Portela AnaCaroline Rodrigues, Hernandez Juliana Merces, Bandeira Renato Silva, Junior Edivaldo Costa Sousa, de Melo Taynah Cohen, Lucena Maria Silvia Sousa, Teixeira Dielle Monteiro, Siqueira Jones Anderson Monteiro, Gabbay Yvone Benchimol, Silva Luciana Damascena
Scientific initiation fellowships program (PIBIC/CNPq), Evandro Chagas Institute, Brazil.
Postgraduate Program in Biology of Infectious and Parasitic Agents, Federal University of Pará, Belém, Pará, Brazil.
Infect Genet Evol. 2021 Dec;96:105130. doi: 10.1016/j.meegid.2021.105130. Epub 2021 Nov 3.
Noroviruses are enteric viruses that cause acute gastroenteritis worldwide. Over two decades, GII.4 genotype was responsible for most cases. However, recombinant strains have emerged and changed the epidemiological context of these infections.
The aim of this study was to identify the recombinant genetic strains of norovirus causing gastroenteritis in Brazilian children from the Amazon region.
We analyzed 534 cases of gastroenteritis between 2015 and 2016. Genotypic characterization was performed by partial sequencing of ORF1 and ORF2. Evolutionary history was inferred by Bayesian inference using MrBayes. Recombinant strains were confirmed by Simplot and RDP4 analysis.
We performed viral detection tests and identified a norovirus frequency of 31.8% (175/534). Based on viral RdRp and VP1 genes, nine genotypes were identified: GIIP31/GII.4, GII·P16/GII.4, GII·P7/GII.6, GII·P21/GII.13, GII·P33/GII.1, GII·P17/GII.17, GI·P7/GI.7, GII·P4/NT, and GII.7/NT. The phylogenetic tree showed evolutionary relationships among the genotypes, including the recombinant strains. This is the first description of GII·P33/GII.1 and GII·P21/GII.13 genotypes in Brazil.
Norovirus evolution has been characterized by the continuous replacement of variants that have new antigenic properties. In recent years, recombinant strains have displaced GII.4, improving the viral fitness and influencing the viral transmissibility and pathogenicity.
诺如病毒是引起全球急性胃肠炎的肠道病毒。二十多年来,GII.4基因型导致了大多数病例。然而,重组毒株已经出现并改变了这些感染的流行病学情况。
本研究的目的是鉴定在巴西亚马逊地区儿童中引起胃肠炎的诺如病毒重组基因毒株。
我们分析了2015年至2016年期间的534例胃肠炎病例。通过对开放阅读框1(ORF1)和开放阅读框2(ORF2)进行部分测序来进行基因分型鉴定。使用MrBayes通过贝叶斯推断来推断进化历史。通过Simplot和RDP4分析确认重组毒株。
我们进行了病毒检测试验,确定诺如病毒感染率为31.8%(175/534)。基于病毒RNA依赖的RNA聚合酶(RdRp)和病毒蛋白1(VP1)基因,鉴定出9种基因型:GII.P31/GII.4、GII·P16/GII.4、GII·P7/GII.6、GII·P21/GII.13、GII·P33/GII.1、GII·P17/GII.17、GI·P7/GI.7、GII·P4/NT和GII.7/NT。系统发育树显示了各基因型之间的进化关系,包括重组毒株。这是巴西首次对GII·P33/GII.1和GII·P21/GII.13基因型进行描述。
诺如病毒的进化特征是具有新抗原特性的变异体不断更替。近年来,重组毒株已取代GII.4,提高了病毒适应性,并影响病毒的传播性和致病性。