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应用焦磷酸测序法和神经氨酸酶抑制试验检测奥司他韦耐药的大流行流感 A(H1N1) 2009 病毒的比较。

A comparison of pyrosequencing and neuraminidase inhibition assays for the detection of oseltamivir-resistant pandemic influenza A(H1N1) 2009 viruses.

机构信息

WHO Collaborating Centre for Reference and Research on Influenza, 10 Wreckyn Street, North Melbourne, VIC 3051, Australia.

出版信息

Antiviral Res. 2011 Apr;90(1):87-91. doi: 10.1016/j.antiviral.2011.02.014. Epub 2011 Mar 2.

Abstract

Currently most pandemic influenza A(H1N1) 2009 (H1N1pdm) viruses are sensitive to oseltamivir, but a single point mutation (H275Y) in the neuraminidase (NA) gene of H1N1pdm can lead to resistance and such viruses have been reported from several countries. In this study we compare the performance of a pyrosequencing-based method for the detection of the H275Y mutation in H1N1pdm viruses with a conventional NA inhibition assay. Pyrosequencing could detect as little as 5% H275Y mutants in a mixed viral population, while mixtures with 25% or greater mutant virus were required before a significant increase in IC50 value could be detected. However, the sensitivity of the NA inhibition assay could be enhanced by using a more sophisticated curve-fitting analysis to generate similar results to the pyrosequencing assay. Of 181 H1N1pdm clinical samples examined by pyrosequencing, nine samples from five patients were found to contain H275Y mutant viruses, four of whom were under oseltamivir treatment. Changes in the ratio of H275Y mutant to wild-type viruses were observed in serial clinical specimens from two patients over the duration of their treatment. This study highlights the need for close monitoring of the H275Y mutation in clinical samples, in particular from severely ill patients infected with H1N1pdm. The use of pyrosequencing and the NA inhibition assay provide powerful tools for the rapid detection and quantitation of resistant influenza viruses in mixed populations.

摘要

目前,大多数大流行流感 A(H1N1) 2009(H1N1pdm)病毒对奥司他韦敏感,但 H1N1pdm 神经氨酸酶(NA)基因中的单点突变(H275Y)可导致耐药性,并且已经有几个国家报告了这种病毒。在这项研究中,我们比较了基于焦磷酸测序的方法和传统的 NA 抑制试验检测 H1N1pdm 病毒中 H275Y 突变的性能。焦磷酸测序可以在混合病毒群中检测到低至 5%的 H275Y 突变体,而在能够检测到 IC50 值显著增加之前,需要混合物中含有 25%或更高比例的突变病毒。然而,通过使用更复杂的曲线拟合分析,NA 抑制试验的灵敏度可以提高,从而产生与焦磷酸测序试验相似的结果。在通过焦磷酸测序检测的 181 份 H1N1pdm 临床样本中,有 9 份来自 5 名患者的样本含有 H275Y 突变病毒,其中 4 名患者正在接受奥司他韦治疗。在两名患者的治疗过程中,从他们的连续临床标本中观察到 H275Y 突变病毒与野生型病毒的比例发生了变化。这项研究强调了需要密切监测临床样本中的 H275Y 突变,特别是来自感染 H1N1pdm 的重症患者的样本。焦磷酸测序和 NA 抑制试验的使用为快速检测和定量混合人群中的耐药流感病毒提供了有力的工具。

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