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Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay
We have developed and evaluated a real-time reverse transcriptase PCR (RT-PCR) assay for the detection of human enterovirus D68 (EV-D68) in clinical specimens. This assay was developed in response to the unprecedented 2014 nationwide EV-D68 outbreak in the United States associated with severe respir...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508392/ https://www.ncbi.nlm.nih.gov/pubmed/26063859 http://dx.doi.org/10.1128/JCM.00923-15 |
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author | Wylie, Todd N. Wylie, Kristine M. Buller, Richard S. Cannella, Maria Storch, Gregory A. |
author_facet | Wylie, Todd N. Wylie, Kristine M. Buller, Richard S. Cannella, Maria Storch, Gregory A. |
author_sort | Wylie, Todd N. |
collection | PubMed |
description | We have developed and evaluated a real-time reverse transcriptase PCR (RT-PCR) assay for the detection of human enterovirus D68 (EV-D68) in clinical specimens. This assay was developed in response to the unprecedented 2014 nationwide EV-D68 outbreak in the United States associated with severe respiratory illness. As part of our evaluation of the outbreak, we sequenced and published the genome sequence of the EV-D68 virus circulating in St. Louis, MO. This sequence, along with other GenBank sequences from past EV-D68 occurrences, was used to computationally select a region of EV-D68 appropriate for targeting in a strain-specific RT-PCR assay. The RT-PCR assay amplifies a segment of the VP1 gene, with an analytic limit of detection of 4 copies per reaction, and it was more sensitive than commercially available assays that detect enteroviruses and rhinoviruses without distinguishing between the two, including three multiplex respiratory panels approved for clinical use by the FDA. The assay did not detect any other enteroviruses or rhinoviruses tested and did detect divergent strains of EV-D68, including the first EV-D68 strain (Fermon) identified in California in 1962. This assay should be useful for identifying and studying current and future outbreaks of EV-D68 viruses. |
format | Online Article Text |
id | pubmed-4508392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-45083922015-07-29 Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay Wylie, Todd N. Wylie, Kristine M. Buller, Richard S. Cannella, Maria Storch, Gregory A. J Clin Microbiol Virology We have developed and evaluated a real-time reverse transcriptase PCR (RT-PCR) assay for the detection of human enterovirus D68 (EV-D68) in clinical specimens. This assay was developed in response to the unprecedented 2014 nationwide EV-D68 outbreak in the United States associated with severe respiratory illness. As part of our evaluation of the outbreak, we sequenced and published the genome sequence of the EV-D68 virus circulating in St. Louis, MO. This sequence, along with other GenBank sequences from past EV-D68 occurrences, was used to computationally select a region of EV-D68 appropriate for targeting in a strain-specific RT-PCR assay. The RT-PCR assay amplifies a segment of the VP1 gene, with an analytic limit of detection of 4 copies per reaction, and it was more sensitive than commercially available assays that detect enteroviruses and rhinoviruses without distinguishing between the two, including three multiplex respiratory panels approved for clinical use by the FDA. The assay did not detect any other enteroviruses or rhinoviruses tested and did detect divergent strains of EV-D68, including the first EV-D68 strain (Fermon) identified in California in 1962. This assay should be useful for identifying and studying current and future outbreaks of EV-D68 viruses. American Society for Microbiology 2015-07-20 2015-08 /pmc/articles/PMC4508392/ /pubmed/26063859 http://dx.doi.org/10.1128/JCM.00923-15 Text en Copyright © 2015, Wylie et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Virology Wylie, Todd N. Wylie, Kristine M. Buller, Richard S. Cannella, Maria Storch, Gregory A. Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay |
title | Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay |
title_full | Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay |
title_fullStr | Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay |
title_full_unstemmed | Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay |
title_short | Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay |
title_sort | development and evaluation of an enterovirus d68 real-time reverse transcriptase pcr assay |
topic | Virology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508392/ https://www.ncbi.nlm.nih.gov/pubmed/26063859 http://dx.doi.org/10.1128/JCM.00923-15 |
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