Cannon Jennifer L, Barclay Leslie, Collins Nikail R, Wikswo Mary E, Castro Christina J, Magaña Laura Cristal, Gregoricus Nicole, Marine Rachel L, Chhabra Preeti, Vinjé Jan
CDC Foundation, Atlanta, Georgia, USA.
Division of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
J Clin Microbiol. 2017 Jul;55(7):2208-2221. doi: 10.1128/JCM.00455-17. Epub 2017 May 10.
Noroviruses are the most frequent cause of epidemic acute gastroenteritis in the United States. Between September 2013 and August 2016, 2,715 genotyped norovirus outbreaks were submitted to CaliciNet. GII.4 Sydney viruses caused 58% of the outbreaks during these years. A GII.4 Sydney virus with a novel GII.P16 polymerase emerged in November 2015, causing 60% of all GII.4 outbreaks in the 2015-2016 season. Several genotypes detected were associated with more than one polymerase type, including GI.3, GII.2, GII.3, GII.4 Sydney, GII.13, and GII.17, four of which harbored GII.P16 polymerases. GII.P16 polymerase sequences associated with GII.2 and GII.4 Sydney viruses were nearly identical, suggesting common ancestry. Other common genotypes, each causing 5 to 17% of outbreaks in a season, included GI.3, GI.5, GII.2, GII.3, GII.6, GII.13, and GII.17 Kawasaki 308. Acquisition of alternative RNA polymerases by recombination is an important mechanism for norovirus evolution and a phenomenon that was shown to occur more frequently than previously recognized in the United States. Continued molecular surveillance of noroviruses, including typing of both polymerase and capsid genes, is important for monitoring emerging strains in our continued efforts to reduce the overall burden of norovirus disease.
诺如病毒是美国流行性急性肠胃炎最常见的病因。在2013年9月至2016年8月期间,2715起基因分型诺如病毒疫情被提交至CaliciNet。在此期间,GII.4悉尼病毒引发了58%的疫情。一种带有新型GII.P16聚合酶的GII.4悉尼病毒于2015年11月出现,在2015 - 2016季节引发了60%的GII.4疫情。检测到的几种基因型与不止一种聚合酶类型相关,包括GI.3、GII.2、GII.3、GII.4悉尼、GII.13和GII.17,其中四种携带GII.P16聚合酶。与GII.2和GII.4悉尼病毒相关的GII.P16聚合酶序列几乎相同,表明有共同的祖先。其他常见基因型,每个季节引发5%至17%的疫情,包括GI.3、GI.5、GII.2、GII.3、GII.6、GII.13和GII.17川崎308。通过重组获得替代RNA聚合酶是诺如病毒进化的重要机制,并且在美国,这一现象的发生频率比之前认为的更高。对诺如病毒持续进行分子监测,包括对聚合酶和衣壳基因进行分型,对于监测新出现的毒株很重要,有助于我们持续努力减轻诺如病毒疾病的总体负担。