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无关其基因簇,肠道病毒 A3(PeV-A3)相关肌痛/肌炎的发生:2003 年至 2016 年日本山形县 PeV-A3 的纵向分子流行病学研究。

Parechovirus A3 (PeV-A3)-associated myalgia/myositis occurs irrespective of its genetic cluster: a longitudinal molecular epidemiology of PeV-A3 in Yamagata, Japan between 2003 and 2016.

机构信息

1​Department of Microbiology, Yamagata Prefectural Institute of Public Health, Yamagata, 990-0031, Japan.

2​Department of Neurology, Yamagata Prefectural Central Hospital, Yamagata, 990-2292, Japan.

出版信息

J Med Microbiol. 2019 Mar;68(3):424-428. doi: 10.1099/jmm.0.000894. Epub 2018 Dec 17.

Abstract

No longitudinal molecular epidemiology of parechovirus A3 (PeV-A3) over a decade is available and PeV-A3-associated myalgia/myositis has been reported only in Japan. Thus, we aimed to clarify the longitudinal molecular epidemiology of PeV-A3 with a major focus on the strains detected from PeV-A3-associated myalgia/myositis cases. We performed sequence and phylogenetic analysis for the VP1 region of PeV-A3 strains in Yamagata, Japan, between 2003 and 2016. The phylogenetic analysis indicated that PeV-A3 strains caused PeV-A3-associated myalgia/myositis as well as a variety of infectious diseases, ranging from mild to severe, in subjects ranging from neonates to adults, irrespective of genetic cluster or variations. PeV-A3 strains are causative agents of a variety of human diseases, irrespective of their genetic cluster. Furthermore, we consider that PeV-A3-associated myalgia/myositis may occur, not only in Japan, but also in other countries, as closely related PeV-A3 strains have been circulating around the world.

摘要

尚无关于肠道病毒 A3 型(PeV-A3)长达十年的纵向分子流行病学资料,且 PeV-A3 相关肌痛/肌炎仅在日本有报道。因此,我们旨在阐明 PeV-A3 的纵向分子流行病学,重点关注从 PeV-A3 相关肌痛/肌炎病例中检测到的毒株。我们对日本山形县 2003 年至 2016 年间的 PeV-A3 毒株的 VP1 区进行了序列和系统发育分析。系统发育分析表明,PeV-A3 毒株可引起 PeV-A3 相关肌痛/肌炎以及各种从轻度到重度的传染病,感染对象从新生儿到成人不等,与遗传聚类或变异无关。PeV-A3 毒株是各种人类疾病的病原体,与其遗传聚类无关。此外,我们认为 PeV-A3 相关肌痛/肌炎不仅在日本,而且在其他国家也可能发生,因为世界各地都有密切相关的 PeV-A3 株在传播。

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