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首页> 外文期刊>Journal of Virological Methods >Rapid molecular detection of the H275Y oseltamivir resistance gene mutation in circulating influenza A (H1N1) viruses.
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Rapid molecular detection of the H275Y oseltamivir resistance gene mutation in circulating influenza A (H1N1) viruses.

机译:快速分子检测循环甲型H1N1流感病毒中的H275Y奥司他韦耐药基因突变。

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摘要

In early 2008, drug susceptibility surveillance of influenza viruses in Europe revealed that some influenza A viruses (subtype H1N1) circulating during the winter season of 2007 and 2008 were resistant to the neuraminidase inhibitor, oseltamivir. This resistance arises due to a histidine to tyrosine substitution in the neuraminidase active site (H275Y in N1 nomenclature). Current methods to detect this mutation involve an end-point reverse transcription polymerase chain reaction followed by nucleotide sequencing. While accurate, this approach has the limitation of being time-consuming, labour-intensive and expensive. Herein we describe a one-step allelic discrimination assay which rapidly (2h) detects this resistance mutation. The sensitivity of the assay was as low as 10 copies per reaction and is capable of detecting the antiviral resistance mutation in a mixture of wild type H275 and mutant H275Y targets.
机译:在2008年初,欧洲对流感病毒的药敏监测显示,在2007年和2008年冬季传播的一些A型流感病毒(H1N1亚型)对神经氨酸酶抑制剂oseltamivir有抗药性。该抗性的产生是由于神经氨酸酶活性位点(N1命名法中的H275Y)中的组氨酸被酪氨酸取代。当前检测这种突变的方法包括终点逆转录聚合酶链反应,然后进行核苷酸测序。尽管这种方法是准确的,但是它具有耗时,劳动密集和昂贵的局限性。在这里,我们描述了一步等位基因鉴别测定法,该测定法迅速(2h)检测到这种抗性突变。该测定法的灵敏度低至每个反应10个拷贝,并且能够检测野生型H275和突变型H275Y靶标混合物中的抗病毒抗性突变。

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