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寡核苷酸微阵列可视化同时检测奥司他韦和金刚烷胺耐药性流感。

Simultaneous detection of oseltamivir- and amantadine-resistant influenza by oligonucleotide microarray visualization.

机构信息

Department of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, People's Republic of China.

出版信息

PLoS One. 2013;8(2):e57154. doi: 10.1371/journal.pone.0057154. Epub 2013 Feb 22.

Abstract

Presently, the resistance of Influenza A virus isolates causes great difficulty for the prevention and treatment of influenza A virus infection. It is important to establish a drug-resistance detection method for epidemiological study and personalized medicine in the clinical setting. Consequently, a cost-effective oligonucleotide microarray visualization method, which was based on quantum dot-catalyzed silver deposition, was developed and evaluated for the simultaneous detection of neuraminidase H275Y and E119V; matrix protein 2 V27A and S31N mutations of influenza A (H3N2), seasonal influenza A (H1N1), and 2009 influenza A (H1N1). Then, 307 clinical throat swab specimens were detected and the drug-resistance results showed that 100% (17/17) of influenza A (H3N2) and 100% (259/259) of 2009 influenza A (H1N1) samples were resistant to amantadine and susceptible to oseltamivir; and 100% (5/5) of seasonal influenza A (H1N1) samples were resistant to both amantadine and oseltamivir.

摘要

目前,甲型流感病毒分离株的耐药性给甲型流感病毒感染的预防和治疗带来了很大的困难。在临床环境中,建立耐药性检测方法对于流行病学研究和个体化医学非常重要。因此,开发并评估了一种基于量子点催化银沉积的具有成本效益的寡核苷酸微阵列可视化方法,用于同时检测甲型流感(H3N2)、季节性流感(H1N1)和 2009 年甲型流感(H1N1)的神经氨酸酶 H275Y 和 E119V、基质蛋白 2 V27A 和 S31N 突变。然后,检测了 307 份临床咽喉拭子标本,耐药性结果表明,17/17 份甲型流感(H3N2)和 259/259 份 2009 年甲型流感(H1N1)样本对金刚烷胺完全耐药,对奥司他韦敏感;5/5 份季节性流感(H1N1)样本对金刚烷胺和奥司他韦均耐药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96cc/3579783/7fe12857f508/pone.0057154.g001.jpg

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