Detection of blood‐transmissible agents: can screening be miniaturized?
Identifieur interne : 001712 ( Istex/Corpus ); précédent : 001711; suivant : 001713Detection of blood‐transmissible agents: can screening be miniaturized?
Auteurs : Chantal Fournier-Wirth ; Nicole Jaffrezic-Renault ; Joliette CosteSource :
- Transfusion [ 0041-1132 ] ; 2010-09.
Abstract
Transfusion safety relating to blood‐transmissible agents is a major public health concern, particularly when faced with the continuing emergence of new infectious agents. These include new viruses appearing alongside other known reemerging viruses (West Nile virus, Chikungunya) as well as new strains of bacteria and parasites (Plasmodium falciparum, Trypanosoma cruzi) and finally pathologic prion protein (variant Creutzfeldt‐Jakob disease). Genomic mutations of known viruses (hepatitis B virus, hepatitis C virus, human immunodeficiency virus) can also be at the origin of variants susceptible to escaping detection by diagnostic tests. New technologies that would allow the simultaneous detection of several blood‐transmissible agents are now needed for the development and improvement of screening strategies. DNA microarrays have been developed for use in immunohematology laboratories for blood group genotyping. Their application in the detection of infectious agents, however, has been hindered by additional technological hurdles. For instance, the variability among and within genomes of interest complicate target amplification and multiplex analysis. Advances in biosensor technologies based on alternative detection strategies have offered new perspectives on pathogen detection; however, whether they are adaptable to diagnostic applications testing biologic fluids is under debate. Elsewhere, current nanotechnologies now offer new tools to improve the sample preparation, target capture, and detection steps. Second‐generation devices combining micro‐ and nanotechnologies have brought us one step closer to the potential development of innovative and multiplexed approaches applicable to the screening of blood for transmissible agents.
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DOI: 10.1111/j.1537-2995.2010.02678.x
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ISTEX:B06107DDCD666E9A614C73045FB89E71BE0477E4Le document en format XML
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Advances in biosensor technologies based on alternative detection strategies have offered new perspectives on pathogen detection; however, whether they are adaptable to diagnostic applications testing biologic fluids is under debate. Elsewhere, current nanotechnologies now offer new tools to improve the sample preparation, target capture, and detection steps. 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Advances in biosensor technologies based on alternative detection strategies have offered new perspectives on pathogen detection; however, whether they are adaptable to diagnostic applications testing biologic fluids is under debate. Elsewhere, current nanotechnologies now offer new tools to improve the sample preparation, target capture, and detection steps. 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and Laboratoire de Sciences Analytiques, Université Claude Bernard Lyon 1, Villeurbanne, France.</addrLine><country key="FR" xml:lang="en">FRANCE</country></address></affiliation></author><author xml:id="author-0001"><persName><forename type="first">Nicole</forename><surname>Jaffrezic‐Renault</surname></persName><affiliation><orgName type="laboratory">From the Laboratoire de R&D‐Agents Transmissibles par Transfusion (R&D‐ATT)</orgName><address><addrLine>Etablissement Français du Sang Pyrénées‐Méditerranée</addrLine><addrLine>Montpellier; and Laboratoire de Sciences Analytiques, Université Claude Bernard Lyon 1, Villeurbanne, France.</addrLine><country key="FR" xml:lang="en">FRANCE</country></address></affiliation></author><author xml:id="author-0002"><persName><forename type="first">Joliette</forename><surname>Coste</surname></persName><affiliation><orgName type="laboratory">From the Laboratoire de R&D‐Agents Transmissibles par Transfusion (R&D‐ATT)</orgName><address><addrLine>Etablissement Français du Sang Pyrénées‐Méditerranée</addrLine><addrLine>Montpellier; 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<ref target="http://www.tei-c.org/">We use TEI</ref></desc></application></appInfo></encodingDesc><profileDesc><abstract xml:lang="en" style="main"><p>Transfusion safety relating to blood‐transmissible agents is a major public health concern, particularly when faced with the continuing emergence of new infectious agents. These include new viruses appearing alongside other known reemerging viruses (West Nile virus, Chikungunya) as well as new strains of bacteria and parasites (<hi rend="italic">Plasmodium falciparum, Trypanosoma cruzi</hi>) and finally pathologic prion protein (variant Creutzfeldt‐Jakob disease). Genomic mutations of known viruses (hepatitis B virus, hepatitis C virus, human immunodeficiency virus) can also be at the origin of variants susceptible to escaping detection by diagnostic tests. New technologies that would allow the simultaneous detection of several blood‐transmissible agents are now needed for the development and improvement of screening strategies. DNA microarrays have been developed for use in immunohematology laboratories for blood group genotyping. Their application in the detection of infectious agents, however, has been hindered by additional technological hurdles. For instance, the variability among and within genomes of interest complicate target amplification and multiplex analysis. Advances in biosensor technologies based on alternative detection strategies have offered new perspectives on pathogen detection; however, whether they are adaptable to diagnostic applications testing biologic fluids is under debate. Elsewhere, current nanotechnologies now offer new tools to improve the sample preparation, target capture, and detection steps. Second‐generation devices combining micro‐ and nanotechnologies have brought us one step closer to the potential development of innovative and multiplexed approaches applicable to the screening of blood for transmissible agents.</p></abstract><textClass><keywords rend="tocHeading1"><term>REVIEW</term></keywords><keywords rend="articleCategory"><term>REVIEW</term></keywords></textClass><langUsage><language ident="en"></language></langUsage></profileDesc><revisionDesc><change when="2019-12-20" who="#istex" xml:id="pub2tei">formatting</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/ark:/67375/WNG-ZCQXJ841-C/fulltext.txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Blackwell Publishing Inc</publisherName><publisherLoc>Malden, USA</publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1537-2995</doi><issn type="print">0041-1132</issn><issn type="electronic">1537-2995</issn><idGroup><id type="product" value="TRF"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="TRANSFUSION">Transfusion</title></titleGroup></publicationMeta><publicationMeta level="part" position="09109"><doi origin="wiley">10.1111/trf.2010.50.issue-9</doi><numberingGroup><numbering type="journalVolume" number="50">50</numbering><numbering type="journalIssue" number="9">9</numbering></numberingGroup><coverDate startDate="2010-09">September 2010</coverDate></publicationMeta><publicationMeta level="unit" type="reviewArticle" position="27" status="forIssue"><doi origin="wiley">10.1111/j.1537-2995.2010.02678.x</doi><idGroup><id type="unit" value="TRF2678"></id></idGroup><countGroup><count type="pageTotal" number="1"></count></countGroup><titleGroup><title type="tocHeading1">REVIEW</title><title type="articleCategory">REVIEW</title></titleGroup><copyright>© 2010 American Association of Blood Banks</copyright><eventGroup><event type="firstOnline" date="2010-06-07"></event><event type="publishedOnlineAcceptedOrEarlyUnpaginated" date="2010-06-07"></event><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.25 mode:FullText source:FullText result:FullText" date="2010-11-10"></event><event type="publishedOnlineFinalForm" date="2010-09-01"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-02-10"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-11-04"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="2032">2032</numbering><numbering type="pageLast" number="2045">2045</numbering></numberingGroup><correspondenceTo>Chantal Fournier‐Wirth, PhD, Etablissement Français du Sang Pyrénées‐Méditerranée, 240 Avenue Emile Jeanbrau, 34 094 Montpellier Cedex 5, France; e‐mail: <email>chantal.fournier@efs.sante.fr</email>.
</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:TRF.TRF2678.pdf"></link></linkGroup></publicationMeta><contentMeta><unparsedEditorialHistory>Received for publication June 12, 2009; revision received December 9, 2009, and accepted February 20, 2010.</unparsedEditorialHistory><countGroup><count type="figureTotal" number="2"></count><count type="tableTotal" number="1"></count><count type="formulaTotal" number="0"></count><count type="referenceTotal" number="122"></count><count type="wordTotal" number="10217"></count><count type="linksPubMed" number="0"></count><count type="linksCrossRef" number="0"></count></countGroup><titleGroup><title type="main">Detection of blood‐transmissible agents: can screening be miniaturized?</title><title type="shortAuthors">FOURNIER‐WIRTH ET AL.</title><title type="short">MINIATURIZATION OF PATHOGEN DETECTION</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#aff-1-1"><personName><givenNames>Chantal</givenNames><familyName>Fournier‐Wirth</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#aff-1-1"><personName><givenNames>Nicole</givenNames><familyName>Jaffrezic‐Renault</familyName></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#aff-1-1"><personName><givenNames>Joliette</givenNames><familyName>Coste</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="aff-1-1" countryCode="FR"><unparsedAffiliation>From the Laboratoire de R&D‐Agents Transmissibles par Transfusion (R&D‐ATT), Etablissement Français du Sang Pyrénées‐Méditerranée, Montpellier; and Laboratoire de Sciences Analytiques, Université Claude Bernard Lyon 1, Villeurbanne, France.</unparsedAffiliation></affiliation></affiliationGroup><abstractGroup><abstract type="main" xml:lang="en"><p>Transfusion safety relating to blood‐transmissible agents is a major public health concern, particularly when faced with the continuing emergence of new infectious agents. These include new viruses appearing alongside other known reemerging viruses (West Nile virus, Chikungunya) as well as new strains of bacteria and parasites (<i>Plasmodium falciparum, Trypanosoma cruzi</i>) and finally pathologic prion protein (variant Creutzfeldt‐Jakob disease). Genomic mutations of known viruses (hepatitis B virus, hepatitis C virus, human immunodeficiency virus) can also be at the origin of variants susceptible to escaping detection by diagnostic tests. New technologies that would allow the simultaneous detection of several blood‐transmissible agents are now needed for the development and improvement of screening strategies. DNA microarrays have been developed for use in immunohematology laboratories for blood group genotyping. Their application in the detection of infectious agents, however, has been hindered by additional technological hurdles. For instance, the variability among and within genomes of interest complicate target amplification and multiplex analysis. Advances in biosensor technologies based on alternative detection strategies have offered new perspectives on pathogen detection; however, whether they are adaptable to diagnostic applications testing biologic fluids is under debate. Elsewhere, current nanotechnologies now offer new tools to improve the sample preparation, target capture, and detection steps. Second‐generation devices combining micro‐ and nanotechnologies have brought us one step closer to the potential development of innovative and multiplexed approaches applicable to the screening of blood for transmissible agents.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Detection of blood‐transmissible agents: can screening be miniaturized?</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>MINIATURIZATION OF PATHOGEN DETECTION</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Detection of blood‐transmissible agents: can screening be miniaturized?</title></titleInfo><name type="personal"><namePart type="given">Chantal</namePart><namePart type="family">Fournier‐Wirth</namePart><affiliation>From the Laboratoire de R&D‐Agents Transmissibles par Transfusion (R&D‐ATT), Etablissement Français du Sang Pyrénées‐Méditerranée, Montpellier; and Laboratoire de Sciences Analytiques, Université Claude Bernard Lyon 1, Villeurbanne, France.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Nicole</namePart><namePart type="family">Jaffrezic‐Renault</namePart><affiliation>From the Laboratoire de R&D‐Agents Transmissibles par Transfusion (R&D‐ATT), Etablissement Français du Sang Pyrénées‐Méditerranée, Montpellier; and Laboratoire de Sciences Analytiques, Université Claude Bernard Lyon 1, Villeurbanne, France.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Joliette</namePart><namePart type="family">Coste</namePart><affiliation>From the Laboratoire de R&D‐Agents Transmissibles par Transfusion (R&D‐ATT), Etablissement Français du Sang Pyrénées‐Méditerranée, Montpellier; and Laboratoire de Sciences Analytiques, Université Claude Bernard Lyon 1, Villeurbanne, France.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="review-article" displayLabel="reviewArticle" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-L5L7X3NF-P">review-article</genre><originInfo><publisher>Blackwell Publishing Inc</publisher><place><placeTerm type="text">Malden, USA</placeTerm></place><dateIssued encoding="w3cdtf">2010-09</dateIssued><edition>Received for publication June 12, 2009; revision received December 9, 2009, and accepted February 20, 2010.</edition><copyrightDate encoding="w3cdtf">2010</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="figures">2</extent><extent unit="tables">1</extent><extent unit="formulas">0</extent><extent unit="references">122</extent><extent unit="linksCrossRef">0</extent><extent unit="words">10217</extent></physicalDescription><abstract lang="en">Transfusion safety relating to blood‐transmissible agents is a major public health concern, particularly when faced with the continuing emergence of new infectious agents. These include new viruses appearing alongside other known reemerging viruses (West Nile virus, Chikungunya) as well as new strains of bacteria and parasites (Plasmodium falciparum, Trypanosoma cruzi) and finally pathologic prion protein (variant Creutzfeldt‐Jakob disease). Genomic mutations of known viruses (hepatitis B virus, hepatitis C virus, human immunodeficiency virus) can also be at the origin of variants susceptible to escaping detection by diagnostic tests. New technologies that would allow the simultaneous detection of several blood‐transmissible agents are now needed for the development and improvement of screening strategies. DNA microarrays have been developed for use in immunohematology laboratories for blood group genotyping. Their application in the detection of infectious agents, however, has been hindered by additional technological hurdles. For instance, the variability among and within genomes of interest complicate target amplification and multiplex analysis. Advances in biosensor technologies based on alternative detection strategies have offered new perspectives on pathogen detection; however, whether they are adaptable to diagnostic applications testing biologic fluids is under debate. Elsewhere, current nanotechnologies now offer new tools to improve the sample preparation, target capture, and detection steps. Second‐generation devices combining micro‐ and nanotechnologies have brought us one step closer to the potential development of innovative and multiplexed approaches applicable to the screening of blood for transmissible agents.</abstract><relatedItem type="host"><titleInfo><title>Transfusion</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><subject><genre>article-category</genre><topic>REVIEW</topic><topic>REVIEW</topic></subject><identifier type="ISSN">0041-1132</identifier><identifier type="eISSN">1537-2995</identifier><identifier type="DOI">10.1111/(ISSN)1537-2995</identifier><identifier type="PublisherID">TRF</identifier><part><date>2010</date><detail type="volume"><caption>vol.</caption><number>50</number></detail><detail type="issue"><caption>no.</caption><number>9</number></detail><extent 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