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一种检测人肠道病毒和柯萨奇病毒A16的实时方法的开发与评估

Development and evaluation of a real-time method for testing human enteroviruses and coxsackievirus A16.

作者信息

Chen Qian, Hu Zheng, Zhang Qihua, Yu Minghui

机构信息

Institute of Pediatrics, Nanjing Children's Hospital affiliated to Nanjing Medical University, No. 72 Guangzhou Road, Gulou Area, Nanjing, Jiangsu 210008, China.

Institute of Pediatrics, Nanjing Children's Hospital affiliated to Nanjing Medical University, No. 72 Guangzhou Road, Gulou Area, Nanjing, Jiangsu 210008, China.

出版信息

Diagn Microbiol Infect Dis. 2016 May;85(1):36-41. doi: 10.1016/j.diagmicrobio.2016.02.003. Epub 2016 Feb 5.

Abstract

Hand, foot, and mouth disease (HFMD) is a common infectious disease caused by a group of the human enteroviruses (HEV), including coxsackievirus A16 (CA16) and enterovirus 71 (EV71). In recent years, another HEV-A serotype, CA6 or CA10, has emerged to be one of the major etiologic agents that can induce HFMD worldwide. The objective of this study is to develop specific, sensitive, and rapid methods to help diagnose HEV and CA16 specifically by using simultaneous amplification testing (SAT) based on isothermal amplification of RNA and real-time detection of fluorescence technique, which were named as SAT-HEV and SAT-CA16, respectively (SAT-HEV/SAT-CA16). The specificity and sensitivity of SAT were tested here. SAT-HEV/SAT-CA16 could measure viral titers that were at least 10-fold lower than those measured by real-time PCR. Non-false cross-reactive amplification indicated that SAT-HEV/SAT-CA16 were highly specific with the addition of internal control (IC) RNA (5000 copies/reaction). A total of 198 clinical specimens were assayed by SAT comparing with real-time PCR. The statistically robust assessment of SAT-HEV and HEV-specific real-time PCR plus sequencing reached 99.0% (196/198), with a kappa value of 0.97, and 99.5% (197/198) and a kappa value of 0.99 for CA16, respectively. Additionally, IC prevented false-negative readings and assured the SAT-HEV/SAT-CA16 method's accuracy. Overall, SAT-HEV/SAT-CA16 method may serve as a platform for the simple and rapid detection of HEV/CA16 in time of HFMD outbreak.

摘要

手足口病(HFMD)是一种由一组人类肠道病毒(HEV)引起的常见传染病,包括柯萨奇病毒A16(CA16)和肠道病毒71型(EV71)。近年来,另一种HEV-A血清型,CA6或CA10,已成为全球范围内可引发手足口病的主要病原体之一。本研究的目的是开发特异性强、灵敏度高且快速的方法,通过基于RNA等温扩增和荧光实时检测技术的同步扩增检测(SAT)来特异性诊断HEV和CA16,分别命名为SAT-HEV和SAT-CA16(SAT-HEV/SAT-CA16)。在此测试了SAT的特异性和灵敏度。SAT-HEV/SAT-CA16能够检测到的病毒滴度比实时PCR检测到的至少低10倍。无假交叉反应扩增表明,添加内部对照(IC)RNA(5000拷贝/反应)时,SAT-HEV/SAT-CA16具有高度特异性。与实时PCR相比,共对198份临床标本进行了SAT检测。SAT-HEV与HEV特异性实时PCR加测序的统计学稳健评估一致性达到99.0%(196/198),kappa值为0.97,CA16的一致性为99.5%(197/198),kappa值为0.99。此外,IC可防止假阴性读数并确保SAT-HEV/SAT-CA16方法的准确性。总体而言,SAT-HEV/SAT-CA16方法可作为在手足口病爆发时简单快速检测HEV/CA16的平台。

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