2P[4]、G3P[8]、G4P[8]和G9P[8]有关。在意大利进行RVA胃肠炎监测期间,2013年从因急性胃肠炎住院的儿童中收集的1112份样本RVA呈阳性,并按照欧洲轮状病毒监测网络的标准化方案进行基因分型。分析的大多数毒株属于五种主要的人类基因型。在这些常见毒株中,对来自意大利不同地区的22株G4P[8] RVA毒株的VP4、VP6、VP7和NSP4基因进行了核苷酸测序,以研究它们的进化。系统发育分析表明,意大利毒株的VP7属于G4-I谱系,VP4属于P[8]-III谱系,与全球儿童中检测到的现代G4P[8] RVA毒株一致。系统发育树显示,本研究中涉及的RVA毒株与先前在欧洲、亚洲和非洲检测到的G4P[8]毒株之间存在高度的核苷酸同一性,但也表明在同一谱系内至少有三个独立的进化簇。根据其高变区推导的氨基酸序列,意大利G4P[8] RVA毒株的VP7和VP8*蛋白在已知中和表位附近均出现了氨基酸替换。