Rapid detection of hand, foot and mouth disease enterovirus genotypes by multiplex PCR

被引:16
作者
Wang, Min [1 ]
Ren, Qian [2 ]
Zhang, Zhenjie [1 ]
Zhang, Lehai [2 ]
Carr, Michael J. [3 ,4 ]
Li, Juan [1 ]
Zhou, Hong [1 ]
Shi, Weifeng [1 ]
机构
[1] Taishan Med Coll, Key Lab Etiol & Epidemiol Emerging Infect Dis Uni, Tai An 271000, Shandong, Peoples R China
[2] Shandong Univ, Dept Childrens Med Lab, Diag Ctr, Qilu Chidrens Hosp, Jinan 250022, Shandong, Peoples R China
[3] Hokkaido Univ, Global Stn Zoonosis Control, Global Inst Collaborat Res & Educ GI CoRE, Sapporo, Hokkaido 0010020, Japan
[4] Univ Coll Dublin, Sch Med, Natl Virus Reference Lab, Dublin 4, Ireland
基金
中国国家自然科学基金;
关键词
Enterovirus; HFMD; Multiplex PCR; CVA6; CVA10; CVA16; EVA71; COXSACKIEVIRUS A6; GENETIC-CHARACTERIZATION; A10; ASSAY; OUTBREAK;
D O I
10.1016/j.jviromet.2018.05.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Hand, foot and mouth disease (HFMD) is a pediatric disease associated with infection by enterovirus (EV) genotypes. The major HFMD EV pathogens are enterovirus A71 (EVA71) and coxsackievirus A16 (CVA16); however, recently, coxsackievirus A6 (CVA6) and coxsackievirus A10 (CVA10) have also emerged. EV genotypes cannot be distinguished on clinical grounds and a new methodology for the rapid detection of the four major HFMD EV genotypes is urgently required. In the present study, a multiplex real-time PCR assay was established for the simultaneous detection of CVA6, CVA10, CVA16 and EVA71. The specificity and sensitivity of the assay was determined on a validation panel of clinical samples, comprising cerebrospinal fluid (n = 51), blood (n = 39), feces (n = 58) and throat swabs (n = 29). The results showed that the multiplex real-time PCR exhibited high specificity, no cross-reactivity with other EV genotypes, lower limits of detection for CVA6, CVA10, CVA16 and EVA71 were 4 x 10(3), 4 x 10(2), 5 x 10(2), and 3 x 10(3) copies/pL, respectively and had comparable sensitivity to singleplex assays testing clinical samples. The multiplex real-time PCR methodology established in this study can be employed for the rapid detection of the four most prevalent HFMD-associated EVs, for epidemiologic surveillance of circulating EV genotypes and for assessing treatment responses and vaccine studies.
引用
收藏
页码:7 / 12
页数:6
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