Barreira Débora Maria Pires Gonçalves, Fumian Túlio Machado, Tonini Marco André Loureiro, Volpini Lays Paula Bondi, Santos Rodrigo Pratte, Ribeiro Anézia Lima Chaves, Leite José Paulo Gagliardi, Souza Márcia Terezinha Baroni de Moraes E, Brasil Patrícia, da Cunha Denise Cotrim, Miagostovich Marize Pereira, Spano Liliana Cruz
Laboratory of Virology and Infectious Gastroenteritis, Pathology Department, Health Science Center, Federal University of Espírito Santo, Av. Marechal Campos 1468, Maruípe, Vitória, ES, Brazil.
Laboratory of Comparative and Environmental Virology, Oswaldo Cruz Institute, Av. Brasil 4365, Rio de Janeiro, RJ, Brazil.
PLoS One. 2017 Dec 13;12(12):e0189504. doi: 10.1371/journal.pone.0189504. eCollection 2017.
Noroviruses are the leading cause of acute gastroenteritis (AGE) in all age groups worldwide. Despite the high genetic diversity of noroviruses, most AGE outbreaks are caused by a single norovirus genotype: GII.4. Since 1995, several different variants of norovirus GII.4 have been associated with pandemics, with each variant circulating for 3 to 8 years. The Sydney_2012 variant was first reported in Australia and then in other countries. A new variant, GII.P16-GII.4, was recently described in Japan and South Korea and then in the USA, France, Germany and England. In our study, 190 faecal specimens were collected from children admitted to a paediatric hospital and a public health facility during a surveillance study of sporadic cases of AGE conducted between January 2015 and July 2016. The norovirus was detected by RT-qPCR in 51 samples (26.8%), and in 37 of them (72.5%), the ORF1-2 junction was successfully sequenced. The new recombinant GII.P16-GII.4 Sydney was revealed for the first time in Brazil in 2016 and predominated among other strains (9 GII.Pe-GII.4, 3 GII.P17-GII.17, 1 GII.Pg-GII.1, 1 GII.P16-GII.3 and 1 GII.PNA-GII.4). The epidemiological significance of this new recombinant is still unknown, but continuous surveillance studies may evaluate its impact on the population, its potential to replace the first recombinant GII.Pe-GII.4 Sydney 2012 variant, and the emergence of new recombinant forms of GII.P16.
诺如病毒是全球所有年龄组急性胃肠炎(AGE)的主要病因。尽管诺如病毒具有高度的遗传多样性,但大多数AGE疫情是由单一的诺如病毒基因型:GII.4引起的。自1995年以来,诺如病毒GII.4的几种不同变体与大流行有关,每种变体流行3至8年。悉尼_2012变体首先在澳大利亚被报道,随后在其他国家也有报道。一种新的变体GII.P16-GII.4最近在日本和韩国被描述,随后在美国、法国、德国和英国也有发现。在我们的研究中,在2015年1月至2016年7月期间对AGE散发病例进行监测研究时,从一家儿科医院和一家公共卫生机构收治的儿童中收集了190份粪便标本。通过RT-qPCR在51份样本(26.8%)中检测到了诺如病毒,其中37份样本(72.5%)的ORF1-2连接处成功测序。新的重组GII.P16-GII.4悉尼变体于2016年首次在巴西被发现,并在其他菌株中占主导地位(9株GII.Pe-GII.4、3株GII.P17-GII.17、1株GII.Pg-GII.1、1株GII.P16-GII.3和1株GII.PNA-GII.4)。这种新重组体的流行病学意义尚不清楚,但持续的监测研究可能会评估其对人群的影响、取代第一个重组GII.Pe-GII.4悉尼2012变体的潜力以及GII.P16新重组形式的出现情况。