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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...
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Published in: | Journal of clinical microbiology 2015-08, Vol.53 (8), p.2641-2647 |
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creator | Wylie, Todd N Wylie, Kristine M Buller, Richard S Cannella, Maria Storch, Gregory A |
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. |
doi_str_mv | 10.1128/JCM.00923-15 |
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J.</contributor><creatorcontrib>Wylie, Todd N ; Wylie, Kristine M ; Buller, Richard S ; Cannella, Maria ; Storch, Gregory A ; Loeffelholz, M. J.</creatorcontrib><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.</description><identifier>ISSN: 0095-1137</identifier><identifier>EISSN: 1098-660X</identifier><identifier>DOI: 10.1128/JCM.00923-15</identifier><identifier>PMID: 26063859</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>DNA Primers - genetics ; Enterovirus ; Enterovirus D, Human - classification ; Enterovirus D, Human - genetics ; Enterovirus D, Human - isolation & purification ; Enterovirus Infections - diagnosis ; Humans ; Molecular Diagnostic Techniques - methods ; Real-Time Polymerase Chain Reaction - methods ; Reverse Transcriptase Polymerase Chain Reaction - methods ; Rhinovirus ; Sensitivity and Specificity ; Virology</subject><ispartof>Journal of clinical microbiology, 2015-08, Vol.53 (8), p.2641-2647</ispartof><rights>Copyright © 2015, Wylie et al.</rights><rights>Copyright © 2015, Wylie et al. 2015 Wylie et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-25ec694a7a531daac1196967739a88213b79255f8bf1589d7bb49fc07038e7653</citedby><cites>FETCH-LOGICAL-c483t-25ec694a7a531daac1196967739a88213b79255f8bf1589d7bb49fc07038e7653</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508392/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508392/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3187,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26063859$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Loeffelholz, M. J.</contributor><creatorcontrib>Wylie, Todd N</creatorcontrib><creatorcontrib>Wylie, Kristine M</creatorcontrib><creatorcontrib>Buller, Richard S</creatorcontrib><creatorcontrib>Cannella, Maria</creatorcontrib><creatorcontrib>Storch, Gregory A</creatorcontrib><title>Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay</title><title>Journal of clinical microbiology</title><addtitle>J Clin Microbiol</addtitle><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.</description><subject>DNA Primers - genetics</subject><subject>Enterovirus</subject><subject>Enterovirus D, Human - classification</subject><subject>Enterovirus D, Human - genetics</subject><subject>Enterovirus D, Human - isolation & purification</subject><subject>Enterovirus Infections - diagnosis</subject><subject>Humans</subject><subject>Molecular Diagnostic Techniques - methods</subject><subject>Real-Time Polymerase Chain Reaction - methods</subject><subject>Reverse Transcriptase Polymerase Chain Reaction - methods</subject><subject>Rhinovirus</subject><subject>Sensitivity and Specificity</subject><subject>Virology</subject><issn>0095-1137</issn><issn>1098-660X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFUctKxEAQHETRdfXmWXL0YHQ6k3ldBNldXyiKrCBehk52opEks84kAf_e-ERPnrq7uii6ugjZAXoAkKjDi8nVAaU6YTHwFTICqlUsBL1fJaMB5jEAkxtkM4RnSiFNOV8nG4mggimuR-RhantbuWVtmzbCZhHNeqw6bEvXRK4YkGjWtNa7vvRdiKZCRbcWq3he1nboeuuDjeYem5D7ctniMN1MbqPjEPB1i6wVWAW7_VXH5O5kNp-cxZfXp-eT48s4TxVr44TbXOgUJXIGC8QcQAstpGQalUqAZVInnBcqK4ArvZBZluoip5IyZaXgbEyOPnWXXVbbRT448ViZpS9r9K_GYWn-bpryyTy63qScKjY8bkz2vgS8e-lsaE1dhtxWFTbWdcGApBoUA8n_pwqtKJMJEwN1_5OaexeCt8XPRUDNe3JmSM58JGfgXXn3t4sf8ndU7A26WJMR</recordid><startdate>20150801</startdate><enddate>20150801</enddate><creator>Wylie, Todd N</creator><creator>Wylie, Kristine M</creator><creator>Buller, Richard S</creator><creator>Cannella, Maria</creator><creator>Storch, Gregory A</creator><general>American Society for Microbiology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7U9</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>20150801</creationdate><title>Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay</title><author>Wylie, Todd N ; Wylie, Kristine M ; Buller, Richard S ; Cannella, Maria ; Storch, Gregory A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-25ec694a7a531daac1196967739a88213b79255f8bf1589d7bb49fc07038e7653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>DNA Primers - genetics</topic><topic>Enterovirus</topic><topic>Enterovirus D, Human - classification</topic><topic>Enterovirus D, Human - genetics</topic><topic>Enterovirus D, Human - isolation & purification</topic><topic>Enterovirus Infections - diagnosis</topic><topic>Humans</topic><topic>Molecular Diagnostic Techniques - methods</topic><topic>Real-Time Polymerase Chain Reaction - methods</topic><topic>Reverse Transcriptase Polymerase Chain Reaction - methods</topic><topic>Rhinovirus</topic><topic>Sensitivity and Specificity</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wylie, Todd N</creatorcontrib><creatorcontrib>Wylie, Kristine M</creatorcontrib><creatorcontrib>Buller, Richard S</creatorcontrib><creatorcontrib>Cannella, Maria</creatorcontrib><creatorcontrib>Storch, Gregory A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wylie, Todd N</au><au>Wylie, Kristine M</au><au>Buller, Richard S</au><au>Cannella, Maria</au><au>Storch, Gregory A</au><au>Loeffelholz, M. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay</atitle><jtitle>Journal of clinical microbiology</jtitle><addtitle>J Clin Microbiol</addtitle><date>2015-08-01</date><risdate>2015</risdate><volume>53</volume><issue>8</issue><spage>2641</spage><epage>2647</epage><pages>2641-2647</pages><issn>0095-1137</issn><eissn>1098-660X</eissn><abstract>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.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>26063859</pmid><doi>10.1128/JCM.00923-15</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | DNA Primers - genetics Enterovirus Enterovirus D, Human - classification Enterovirus D, Human - genetics Enterovirus D, Human - isolation & purification Enterovirus Infections - diagnosis Humans Molecular Diagnostic Techniques - methods Real-Time Polymerase Chain Reaction - methods Reverse Transcriptase Polymerase Chain Reaction - methods Rhinovirus Sensitivity and Specificity Virology |
title | Development and Evaluation of an Enterovirus D68 Real-Time Reverse Transcriptase PCR Assay |
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