Xue Liang, Wu Qingping, Cai Weicheng, Zhang Jumei, Guo Weipeng
Guangdong Institute of Microbiology, State Key Laboratory of Applied Microbiology Southern China, Guangzhou 510070, PR China; Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangdong Open Laboratory of Applied Microbiology, Guangzhou 510070, PR China.
Guangdong Institute of Microbiology, State Key Laboratory of Applied Microbiology Southern China, Guangzhou 510070, PR China; Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangdong Open Laboratory of Applied Microbiology, Guangzhou 510070, PR China.
Infect Genet Evol. 2016 Jun;40:1-7. doi: 10.1016/j.meegid.2016.02.026. Epub 2016 Feb 23.
Noroviruses are still the primary cause of non-bacterial acute gastroenteritis worldwide. Recently, a novel GII.17 norovirus variant emerged and caused an infection peak in the cold season of 2014/2015 in some Asian countries, including China. In this study, in order to understand the evolutionary advantage of the novel variant, complete genomic sequences of GII.17 NoV strains from South China were comprehensively analyzed. Pairwise alignments of new GII.17 genomes with representative sequences of each GII genotype were performed. Inconsistent homology was observed between different protein-encoding regions, of which VPg (NS5) and P2 were found to be the most conserved and variable ones, respectively. The differences between new sequences and other reported GII.17 genomes were also compared, and 84 mismatched nucleotides were found, resulting in 15 amino acid changes. Then, all capsid sequences of different GII.17 NoV variants were collected for multiple alignments, and a total of 87 spots were identified during their evolution process. Homology modeling of capsid proteins of four GII.17 variants was carried out based on comparison with GII.4 VA387 strain, and structural differences were mainly embodied in five extended loops. Furthermore, positions of potential conformational epitope regions of new GII.17 variants were found more similar or adjacent to those of GII.4 rather than those of the former GII.17 variants. In summary, nine GII.17 strains from South China were extensively characterized based on their complete genomes, and a different distribution pattern of epitope residues was predicted on the new GII.17 variant capsid from that of the former ones.
诺如病毒仍然是全球非细菌性急性肠胃炎的主要病因。最近,一种新型GII.17诺如病毒变体出现,并于2014/2015年寒冷季节在包括中国在内的一些亚洲国家引发了感染高峰。在本研究中,为了解该新型变体的进化优势,对来自中国南方的GII.17 NoV毒株的完整基因组序列进行了全面分析。将新的GII.17基因组与各GII基因型的代表性序列进行了两两比对。在不同的蛋白质编码区域观察到不一致的同源性,其中发现VPg(NS5)和P2分别是最保守和最可变的区域。还比较了新序列与其他已报道的GII.17基因组之间的差异,发现84个错配核苷酸,导致15个氨基酸变化。然后,收集不同GII.17 NoV变体的所有衣壳序列进行多重比对,在其进化过程中总共鉴定出87个位点。基于与GII.4 VA387毒株的比较,对四种GII.17变体的衣壳蛋白进行了同源建模,结构差异主要体现在五个延伸环上。此外,发现新的GII.17变体潜在构象表位区域的位置与GII.4的更相似或相邻,而不是与先前的GII.17变体。总之,基于来自中国南方的9株GII.17毒株的完整基因组进行了广泛表征,并预测新的GII.17变体衣壳上的表位残基分布模式与先前的不同。