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Frequency and distribution of H1N1 influenza A viruses with oseltamivir‐resistant mutations worldwide before and after the 2009 pandemic

奥司他韦 神经氨酸酶 神经氨酸酶抑制剂 病毒学 大流行 抗药性 生物 甲型流感病毒 病毒 抗病毒药物 抗性突变 2019年冠状病毒病(COVID-19) 遗传学 医学 基因 传染病(医学专业) 聚合酶链反应 内科学 逆转录酶 疾病
作者
Weixu Zhang,Hefeng Xu,Shuxuan Guan,Chengmin Wang,Guoying Dong
出处
期刊:Journal of Medical Virology [Wiley]
卷期号:94 (9): 4406-4416 被引量:19
标识
DOI:10.1002/jmv.27870
摘要

H1N1 influenza has brought serious threats to people's health and a high socioeconomic burden to society. Oseltamivir, a kind of neuraminidase (NA) inhibitor, is the second-generation specific drug that is broadly used currently. However, H1N1 influenza viruses have exhibited oseltamivir resistance in the past decades, which might be a hidden danger. To understand the frequency and distribution laws of oseltamivir-resistant viruses, we conducted a thorough and deep analysis of the available NA protein sequences of H1N1 influenza viruses worldwide from 1918 to 2020. The differences and similarities before and after 2009 were also considered since the dominant viruses changed in this period. Results showed that 3.76% of H1N1 viruses harbored oseltamivir resistance currently. Among various significative mutations, H274Y had the highest frequency of 3.30%, while the frequencies of the other mutations were far below this whether before or after 2009. The oseltamivir resistance was mainly found in three hosts, humans, swine, and avian. Different mutation sites could exhibit different distributions in each host. Our results showed that the resistance level reached a peak during the 2007-2008 influenza season and then quickly decreased in 2009. The resistance also displayed a global distribution. The densely populated countries usually had a high resistance level. However, frequent significative mutations were also found in some small countries. Our findings indicated the necessity of monitoring oseltamivir resistance around the world. The study could provide a unique perspective toward the cognition of viruses and facilitate the future study of both pandemic and drug development.
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