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

机译:神经氨酸酶的允许变化在提高耐奥司他韦的季节性甲型流感病毒(H1N1)的病毒适应性中起主要作用

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摘要

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. (C) 2014 Elsevier B.V. All rights reserved.
机译:允许的神经氨酸酶(NA)替代,例如R222Q,V234M和D344N,已经促进了耐奥司他韦的A / Brisbane / 59/2007(H1N1)-H275Y流感病毒的出现和在世界范围内的传播。但是,其他病毒部分的遗传变化对病毒适应性的潜在贡献仍未得到很好的研究。一系列重组A(H1N1)pdm09和A / WSN / 33 7:1重配子,包含野生型(WT)A /布里斯班/ 59/2007 NA基因或其单个(H275Y)和双(H275Y / Q222R,H275Y产生/ M234V和H275Y / N344D)变异体,并在体外评估其复制特性。当在A(H1N1)pdm09和A / WSN / 33背景中进行评估时,Q222R还原取代显着降低了病毒滴度。使用含有对奥司他韦敏感或对奥司他韦耐药的A /密西西比/ 03/2001株的NA基因的A / WSN / 33 7:1重配子,进一步证实了R222Q的许可作用。因此,NA允许取代在体外增强对奥司他韦抗性A(H1N1)-H275Y病毒的病毒复制中起着主导作用。 (C)2014 Elsevier B.V.保留所有权利。

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