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使用多重实时聚合酶链反应快速鉴定氨基糖苷类药物致聋基因突变

Rapid identification of aminoglycoside-induced deafness gene mutations using multiplex real-time polymerase chain reaction.

作者信息

Huang Shasha, Xiang Guangxin, Kang Dongyang, Wang Chen, Kong Yanling, Zhang Xun, Liang Shujian, Mitchelson Keith, Xing Wanli, Dai Pu

机构信息

Department of Otolaryngology, PLA General Hospital, Do. 28 Fuxing Rode, Beijing 100853, People's Republic of China.

Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Hangzhou 310003, P. R. China; National Engineering Research Center for Beijing Biochip Technology, Beijing 102206, P. R. China; CapitaBio Corporation, Beijing 102206, P. R. China.

出版信息

Int J Pediatr Otorhinolaryngol. 2015 Jul;79(7):1067-72. doi: 10.1016/j.ijporl.2015.04.028. Epub 2015 Apr 25.

Abstract

BACKGROUND

Exposure to aminoglycoside antibiotics can induce ototoxicity in genetically susceptible individuals carrying certain mitochondrial DNA (mtDNA) mutations (C1494T and A1555G), resulting in hearing loss. So, a rapid diagnostic approach is needed to accurately identify subjects carrying such gene mutations.

METHODS

In the present study, we describe a rapid and reliable four-color, real-time quantitative polymerase chain reaction (qPCR) assay for simultaneously detecting two mtDNA 12S rRNA gene variants, A1555G and C1494T, which are prevalent in the Han Chinese population. This multiplex assay incorporates three allele-specific TaqMan probes labeled with different fluorophores in a single reaction, providing high genotyping accuracy for clinical blood samples.

RESULTS

Tests with C1494T, A1555G and wild-type DNA exhibited high sensitivity, specificity, reproducibility and accuracy of discriminating mutations from wild-type.

CONCLUSIONS

This study shows that this simple and inexpensive method can be used for routine molecular diagnostics and potentially for large-scale genetic screening.

摘要

背景

接触氨基糖苷类抗生素可在携带某些线粒体DNA(mtDNA)突变(C1494T和A1555G)的遗传易感个体中诱发耳毒性,导致听力丧失。因此,需要一种快速诊断方法来准确识别携带此类基因突变的个体。

方法

在本研究中,我们描述了一种快速可靠的四色实时定量聚合酶链反应(qPCR)检测方法,用于同时检测两个mtDNA 12S rRNA基因变体A1555G和C1494T,这两个变体在汉族人群中很常见。这种多重检测方法在单个反应中整合了三个用不同荧光团标记的等位基因特异性TaqMan探针,为临床血液样本提供了高基因分型准确性。

结果

对C1494T、A1555G和野生型DNA进行检测,结果显示该方法在区分突变型和野生型时具有高灵敏度、特异性、可重复性和准确性。

结论

本研究表明,这种简单且成本低廉的方法可用于常规分子诊断,并有可能用于大规模基因筛查。

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