Mishin Vasiliy P, Hayden Frederick G, Gubareva Larisa V
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.
Antimicrob Agents Chemother. 2005 Nov;49(11):4515-20. doi: 10.1128/AAC.49.11.4515-4520.2005.
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.
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。