A simple method for the detection of measles virus genome by loop‐mediated isothermal amplification (LAMP)
Identifieur interne : 000632 ( Istex/Corpus ); précédent : 000631; suivant : 000633A simple method for the detection of measles virus genome by loop‐mediated isothermal amplification (LAMP)
Auteurs : Motoko Fujino ; Naoko Yoshida ; Shinya Yamaguchi ; Norimitsu Hosaka ; Yoshinori Ota ; Tsugunori Notomi ; Tetsuo NakayamaSource :
- Journal of Medical Virology [ 0146-6615 ] ; 2005-07.
Abstract
Approximately 20,000–30,000 measles patients were reported in a surveillance of infectious diseases because of low vaccine coverage of 80% in Japan. Among them, some were thought to be secondary vaccine failure (SVF) with generally mild or non‐typical measles illness and sometimes became a source of further transmission. We have developed a new, sensitive, and rapid method to detect the measles virus genome by reverse transcription loop‐mediated isothermal amplification (RT‐LAMP). We examined 50 nasopharyngeal secretion (NPS) samples that were obtained during the 1999 outbreak and stored at −70°C and fresh NPS, lymphocytes and sera from 11 patients in 2003. Total RNA was extracted from the samples and subjected to reverse transcription‐polymerase chain reaction (RT‐PCR) and RT‐LAMP. We detected the genomic RNA corresponding to at least 0.01–0.04 TCID50, 30–100 copies in samples by RT‐LAMP within 60 min after extraction of RNA, and all four genotypes isolated in Japan were equally amplified. Specific DNA amplification was monitored spectrophotometrically by real time turbidimeter and the quantity of RNA was calculated. Measles virus genome was detected in 44 of 50 stored NPS by RT‐PCR and in 49 by RT‐LAMP. The vaccine strain was discriminated from wild strains after sequencing the LAMP products. RT‐LAMP is a useful rapid diagnostic method for the detection of measles virus without any special apparatus, showing higher sensitivity than RT‐PCR, and expected to be applied for hospital‐based infection control and for laboratory‐based measles surveillance. J. Med. Virol. 76:406–413, 2005. © 2005 Wiley‐Liss, Inc.
Url:
DOI: 10.1002/jmv.20371
Links to Exploration step
ISTEX:DF1455206F714BAA11C1A5FBCC3C3C60BF5B9A2ALe document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">A simple method for the detection of measles virus genome by loop‐mediated isothermal amplification (LAMP)</title><author><name sortKey="Fujino, Motoko" sort="Fujino, Motoko" uniqKey="Fujino M" first="Motoko" last="Fujino">Motoko Fujino</name><affiliation><mods:affiliation>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Minato‐ku, Tokyo, Japan</mods:affiliation></affiliation></author><author><name sortKey="Yoshida, Naoko" sort="Yoshida, Naoko" uniqKey="Yoshida N" first="Naoko" last="Yoshida">Naoko Yoshida</name><affiliation><mods:affiliation>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Minato‐ku, Tokyo, Japan</mods:affiliation></affiliation></author><author><name sortKey="Yamaguchi, Shinya" sort="Yamaguchi, Shinya" uniqKey="Yamaguchi S" first="Shinya" last="Yamaguchi">Shinya Yamaguchi</name><affiliation><mods:affiliation>Department of Pediatrics, National Kasumigaura Hospital, Tsuchiura, Ibaraki, Japan</mods:affiliation></affiliation></author><author><name sortKey="Hosaka, Norimitsu" sort="Hosaka, Norimitsu" uniqKey="Hosaka N" first="Norimitsu" last="Hosaka">Norimitsu Hosaka</name><affiliation><mods:affiliation>Eiken Chemical Co. Ltd., Kita‐ku, Tokyo, Japan</mods:affiliation></affiliation></author><author><name sortKey="Ota, Yoshinori" sort="Ota, Yoshinori" uniqKey="Ota Y" first="Yoshinori" last="Ota">Yoshinori Ota</name><affiliation><mods:affiliation>Eiken Chemical Co. Ltd., Kita‐ku, Tokyo, Japan</mods:affiliation></affiliation></author><author><name sortKey="Notomi, Tsugunori" sort="Notomi, Tsugunori" uniqKey="Notomi T" first="Tsugunori" last="Notomi">Tsugunori Notomi</name><affiliation><mods:affiliation>Eiken Chemical Co. Ltd., Kita‐ku, Tokyo, Japan</mods:affiliation></affiliation></author><author><name sortKey="Nakayama, Tetsuo" sort="Nakayama, Tetsuo" uniqKey="Nakayama T" first="Tetsuo" last="Nakayama">Tetsuo Nakayama</name><affiliation><mods:affiliation>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Minato‐ku, Tokyo, Japan</mods:affiliation></affiliation><affiliation><mods:affiliation>E-mail: tetsuo‐n@lisci.kitasato‐u.ac.jp</mods:affiliation></affiliation><affiliation><mods:affiliation>Correspondence address: Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Kitasato University, Shirokane 5‐9‐1, Minato‐ku, Tokyo 108‐8641, Japan.===</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:DF1455206F714BAA11C1A5FBCC3C3C60BF5B9A2A</idno><date when="2005" year="2005">2005</date><idno type="doi">10.1002/jmv.20371</idno><idno type="url">https://api.istex.fr/ark:/67375/WNG-ZH92N2WX-C/fulltext.pdf</idno><idno type="wicri:Area/Istex/Corpus">000632</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000632</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main">A simple method for the detection of measles virus genome by loop‐mediated isothermal amplification (LAMP)</title><author><name sortKey="Fujino, Motoko" sort="Fujino, Motoko" uniqKey="Fujino M" first="Motoko" last="Fujino">Motoko Fujino</name><affiliation><mods:affiliation>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Minato‐ku, Tokyo, Japan</mods:affiliation></affiliation></author><author><name sortKey="Yoshida, Naoko" sort="Yoshida, Naoko" uniqKey="Yoshida N" first="Naoko" last="Yoshida">Naoko Yoshida</name><affiliation><mods:affiliation>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Minato‐ku, Tokyo, Japan</mods:affiliation></affiliation></author><author><name sortKey="Yamaguchi, Shinya" sort="Yamaguchi, Shinya" uniqKey="Yamaguchi S" first="Shinya" last="Yamaguchi">Shinya Yamaguchi</name><affiliation><mods:affiliation>Department of Pediatrics, National Kasumigaura Hospital, Tsuchiura, Ibaraki, Japan</mods:affiliation></affiliation></author><author><name sortKey="Hosaka, Norimitsu" sort="Hosaka, Norimitsu" uniqKey="Hosaka N" first="Norimitsu" last="Hosaka">Norimitsu Hosaka</name><affiliation><mods:affiliation>Eiken Chemical Co. Ltd., Kita‐ku, Tokyo, Japan</mods:affiliation></affiliation></author><author><name sortKey="Ota, Yoshinori" sort="Ota, Yoshinori" uniqKey="Ota Y" first="Yoshinori" last="Ota">Yoshinori Ota</name><affiliation><mods:affiliation>Eiken Chemical Co. Ltd., Kita‐ku, Tokyo, Japan</mods:affiliation></affiliation></author><author><name sortKey="Notomi, Tsugunori" sort="Notomi, Tsugunori" uniqKey="Notomi T" first="Tsugunori" last="Notomi">Tsugunori Notomi</name><affiliation><mods:affiliation>Eiken Chemical Co. Ltd., Kita‐ku, Tokyo, Japan</mods:affiliation></affiliation></author><author><name sortKey="Nakayama, Tetsuo" sort="Nakayama, Tetsuo" uniqKey="Nakayama T" first="Tetsuo" last="Nakayama">Tetsuo Nakayama</name><affiliation><mods:affiliation>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Minato‐ku, Tokyo, Japan</mods:affiliation></affiliation><affiliation><mods:affiliation>E-mail: tetsuo‐n@lisci.kitasato‐u.ac.jp</mods:affiliation></affiliation><affiliation><mods:affiliation>Correspondence address: Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Kitasato University, Shirokane 5‐9‐1, Minato‐ku, Tokyo 108‐8641, Japan.===</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Journal of Medical Virology</title><title level="j" type="alt">JOURNAL OF MEDICAL VIROLOGY</title><idno type="ISSN">0146-6615</idno><idno type="eISSN">1096-9071</idno><imprint><biblScope unit="vol">76</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="406">406</biblScope><biblScope unit="page" to="413">413</biblScope><biblScope unit="page-count">8</biblScope><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="2005-07">2005-07</date></imprint><idno type="ISSN">0146-6615</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0146-6615</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Approximately 20,000–30,000 measles patients were reported in a surveillance of infectious diseases because of low vaccine coverage of 80% in Japan. Among them, some were thought to be secondary vaccine failure (SVF) with generally mild or non‐typical measles illness and sometimes became a source of further transmission. We have developed a new, sensitive, and rapid method to detect the measles virus genome by reverse transcription loop‐mediated isothermal amplification (RT‐LAMP). We examined 50 nasopharyngeal secretion (NPS) samples that were obtained during the 1999 outbreak and stored at −70°C and fresh NPS, lymphocytes and sera from 11 patients in 2003. Total RNA was extracted from the samples and subjected to reverse transcription‐polymerase chain reaction (RT‐PCR) and RT‐LAMP. We detected the genomic RNA corresponding to at least 0.01–0.04 TCID50, 30–100 copies in samples by RT‐LAMP within 60 min after extraction of RNA, and all four genotypes isolated in Japan were equally amplified. Specific DNA amplification was monitored spectrophotometrically by real time turbidimeter and the quantity of RNA was calculated. Measles virus genome was detected in 44 of 50 stored NPS by RT‐PCR and in 49 by RT‐LAMP. The vaccine strain was discriminated from wild strains after sequencing the LAMP products. RT‐LAMP is a useful rapid diagnostic method for the detection of measles virus without any special apparatus, showing higher sensitivity than RT‐PCR, and expected to be applied for hospital‐based infection control and for laboratory‐based measles surveillance. J. Med. Virol. 76:406–413, 2005. © 2005 Wiley‐Liss, Inc.</div></front></TEI><istex><corpusName>wiley</corpusName><keywords><teeft><json:string>genome</json:string><json:string>primer</json:string><json:string>genotype</json:string><json:string>measles</json:string><json:string>measles virus genome</json:string><json:string>measles virus</json:string><json:string>nakayama</json:string><json:string>virol</json:string><json:string>isothermal amplification</json:string><json:string>lamp product</json:string><json:string>isothermal</json:string><json:string>notomi</json:string><json:string>microbiol</json:string><json:string>detection limit</json:string><json:string>clin</json:string><json:string>loop structure</json:string><json:string>amplification</json:string><json:string>lamp reaction</json:string><json:string>chain reaction</json:string><json:string>high sensitivity</json:string><json:string>sequence alignment</json:string><json:string>measles genome</json:string><json:string>virus infection</json:string><json:string>higher sensitivity</json:string><json:string>genome position</json:string><json:string>vaccine</json:string><json:string>england biolabs</json:string><json:string>different genotype</json:string><json:string>virus isolation</json:string><json:string>human herpesvirus</json:string><json:string>rapid diagnosis</json:string><json:string>clinical sample</json:string><json:string>nasopharyngeal secretion</json:string><json:string>in primer</json:string><json:string>loop primer</json:string><json:string>rapid detection</json:string><json:string>double strand</json:string><json:string>virus</json:string><json:string>lamp primer design</json:string><json:string>secondary vaccine failure</json:string><json:string>variable region</json:string><json:string>peripheral blood mononuclear cell</json:string><json:string>fresh sample</json:string><json:string>transcription isothermal amplification</json:string><json:string>magnetic bead</json:string><json:string>takara biomedicals</json:string><json:string>negative sense</json:string><json:string>primer design</json:string><json:string>lamp primer</json:string><json:string>vaccine coverage</json:string><json:string>genetic characteristic</json:string><json:string>rapid diagnostic tool</json:string><json:string>amplification method</json:string><json:string>loopmediated isothermal amplification</json:string><json:string>measles patient</json:string><json:string>eiken chemical</json:string><json:string>reaction mixture</json:string><json:string>further transmission</json:string><json:string>protein expression plasmid</json:string><json:string>lamp method</json:string><json:string>spectrophotometric value</json:string><json:string>life science</json:string><json:string>micro liter</json:string><json:string>linear correlation</json:string><json:string>measles infection</json:string><json:string>reaction time</json:string><json:string>primer region</json:string><json:string>measles virus strain</json:string><json:string>west nile virus</json:string><json:string>mumps virus</json:string><json:string>comparative evaluation</json:string><json:string>kitasato institute</json:string><json:string>viral infection</json:string><json:string>measles illness</json:string><json:string>wkly epidemiol</json:string></teeft></keywords><author><json:item><name>Motoko Fujino</name><affiliations><json:string>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Minato‐ku, Tokyo, Japan</json:string></affiliations></json:item><json:item><name>Naoko Yoshida</name><affiliations><json:string>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Minato‐ku, Tokyo, Japan</json:string></affiliations></json:item><json:item><name>Shinya Yamaguchi</name><affiliations><json:string>Department of Pediatrics, National Kasumigaura Hospital, Tsuchiura, Ibaraki, Japan</json:string></affiliations></json:item><json:item><name>Norimitsu Hosaka</name><affiliations><json:string>Eiken Chemical Co. Ltd., Kita‐ku, Tokyo, Japan</json:string></affiliations></json:item><json:item><name>Yoshinori Ota</name><affiliations><json:string>Eiken Chemical Co. Ltd., Kita‐ku, Tokyo, Japan</json:string></affiliations></json:item><json:item><name>Tsugunori Notomi</name><affiliations><json:string>Eiken Chemical Co. Ltd., Kita‐ku, Tokyo, Japan</json:string></affiliations></json:item><json:item><name>Tetsuo Nakayama</name><affiliations><json:string>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Minato‐ku, Tokyo, Japan</json:string><json:string>E-mail: tetsuo‐n@lisci.kitasato‐u.ac.jp</json:string><json:string>Correspondence address: Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Kitasato University, Shirokane 5‐9‐1, Minato‐ku, Tokyo 108‐8641, Japan.===</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>measles virus</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>reverse transcription‐polymerase reaction (RT‐PCR)</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>reverse transcription‐loop‐mediated isothermal amplification (RT‐LAMP)</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>rapid diagnosis</value></json:item></subject><articleId><json:string>JMV20371</json:string></articleId><arkIstex>ark:/67375/WNG-ZH92N2WX-C</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>article</json:string></originalGenre><abstract>Approximately 20,000–30,000 measles patients were reported in a surveillance of infectious diseases because of low vaccine coverage of 80% in Japan. Among them, some were thought to be secondary vaccine failure (SVF) with generally mild or non‐typical measles illness and sometimes became a source of further transmission. We have developed a new, sensitive, and rapid method to detect the measles virus genome by reverse transcription loop‐mediated isothermal amplification (RT‐LAMP). We examined 50 nasopharyngeal secretion (NPS) samples that were obtained during the 1999 outbreak and stored at −70°C and fresh NPS, lymphocytes and sera from 11 patients in 2003. Total RNA was extracted from the samples and subjected to reverse transcription‐polymerase chain reaction (RT‐PCR) and RT‐LAMP. We detected the genomic RNA corresponding to at least 0.01–0.04 TCID50, 30–100 copies in samples by RT‐LAMP within 60 min after extraction of RNA, and all four genotypes isolated in Japan were equally amplified. Specific DNA amplification was monitored spectrophotometrically by real time turbidimeter and the quantity of RNA was calculated. Measles virus genome was detected in 44 of 50 stored NPS by RT‐PCR and in 49 by RT‐LAMP. The vaccine strain was discriminated from wild strains after sequencing the LAMP products. RT‐LAMP is a useful rapid diagnostic method for the detection of measles virus without any special apparatus, showing higher sensitivity than RT‐PCR, and expected to be applied for hospital‐based infection control and for laboratory‐based measles surveillance. J. Med. Virol. 76:406–413, 2005. © 2005 Wiley‐Liss, Inc.</abstract><qualityIndicators><score>8.979</score><pdfWordCount>4075</pdfWordCount><pdfCharCount>25025</pdfCharCount><pdfVersion>1.3</pdfVersion><pdfPageCount>8</pdfPageCount><pdfPageSize>594 x 792 pts</pdfPageSize><pdfWordsPerPage>509</pdfWordsPerPage><pdfText>true</pdfText><refBibsNative>true</refBibsNative><abstractWordCount>242</abstractWordCount><abstractCharCount>1633</abstractCharCount><keywordCount>4</keywordCount></qualityIndicators><title>A simple method for the detection of measles virus genome by loop‐mediated isothermal amplification (LAMP)</title><pmid><json:string>15902708</json:string></pmid><genre><json:string>article</json:string></genre><host><title>Journal of Medical Virology</title><language><json:string>unknown</json:string></language><doi><json:string>10.1002/(ISSN)1096-9071</json:string></doi><issn><json:string>0146-6615</json:string></issn><eissn><json:string>1096-9071</json:string></eissn><publisherId><json:string>JMV</json:string></publisherId><volume>76</volume><issue>3</issue><pages><first>406</first><last>413</last><total>8</total></pages><genre><json:string>journal</json:string></genre><subject><json:item><value>Research Article</value></json:item></subject></host><namedEntities><unitex><date><json:string>2000</json:string><json:string>2005</json:string><json:string>21st Century</json:string><json:string>1987</json:string><json:string>from the 21st Century</json:string><json:string>1999</json:string><json:string>1990</json:string><json:string>5-9-1</json:string><json:string>2003</json:string><json:string>1984</json:string><json:string>1985</json:string></date><geogName></geogName><orgName><json:string>WHO</json:string><json:string>Ministry of Education, Culture, Sports, Science and Technology</json:string><json:string>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Kitasato University, Shirokane</json:string><json:string>Life Technologies, Inc.</json:string><json:string>Eiken Chemical Co.</json:string><json:string>Ministry of Education, Culture, Sports, Science and Technology of Japan</json:string><json:string>Japan Department of Pediatrics, National Kasumigaura Hospital, Tsuchiura, Ibaraki, Japan</json:string><json:string>Wiley-Liss, Inc</json:string><json:string>TOYOBO Co.</json:string><json:string>LISS, INC.</json:string></orgName><orgName_funder></orgName_funder><orgName_provider></orgName_provider><persName><json:string>TaKaRa BioMedicals</json:string><json:string>I. Detection</json:string></persName><placeName><json:string>Nile</json:string><json:string>Yamaguchi</json:string><json:string>Kyoto</json:string><json:string>Madison</json:string><json:string>Japan</json:string><json:string>Gaithesburg</json:string><json:string>MD</json:string><json:string>Tokyo</json:string><json:string>Chicago</json:string><json:string>WI</json:string><json:string>Osaka</json:string></placeName><ref_url></ref_url><ref_bibl><json:string>Fujino et al.</json:string><json:string>Okafuji et al., 2005</json:string><json:string>Yoshikawa et al. [2004]</json:string><json:string>Kumada et al., 2004</json:string><json:string>Wild et al., 1991</json:string><json:string>Mori et al., 2004</json:string><json:string>Lievano et al., 2004</json:string><json:string>Helfand et al., 1998</json:string><json:string>Nagamine et al., 2002</json:string><json:string>Iwamoto et al., 2003</json:string><json:string>ref of WHO, 2001</json:string><json:string>Thai et al., 2004</json:string><json:string>Kuboki et al., 2003</json:string><json:string>Takahashi et al., 2000</json:string><json:string>Ozoemena et al., 2004</json:string><json:string>Yoshikawa et al., 2004</json:string><json:string>Mossong et al., 1999</json:string><json:string>Schalk et al., 2004</json:string><json:string>Ozoemena et al. [2004]</json:string><json:string>Stein et al., 2003</json:string><json:string>Okamoto et al., 2004</json:string><json:string>Maruyama et al., 2003</json:string><json:string>Kobune et al., 1990</json:string><json:string>Ihira et al., 2004</json:string><json:string>Notomi et al., 2000</json:string><json:string>Zhou et al., 2003</json:string><json:string>Nakayama et al., 2003</json:string><json:string>Parida et al., 2004</json:string><json:string>Afzal et al., 2003</json:string><json:string>Nakayama et al., 1995</json:string></ref_bibl><bibl></bibl></unitex></namedEntities><ark><json:string>ark:/67375/WNG-ZH92N2WX-C</json:string></ark><categories><wos><json:string>1 - science</json:string><json:string>2 - virology</json:string></wos><scienceMetrix><json:string>1 - health sciences</json:string><json:string>2 - biomedical research</json:string><json:string>3 - virology</json:string></scienceMetrix><scopus><json:string>1 - Health Sciences</json:string><json:string>2 - Medicine</json:string><json:string>3 - Infectious Diseases</json:string><json:string>1 - Life Sciences</json:string><json:string>2 - Immunology and Microbiology</json:string><json:string>3 - Virology</json:string></scopus><inist><json:string>1 - sciences appliquees, technologies et medecines</json:string><json:string>2 - sciences biologiques et medicales</json:string><json:string>3 - sciences medicales</json:string><json:string>4 - maladies metaboliques</json:string></inist></categories><publicationDate>2005</publicationDate><copyrightDate>2005</copyrightDate><doi><json:string>10.1002/jmv.20371</json:string></doi><id>DF1455206F714BAA11C1A5FBCC3C3C60BF5B9A2A</id><score>1</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/ark:/67375/WNG-ZH92N2WX-C/fulltext.pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/ark:/67375/WNG-ZH92N2WX-C/bundle.zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/ark:/67375/WNG-ZH92N2WX-C/fulltext.tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main">A simple method for the detection of measles virus genome by loop‐mediated isothermal amplification (LAMP)</title><title level="a" type="short" xml:lang="en">Detection of Measles Virus Genome by LAMP</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><availability><licence>Copyright © 2005 Wiley‐Liss, Inc.</licence></availability><date type="published" when="2005-07"></date></publicationStmt><notesStmt><note type="content-type" subtype="article" source="article" scheme="https://content-type.data.istex.fr/ark:/67375/XTP-6N5SZHKN-D">article</note><note type="publication-type" subtype="journal" scheme="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</note></notesStmt><sourceDesc><biblStruct type="article"><analytic><title level="a" type="main">A simple method for the detection of measles virus genome by loop‐mediated isothermal amplification (LAMP)</title><title level="a" type="short" xml:lang="en">Detection of Measles Virus Genome by LAMP</title><author xml:id="author-0000"><persName><forename type="first">Motoko</forename><surname>Fujino</surname></persName><affiliation><orgName type="laboratory">Laboratory of Viral Infection I</orgName><orgName type="institution">Kitasato Institute for Life Sciences</orgName><address><addrLine>Minato‐ku</addrLine><addrLine>Tokyo, Japan</addrLine><country key="JP" xml:lang="en">JAPAN</country></address></affiliation></author><author xml:id="author-0001"><persName><forename type="first">Naoko</forename><surname>Yoshida</surname></persName><affiliation><orgName type="laboratory">Laboratory of Viral Infection I</orgName><orgName type="institution">Kitasato Institute for Life Sciences</orgName><address><addrLine>Minato‐ku</addrLine><addrLine>Tokyo, Japan</addrLine><country key="JP" xml:lang="en">JAPAN</country></address></affiliation></author><author xml:id="author-0002"><persName><forename type="first">Shinya</forename><surname>Yamaguchi</surname></persName><affiliation><orgName type="division">Department of Pediatrics</orgName><orgName type="institution">National Kasumigaura Hospital</orgName><address><addrLine>Tsuchiura</addrLine><addrLine>Ibaraki, Japan</addrLine><country key="JP" xml:lang="en">JAPAN</country></address></affiliation></author><author xml:id="author-0003"><persName><forename type="first">Norimitsu</forename><surname>Hosaka</surname></persName><affiliation><address><addrLine>Eiken Chemical Co. Ltd.</addrLine><addrLine>Kita‐ku, Tokyo, Japan</addrLine><country key="JP" xml:lang="en">JAPAN</country></address></affiliation></author><author xml:id="author-0004"><persName><forename type="first">Yoshinori</forename><surname>Ota</surname></persName><affiliation><address><addrLine>Eiken Chemical Co. Ltd.</addrLine><addrLine>Kita‐ku, Tokyo, Japan</addrLine><country key="JP" xml:lang="en">JAPAN</country></address></affiliation></author><author xml:id="author-0005"><persName><forename type="first">Tsugunori</forename><surname>Notomi</surname></persName><affiliation><address><addrLine>Eiken Chemical Co. Ltd.</addrLine><addrLine>Kita‐ku, Tokyo, Japan</addrLine><country key="JP" xml:lang="en">JAPAN</country></address></affiliation></author><author xml:id="author-0006" role="corresp"><persName><forename type="first">Tetsuo</forename><surname>Nakayama</surname></persName><email>tetsuo‐n@lisci.kitasato‐u.ac.jp</email><affiliation><orgName type="laboratory">Laboratory of Viral Infection I</orgName><orgName type="institution">Kitasato Institute for Life Sciences</orgName><address><addrLine>Minato‐ku</addrLine><addrLine>Tokyo, Japan</addrLine><country key="JP" xml:lang="en">JAPAN</country></address></affiliation></author><idno type="istex">DF1455206F714BAA11C1A5FBCC3C3C60BF5B9A2A</idno><idno type="ark">ark:/67375/WNG-ZH92N2WX-C</idno><idno type="DOI">10.1002/jmv.20371</idno><idno type="unit">JMV20371</idno><idno type="toTypesetVersion">file:JMV.JMV20371.pdf</idno></analytic><monogr><title level="j" type="main">Journal of Medical Virology</title><title level="j" type="alt">JOURNAL OF MEDICAL VIROLOGY</title><idno type="pISSN">0146-6615</idno><idno type="eISSN">1096-9071</idno><idno type="book-DOI">10.1002/(ISSN)1096-9071</idno><idno type="book-part-DOI">10.1002/jmv.v76:3</idno><idno type="product">JMV</idno><imprint><biblScope unit="vol">76</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="406">406</biblScope><biblScope unit="page" to="413">413</biblScope><biblScope unit="page-count">8</biblScope><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="2005-07"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><encodingDesc><schemaRef type="ODD" url="https://xml-schema.delivery.istex.fr/tei-istex.odd"></schemaRef><appInfo><application ident="pub2tei" version="1.0.10" when="2019-12-20"><label>pub2TEI-ISTEX</label><desc>A set of style sheets for converting XML documents encoded in various scientific publisher formats into a common TEI format.
<ref target="http://www.tei-c.org/">We use TEI</ref></desc></application></appInfo></encodingDesc><profileDesc><abstract xml:lang="en" style="main"><head>Abstract</head><p>Approximately 20,000–30,000 measles patients were reported in a surveillance of infectious diseases because of low vaccine coverage of 80% in Japan. Among them, some were thought to be secondary vaccine failure (SVF) with generally mild or non‐typical measles illness and sometimes became a source of further transmission. We have developed a new, sensitive, and rapid method to detect the measles virus genome by reverse transcription loop‐mediated isothermal amplification (RT‐LAMP). We examined 50 nasopharyngeal secretion (NPS) samples that were obtained during the 1999 outbreak and stored at −70°C and fresh NPS, lymphocytes and sera from 11 patients in 2003. Total RNA was extracted from the samples and subjected to reverse transcription‐polymerase chain reaction (RT‐PCR) and RT‐LAMP. We detected the genomic RNA corresponding to at least 0.01–0.04 TCID50, 30–100 copies in samples by RT‐LAMP within 60 min after extraction of RNA, and all four genotypes isolated in Japan were equally amplified. Specific DNA amplification was monitored spectrophotometrically by real time turbidimeter and the quantity of RNA was calculated. Measles virus genome was detected in 44 of 50 stored NPS by RT‐PCR and in 49 by RT‐LAMP. The vaccine strain was discriminated from wild strains after sequencing the LAMP products. RT‐LAMP is a useful rapid diagnostic method for the detection of measles virus without any special apparatus, showing higher sensitivity than RT‐PCR, and expected to be applied for hospital‐based infection control and for laboratory‐based measles surveillance. J. Med. Virol. 76:406–413, 2005. © 2005 Wiley‐Liss, Inc.</p></abstract><textClass><keywords xml:lang="en"><term xml:id="kwd1">measles virus</term><term xml:id="kwd2">reverse transcription‐polymerase reaction (RT‐PCR)</term><term xml:id="kwd3">reverse transcription‐loop‐mediated isothermal amplification (RT‐LAMP)</term><term xml:id="kwd4">rapid diagnosis</term></keywords><keywords rend="articleCategory"><term>Research Article</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-ZH92N2WX-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>Wiley Subscription Services, Inc., A Wiley Company</publisherName><publisherLoc>Hoboken</publisherLoc></publisherInfo><doi registered="yes">10.1002/(ISSN)1096-9071</doi><issn type="print">0146-6615</issn><issn type="electronic">1096-9071</issn><idGroup><id type="product" value="JMV"></id></idGroup><titleGroup><title type="main" xml:lang="en" sort="JOURNAL OF MEDICAL VIROLOGY">Journal of Medical Virology</title><title type="short">J. Med. Virol.</title></titleGroup></publicationMeta><publicationMeta level="part" position="30"><doi origin="wiley" registered="yes">10.1002/jmv.v76:3</doi><numberingGroup><numbering type="journalVolume" number="76">76</numbering><numbering type="journalIssue">3</numbering></numberingGroup><coverDate startDate="2005-07">July 2005</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="18" status="forIssue"><doi origin="wiley" registered="yes">10.1002/jmv.20371</doi><idGroup><id type="unit" value="JMV20371"></id></idGroup><countGroup><count type="pageTotal" number="8"></count></countGroup><titleGroup><title type="articleCategory">Research Article</title></titleGroup><copyright ownership="publisher">Copyright © 2005 Wiley‐Liss, Inc.</copyright><eventGroup><event type="manuscriptAccepted" date="2005-03-14"></event><event type="firstOnline" date="2005-05-18"></event><event type="publishedOnlineFinalForm" date="2005-05-18"></event><event type="xmlConverted" agent="Converter:JWSART34_TO_WML3G version:2.3.2 mode:FullText source:HeaderRef result:HeaderRef" date="2010-03-15"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:4.0.1" date="2014-03-20"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-30"></event></eventGroup><numberingGroup><numbering type="pageFirst">406</numbering><numbering type="pageLast">413</numbering></numberingGroup><correspondenceTo>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Kitasato University, Shirokane 5‐9‐1, Minato‐ku, Tokyo 108‐8641, Japan.===</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:JMV.JMV20371.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="5"></count><count type="tableTotal" number="1"></count><count type="referenceTotal" number="30"></count><count type="wordTotal" number="1080"></count></countGroup><titleGroup><title type="main" xml:lang="en">A simple method for the detection of measles virus genome by loop‐mediated isothermal amplification (LAMP)</title><title type="short" xml:lang="en">Detection of Measles Virus Genome by LAMP</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Motoko</givenNames><familyName>Fujino</familyName></personName></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Naoko</givenNames><familyName>Yoshida</familyName></personName></creator><creator xml:id="au3" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Shinya</givenNames><familyName>Yamaguchi</familyName></personName></creator><creator xml:id="au4" creatorRole="author" affiliationRef="#af3"><personName><givenNames>Norimitsu</givenNames><familyName>Hosaka</familyName></personName></creator><creator xml:id="au5" creatorRole="author" affiliationRef="#af3"><personName><givenNames>Yoshinori</givenNames><familyName>Ota</familyName></personName></creator><creator xml:id="au6" creatorRole="author" affiliationRef="#af3"><personName><givenNames>Tsugunori</givenNames><familyName>Notomi</familyName></personName></creator><creator xml:id="au7" creatorRole="author" affiliationRef="#af1" corresponding="yes"><personName><givenNames>Tetsuo</givenNames><familyName>Nakayama</familyName></personName><contactDetails><email normalForm="tetsuo-n@lisci.kitasato-u.ac.jp">tetsuo‐n@lisci.kitasato‐u.ac.jp</email></contactDetails></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="JP" type="organization"><unparsedAffiliation>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Minato‐ku, Tokyo, Japan</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="JP" type="organization"><unparsedAffiliation>Department of Pediatrics, National Kasumigaura Hospital, Tsuchiura, Ibaraki, Japan</unparsedAffiliation></affiliation><affiliation xml:id="af3" countryCode="JP" type="organization"><unparsedAffiliation>Eiken Chemical Co. Ltd., Kita‐ku, Tokyo, Japan</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">measles virus</keyword><keyword xml:id="kwd2">reverse transcription‐polymerase reaction (RT‐PCR)</keyword><keyword xml:id="kwd3">reverse transcription‐loop‐mediated isothermal amplification (RT‐LAMP)</keyword><keyword xml:id="kwd4">rapid diagnosis</keyword></keywordGroup><fundingInfo><fundingAgency>21st Century COE Program of the Ministry of Education, Culture, Sports, Science and Technology (Japan)</fundingAgency></fundingInfo><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>Approximately 20,000–30,000 measles patients were reported in a surveillance of infectious diseases because of low vaccine coverage of 80% in Japan. Among them, some were thought to be secondary vaccine failure (SVF) with generally mild or non‐typical measles illness and sometimes became a source of further transmission. We have developed a new, sensitive, and rapid method to detect the measles virus genome by reverse transcription loop‐mediated isothermal amplification (RT‐LAMP). We examined 50 nasopharyngeal secretion (NPS) samples that were obtained during the 1999 outbreak and stored at −70°C and fresh NPS, lymphocytes and sera from 11 patients in 2003. Total RNA was extracted from the samples and subjected to reverse transcription‐polymerase chain reaction (RT‐PCR) and RT‐LAMP. We detected the genomic RNA corresponding to at least 0.01–0.04 TCID50, 30–100 copies in samples by RT‐LAMP within 60 min after extraction of RNA, and all four genotypes isolated in Japan were equally amplified. Specific DNA amplification was monitored spectrophotometrically by real time turbidimeter and the quantity of RNA was calculated. Measles virus genome was detected in 44 of 50 stored NPS by RT‐PCR and in 49 by RT‐LAMP. The vaccine strain was discriminated from wild strains after sequencing the LAMP products. RT‐LAMP is a useful rapid diagnostic method for the detection of measles virus without any special apparatus, showing higher sensitivity than RT‐PCR, and expected to be applied for hospital‐based infection control and for laboratory‐based measles surveillance. J. Med. Virol. 76:406–413, 2005. © 2005 Wiley‐Liss, Inc.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>A simple method for the detection of measles virus genome by loop‐mediated isothermal amplification (LAMP)</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Detection of Measles Virus Genome by LAMP</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>A simple method for the detection of measles virus genome by loop‐mediated isothermal amplification (LAMP)</title></titleInfo><name type="personal"><namePart type="given">Motoko</namePart><namePart type="family">Fujino</namePart><affiliation>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Minato‐ku, Tokyo, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Naoko</namePart><namePart type="family">Yoshida</namePart><affiliation>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Minato‐ku, Tokyo, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Shinya</namePart><namePart type="family">Yamaguchi</namePart><affiliation>Department of Pediatrics, National Kasumigaura Hospital, Tsuchiura, Ibaraki, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Norimitsu</namePart><namePart type="family">Hosaka</namePart><affiliation>Eiken Chemical Co. Ltd., Kita‐ku, Tokyo, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Yoshinori</namePart><namePart type="family">Ota</namePart><affiliation>Eiken Chemical Co. Ltd., Kita‐ku, Tokyo, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Tsugunori</namePart><namePart type="family">Notomi</namePart><affiliation>Eiken Chemical Co. Ltd., Kita‐ku, Tokyo, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Tetsuo</namePart><namePart type="family">Nakayama</namePart><affiliation>Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Minato‐ku, Tokyo, Japan</affiliation><affiliation>E-mail: tetsuo‐n@lisci.kitasato‐u.ac.jp</affiliation><affiliation>Correspondence address: Laboratory of Viral Infection I, Kitasato Institute for Life Sciences, Kitasato University, Shirokane 5‐9‐1, Minato‐ku, Tokyo 108‐8641, Japan.===</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-6N5SZHKN-D">article</genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">2005-07</dateIssued><dateValid encoding="w3cdtf">2005-03-14</dateValid><copyrightDate encoding="w3cdtf">2005</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="figures">5</extent><extent unit="tables">1</extent><extent unit="references">30</extent><extent unit="words">1080</extent></physicalDescription><abstract lang="en">Approximately 20,000–30,000 measles patients were reported in a surveillance of infectious diseases because of low vaccine coverage of 80% in Japan. Among them, some were thought to be secondary vaccine failure (SVF) with generally mild or non‐typical measles illness and sometimes became a source of further transmission. We have developed a new, sensitive, and rapid method to detect the measles virus genome by reverse transcription loop‐mediated isothermal amplification (RT‐LAMP). We examined 50 nasopharyngeal secretion (NPS) samples that were obtained during the 1999 outbreak and stored at −70°C and fresh NPS, lymphocytes and sera from 11 patients in 2003. Total RNA was extracted from the samples and subjected to reverse transcription‐polymerase chain reaction (RT‐PCR) and RT‐LAMP. We detected the genomic RNA corresponding to at least 0.01–0.04 TCID50, 30–100 copies in samples by RT‐LAMP within 60 min after extraction of RNA, and all four genotypes isolated in Japan were equally amplified. Specific DNA amplification was monitored spectrophotometrically by real time turbidimeter and the quantity of RNA was calculated. Measles virus genome was detected in 44 of 50 stored NPS by RT‐PCR and in 49 by RT‐LAMP. The vaccine strain was discriminated from wild strains after sequencing the LAMP products. RT‐LAMP is a useful rapid diagnostic method for the detection of measles virus without any special apparatus, showing higher sensitivity than RT‐PCR, and expected to be applied for hospital‐based infection control and for laboratory‐based measles surveillance. J. Med. Virol. 76:406–413, 2005. © 2005 Wiley‐Liss, Inc.</abstract><note type="funding">21st Century COE Program of the Ministry of Education, Culture, Sports, Science and Technology (Japan)</note><subject lang="en"><genre>keywords</genre><topic>measles virus</topic><topic>reverse transcription‐polymerase reaction (RT‐PCR)</topic><topic>reverse transcription‐loop‐mediated isothermal amplification (RT‐LAMP)</topic><topic>rapid diagnosis</topic></subject><relatedItem type="host"><titleInfo><title>Journal of Medical Virology</title></titleInfo><titleInfo type="abbreviated"><title>J. Med. Virol.</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>Research Article</topic></subject><identifier type="ISSN">0146-6615</identifier><identifier type="eISSN">1096-9071</identifier><identifier type="DOI">10.1002/(ISSN)1096-9071</identifier><identifier type="PublisherID">JMV</identifier><part><date>2005</date><detail type="volume"><caption>vol.</caption><number>76</number></detail><detail type="issue"><caption>no.</caption><number>3</number></detail><extent unit="pages"><start>406</start><end>413</end><total>8</total></extent></part></relatedItem><relatedItem type="references" displayLabel="cit1"><titleInfo><title>Comparative evaluation of measles virus‐specific RT‐PCR methods through an international collaborative study</title></titleInfo><name type="personal"><namePart type="given">MA</namePart><namePart type="family">Afzal</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">ADME</namePart><namePart type="family">Osterhaus</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">SL</namePart><namePart type="family">Cosby</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">L</namePart><namePart type="family">Jin</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">J</namePart><namePart type="family">Beeler</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">K</namePart><namePart type="family">Takeuchi</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">H</namePart><namePart type="family">Kawashima</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Afzal MA, Osterhaus ADME, Cosby SL, Jin L, Beeler J, Takeuchi K, Kawashima H. 2003. Comparative evaluation of measles virus‐specific RT‐PCR methods through an international collaborative study. J Med Virol 70: 171–176.</note><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>70</number></detail><extent unit="pages"><start>171</start><end>176</end></extent></part><relatedItem type="host"><titleInfo><title>J Med Virol</title></titleInfo><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>70</number></detail><extent unit="pages"><start>171</start><end>176</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit2"><titleInfo><title>Measles virus</title></titleInfo><name type="personal"><namePart type="given">DE</namePart><namePart type="family">Griffin</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">WJ</namePart><namePart type="family">Bellini</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>book-chapter</genre><relatedItem type="host"><titleInfo><title>Fields virology</title></titleInfo><originInfo><publisher>Lippincott Williams & Wilkins</publisher><place><placeTerm type="text">Philadelphia</placeTerm></place></originInfo><part><date>2001</date><extent unit="pages"><start>1401</start><end>1441</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit3"><titleInfo><title>Nonclassic measles infections in an immune population exposed to measles during a college bus trip</title></titleInfo><name type="personal"><namePart type="given">RF</namePart><namePart type="family">Helfand</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">DK</namePart><namePart type="family">Kim</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">HE</namePart><namePart type="family">Gary Jr.</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">GL</namePart><namePart type="family">Edwards</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">GP</namePart><namePart type="family">Bisson</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">MJ</namePart><namePart type="family">Papania</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">JL</namePart><namePart type="family">Heath</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">DL</namePart><namePart type="family">Schaff</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">WJ</namePart><namePart type="family">Bellini</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">SC</namePart><namePart type="family">Redd</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">LJ</namePart><namePart type="family">Anderson</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Helfand RF, Kim DK, Gary HE, Jr., Edwards GL, Bisson GP, Papania MJ, Heath JL, Schaff DL, Bellini WJ, Redd SC, Anderson LJ. 1998. Nonclassic measles infections in an immune population exposed to measles during a college bus trip. J Med Virol 56: 337–341.</note><part><date>1998</date><detail type="volume"><caption>vol.</caption><number>56</number></detail><extent unit="pages"><start>337</start><end>341</end></extent></part><relatedItem type="host"><titleInfo><title>J Med Virol</title></titleInfo><part><date>1998</date><detail type="volume"><caption>vol.</caption><number>56</number></detail><extent unit="pages"><start>337</start><end>341</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit4"><titleInfo><title>Rapid diagnosis of human herpesvirus 6 infection by a novel DNA amplification method, loop‐mediated isothermal amplification</title></titleInfo><name type="personal"><namePart type="given">M</namePart><namePart type="family">Ihira</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Yoshikawa</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Enomoto</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">S</namePart><namePart type="family">Akimoto</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M</namePart><namePart type="family">Ohashi</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">S</namePart><namePart type="family">Suga</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">N</namePart><namePart type="family">Nishimura</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Ozaki</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Nishiyama</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Notomi</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Ohta</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Asano</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Ihira M, Yoshikawa T, Enomoto Y, Akimoto S, Ohashi M, Suga S, Nishimura N, Ozaki T, Nishiyama Y, Notomi T, Ohta Y, Asano Y. 2004. Rapid diagnosis of human herpesvirus 6 infection by a novel DNA amplification method, loop‐mediated isothermal amplification. J Clin Microbiol 42: 140–145.</note><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>42</number></detail><extent unit="pages"><start>140</start><end>145</end></extent></part><relatedItem type="host"><titleInfo><title>J Clin Microbiol</title></titleInfo><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>42</number></detail><extent unit="pages"><start>140</start><end>145</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit5"><titleInfo><title>Loop‐mediated isothermal amplification for direct detection of Mycobacterium tuberculosis complex, M. avium, and M. intracellulare in sputum samples</title></titleInfo><name type="personal"><namePart type="given">T</namePart><namePart type="family">Iwamoto</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Sonobe</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">K</namePart><namePart type="family">Hayashi</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Iwamoto T, Sonobe T, Hayashi K. 2003. Loop‐mediated isothermal amplification for direct detection of Mycobacterium tuberculosis complex, M. avium, and M. intracellulare in sputum samples. J Clin Microbiol 41: 2616–2622.</note><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>41</number></detail><extent unit="pages"><start>2616</start><end>2622</end></extent></part><relatedItem type="host"><titleInfo><title>J Clin Microbiol</title></titleInfo><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>41</number></detail><extent unit="pages"><start>2616</start><end>2622</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit6"><titleInfo><title>Marmoset lymphoblastoid cells as a sensitive host for isolation of measles virus</title></titleInfo><name type="personal"><namePart type="given">F</namePart><namePart type="family">Kobune</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">H</namePart><namePart type="family">Sakata</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">A</namePart><namePart type="family">Sugiura</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Kobune F, Sakata H, Sugiura A. 1990. Marmoset lymphoblastoid cells as a sensitive host for isolation of measles virus. J Virol 64: 700–705.</note><part><date>1990</date><detail type="volume"><caption>vol.</caption><number>64</number></detail><extent unit="pages"><start>700</start><end>705</end></extent></part><relatedItem type="host"><titleInfo><title>J Virol</title></titleInfo><part><date>1990</date><detail type="volume"><caption>vol.</caption><number>64</number></detail><extent unit="pages"><start>700</start><end>705</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit7"><titleInfo><title>Loop‐mediated isothermal amplification for detection of African trypanosomes</title></titleInfo><name type="personal"><namePart type="given">N</namePart><namePart type="family">Kuboki</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">N</namePart><namePart type="family">Inoue</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Sakurai</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">F</namePart><namePart type="family">Di Cello</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">DJ</namePart><namePart type="family">Grab</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">H</namePart><namePart type="family">Suzuki</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">C</namePart><namePart type="family">Sugimoto</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">I</namePart><namePart type="family">Igarashi</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Kuboki N, Inoue N, Sakurai T, Di Cello F, Grab DJ, Suzuki H, Sugimoto C, Igarashi I. 2003. Loop‐mediated isothermal amplification for detection of African trypanosomes. J Clin Microbiol 41: 5517–5524.</note><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>41</number></detail><extent unit="pages"><start>5517</start><end>5524</end></extent></part><relatedItem type="host"><titleInfo><title>J Clin Microbiol</title></titleInfo><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>41</number></detail><extent unit="pages"><start>5517</start><end>5524</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit8"><titleInfo><title>Recombinant measles AIK‐C strain expressing current wild‐type hemagglutinin protein</title></titleInfo><name type="personal"><namePart type="given">A</namePart><namePart type="family">Kumada</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">K</namePart><namePart type="family">Komase</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Nakayana</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Kumada A, Komase K, Nakayana T. 2004. Recombinant measles AIK‐C strain expressing current wild‐type hemagglutinin protein. Vaccine 22: 309–316.</note><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>22</number></detail><extent unit="pages"><start>309</start><end>316</end></extent></part><relatedItem type="host"><titleInfo><title>Vaccine</title></titleInfo><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>22</number></detail><extent unit="pages"><start>309</start><end>316</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit9"><titleInfo><title>Lack of evidence of measles virus shedding in people with inapparent measles virus infections</title></titleInfo><name type="personal"><namePart type="given">FA</namePart><namePart type="family">Lievano</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">MJ</namePart><namePart type="family">Papania</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">RF</namePart><namePart type="family">Helfand</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Lievano FA, Papania MJ, Helfand RF. 2004. Lack of evidence of measles virus shedding in people with inapparent measles virus infections J Infect Dis 189: S165–S170.</note><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>189</number></detail><extent unit="pages"><start>S165</start><end>S170</end></extent></part><relatedItem type="host"><titleInfo><title>J Infect Dis</title></titleInfo><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>189</number></detail><extent unit="pages"><start>S165</start><end>S170</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit10"><titleInfo><title>Detection of bacteria carrying the stx2 gene by in situ loop‐mediated isothermal amplification</title></titleInfo><name type="personal"><namePart type="given">F</namePart><namePart type="family">Maruyama</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Kenzaka</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">N</namePart><namePart type="family">Yamaguchi</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">K</namePart><namePart type="family">Tani</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M</namePart><namePart type="family">Nasu</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Maruyama F, Kenzaka T, Yamaguchi N, Tani K, Nasu M. 2003. Detection of bacteria carrying the stx2 gene by in situ loop‐mediated isothermal amplification. Appl Environ Microbiol 69: 5023–5028.</note><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>69</number></detail><extent unit="pages"><start>5023</start><end>5028</end></extent></part><relatedItem type="host"><titleInfo><title>Appl Environ Microbiol</title></titleInfo><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>69</number></detail><extent unit="pages"><start>5023</start><end>5028</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit11"><titleInfo><title>Real‐time turbidimetry of LAMP reaction for quantifying template DNA</title></titleInfo><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Mori</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M</namePart><namePart type="family">Kitao</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">N</namePart><namePart type="family">Tomita</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Notomi</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Mori Y, Kitao M, Tomita N, Notomi T. 2004. Real‐time turbidimetry of LAMP reaction for quantifying template DNA. J Biochem Biophys Methods 59: 145–157.</note><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>59</number></detail><extent unit="pages"><start>145</start><end>157</end></extent></part><relatedItem type="host"><titleInfo><title>J Biochem Biophys Methods</title></titleInfo><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>59</number></detail><extent unit="pages"><start>145</start><end>157</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit12"><titleInfo><title>Modeling the impact of inapparent measles transmission in vaccinated populations with waning immunity</title></titleInfo><name type="personal"><namePart type="given">J</namePart><namePart type="family">Mossong</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">DJ</namePart><namePart type="family">Nokes</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">WJ</namePart><namePart type="family">Edmunds</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">MJ</namePart><namePart type="family">Cox</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">S</namePart><namePart type="family">Ratnam</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">CP</namePart><namePart type="family">Muller</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Mossong J, Nokes DJ, Edmunds WJ, Cox MJ, Ratnam S, Muller CP. 1999. Modeling the impact of inapparent measles transmission in vaccinated populations with waning immunity. Am J Epidemiol 150: 1238–1249.</note><part><date>1999</date><detail type="volume"><caption>vol.</caption><number>150</number></detail><extent unit="pages"><start>1238</start><end>1249</end></extent></part><relatedItem type="host"><titleInfo><title>Am J Epidemiol</title></titleInfo><part><date>1999</date><detail type="volume"><caption>vol.</caption><number>150</number></detail><extent unit="pages"><start>1238</start><end>1249</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit13"><titleInfo><title>Accelerated reaction by loop‐mediated isothermal amplification using loop primers</title></titleInfo><name type="personal"><namePart type="given">K</namePart><namePart type="family">Nagamine</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Hase</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Notomi</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Nagamine K, Hase T, Notomi T. 2002. Accelerated reaction by loop‐mediated isothermal amplification using loop primers. Mol Cell Probes 16: 223–229.</note><part><date>2002</date><detail type="volume"><caption>vol.</caption><number>16</number></detail><extent unit="pages"><start>223</start><end>229</end></extent></part><relatedItem type="host"><titleInfo><title>Mol Cell Probes</title></titleInfo><part><date>2002</date><detail type="volume"><caption>vol.</caption><number>16</number></detail><extent unit="pages"><start>223</start><end>229</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit14"><titleInfo><title>Detection of measles virus genome directly from clinical samples by reverse transcriptase‐polymerase chain reaction and genetic variability</title></titleInfo><name type="personal"><namePart type="given">T</namePart><namePart type="family">Nakayama</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Mori</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">S</namePart><namePart type="family">Yamaguchi</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">S</namePart><namePart type="family">Sonoda</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">S</namePart><namePart type="family">Asamura</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">R</namePart><namePart type="family">Yamashita</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Takeuchi</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Urano</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Nakayama T, Mori T, Yamaguchi S, Sonoda S, Asamura S, Yamashita R, Takeuchi Y, Urano T. 1995. Detection of measles virus genome directly from clinical samples by reverse transcriptase‐polymerase chain reaction and genetic variability. Virus Res 35: 1–16.</note><part><date>1995</date><detail type="volume"><caption>vol.</caption><number>35</number></detail><extent unit="pages"><start>1</start><end>16</end></extent></part><relatedItem type="host"><titleInfo><title>Virus Res</title></titleInfo><part><date>1995</date><detail type="volume"><caption>vol.</caption><number>35</number></detail><extent unit="pages"><start>1</start><end>16</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit15"><titleInfo><title>Current status of measles in Japan</title></titleInfo><name type="personal"><namePart type="given">T</namePart><namePart type="family">Nakayama</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">J</namePart><namePart type="family">Zhou</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M</namePart><namePart type="family">Fujino</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Nakayama T, Zhou J, Fujino M. 2003. Current status of measles in Japan. J Infect Chemother 9: 1–7.</note><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>9</number></detail><extent unit="pages"><start>1</start><end>7</end></extent></part><relatedItem type="host"><titleInfo><title>J Infect Chemother</title></titleInfo><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>9</number></detail><extent unit="pages"><start>1</start><end>7</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit16"><titleInfo><title>Loop‐mediated isothermal amplification of DNA</title></titleInfo><name type="personal"><namePart type="given">T</namePart><namePart type="family">Notomi</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">H</namePart><namePart type="family">Okayama</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">H</namePart><namePart type="family">Masubuchi</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Yonekawa</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">K</namePart><namePart type="family">K. Watanabe</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">N</namePart><namePart type="family">Amino</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Hase</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Notomi T, Okayama H, Masubuchi H, Yonekawa T, K. Watanabe K, Amino N, Hase T. 2000. Loop‐mediated isothermal amplification of DNA. Nucleic Acids Res 28: e63.</note><part><date>2000</date><detail type="volume"><caption>vol.</caption><number>28</number></detail><extent unit="pages"><start>e63</start></extent></part><relatedItem type="host"><titleInfo><title>Nucleic Acids Res</title></titleInfo><part><date>2000</date><detail type="volume"><caption>vol.</caption><number>28</number></detail><extent unit="pages"><start>e63</start></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit17"><titleInfo><title>Rapid diagnostic method for the detection of mumps virus genome by loop‐mediated isothermal amplification</title></titleInfo><name type="personal"><namePart type="given">T</namePart><namePart type="family">Okafuji</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">N</namePart><namePart type="family">Yoshida</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M</namePart><namePart type="family">Fujino</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Motegi</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Ihara</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Ota</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Notomi</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Nakayama</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Okafuji T, Yoshida N, Fujino M, Motegi Y, Ihara T, Ota Y, Notomi T, Nakayama T. 2005. Rapid diagnostic method for the detection of mumps virus genome by loop‐mediated isothermal amplification. J Clin Microbiol 43: 1625–1631.</note><part><date>2005</date><detail type="volume"><caption>vol.</caption><number>43</number></detail><extent unit="pages"><start>1625</start><end>1631</end></extent></part><relatedItem type="host"><titleInfo><title>J Clin Microbiol</title></titleInfo><part><date>2005</date><detail type="volume"><caption>vol.</caption><number>43</number></detail><extent unit="pages"><start>1625</start><end>1631</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit18"><titleInfo><title>Rapid detection of varicella‐zoster virus infection by a loop‐mediated isothermal amplification method</title></titleInfo><name type="personal"><namePart type="given">S</namePart><namePart type="family">Okamoto</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Yoshikawa</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M</namePart><namePart type="family">Ihira</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">K</namePart><namePart type="family">Suzuki</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">K</namePart><namePart type="family">Shimokata</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Nishiyama</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Asano</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Okamoto S, Yoshikawa T, Ihira M, Suzuki K, Shimokata K, Nishiyama Y, Asano Y. 2004. Rapid detection of varicella‐zoster virus infection by a loop‐mediated isothermal amplification method. J Med Virol 74: 677–682.</note><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>74</number></detail><extent unit="pages"><start>677</start><end>682</end></extent></part><relatedItem type="host"><titleInfo><title>J Med Virol</title></titleInfo><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>74</number></detail><extent unit="pages"><start>677</start><end>682</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit19"><titleInfo><title>Comparative evaluation of measles virus specific TaqMan PCR and conventional PCR using synthetic and natural RNA templates</title></titleInfo><name type="personal"><namePart type="given">LC</namePart><namePart type="family">Ozoemena</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">PD</namePart><namePart type="family">Minor</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">MA</namePart><namePart type="family">Afzahl</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Ozoemena LC, Minor PD, Afzahl MA. 2004. Comparative evaluation of measles virus specific TaqMan PCR and conventional PCR using synthetic and natural RNA templates. J Med Virol 73: 79–84.</note><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>73</number></detail><extent unit="pages"><start>79</start><end>84</end></extent></part><relatedItem type="host"><titleInfo><title>J Med Virol</title></titleInfo><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>73</number></detail><extent unit="pages"><start>79</start><end>84</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit20"><titleInfo><title>Real‐time reverse transcription loop‐mediated isothermal amplification for rapid detection of West Nile virus</title></titleInfo><name type="personal"><namePart type="given">M</namePart><namePart type="family">Parida</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">G</namePart><namePart type="family">Posadas</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">S</namePart><namePart type="family">Inoue</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">F</namePart><namePart type="family">Hasebe</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">K</namePart><namePart type="family">Morita</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Parida M, Posadas G, Inoue S, Hasebe F, Morita K. 2004. Real‐time reverse transcription loop‐mediated isothermal amplification for rapid detection of West Nile virus. J Clin Microbiol 42: 257–263.</note><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>42</number></detail><extent unit="pages"><start>257</start><end>263</end></extent></part><relatedItem type="host"><titleInfo><title>J Clin Microbiol</title></titleInfo><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>42</number></detail><extent unit="pages"><start>257</start><end>263</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit21"><titleInfo><title>Estimation of the number of infectious measles viruses in live virus vaccine using real‐time PCR</title></titleInfo><name type="personal"><namePart type="given">JAC</namePart><namePart type="family">Schalk</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">C</namePart><namePart type="family">Van den Elzen</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">H</namePart><namePart type="family">Ovelgonne</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">C</namePart><namePart type="family">Baas</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">PMJM</namePart><namePart type="family">Jongen</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Schalk JAC, Van den Elzen C, Ovelgonne H, Baas C, Jongen PMJM. 2004. Estimation of the number of infectious measles viruses in live virus vaccine using real‐time PCR. J Virol Methods 117: 179–187.</note><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>117</number></detail><extent unit="pages"><start>179</start><end>187</end></extent></part><relatedItem type="host"><titleInfo><title>J Virol Methods</title></titleInfo><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>117</number></detail><extent unit="pages"><start>179</start><end>187</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit22"><titleInfo><title>The global burden of measles in the year 2000—a model that uses country‐specific indicators</title></titleInfo><name type="personal"><namePart type="given">CE</namePart><namePart type="family">Stein</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M</namePart><namePart type="family">Birmingham</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M</namePart><namePart type="family">Kurian</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">P</namePart><namePart type="family">Duclos</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">P</namePart><namePart type="family">Strebel</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Stein CE, Birmingham M, Kurian M, Duclos P, Strebel P. 2003. The global burden of measles in the year 2000—a model that uses country‐specific indicators. J Infect Dis 187: S8–S14.</note><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>187</number></detail><extent unit="pages"><start>S8</start><end>S14</end></extent></part><relatedItem type="host"><titleInfo><title>J Infect Dis</title></titleInfo><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>187</number></detail><extent unit="pages"><start>S8</start><end>S14</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit23"><titleInfo><title>A single genotype of measles virus is dominant whereas several genotypes of mumps virus are co‐circulating</title></titleInfo><name type="personal"><namePart type="given">M</namePart><namePart type="family">Takahashi</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Nakayama</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Kashiwagi</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Takami</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">S</namePart><namePart type="family">Sonoda</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Yamanaka</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">H</namePart><namePart type="family">Ochiai</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Ihara</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Tajima</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Takahashi M, Nakayama T, Kashiwagi Y, Takami T, Sonoda S, Yamanaka T, Ochiai H, Ihara T, Tajima T. 2000. A single genotype of measles virus is dominant whereas several genotypes of mumps virus are co‐circulating. J Med Virol 62: 278–285.</note><part><date>2000</date><detail type="volume"><caption>vol.</caption><number>62</number></detail><extent unit="pages"><start>278</start><end>285</end></extent></part><relatedItem type="host"><titleInfo><title>J Med Virol</title></titleInfo><part><date>2000</date><detail type="volume"><caption>vol.</caption><number>62</number></detail><extent unit="pages"><start>278</start><end>285</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit24"><titleInfo><title>Development and evaluation of a novel loop‐mediated isothermal amplification method for rapid detection of severe acute respiratory syndrome coronavirus</title></titleInfo><name type="personal"><namePart type="given">HTC</namePart><namePart type="family">Thai</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">MQ</namePart><namePart type="family">Le</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">CD</namePart><namePart type="family">Vuong</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M</namePart><namePart type="family">Parida</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">H</namePart><namePart type="family">Minekawa</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Notomi</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">F</namePart><namePart type="family">Hasebe</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">K</namePart><namePart type="family">Morita</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Thai HTC, Le MQ, Vuong CD, Parida M, Minekawa H, Notomi T, Hasebe F, Morita K. 2004. Development and evaluation of a novel loop‐mediated isothermal amplification method for rapid detection of severe acute respiratory syndrome coronavirus. J Clin Microbiol 42: 1956–1961.</note><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>42</number></detail><extent unit="pages"><start>1956</start><end>1961</end></extent></part><relatedItem type="host"><titleInfo><title>J Clin Microbiol</title></titleInfo><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>42</number></detail><extent unit="pages"><start>1956</start><end>1961</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit25"><titleInfo><title>Standardization of the nomenclature for describing the genetic characteristics of wild‐type measles viruses</title></titleInfo><name type="corporate"><namePart>WHO</namePart></name><genre>journal-article</genre><note type="citation/reference">WHO. 2001. Standardization of the nomenclature for describing the genetic characteristics of wild‐type measles viruses. Wkly Epidemiol Rec 76: 241–248.</note><part><date>2001</date><detail type="volume"><caption>vol.</caption><number>76</number></detail><extent unit="pages"><start>241</start><end>248</end></extent></part><relatedItem type="host"><titleInfo><title>Wkly Epidemiol Rec</title></titleInfo><part><date>2001</date><detail type="volume"><caption>vol.</caption><number>76</number></detail><extent unit="pages"><start>241</start><end>248</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit26"><titleInfo><title>WHO‐UNICEF joint statement on strategies to reduce measles mortality worldwide</title></titleInfo><name type="corporate"><namePart>WHO</namePart></name><genre>journal-article</genre><note type="citation/reference">WHO. 2002. WHO‐UNICEF joint statement on strategies to reduce measles mortality worldwide. Wkly Epidemiol Rec 77: 224–228.</note><part><date>2002</date><detail type="volume"><caption>vol.</caption><number>77</number></detail><extent unit="pages"><start>224</start><end>228</end></extent></part><relatedItem type="host"><titleInfo><title>Wkly Epidemiol Rec</title></titleInfo><part><date>2002</date><detail type="volume"><caption>vol.</caption><number>77</number></detail><extent unit="pages"><start>224</start><end>228</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit27"><titleInfo><title>Measles virus: Both haemagglutinin and the fusion glycoproteins are required for fusion</title></titleInfo><name type="personal"><namePart type="given">TF</namePart><namePart type="family">Wild</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">E</namePart><namePart type="family">Malvoisin</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">R</namePart><namePart type="family">Buckland</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Wild TF, Malvoisin E, Buckland R. 1991. Measles virus: Both haemagglutinin and the fusion glycoproteins are required for fusion. J Gen Virol 72: 439–442.</note><part><date>1991</date><detail type="volume"><caption>vol.</caption><number>72</number></detail><extent unit="pages"><start>439</start><end>442</end></extent></part><relatedItem type="host"><titleInfo><title>J Gen Virol</title></titleInfo><part><date>1991</date><detail type="volume"><caption>vol.</caption><number>72</number></detail><extent unit="pages"><start>439</start><end>442</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit28"><titleInfo><title>Identification of three lineages of wild measles virus by nucleotide sequence analysis of N, P, M, F and L genes in Japan</title></titleInfo><name type="personal"><namePart type="given">S</namePart><namePart type="family">Yamaguchi</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Yamaguchi S. 1997. Identification of three lineages of wild measles virus by nucleotide sequence analysis of N, P, M, F and L genes in Japan. J Med Virol l 52: 113–120.</note><part><date>1997</date><detail type="volume"><caption>vol.</caption><number>52</number></detail><extent unit="pages"><start>113</start><end>120</end></extent></part><relatedItem type="host"><titleInfo><title>J Med Virol l</title></titleInfo><part><date>1997</date><detail type="volume"><caption>vol.</caption><number>52</number></detail><extent unit="pages"><start>113</start><end>120</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit29"><titleInfo><title>Detection of human herpesvirus 7 DNA by loop‐mediated isothermal amplification</title></titleInfo><name type="personal"><namePart type="given">T</namePart><namePart type="family">Yoshikawa</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M</namePart><namePart type="family">Ihira</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">S</namePart><namePart type="family">Akimoto</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">C</namePart><namePart type="family">Usui</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">F</namePart><namePart type="family">Miyake</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">S</namePart><namePart type="family">Suga</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Enomoto</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Suzuki</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y</namePart><namePart type="family">Nishiyama</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">A</namePart><namePart type="family">Asano</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Yoshikawa T, Ihira M, Akimoto S, Usui C, Miyake F, Suga S, Enomoto Y, Suzuki Y, Nishiyama Y, Asano A. 2004. Detection of human herpesvirus 7 DNA by loop‐mediated isothermal amplification. J Clin Microbiol 42: 1348–1352.</note><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>42</number></detail><extent unit="pages"><start>1348</start><end>1352</end></extent></part><relatedItem type="host"><titleInfo><title>J Clin Microbiol</title></titleInfo><part><date>2004</date><detail type="volume"><caption>vol.</caption><number>42</number></detail><extent unit="pages"><start>1348</start><end>1352</end></extent></part></relatedItem></relatedItem><relatedItem type="references" displayLabel="cit30"><titleInfo><title>H1 genotype of measles virus was detected in outbreaks in Japan after 2000</title></titleInfo><name type="personal"><namePart type="given">J</namePart><namePart type="family">Zhou</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M</namePart><namePart type="family">Fujino</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T</namePart><namePart type="family">Nakayama</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Zhou J, Fujino M, Nakayama T. 2003. H1 genotype of measles virus was detected in outbreaks in Japan after 2000. J Med Virol 70: 642–648.</note><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>70</number></detail><extent unit="pages"><start>642</start><end>648</end></extent></part><relatedItem type="host"><titleInfo><title>J Med Virol</title></titleInfo><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>70</number></detail><extent unit="pages"><start>642</start><end>648</end></extent></part></relatedItem></relatedItem><identifier type="istex">DF1455206F714BAA11C1A5FBCC3C3C60BF5B9A2A</identifier><identifier type="ark">ark:/67375/WNG-ZH92N2WX-C</identifier><identifier type="DOI">10.1002/jmv.20371</identifier><identifier type="ArticleID">JMV20371</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2005 Wiley‐Liss, Inc.</accessCondition><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-L0C46X92-X">wiley</recordContentSource><recordOrigin>Converted from (version ) to MODS version 3.6.</recordOrigin><recordCreationDate encoding="w3cdtf">2019-11-15</recordCreationDate></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/ark:/67375/WNG-ZH92N2WX-C/record.json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/CovidV1/Data/Istex/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000632 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 000632 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= CovidV1
|flux= Istex
|étape= Corpus
|type= RBID
|clé= ISTEX:DF1455206F714BAA11C1A5FBCC3C3C60BF5B9A2A
|texte= A simple method for the detection of measles virus genome by loop‐mediated isothermal amplification (LAMP)
}}
| This area was generated with Dilib version V0.6.33. |  |