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中国大陆2016 - 2017年流感季节期间人类流感病毒的神经氨酸酶抑制剂敏感性概况。

Neuraminidase inhibitor susceptibility profile of human influenza viruses during the 2016-2017 influenza season in Mainland China.

作者信息

Huang Weijuan, Cheng Yanhui, Li Xiyan, Tan Minju, Wei Hejiang, Zhao Xiang, Xiao Ning, Dong Jie, Wang Dayan

机构信息

Chinese National Influenza Center, National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention, Key Laboratory for Medical Virology, National Health Commission, Beijing, 102206, PR China.

Chinese National Influenza Center, National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention, Key Laboratory for Medical Virology, National Health Commission, Beijing, 102206, PR China.

出版信息

J Infect Chemother. 2018 Sep;24(9):729-733. doi: 10.1016/j.jiac.2018.05.003. Epub 2018 Jun 14.

Abstract

To understand the current situation of antiviral-resistance of influenza viruses to neuraminidase inhibitors (NAIs) in Mainland China, The antiviral-resistant surveillance data of the circulating influenza viruses in Mainland China during the 2016-2017 influenza season were analyzed. The total 3215 influenza viruses were studied to determine 50% inhibitory concentration (IC) for oseltamivir and zanamivir using a fluorescence-based assay. Approximately 0.3% (n = 10) of viruses showed either highly reduced inhibition (HRI) or reduced inhibition (RI) against at least one NAI. The most common neuraminidase (NA) amino acid substitution was H275Y in A (H1N1)pdm09 virus, which confers HRI by oseltamivir. Two A (H1N1)pdm09 viruses contained a new NA amino acid substitution respectively, S110F and D151E, which confers RI by oseltamivir or/and zanamivir. Two B/Victoria-lineage viruses harbored a new NA amino acid substitution respectively, H134Q and S246P, which confers RI by zanamivir. One B/Victoria-lineage virus contained dual amino acid substitution NA P124T and V422I, which confers HRI by zanamivir. One B/Yamagata-lineage virus was a reassortant virus that haemagglutinin (HA) from B/Yamagata-lineage virus and NA from B/Victoria-lineage virus, defined as B/Yamagata-lineage virus confers RI by oseltamivir, but as B/Victoria-lineage virus confers normal inhibition by oseltamivir. All new substitutions that have not been reported before, the correlation of these substitutions and observed changes in IC should be further assessed. During the 2016-2017 influenza season in Mainland China the majority tested viruses were susceptible to oseltamivir and zanamivir. Hence, NAIs remain the recommended antiviral for treatment and prophylaxis of influenza virus infections.

摘要

为了解中国大陆地区流感病毒对神经氨酸酶抑制剂(NAIs)的耐药现状,分析了2016 - 2017流感季中国大陆地区流行流感病毒的耐药监测数据。共研究了3215株流感病毒,采用基于荧光的检测方法测定其对奥司他韦和扎那米韦的50%抑制浓度(IC)。约0.3%(n = 10)的病毒对至少一种NAI表现出高度降低抑制(HRI)或降低抑制(RI)。最常见的神经氨酸酶(NA)氨基酸替代是A(H1N1)pdm09病毒中的H275Y,其导致对奥司他韦的HRI。两株A(H1N1)pdm09病毒分别含有新的NA氨基酸替代S110F和D151E,其导致对奥司他韦或/和扎那米韦的RI。两株B/维多利亚系病毒分别含有新的NA氨基酸替代H134Q和S246P,其导致对扎那米韦的RI。一株B/维多利亚系病毒含有双重氨基酸替代NA P124T和V422I,其导致对扎那米韦的HRI。一株B/山形系病毒是一种重组病毒,其血凝素(HA)来自B/山形系病毒,NA来自B/维多利亚系病毒,定义为B/山形系病毒对奥司他韦表现出RI,但作为B/维多利亚系病毒对奥司他韦表现出正常抑制。所有此前未报道过的新替代,这些替代与观察到的IC变化之间的相关性应进一步评估。在2016 - 2017年中国大陆流感季,大多数检测的病毒对奥司他韦和扎那米韦敏感。因此,NAIs仍然是推荐用于治疗和预防流感病毒感染的抗病毒药物。

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