Hussain Saira, Meijer Adam, Govorkova Elena A, Dapat Clyde, Gubareva Larisa V, Barr Ian G, Brown Sook Kwan, Daniels Rod S, Fujisaki Seiichiro, Galiano Monica, Huang Weijuan, Kondor Rebecca J, Lackenby Angie, Lewis Nicola, Lo Janice, Nguyen Ha T, Patel Mira C, Pereyaslov Dmitriy, Rattigan Aine, Samaan Magdi, Wang Dayan, Webby Richard J, Yen Hui-Ling, Zhang Wenqing, Takashita Emi
WHO Collaborating Centre for Reference and Research on Influenza, Peter Doherty Institute for Infection and Immunity, 792 Elizabeth Street, Melbourne, Victoria, 3000, Australia.
National Institute for Public Health and the Environment, PO Box 1, 3720, BA, Bilthoven, the Netherlands.
Antiviral Res. 2025 Sep;241:106217. doi: 10.1016/j.antiviral.2025.106217. Epub 2025 Jun 24.
Antiviral susceptibility of influenza viruses is monitored by the World Health Organization Global Influenza Surveillance and Response System. This study describes a global analysis of the susceptibility of influenza viruses to neuraminidase (NA) inhibitors (NAIs, oseltamivir, zanamivir, peramivir, laninamivir) and the cap-dependent endonuclease inhibitor (CENI, baloxavir) for three periods (May to May for 2020-2021, 2021-2022 and 2022-2023). In particular, global influenza activity declined significantly in 2020-2021 and 2021-2022 when compared to the pre-pandemic period of COVID-19. Combined phenotypic and NA sequence-based analysis revealed that the global frequency of seasonal influenza viruses with reduced or highly reduced inhibition (RI/HRI) by NAIs remained low, 0.09% (2/2224), 0.12% (27/23465) and 0.23% (124/53917) for 2020-2021, 2021-2022 and 2022-2023, respectively. As in previous years, NA-H275Y in A(H1N1)pdm09 viruses was the most frequent substitution causing HRI by oseltamivir and peramivir. Sequence-based analysis of polymerase acidic (PA) protein supplemented with phenotypic testing revealed low global frequencies of seasonal influenza viruses with reduced susceptibility (RS) to baloxavir, 0.07% (1/1376), 0.05% (9/18380) and 0.12% (48/39945) for 2020-2021, 2021-2022 and 2022-2023, respectively; commonly associated substitutions were PA-I38T/M/L. In Japan, the rate was 3.3% (16/488) during 2022-2023, with 11 A(H3N2) viruses having PA-I38T/M substitutions. For zoonotic viruses, 2.7% (3/111) contained substitutions, one each NA-H275Y, NA-S247N and NA-N295S, associated with RI/HRI NAI phenotypes, and none contained PA substitutions associated with RS to baloxavir. In conclusion, the great majority of seasonal and zoonotic influenza viruses remained susceptible to NAIs and CENI baloxavir.
世界卫生组织全球流感监测与应对系统对流感病毒的抗病毒敏感性进行监测。本研究描述了对三个时期(2020 - 2021年5月至5月、2021 - 2022年、2022 - 2023年)流感病毒对神经氨酸酶(NA)抑制剂(NAIs,奥司他韦、扎那米韦、帕拉米韦、拉尼米韦)和帽依赖性内切核酸酶抑制剂(CENI,巴洛沙韦)敏感性的全球分析。特别是,与新冠疫情大流行前时期相比,2020 - 2021年和2021 - 2022年全球流感活动显著下降。结合表型和基于NA序列的分析表明,对NAIs抑制作用降低或高度降低(RI/HRI)的季节性流感病毒的全球频率仍然较低,2020 - 2021年、2021 - 2022年和2022 - 2023年分别为0.09%(2/2224)、0.12%(27/23465)和0.23%(124/53917)。与往年一样,A(H1N¹)pdm09病毒中的NA - H275Y是导致对奥司他韦和帕拉米韦产生HRI的最常见替代。补充表型检测的聚合酶酸性(PA)蛋白的基于序列的分析表明,对巴洛沙韦敏感性降低(RS)的季节性流感病毒的全球频率较低,2020 - 2021年、2021 - 2022年和2022 - 2023年分别为0.07%(1/1376)、0.05%(9/18380)和0.12%(48/39945);常见的相关替代是PA - I38T/M/L。在日本,2022 - 2023年期间这一比例为3.3%(16/488),有11株A(H³N²)病毒具有PA - I38T/M替代。对于人畜共患病毒,2.7%(3/111)含有替代,分别为一个NA - H275Y、NA - S247N和NA - N295S,与RI/HRI NAI表型相关,且没有包含与对巴洛沙韦RS相关的PA替代。总之,绝大多数季节性和人畜共患流感病毒对NAIs和CENI巴洛沙韦仍然敏感。