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Rapid detection of human mastadenovirus species B by recombinase polymerase amplification assay
BACKGROUND: As an important component of the causative agent of respiratory tract infections, enteric and eye infections, Human mastadenoviruses (HAdVs) species B spread easily in the crowd. In this study, we developed a recombinase polymerase amplification (RPA) assay for rapidly detecting HAdVs sp...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325725/ https://www.ncbi.nlm.nih.gov/pubmed/30621594 http://dx.doi.org/10.1186/s12866-018-1365-7 |
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author | Wu, Tao Wu, Haizhen Zhao, Kangchen Hu, Chaoyou Ge, Yiyue Zhu, Xiaojuan Zhang, Xingchen Zhou, Minghao Zhu, Fengcai Cui, Lunbiao |
author_facet | Wu, Tao Wu, Haizhen Zhao, Kangchen Hu, Chaoyou Ge, Yiyue Zhu, Xiaojuan Zhang, Xingchen Zhou, Minghao Zhu, Fengcai Cui, Lunbiao |
author_sort | Wu, Tao |
collection | PubMed |
description | BACKGROUND: As an important component of the causative agent of respiratory tract infections, enteric and eye infections, Human mastadenoviruses (HAdVs) species B spread easily in the crowd. In this study, we developed a recombinase polymerase amplification (RPA) assay for rapidly detecting HAdVs species B which was comprised of two different formats (real-time and lateral-flow device). RESULTS: This assay was confirmed to be able to detect 5 different HAdVs species B subtypes (HAdV-B3, HAdV-B7, HAdV-B11, HAdV-B14 and HAdV-B55) without cross-reactions with other subtypes and other respiratory tract pathogens. This RPA assay has not only highly sensitivity with low detection limit of 50 copies per reaction but also short reaction time (< 15 min per detection). Furthermore, the real-time RPA assay has excellent correlation with real-time PCR assay for detection of HAdVs species B presented in clinical samples. CONCLUSIONS: Thus, the RPA assay developed in this study provides an effective and portable approach for the rapid detection of HAdVs species B. |
format | Online Article Text |
id | pubmed-6325725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63257252019-01-11 Rapid detection of human mastadenovirus species B by recombinase polymerase amplification assay Wu, Tao Wu, Haizhen Zhao, Kangchen Hu, Chaoyou Ge, Yiyue Zhu, Xiaojuan Zhang, Xingchen Zhou, Minghao Zhu, Fengcai Cui, Lunbiao BMC Microbiol Research Article BACKGROUND: As an important component of the causative agent of respiratory tract infections, enteric and eye infections, Human mastadenoviruses (HAdVs) species B spread easily in the crowd. In this study, we developed a recombinase polymerase amplification (RPA) assay for rapidly detecting HAdVs species B which was comprised of two different formats (real-time and lateral-flow device). RESULTS: This assay was confirmed to be able to detect 5 different HAdVs species B subtypes (HAdV-B3, HAdV-B7, HAdV-B11, HAdV-B14 and HAdV-B55) without cross-reactions with other subtypes and other respiratory tract pathogens. This RPA assay has not only highly sensitivity with low detection limit of 50 copies per reaction but also short reaction time (< 15 min per detection). Furthermore, the real-time RPA assay has excellent correlation with real-time PCR assay for detection of HAdVs species B presented in clinical samples. CONCLUSIONS: Thus, the RPA assay developed in this study provides an effective and portable approach for the rapid detection of HAdVs species B. BioMed Central 2019-01-08 /pmc/articles/PMC6325725/ /pubmed/30621594 http://dx.doi.org/10.1186/s12866-018-1365-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Wu, Tao Wu, Haizhen Zhao, Kangchen Hu, Chaoyou Ge, Yiyue Zhu, Xiaojuan Zhang, Xingchen Zhou, Minghao Zhu, Fengcai Cui, Lunbiao Rapid detection of human mastadenovirus species B by recombinase polymerase amplification assay |
title | Rapid detection of human mastadenovirus species B by recombinase polymerase amplification assay |
title_full | Rapid detection of human mastadenovirus species B by recombinase polymerase amplification assay |
title_fullStr | Rapid detection of human mastadenovirus species B by recombinase polymerase amplification assay |
title_full_unstemmed | Rapid detection of human mastadenovirus species B by recombinase polymerase amplification assay |
title_short | Rapid detection of human mastadenovirus species B by recombinase polymerase amplification assay |
title_sort | rapid detection of human mastadenovirus species b by recombinase polymerase amplification assay |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325725/ https://www.ncbi.nlm.nih.gov/pubmed/30621594 http://dx.doi.org/10.1186/s12866-018-1365-7 |
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