Cargando…

The Development and Application of the Two Real-Time RT-PCR Assays to Detect the Pathogen of HFMD

Large-scale Hand, Foot, and Mouth Disease (HFMD) outbreaks have frequently occurred in China since 2008, affecting more than one million children and causing several hundred children deaths every year. The pathogens of HFMD are mainly human enteroviruses (HEVs). Among them, human enterovirus 71 (HEV...

Descripción completa

Detalles Bibliográficos
Autores principales: Cui, Aili, Xu, Changping, Tan, Xiaojuan, Zhang, Yan, Zhu, Zhen, Mao, Naiying, Lu, Yiyu, Xu, Wenbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3630163/
https://www.ncbi.nlm.nih.gov/pubmed/23637836
http://dx.doi.org/10.1371/journal.pone.0061451
_version_ 1782266669779910656
author Cui, Aili
Xu, Changping
Tan, Xiaojuan
Zhang, Yan
Zhu, Zhen
Mao, Naiying
Lu, Yiyu
Xu, Wenbo
author_facet Cui, Aili
Xu, Changping
Tan, Xiaojuan
Zhang, Yan
Zhu, Zhen
Mao, Naiying
Lu, Yiyu
Xu, Wenbo
author_sort Cui, Aili
collection PubMed
description Large-scale Hand, Foot, and Mouth Disease (HFMD) outbreaks have frequently occurred in China since 2008, affecting more than one million children and causing several hundred children deaths every year. The pathogens of HFMD are mainly human enteroviruses (HEVs). Among them, human enterovirus 71 (HEV71) and coxsackievirus A16 (CVA16) are the most common pathogens of HFMD. However, other HEVs could also cause HFMD. To rapidly detect HEV71 and CVA16, and ensure detection of all HEVs causing HFMD, two real-time hybridization probe-based RT-PCR assays were developed in this study. One is a multiplex real-time RT-PCR assay, which was developed to detect and differentiate HEV71 specifically from CVA16 directly from clinical specimens within 1–2 h, and the other is a broad-spectrum real-time RT-PCR assay, which targeted almost all HEVs. The experiments confirmed that the two assays have high sensitivity and specificity, and the sensitivity was up to 0.1 TCID(50)/ml for detection of HEVs, HEV71, and CVA16, respectively. A total of 213 clinical specimens were simultaneously detected by three kinds of assays, including the two real-time RT-PCR assays, direct conventional RT-PCR assay, and virus isolation assay on human rhabdomyosarcoma cells (RD cells). The total positive rate of both HEV71 and CVA16 was 69.48% with real-time RT-PCR assay, 47.42% with RT-PCR assay, and 34.58% with virus isolation assay. One HFMD clinical specimen was positive for HEV, but negative for HEV71 or CVA16, which was identified as Echovirus 11 (Echo11) by virus isolation, RT-PCR, and sequencing for the VP1 gene. The two real-time RT-PCR assays had been applied in 31 provincial HFMD labs to detect the pathogens of HFMD, which has contributed to the rapid identification of the pathogens in the early stages of HFMD outbreaks, and helped to clarify the etiologic agents of HFMD in China.
format Online
Article
Text
id pubmed-3630163
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-36301632013-05-01 The Development and Application of the Two Real-Time RT-PCR Assays to Detect the Pathogen of HFMD Cui, Aili Xu, Changping Tan, Xiaojuan Zhang, Yan Zhu, Zhen Mao, Naiying Lu, Yiyu Xu, Wenbo PLoS One Research Article Large-scale Hand, Foot, and Mouth Disease (HFMD) outbreaks have frequently occurred in China since 2008, affecting more than one million children and causing several hundred children deaths every year. The pathogens of HFMD are mainly human enteroviruses (HEVs). Among them, human enterovirus 71 (HEV71) and coxsackievirus A16 (CVA16) are the most common pathogens of HFMD. However, other HEVs could also cause HFMD. To rapidly detect HEV71 and CVA16, and ensure detection of all HEVs causing HFMD, two real-time hybridization probe-based RT-PCR assays were developed in this study. One is a multiplex real-time RT-PCR assay, which was developed to detect and differentiate HEV71 specifically from CVA16 directly from clinical specimens within 1–2 h, and the other is a broad-spectrum real-time RT-PCR assay, which targeted almost all HEVs. The experiments confirmed that the two assays have high sensitivity and specificity, and the sensitivity was up to 0.1 TCID(50)/ml for detection of HEVs, HEV71, and CVA16, respectively. A total of 213 clinical specimens were simultaneously detected by three kinds of assays, including the two real-time RT-PCR assays, direct conventional RT-PCR assay, and virus isolation assay on human rhabdomyosarcoma cells (RD cells). The total positive rate of both HEV71 and CVA16 was 69.48% with real-time RT-PCR assay, 47.42% with RT-PCR assay, and 34.58% with virus isolation assay. One HFMD clinical specimen was positive for HEV, but negative for HEV71 or CVA16, which was identified as Echovirus 11 (Echo11) by virus isolation, RT-PCR, and sequencing for the VP1 gene. The two real-time RT-PCR assays had been applied in 31 provincial HFMD labs to detect the pathogens of HFMD, which has contributed to the rapid identification of the pathogens in the early stages of HFMD outbreaks, and helped to clarify the etiologic agents of HFMD in China. Public Library of Science 2013-04-18 /pmc/articles/PMC3630163/ /pubmed/23637836 http://dx.doi.org/10.1371/journal.pone.0061451 Text en © 2013 Cui et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cui, Aili
Xu, Changping
Tan, Xiaojuan
Zhang, Yan
Zhu, Zhen
Mao, Naiying
Lu, Yiyu
Xu, Wenbo
The Development and Application of the Two Real-Time RT-PCR Assays to Detect the Pathogen of HFMD
title The Development and Application of the Two Real-Time RT-PCR Assays to Detect the Pathogen of HFMD
title_full The Development and Application of the Two Real-Time RT-PCR Assays to Detect the Pathogen of HFMD
title_fullStr The Development and Application of the Two Real-Time RT-PCR Assays to Detect the Pathogen of HFMD
title_full_unstemmed The Development and Application of the Two Real-Time RT-PCR Assays to Detect the Pathogen of HFMD
title_short The Development and Application of the Two Real-Time RT-PCR Assays to Detect the Pathogen of HFMD
title_sort development and application of the two real-time rt-pcr assays to detect the pathogen of hfmd
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3630163/
https://www.ncbi.nlm.nih.gov/pubmed/23637836
http://dx.doi.org/10.1371/journal.pone.0061451
work_keys_str_mv AT cuiaili thedevelopmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT xuchangping thedevelopmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT tanxiaojuan thedevelopmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT zhangyan thedevelopmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT zhuzhen thedevelopmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT maonaiying thedevelopmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT luyiyu thedevelopmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT xuwenbo thedevelopmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT cuiaili developmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT xuchangping developmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT tanxiaojuan developmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT zhangyan developmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT zhuzhen developmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT maonaiying developmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT luyiyu developmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd
AT xuwenbo developmentandapplicationofthetworealtimertpcrassaystodetectthepathogenofhfmd