扎那米韦
奥司他韦
神经氨酸酶
神经氨酸酶抑制剂
病毒学
生物
突变
抗性突变
突变体
甲型流感病毒
病毒
野生型
微生物学
作者
Yacine Abed,Mariana Baz,Guy Boivin
出处
期刊:Antiviral Therapy
[International Medical Press]
日期:2006-11-01
卷期号:11 (8): 971-976
被引量:108
标识
DOI:10.1177/135965350601100804
摘要
Subtype-specific neuraminidase (NA) mutations conferring resistance to NA inhibitors (NAIs) have been reported during in vitro passages and in clinic. In this study, we evaluated the impact of various NA mutations (E119A/G/V, H274Y, R292K and N294S) on the susceptibility profiles to different NAIs (oseltamivir, zanamivir and peramivir) using recombinant NA proteins of influenza A/WSN/33 (H1N1) and A/Sydney/5/97-like (H3N2) viruses. In the N1 subtype, the E119V mutation conferred cross-resistance to oseltamivir, zanamivir and peramivir [1,727–2,144 and 5,050-fold increase in IC 50 values compared with wild-type (WT)] whereas only oseltamivir-resistance (1,028-fold increase in IC 50 ) was conferred by the same mutation in the N2 subtype. The N294S mutation conferred resistance to oseltamivir in both the N1 and N2 subtypes (197- and 1,879-fold increase in IC 50 values, respectively) whereas the H274Y mutation conferred resistance to oseltamivir (754-fold increase) and peramivir (260-fold increase) in the N1 subtype only. The virulence of reverse genetics-rescued A/WSN/33 viruses harbouring H274Y and N294S NA mutations was investigated in Balb/c mice. The WT and H274Y recombinants had identical LD 50 values (10 3 PFUs) and generated similar viral lung titres, whereas a higher LD 50 (10 4 PFUs) and a 1-log decrease in viral lung titres were obtained with the N294S mutant. This study shows that some NA mutations at framework residues may confer resistance to one or three NAIs depending on the viral subtype. It suggests that certain drug-resistant NA mutants may still be virulent although additional studies using clinical isolates are needed to confirm our results.
科研通智能强力驱动
Strongly Powered by AbleSci AI