A simple and rapid DNA extraction method from whole blood for highly sensitive detection and quantitation of HIV-1 proviral DNA by real-time PCR

•This FINA method with internal control (IC) was developed to detect proviral HIV-1 DNA from whole blood samples using a modification of Abbott's HIV-1 RealTime Assay for early infant diagnosis.•The limit of quantification is 10copies/100μl whole blood and as little as a single proviral copy ca...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of virological methods 2015-03, Vol.214, p.37-42
Hauptverfasser: McFall, Sally M., Wagner, Robin L., Jangam, Sujit R., Yamada, Douglas H., Hardie, Diana, Kelso, David M.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 42
container_issue
container_start_page 37
container_title Journal of virological methods
container_volume 214
creator McFall, Sally M.
Wagner, Robin L.
Jangam, Sujit R.
Yamada, Douglas H.
Hardie, Diana
Kelso, David M.
description •This FINA method with internal control (IC) was developed to detect proviral HIV-1 DNA from whole blood samples using a modification of Abbott's HIV-1 RealTime Assay for early infant diagnosis.•The limit of quantification is 10copies/100μl whole blood and as little as a single proviral copy can be detected.•In a preliminary field test with 61 South African infant specimens, the FINA assay demonstrated 100% sensitivity and specificity. Early diagnosis and access to treatment for infants with human immunodeficiency virus-1 (HIV-1) is critical to reduce infant mortality. The lack of simple point-of-care tests impedes the timely initiation of antiretroviral therapy. The development of FINA, filtration isolation of nucleic acids, a novel DNA extraction method that can be performed by clinic personnel in less than 2min has been reported previously. In this report, significant improvements in the DNA extraction and amplification methods are detailed that allow sensitive quantitation of as little as 10 copies of HIV-1 proviral DNA and detection of 3 copies extracted from 100μl of whole blood. An internal control to detect PCR inhibition was also incorporated. In a preliminary field evaluation of 61 South African infants, the FINA test demonstrated 100% sensitivity and specificity. The proviral copy number of the infant specimens was quantified, and it was established that 100 microliters of whole blood is required for sensitive diagnosis of infants.
doi_str_mv 10.1016/j.jviromet.2015.01.005
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1727680817</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0166093415000208</els_id><sourcerecordid>1727680817</sourcerecordid><originalsourceid>FETCH-LOGICAL-c449t-e00c745845daa4f54ebc79b9901c1ff00bf7ccfd44b15dd0017ccd5cabbfde5e3</originalsourceid><addsrcrecordid>eNqFkc9uEzEQxi0EoqHlFSofuewyztr750YUCq1UQVVBr5bXHhNHu-vUdgJ5iz5ynabl2pPHo98332g-Qs4ZlAxY_Xldrncu-BFTOQcmSmAlgHhDZqxtugK6lr8lswzWua74CfkQ4xoy0VTVe3IyF3XLxJzPyMOCRjduBqRqMjSojTP0648FxX8pKJ2cn2j2WHlDbXajf1c-o_3gDw0f6Mr9WQ17GnGKLrkdUoMJj7LDvPutmpJL6qnhLb28uisY3QSfd1fDk1G_pwHVUCQ3Ir1Z3p6Rd1YNET8-v6fk97eLX8vL4vrn96vl4rrQnHepQADdcNFyYZTiVnDsddP1XQdMM2sBettobQ3nPRPGALD8NUKrvrcGBVan5NNxbt7mfosxydFFjcOgJvTbKFkzb-oWWta8jtY1y8ZVzTJaH1EdfIwBrdwEN6qwlwzkITi5li_ByUNwEpjMsWTh-bPHth_R_Je9JJWBL0cA81F2DoOM2uGk0biQLy6Nd695PAJKTK9G</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1661990361</pqid></control><display><type>article</type><title>A simple and rapid DNA extraction method from whole blood for highly sensitive detection and quantitation of HIV-1 proviral DNA by real-time PCR</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>McFall, Sally M. ; Wagner, Robin L. ; Jangam, Sujit R. ; Yamada, Douglas H. ; Hardie, Diana ; Kelso, David M.</creator><creatorcontrib>McFall, Sally M. ; Wagner, Robin L. ; Jangam, Sujit R. ; Yamada, Douglas H. ; Hardie, Diana ; Kelso, David M.</creatorcontrib><description>•This FINA method with internal control (IC) was developed to detect proviral HIV-1 DNA from whole blood samples using a modification of Abbott's HIV-1 RealTime Assay for early infant diagnosis.•The limit of quantification is 10copies/100μl whole blood and as little as a single proviral copy can be detected.•In a preliminary field test with 61 South African infant specimens, the FINA assay demonstrated 100% sensitivity and specificity. Early diagnosis and access to treatment for infants with human immunodeficiency virus-1 (HIV-1) is critical to reduce infant mortality. The lack of simple point-of-care tests impedes the timely initiation of antiretroviral therapy. The development of FINA, filtration isolation of nucleic acids, a novel DNA extraction method that can be performed by clinic personnel in less than 2min has been reported previously. In this report, significant improvements in the DNA extraction and amplification methods are detailed that allow sensitive quantitation of as little as 10 copies of HIV-1 proviral DNA and detection of 3 copies extracted from 100μl of whole blood. An internal control to detect PCR inhibition was also incorporated. In a preliminary field evaluation of 61 South African infants, the FINA test demonstrated 100% sensitivity and specificity. The proviral copy number of the infant specimens was quantified, and it was established that 100 microliters of whole blood is required for sensitive diagnosis of infants.</description><identifier>ISSN: 0166-0934</identifier><identifier>EISSN: 1879-0984</identifier><identifier>DOI: 10.1016/j.jviromet.2015.01.005</identifier><identifier>PMID: 25681524</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Blood - virology ; DNA, Viral - genetics ; DNA, Viral - isolation &amp; purification ; Early infant diagnosis ; HIV ; HIV Infections - virology ; HIV-1 - genetics ; HIV-1 - isolation &amp; purification ; Human immunodeficiency virus 1 ; Humans ; Infant ; Infant, Newborn ; Polymerase chain reaction ; Provirus ; Proviruses - genetics ; Proviruses - isolation &amp; purification ; Real-Time Polymerase Chain Reaction - methods ; Real-Time Polymerase Chain Reaction - standards ; Reference Standards ; Sensitivity and Specificity ; Specimen Handling - methods ; Specimen Handling - standards ; Time Factors ; Viral Load - methods</subject><ispartof>Journal of virological methods, 2015-03, Vol.214, p.37-42</ispartof><rights>2015 The Authors</rights><rights>Copyright © 2015 The Authors. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c449t-e00c745845daa4f54ebc79b9901c1ff00bf7ccfd44b15dd0017ccd5cabbfde5e3</citedby><cites>FETCH-LOGICAL-c449t-e00c745845daa4f54ebc79b9901c1ff00bf7ccfd44b15dd0017ccd5cabbfde5e3</cites><orcidid>0000-0001-5554-6615</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jviromet.2015.01.005$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25681524$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McFall, Sally M.</creatorcontrib><creatorcontrib>Wagner, Robin L.</creatorcontrib><creatorcontrib>Jangam, Sujit R.</creatorcontrib><creatorcontrib>Yamada, Douglas H.</creatorcontrib><creatorcontrib>Hardie, Diana</creatorcontrib><creatorcontrib>Kelso, David M.</creatorcontrib><title>A simple and rapid DNA extraction method from whole blood for highly sensitive detection and quantitation of HIV-1 proviral DNA by real-time PCR</title><title>Journal of virological methods</title><addtitle>J Virol Methods</addtitle><description>•This FINA method with internal control (IC) was developed to detect proviral HIV-1 DNA from whole blood samples using a modification of Abbott's HIV-1 RealTime Assay for early infant diagnosis.•The limit of quantification is 10copies/100μl whole blood and as little as a single proviral copy can be detected.•In a preliminary field test with 61 South African infant specimens, the FINA assay demonstrated 100% sensitivity and specificity. Early diagnosis and access to treatment for infants with human immunodeficiency virus-1 (HIV-1) is critical to reduce infant mortality. The lack of simple point-of-care tests impedes the timely initiation of antiretroviral therapy. The development of FINA, filtration isolation of nucleic acids, a novel DNA extraction method that can be performed by clinic personnel in less than 2min has been reported previously. In this report, significant improvements in the DNA extraction and amplification methods are detailed that allow sensitive quantitation of as little as 10 copies of HIV-1 proviral DNA and detection of 3 copies extracted from 100μl of whole blood. An internal control to detect PCR inhibition was also incorporated. In a preliminary field evaluation of 61 South African infants, the FINA test demonstrated 100% sensitivity and specificity. The proviral copy number of the infant specimens was quantified, and it was established that 100 microliters of whole blood is required for sensitive diagnosis of infants.</description><subject>Blood - virology</subject><subject>DNA, Viral - genetics</subject><subject>DNA, Viral - isolation &amp; purification</subject><subject>Early infant diagnosis</subject><subject>HIV</subject><subject>HIV Infections - virology</subject><subject>HIV-1 - genetics</subject><subject>HIV-1 - isolation &amp; purification</subject><subject>Human immunodeficiency virus 1</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Polymerase chain reaction</subject><subject>Provirus</subject><subject>Proviruses - genetics</subject><subject>Proviruses - isolation &amp; purification</subject><subject>Real-Time Polymerase Chain Reaction - methods</subject><subject>Real-Time Polymerase Chain Reaction - standards</subject><subject>Reference Standards</subject><subject>Sensitivity and Specificity</subject><subject>Specimen Handling - methods</subject><subject>Specimen Handling - standards</subject><subject>Time Factors</subject><subject>Viral Load - methods</subject><issn>0166-0934</issn><issn>1879-0984</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9uEzEQxi0EoqHlFSofuewyztr750YUCq1UQVVBr5bXHhNHu-vUdgJ5iz5ynabl2pPHo98332g-Qs4ZlAxY_Xldrncu-BFTOQcmSmAlgHhDZqxtugK6lr8lswzWua74CfkQ4xoy0VTVe3IyF3XLxJzPyMOCRjduBqRqMjSojTP0648FxX8pKJ2cn2j2WHlDbXajf1c-o_3gDw0f6Mr9WQ17GnGKLrkdUoMJj7LDvPutmpJL6qnhLb28uisY3QSfd1fDk1G_pwHVUCQ3Ir1Z3p6Rd1YNET8-v6fk97eLX8vL4vrn96vl4rrQnHepQADdcNFyYZTiVnDsddP1XQdMM2sBettobQ3nPRPGALD8NUKrvrcGBVan5NNxbt7mfosxydFFjcOgJvTbKFkzb-oWWta8jtY1y8ZVzTJaH1EdfIwBrdwEN6qwlwzkITi5li_ByUNwEpjMsWTh-bPHth_R_Je9JJWBL0cA81F2DoOM2uGk0biQLy6Nd695PAJKTK9G</recordid><startdate>201503</startdate><enddate>201503</enddate><creator>McFall, Sally M.</creator><creator>Wagner, Robin L.</creator><creator>Jangam, Sujit R.</creator><creator>Yamada, Douglas H.</creator><creator>Hardie, Diana</creator><creator>Kelso, David M.</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><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>7TM</scope><scope>7U9</scope><scope>H94</scope><orcidid>https://orcid.org/0000-0001-5554-6615</orcidid></search><sort><creationdate>201503</creationdate><title>A simple and rapid DNA extraction method from whole blood for highly sensitive detection and quantitation of HIV-1 proviral DNA by real-time PCR</title><author>McFall, Sally M. ; Wagner, Robin L. ; Jangam, Sujit R. ; Yamada, Douglas H. ; Hardie, Diana ; Kelso, David M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c449t-e00c745845daa4f54ebc79b9901c1ff00bf7ccfd44b15dd0017ccd5cabbfde5e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Blood - virology</topic><topic>DNA, Viral - genetics</topic><topic>DNA, Viral - isolation &amp; purification</topic><topic>Early infant diagnosis</topic><topic>HIV</topic><topic>HIV Infections - virology</topic><topic>HIV-1 - genetics</topic><topic>HIV-1 - isolation &amp; purification</topic><topic>Human immunodeficiency virus 1</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Polymerase chain reaction</topic><topic>Provirus</topic><topic>Proviruses - genetics</topic><topic>Proviruses - isolation &amp; purification</topic><topic>Real-Time Polymerase Chain Reaction - methods</topic><topic>Real-Time Polymerase Chain Reaction - standards</topic><topic>Reference Standards</topic><topic>Sensitivity and Specificity</topic><topic>Specimen Handling - methods</topic><topic>Specimen Handling - standards</topic><topic>Time Factors</topic><topic>Viral Load - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McFall, Sally M.</creatorcontrib><creatorcontrib>Wagner, Robin L.</creatorcontrib><creatorcontrib>Jangam, Sujit R.</creatorcontrib><creatorcontrib>Yamada, Douglas H.</creatorcontrib><creatorcontrib>Hardie, Diana</creatorcontrib><creatorcontrib>Kelso, David M.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Journal of virological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McFall, Sally M.</au><au>Wagner, Robin L.</au><au>Jangam, Sujit R.</au><au>Yamada, Douglas H.</au><au>Hardie, Diana</au><au>Kelso, David M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A simple and rapid DNA extraction method from whole blood for highly sensitive detection and quantitation of HIV-1 proviral DNA by real-time PCR</atitle><jtitle>Journal of virological methods</jtitle><addtitle>J Virol Methods</addtitle><date>2015-03</date><risdate>2015</risdate><volume>214</volume><spage>37</spage><epage>42</epage><pages>37-42</pages><issn>0166-0934</issn><eissn>1879-0984</eissn><abstract>•This FINA method with internal control (IC) was developed to detect proviral HIV-1 DNA from whole blood samples using a modification of Abbott's HIV-1 RealTime Assay for early infant diagnosis.•The limit of quantification is 10copies/100μl whole blood and as little as a single proviral copy can be detected.•In a preliminary field test with 61 South African infant specimens, the FINA assay demonstrated 100% sensitivity and specificity. Early diagnosis and access to treatment for infants with human immunodeficiency virus-1 (HIV-1) is critical to reduce infant mortality. The lack of simple point-of-care tests impedes the timely initiation of antiretroviral therapy. The development of FINA, filtration isolation of nucleic acids, a novel DNA extraction method that can be performed by clinic personnel in less than 2min has been reported previously. In this report, significant improvements in the DNA extraction and amplification methods are detailed that allow sensitive quantitation of as little as 10 copies of HIV-1 proviral DNA and detection of 3 copies extracted from 100μl of whole blood. An internal control to detect PCR inhibition was also incorporated. In a preliminary field evaluation of 61 South African infants, the FINA test demonstrated 100% sensitivity and specificity. The proviral copy number of the infant specimens was quantified, and it was established that 100 microliters of whole blood is required for sensitive diagnosis of infants.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>25681524</pmid><doi>10.1016/j.jviromet.2015.01.005</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-5554-6615</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0166-0934
ispartof Journal of virological methods, 2015-03, Vol.214, p.37-42
issn 0166-0934
1879-0984
language eng
recordid cdi_proquest_miscellaneous_1727680817
source MEDLINE; Elsevier ScienceDirect Journals
subjects Blood - virology
DNA, Viral - genetics
DNA, Viral - isolation & purification
Early infant diagnosis
HIV
HIV Infections - virology
HIV-1 - genetics
HIV-1 - isolation & purification
Human immunodeficiency virus 1
Humans
Infant
Infant, Newborn
Polymerase chain reaction
Provirus
Proviruses - genetics
Proviruses - isolation & purification
Real-Time Polymerase Chain Reaction - methods
Real-Time Polymerase Chain Reaction - standards
Reference Standards
Sensitivity and Specificity
Specimen Handling - methods
Specimen Handling - standards
Time Factors
Viral Load - methods
title A simple and rapid DNA extraction method from whole blood for highly sensitive detection and quantitation of HIV-1 proviral DNA by real-time PCR
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T09%3A19%3A52IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20simple%20and%20rapid%20DNA%20extraction%20method%20from%20whole%20blood%20for%20highly%20sensitive%20detection%20and%20quantitation%20of%20HIV-1%20proviral%20DNA%20by%20real-time%20PCR&rft.jtitle=Journal%20of%20virological%20methods&rft.au=McFall,%20Sally%20M.&rft.date=2015-03&rft.volume=214&rft.spage=37&rft.epage=42&rft.pages=37-42&rft.issn=0166-0934&rft.eissn=1879-0984&rft_id=info:doi/10.1016/j.jviromet.2015.01.005&rft_dat=%3Cproquest_cross%3E1727680817%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1661990361&rft_id=info:pmid/25681524&rft_els_id=S0166093415000208&rfr_iscdi=true