National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing.
Key Laboratory of Special Pathogens and Biosafety, Center for Emerging Infectious Diseases, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan.
J Infect Dis. 2018 Jun 5;218(1):133-143. doi: 10.1093/infdis/jiy182.
During 2016-2017, the previously rare GII.P16-GII.2 norovirus suddenly emerged as the predominant genotype causing gastroenteritis outbreaks in China and other countries. Its origin, phylodynamics, and mechanism behind the predominance remain unclear.
Bayesian phylogenetic analyses were performed on 180 full capsid and 150 polymerase sequences of 2016-2017 GII.P16-GII.2 noroviruses in China, and those for all publicly available GII.P16 and GII.2 sequences. Saliva-based histo-blood group antigen (HBGA) binding assays and crystal structural analysis were conducted by using the P proteins of 2016-2017 GII.P16-GII.2 noroviruses.
The reemerging GII.P16-GII.2 norovirus showed a rapid genetic diversification after its emergence in 2012-2013. The antigenicity and HBGA binding profile of the early 2016-2017 and pre-2016 GII.2 noroviruses were similar. A further variant with a single Val256Ile mutation and the conventionally orientated Asp382 in the VP1 protein showed an expanded HBGA-binding spectrum. Mutations on the surface of polymerase that could alter its function were seen, which may help to accelerate the VP1 gene evolution to 5.5 × 10-3 substitutions per site per year. This virus can be traced back to Pearl River Delta, China.
Our findings provide new insights into GII.2 norovirus epidemics and highlight the necessity of enhanced global surveillance for potential epidemics of rare-genotype noroviruses.
2016-2017 年期间,原本罕见的 GII.P16-GII.2 诺如病毒突然成为中国和其他国家引发胃肠炎暴发的主要基因型。其起源、系统发育动力学和优势背后的机制仍不清楚。
对中国 2016-2017 年 GII.P16-GII.2 诺如病毒的 180 个全衣壳和 150 个聚合酶序列以及所有公开的 GII.P16 和 GII.2 序列进行贝叶斯系统发育分析。通过使用 2016-2017 年 GII.P16-GII.2 诺如病毒的 P 蛋白进行基于唾液的组织血型抗原(HBGA)结合测定和晶体结构分析。
重新出现的 GII.P16-GII.2 诺如病毒在 2012-2013 年出现后迅速发生遗传多样化。早期 2016-2017 年和 2016 年前的 GII.2 诺如病毒的抗原性和 HBGA 结合特征相似。具有单个 Val256Ile 突变和 VP1 蛋白中常规定向 Asp382 的进一步变体显示出扩展的 HBGA 结合谱。在聚合酶表面发现了可以改变其功能的突变,这可能有助于加速 VP1 基因进化到每年每个位点 5.5×10-3 个取代。该病毒可追溯到中国珠江三角洲。
我们的研究结果为 GII.2 诺如病毒流行提供了新的见解,并强调了加强全球监测以预防罕见基因型诺如病毒潜在流行的必要性。