Department of Virology, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.
J Virol Methods. 2010 Dec;170(1-2):165-8. doi: 10.1016/j.jviromet.2010.09.005. Epub 2010 Sep 15.
The sudden emergence of the pandemic influenza A (H1N1) 2009 virus in early 2009 has resulted in a rapid transmission of this virus worldwide. Within a short time span, sporadic cases infected with this virus that shows oseltamivir resistance have also been reported. These resistant viruses have an amino acid change from histidine to tyrosine at position 275 (H275Y) of the neuraminidase gene. In this study, a reverse transcriptase PCR/restriction fragment length polymorphism (RT-PCR/RFLP) assay was developed to detect the H275Y mutation. Resistant and sensitive viruses could be differentiated using the RFLP patterns. This RT-PCR/RFLP assay is a simple method and also very specific and sensitive for detecting the H275Y mutation of pandemic influenza A (H1N1) 2009 viruses, and can be used in resource-limited settings.
2009 年初,大流行性流感 A(H1N1)病毒的突然出现导致该病毒在全球范围内迅速传播。在短时间内,也报告了零星感染具有奥司他韦耐药性的此类病毒的病例。这些耐药病毒的神经氨酸酶基因 275 位的组氨酸突变为酪氨酸(H275Y)。在这项研究中,开发了逆转录酶 PCR/限制性片段长度多态性(RT-PCR/RFLP)检测方法,以检测 H275Y 突变。可以使用 RFLP 模式来区分耐药病毒和敏感病毒。该 RT-PCR/RFLP 检测方法是一种简单的方法,对于检测大流行性流感 A(H1N1)2009 病毒的 H275Y 突变非常特异和敏感,可在资源有限的情况下使用。