Suppr超能文献

抗病毒耐药流感病毒对新型神经氨酸酶抑制剂的敏感性。

Susceptibilities of antiviral-resistant influenza viruses to novel neuraminidase inhibitors.

作者信息

Mishin Vasiliy P, Hayden Frederick G, Gubareva Larisa V

机构信息

Division of Infectious Diseases and International Health, Department of Internal Medicine, University of Virginia Health Sciences Center, P.O. Box 800473, 1300 Jefferson Ave., Rm. 2231, Charlottesville, Virginia 22908, USA.

出版信息

Antimicrob Agents Chemother. 2005 Nov;49(11):4515-20. doi: 10.1128/AAC.49.11.4515-4520.2005.

Abstract

The susceptibilities of five zanamivir-resistant and six oseltamivir-resistant influenza viruses were assessed against four neuraminidase (NA) inhibitors, including peramivir and A-315675, by a fluorometric NA activity inhibition assay. The enzyme activity of a majority of the variants was effectively inhibited by either A-315675 or both peramivir and A-315675 (50% inhibitory concentration, <10 nM). A novel oseltamivir-resistant influenza virus B variant carrying substitution at residue 198 (Asp-->Asn) (N2 numbering) retained susceptibility to peramivir and A-315675. In vivo, the Asn198 variant showed no apparent fitness impairment as judged by its recovery on day 5 from the nasal washes of ferrets coinfected with equal doses of the wild-type virus and the Asn198 variant. Based on the sequence analysis of the virus in the nasal washes, oseltamivir treatment (5 mg/kg twice daily for 5 days) did not provide growth advantage to the Asn198 variant. Nevertheless, treatment with A-315675 (prodrug A-322278) reduced the number of the animals (two of seven) shedding the Asn198 variant. These studies indicate that different patterns of susceptibility and cross-resistance between NA inhibitors may prove important if antiviral resistance to zanamivir and oseltamivir were to emerge.

摘要

通过荧光神经氨酸酶(NA)活性抑制试验,评估了5株对扎那米韦耐药和6株对奥司他韦耐药的流感病毒对4种神经氨酸酶抑制剂(包括帕拉米韦和A-315675)的敏感性。大多数变异株的酶活性可被A-315675或帕拉米韦与A-315675二者有效抑制(50%抑制浓度,<10 nM)。一种新型的对奥司他韦耐药的B型流感病毒变异株,其198位残基(天冬氨酸→天冬酰胺)(N2编号)发生置换,对帕拉米韦和A-315675仍敏感。在体内,根据从同时感染等量野生型病毒和Asn198变异株的雪貂鼻腔冲洗液中第5天的病毒回收情况判断,Asn198变异株未显示出明显的适应性损害。基于鼻腔冲洗液中病毒的序列分析,奥司他韦治疗(5 mg/kg,每日2次,共5天)未使Asn198变异株获得生长优势。然而,用A-315675(前体药物A-322278)治疗减少了排出Asn198变异株的动物数量(7只中有2只)。这些研究表明,如果出现对扎那米韦和奥司他韦的抗病毒耐药性,NA抑制剂之间不同的敏感性和交叉耐药模式可能会很重要。

相似文献

1
Susceptibilities of antiviral-resistant influenza viruses to novel neuraminidase inhibitors.
Antimicrob Agents Chemother. 2005 Nov;49(11):4515-20. doi: 10.1128/AAC.49.11.4515-4520.2005.
7
Neuraminidase Mutations Conferring Resistance to Oseltamivir in Influenza A(H7N9) Viruses.
J Virol. 2015 May;89(10):5419-26. doi: 10.1128/JVI.03513-14. Epub 2015 Mar 4.
9
Neuraminidase inhibitor-resistant influenza viruses may differ substantially in fitness and transmissibility.
Antimicrob Agents Chemother. 2005 Oct;49(10):4075-84. doi: 10.1128/AAC.49.10.4075-4084.2005.

引用本文的文献

1
Drug resistance and possible therapeutic options against influenza A virus infection over past years.
Arch Microbiol. 2024 Nov 5;206(12):458. doi: 10.1007/s00203-024-04181-3.
2
Antiviral Potential of Natural Resources against Influenza Virus Infections.
Viruses. 2022 Nov 5;14(11):2452. doi: 10.3390/v14112452.
3
Inhibition of Influenza Virus Replication by Oseltamivir Derivatives.
Pathogens. 2022 Feb 11;11(2):237. doi: 10.3390/pathogens11020237.
4
A Novel Bifunctional Fusion Protein, Vunakizumab-IL22, for Protection Against Pulmonary Immune Injury Caused by Influenza Virus.
Front Immunol. 2021 Aug 24;12:727941. doi: 10.3389/fimmu.2021.727941. eCollection 2021.
5
Baloxavir Treatment Delays Influenza B Virus Transmission in Ferrets and Results in Limited Generation of Drug-Resistant Variants.
Antimicrob Agents Chemother. 2021 Oct 18;65(11):e0113721. doi: 10.1128/AAC.01137-21. Epub 2021 Aug 23.
8
Anti-Influenza Strategies Based on Nanoparticle Applications.
Pathogens. 2020 Dec 3;9(12):1020. doi: 10.3390/pathogens9121020.
9
Prion protein signaling induces M2 macrophage polarization and protects from lethal influenza infection in mice.
PLoS Pathog. 2020 Aug 26;16(8):e1008823. doi: 10.1371/journal.ppat.1008823. eCollection 2020 Aug.
10
Status presens of antiviral drugs and strategies: Part II: RNA VIRUSES (EXCEPT RETROVIRUSES).
Adv Antivir Drug Des. 2007;5:59-112. doi: 10.1016/S1075-8593(06)05002-7. Epub 2007 Sep 2.

本文引用的文献

2
Characterization of recombinant influenza B viruses with key neuraminidase inhibitor resistance mutations.
J Antimicrob Chemother. 2005 Feb;55(2):162-9. doi: 10.1093/jac/dkh528. Epub 2005 Jan 21.
3
Influenza viruses resistant to the antiviral drug oseltamivir: transmission studies in ferrets.
J Infect Dis. 2004 Nov 1;190(9):1627-30. doi: 10.1086/424572. Epub 2004 Sep 28.
6
Resistant influenza A viruses in children treated with oseltamivir: descriptive study.
Lancet. 2004;364(9436):759-65. doi: 10.1016/S0140-6736(04)16934-1.
7
Genesis of a highly pathogenic and potentially pandemic H5N1 influenza virus in eastern Asia.
Nature. 2004 Jul 8;430(6996):209-13. doi: 10.1038/nature02746.
8
Identification of a human influenza type B strain with reduced sensitivity to neuraminidase inhibitor drugs.
Virus Res. 2004 Jul;103(1-2):205-11. doi: 10.1016/j.virusres.2004.02.035.
9
Molecular mechanisms of influenza virus resistance to neuraminidase inhibitors.
Virus Res. 2004 Jul;103(1-2):199-203. doi: 10.1016/j.virusres.2004.02.034.
10
Avian influenza: a new pandemic threat?
Mayo Clin Proc. 2004 Apr;79(4):523-30; quiz 530. doi: 10.4065/79.4.523.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验