1Veterinary Virology and Animal Viral Diseases, Department of Infectious and Parasitic Diseases, FARAH Research Centre, Faculty of Veterinary Medicine, Liège University, B43b, Quartier Vallée 2, Avenue de Cureghem, 10, B-4000 Liège, Belgium.
2Staff direction for risk assessment, Control Policy, Federal Agency for the Safety of the Food Chain, Blv du Jardin Botanique 55, 1000 Brussels, Belgium.
J Gen Virol. 2018 Aug;99(8):970-988. doi: 10.1099/jgv.0.001103. Epub 2018 Jun 15.
Noroviruses are recognized as the major global cause of sporadic and epidemic non-bacterial gastroenteritis in humans. Molecular mechanisms driving norovirus evolution are the accumulation of point mutations and recombination. Intragenotypic recombination has long been postulated to be a driving force of GII.4 noroviruses, the predominant genotype circulating in humans for over two decades. Increasingly, emergence and re-emergence of different intragenotype recombinants have been reported. The number and types of norovirus recombinants remained undefined until the 2007 Journal of General Virology research article 'Norovirus recombination' reported an assembly of 20 hitherto unclassified intergenotypic norovirus recombinant types. In the intervening decade, a host of novel recombinants has been analysed. New recombination breakpoints have been described, in vitro and in vivo studies supplement in silico analyses, and advances have been made in analysing factors driving norovirus recombination. This work presents a timely overview of these data and focuses on important aspects of norovirus recombination and its role in norovirus molecular evolution. An overview of intergenogroup, intergenotype, intragenotype and 'obligatory' norovirus recombinants as detected via in silico methods in the field is provided, enlarging the scope of intergenotypic recombinant types to 80 in total, and notably including three intergenogroup recombinants. A recap of advances made studying norovirus recombination in the laboratory is given. Putative drivers and constraints of norovirus recombination are discussed and the potential link between recombination and norovirus zoonosis risk is examined.
诺如病毒被认为是人类散发和流行的非细菌性胃肠炎的主要全球病因。推动诺如病毒进化的分子机制是点突变的积累和重组。种内重组长期以来一直被认为是 GII.4 诺如病毒的驱动力,GII.4 诺如病毒是人类流行超过二十年的主要基因型。越来越多的不同种内重组体的出现和再现被报道。直到 2007 年《普通病毒学杂志》的研究文章“诺如病毒重组”报道了 20 种以前未分类的种间诺如病毒重组类型,诺如病毒重组体的数量和类型仍未确定。在这十年中,分析了许多新的重组体。描述了新的重组断点,体外和体内研究补充了计算机分析,并且在分析推动诺如病毒重组的因素方面取得了进展。本文及时概述了这些数据,并重点介绍了诺如病毒重组及其在诺如病毒分子进化中的作用的重要方面。概述了通过现场的计算机方法检测到的种间、种内、种内和“强制性”诺如病毒重组体,将种间重组体的类型总数扩大到 80 种,值得注意的是包括三种种间重组体。总结了在实验室中研究诺如病毒重组的进展。讨论了诺如病毒重组的潜在驱动因素和限制因素,并检查了重组与诺如病毒人畜共患病风险之间的潜在联系。