Key Laboratory of Etiology and Epidemiology of Emerging Infectious Diseases in Universities of Shandong, Taishan Medical College, Taian, 271000, Shandong, China.
Department of Children's Medical Laboratory Diagnosis Center, Qilu Chidren's Hospital of Shandong University, Jinan, Shandong, 250022, China.
J Virol Methods. 2018 Aug;258:7-12. doi: 10.1016/j.jviromet.2018.05.005. Epub 2018 May 26.
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 × 10, 4 × 10, 5 × 10, and 3 × 10 copies/μL, 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.
手足口病(HFMD)是一种与肠道病毒(EV)基因型感染相关的儿科疾病。主要的 HFMD EV 病原体是肠道病毒 A71(EVA71)和柯萨奇病毒 A16(CVA16);然而,最近,柯萨奇病毒 A6(CVA6)和柯萨奇病毒 A10(CVA10)也出现了。临床上无法区分 EV 基因型,因此迫切需要一种快速检测四种主要 HFMD EV 基因型的新方法。在本研究中,建立了一种用于同时检测 CVA6、CVA10、CVA16 和 EVA71 的多重实时 PCR 检测方法。该方法在包含脑脊液(n=51)、血液(n=39)、粪便(n=58)和咽喉拭子(n=29)的临床样本验证组中进行了特异性和灵敏度的确定。结果表明,该多重实时 PCR 具有高特异性,与其他 EV 基因型无交叉反应,CVA6、CVA10、CVA16 和 EVA71 的检测下限分别为 4×10、4×10、5×10 和 3×10 拷贝/μL,与单重检测临床样本的灵敏度相当。本研究建立的多重实时 PCR 方法可用于快速检测四种最常见的 HFMD 相关 EV,进行循环 EV 基因型的流行病学监测,以及评估治疗反应和疫苗研究。