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比利时轮状病毒疫苗衍生病例:减毒突变回复和其他肠胃炎病因的证据。

Rotavirus vaccine-derived cases in Belgium: Evidence for reversion of attenuating mutations and alternative causes of gastroenteritis.

机构信息

KU Leuven - University of Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, Leuven, Belgium.

Department of Laboratory Medicine, Medical Microbiology, AZ Sint-Jan, Brugge-Oostende AV, Bruges, Belgium.

出版信息

Vaccine. 2022 Aug 19;40(35):5114-5125. doi: 10.1016/j.vaccine.2022.06.082. Epub 2022 Jul 22.

Abstract

Since the introduction of live-attenuated rotavirus vaccines in Belgium in 2006, surveillance has routinely detected rotavirus vaccine-derived strains. However, their genomic landscape and potential role in gastroenteritis have not been thoroughly investigated. We compared VP7 and VP4 nucleotide sequences obtained from rotavirus surveillance with the Rotarix vaccine sequence. As a result, we identified 80 vaccine-derived strains in 5125 rotavirus-positive infants with gastroenteritis from 2007 to 2018. Using both viral metagenomics and reverse transcription qPCR, we evaluated the vaccine strains and screened for co-infecting enteropathogens. Among the 45 patients with known vaccination status, 39 were vaccinated and 87% received the vaccine less than a month before the gastroenteritis episode. Reconstruction of 30 near complete vaccine-derived genomes revealed 0-11 mutations per genome, with 88% of them being non-synonymous. This, in combination with several shared amino acid changes among strains, pointed at selection of minor variant(s) present in the vaccine. We also found that some of these substitutions were true revertants (e.g., F167L on VP4, and I45T on NSP4). Finally, co-infections with known (e.g., Clostridioides difficile and norovirus) and divergent or emerging (e.g., human parechovirus A1, salivirus A2) pathogens were detected, and we estimated that 35% of the infants likely had gastroenteritis due to a 'non-rotavirus' cause. Conversely, we could not rule out the vaccine-derived gastroenteritis in over half of the cases. Continued studies inspecting reversion to pathogenicity should monitor the long-time safety of live-attenuated rotavirus vaccines. All in all, the complementary approach with NGS and qPCR provided a better understanding of rotavirus vaccine strain evolution in the Belgian population and epidemiology of co-infecting enteropathogens in suspected rotavirus vaccine-derived gastroenteritis cases.

摘要

自 2006 年比利时引入减毒活轮状病毒疫苗以来,监测工作已常规检测到轮状病毒疫苗衍生株。然而,它们的基因组特征及其在胃肠炎中的潜在作用尚未得到深入研究。我们比较了从轮状病毒监测中获得的 VP7 和 VP4 核苷酸序列与 Rotarix 疫苗序列。结果,我们在 2007 年至 2018 年间,从 5125 例胃肠炎轮状病毒阳性婴儿中发现了 80 株疫苗衍生株。我们使用病毒宏基因组学和逆转录 qPCR 评估了疫苗株,并筛选了共同感染的肠道病原体。在 45 名已知接种状态的患者中,39 名接种了疫苗,87%的患者在胃肠炎发作前不到一个月接种了疫苗。对 30 个近乎完整的疫苗衍生基因组的重建显示每个基因组有 0-11 个突变,其中 88%为非同义突变。这与株间存在的少数变异(minor variant)选择一致,这些变异存在于疫苗中。我们还发现,其中一些突变是真正的回复突变(例如 VP4 上的 F167L 和 NSP4 上的 I45T)。最后,检测到已知(如艰难梭菌和诺如病毒)和不同或新兴(如人肠道病毒 A1、唾液病毒 A2)病原体的合并感染,我们估计,35%的婴儿可能患有由“非轮状病毒”引起的胃肠炎。相反,我们不能排除一半以上病例的疫苗衍生胃肠炎。持续进行的研究监测回复到致病性,应该监测减毒活轮状病毒疫苗的长期安全性。总之,使用 NGS 和 qPCR 的互补方法,更好地了解了比利时人群中轮状病毒疫苗株的进化以及疑似轮状病毒疫苗衍生胃肠炎病例中共同感染的肠道病原体的流行病学。

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