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神经氨酸酶的适应性变化在提高对奥司他韦耐药的季节性甲型H1N1流感病毒株的病毒适应性方面起主导作用。

Permissive changes in the neuraminidase play a dominant role in improving the viral fitness of oseltamivir-resistant seasonal influenza A(H1N1) strains.

作者信息

Abed Yacine, Pizzorno Andrés, Bouhy Xavier, Boivin Guy

机构信息

Research Center in Infectious Diseases of the CHUQ-CHUL and Laval University, Québec City, QC, Canada.

Research Center in Infectious Diseases of the CHUQ-CHUL and Laval University, Québec City, QC, Canada.

出版信息

Antiviral Res. 2015 Feb;114:57-61. doi: 10.1016/j.antiviral.2014.12.006. Epub 2014 Dec 12.

Abstract

Permissive neuraminidase (NA) substitutions such as R222Q, V234M and D344N have facilitated the emergence and worldwide spread of oseltamivir-resistant influenza A/Brisbane/59/2007 (H1N1)-H275Y viruses. However, the potential contribution of genetic changes in other viral segments on viral fitness remains poorly investigated. A series of recombinant A(H1N1)pdm09 and A/WSN/33 7:1 reassortants containing the wild-type (WT) A/Brisbane/59/2007 NA gene or its single (H275Y) and double (H275Y/Q222R, H275Y/M234V and H275Y/N344D) variants were generated and their replicative properties were assessed in vitro. The Q222R reversion substitution significantly reduced viral titers when evaluated in both A(H1N1)pdm09 and A/WSN/33 backgrounds. The permissive role of the R222Q was further confirmed using A/WSN/33 7:1 reassortants containing the NA gene of the oseltamivir-susceptible or oseltamivir-resistant influenza A/Mississippi/03/2001 strains. Therefore, NA permissive substitutions play a dominant role for improving viral replication of oseltamivir-resistant A (H1N1)-H275Y viruses in vitro.

摘要

诸如R222Q、V234M和D344N等允许性神经氨酸酶(NA)替换促进了对奥司他韦耐药的甲型流感病毒/布里斯班/59/2007(H1N1)-H275Y病毒的出现和全球传播。然而,其他病毒片段的基因变化对病毒适应性的潜在贡献仍未得到充分研究。构建了一系列包含野生型(WT)A/布里斯班/59/2007 NA基因或其单突变(H275Y)和双突变(H275Y/Q222R、H275Y/M234V和H275Y/N344D)变体的重组A(H1N1)pdm09和A/WSN/33 7:1重配体,并在体外评估了它们的复制特性。当在A(H1N1)pdm09和A/WSN/33背景中评估时,Q222R回复替换显著降低了病毒滴度。使用包含对奥司他韦敏感或耐药的甲型流感病毒/密西西比/03/2001株NA基因的A/WSN/33 7:1重配体进一步证实了R222Q的允许作用。因此,NA允许性替换在体外改善对奥司他韦耐药的甲型(H1N1)-H275Y病毒的复制中起主导作用。

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