Nucleotide sequence of the avian influenza A/Mallard/NY/6750/78 virus polymerase genes
Identifieur interne : 000189 ( Istex/Corpus ); précédent : 000188; suivant : 000190Nucleotide sequence of the avian influenza A/Mallard/NY/6750/78 virus polymerase genes
Auteurs : John Treanor ; Kawaoka Yoshihiro ; Roger Miller ; Robert G. Webster ; Brian MurphySource :
- Virus Research [ 0168-1702 ] ; 1989.
English descriptors
- Teeft :
- Amino, Amino acid sequence, Amino acid sequences, Amino acids, Animal influenza, Attenuated, Avian, Avian influenza, Avian influenza virus, Avian virus, Embryonated eggs, Encoding, Gene, Gene segment, Gene segments, Hlnl, Homology, Human influenza, Human influenza virus, Human virus, Human viruses, Influenza, Influenza virus, Internal genes, Location signals, Nuclear location signal, Nucleoprotein, Nucleotide, Nucleotide sequence, Nucleotide sequences, Polymerase, Polymerase gene segments, Polymerase genes, Polymerase proteins, Reassortant, Reassortant virus, Reassortant viruses, Replication, Sequencing, Squirrel monkeys, Vaccine, Virology, Virus.
Abstract
Abstract: The avian influenza A/Mallard/NY/6750/78 virus is currently being evaluated as a donor of attenuating genes in the construction of live avian-human influenza A reassortant virus vaccines for use in humans. We determined the nucleotide sequences of the three polymerase gene segments of this virus. This completes the nucleotide sequence of the six transferrable genes of the avian donor virus. Comparison of the nucleotide and deduced amino acid sequences of the non-glycoprotein genes of the avian A/Mallard/78 virus with representative avian and human influenza A viruses suggests that the PB1 gene of H2N2 subtype human influenza A viruses may have been derived from a non-human, possibly avian influenza A virus by genetic reassortment. In addition, several regions of conserved amino acids with potential functional significance were identified in the deduced amino acid sequences of the polymerase proteins.
Url:
DOI: 10.1016/0168-1702(89)90006-3
Links to Exploration step
ISTEX:5174CC987A39013BB6ADFFBCD08CABDFC01216C1Le document en format XML
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Webster</name><affiliation><mods:affiliation>Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, Memphis, Tennessee U.S.A.</mods:affiliation></affiliation></author><author><name sortKey="Murphy, Brian" sort="Murphy, Brian" uniqKey="Murphy B" first="Brian" last="Murphy">Brian Murphy</name><affiliation><mods:affiliation>Respiratory Laboratory of Infectious Disease, NIAID, Bethesda, MarylandUSA</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Virus Research</title><title level="j" type="abbrev">VIRUS</title><idno type="ISSN">0168-1702</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1989">1989</date><biblScope unit="volume">14</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="257">257</biblScope><biblScope unit="page" to="269">269</biblScope></imprint><idno type="ISSN">0168-1702</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0168-1702</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Amino</term><term>Amino acid sequence</term><term>Amino acid sequences</term><term>Amino acids</term><term>Animal influenza</term><term>Attenuated</term><term>Avian</term><term>Avian influenza</term><term>Avian influenza virus</term><term>Avian virus</term><term>Embryonated eggs</term><term>Encoding</term><term>Gene</term><term>Gene segment</term><term>Gene segments</term><term>Hlnl</term><term>Homology</term><term>Human influenza</term><term>Human influenza virus</term><term>Human virus</term><term>Human viruses</term><term>Influenza</term><term>Influenza virus</term><term>Internal genes</term><term>Location signals</term><term>Nuclear location signal</term><term>Nucleoprotein</term><term>Nucleotide</term><term>Nucleotide sequence</term><term>Nucleotide sequences</term><term>Polymerase</term><term>Polymerase gene segments</term><term>Polymerase genes</term><term>Polymerase proteins</term><term>Reassortant</term><term>Reassortant virus</term><term>Reassortant viruses</term><term>Replication</term><term>Sequencing</term><term>Squirrel monkeys</term><term>Vaccine</term><term>Virology</term><term>Virus</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: The avian influenza A/Mallard/NY/6750/78 virus is currently being evaluated as a donor of attenuating genes in the construction of live avian-human influenza A reassortant virus vaccines for use in humans. We determined the nucleotide sequences of the three polymerase gene segments of this virus. This completes the nucleotide sequence of the six transferrable genes of the avian donor virus. Comparison of the nucleotide and deduced amino acid sequences of the non-glycoprotein genes of the avian A/Mallard/78 virus with representative avian and human influenza A viruses suggests that the PB1 gene of H2N2 subtype human influenza A viruses may have been derived from a non-human, possibly avian influenza A virus by genetic reassortment. 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Webster</name><affiliations><json:string>Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, Memphis, Tennessee U.S.A.</json:string></affiliations></json:item><json:item><name>Brian Murphy</name><affiliations><json:string>Respiratory Laboratory of Infectious Disease, NIAID, Bethesda, MarylandUSA</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Influenza A virus</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Polymerase gene sequence</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Influenza vaccine</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Influenza virus evolution</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Avian influenza A virus</value></json:item></subject><arkIstex>ark:/67375/6H6-VVKR89MJ-M</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>Full-length article</json:string></originalGenre><abstract>Abstract: The avian influenza A/Mallard/NY/6750/78 virus is currently being evaluated as a donor of attenuating genes in the construction of live avian-human influenza A reassortant virus vaccines for use in humans. We determined the nucleotide sequences of the three polymerase gene segments of this virus. This completes the nucleotide sequence of the six transferrable genes of the avian donor virus. Comparison of the nucleotide and deduced amino acid sequences of the non-glycoprotein genes of the avian A/Mallard/78 virus with representative avian and human influenza A viruses suggests that the PB1 gene of H2N2 subtype human influenza A viruses may have been derived from a non-human, possibly avian influenza A virus by genetic reassortment. In addition, several regions of conserved amino acids with potential functional significance were identified in the deduced amino acid sequences of the polymerase proteins.</abstract><qualityIndicators><refBibsNative>true</refBibsNative><abstractWordCount>137</abstractWordCount><abstractCharCount>923</abstractCharCount><keywordCount>5</keywordCount><score>7.266</score><pdfWordCount>3622</pdfWordCount><pdfCharCount>28616</pdfCharCount><pdfVersion>1.2</pdfVersion><pdfPageCount>13</pdfPageCount><pdfPageSize>432 x 648 pts</pdfPageSize></qualityIndicators><title>Nucleotide sequence of the avian influenza A/Mallard/NY/6750/78 virus polymerase genes</title><pmid><json:string>2483012</json:string></pmid><pii><json:string>0168-1702(89)90006-3</json:string></pii><genre><json:string>research-article</json:string></genre><serie><title>Virology</title><language><json:string>unknown</json:string></language><pages><first>1179</first><last>1240</last></pages></serie><host><title>Virus Research</title><language><json:string>unknown</json:string></language><publicationDate>1989</publicationDate><issn><json:string>0168-1702</json:string></issn><pii><json:string>S0168-1702(00)X0099-8</json:string></pii><volume>14</volume><issue>3</issue><pages><first>257</first><last>269</last></pages><genre><json:string>journal</json:string></genre></host><namedEntities><unitex><date><json:string>1934</json:string><json:string>1968</json:string><json:string>1989</json:string></date><geogName></geogName><orgName><json:string>and American Lebanese Syrian Associated Charities</json:string><json:string>Cancer Center Support</json:string><json:string>Jude Children’s Research Hospital, Memphis, Tennessee</json:string><json:string>BIONET National Computer Resource for Molecular Biology</json:string><json:string>CORE</json:string><json:string>Department of Virology and Molecular Biology</json:string><json:string>National Institutes of Health grant U41-0168505</json:string><json:string>Grant CA 21765</json:string></orgName><orgName_funder><json:string>National Institutes of Health grant U41-0168505</json:string><json:string>Grant CA 21765</json:string></orgName_funder><orgName_provider></orgName_provider><persName><json:string>G. Webster</json:string><json:string>Katzunor Okazaki</json:string><json:string>J. Treanor</json:string><json:string>Kathy Alexander</json:string><json:string>Peter Collins</json:string><json:string>Eveline</json:string><json:string>Brian Murphy</json:string><json:string>Ann Arbor</json:string><json:string>Myron Hill</json:string><json:string>AlAnn Arbor</json:string><json:string>Roger Miller</json:string></persName><placeName><json:string>Singapore</json:string><json:string>Germany</json:string><json:string>York</json:string></placeName><ref_url></ref_url><ref_bibl><json:string>Sanger et al., 1977</json:string><json:string>Sears et al., 1988</json:string><json:string>Krug et al.. 1975</json:string><json:string>Snyder et al., 1987</json:string><json:string>Tian et al., 1985</json:string><json:string>Buckler-White and Murphy, 1986</json:string><json:string>Treanor et al., 1989</json:string><json:string>Murphy et al., 1982b</json:string><json:string>Smith et al., 1987</json:string><json:string>Coelingh et al., 1986</json:string><json:string>Snyder et al., 1986</json:string><json:string>McCurley et al., 1982</json:string><json:string>Jones et al., 1983</json:string><json:string>Roditi and Robertson, 1984</json:string><json:string>Fields and Winter, 1982</json:string><json:string>Cox et al., 1988</json:string><json:string>Kida et al., 1987</json:string><json:string>Murphy et al., 1982a</json:string><json:string>Buckler-White et al., 1986</json:string><json:string>Kenderim et al., 1986</json:string><json:string>Winter and Fields, 1980, 1981, 1982</json:string><json:string>Smith et al., 1985</json:string><json:string>Lamb and Lai, 1981</json:string><json:string>Bishop et al., 1982a, b</json:string><json:string>DeBorde et al., 1988</json:string><json:string>Robertson et al., 1984</json:string><json:string>Buonagurio et al., 1986</json:string><json:string>Wilbur and Lipman (1983)</json:string><json:string>Tomley and Roditi, 1984</json:string><json:string>Massicot et al., 1980</json:string><json:string>Scholtissek et al., 1978</json:string><json:string>Chen and Seeberg (1985)</json:string><json:string>Argos, 1988</json:string><json:string>Huddleston and Brownlee, 1982</json:string><json:string>Murphy et al., 1985</json:string><json:string>Braam et al., 1983</json:string><json:string>DeBorde et al., 1986</json:string></ref_bibl><bibl></bibl></unitex></namedEntities><ark><json:string>ark:/67375/6H6-VVKR89MJ-M</json:string></ark><categories><wos><json:string>1 - 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Treanor, Respiratory Section, Laboratory, of Infectious Disease, NIAID, Bethesda, Maryland U.S.A..</p></note><affiliation>Respiratory Laboratory of Infectious Disease, NIAID, Bethesda, MarylandUSA</affiliation></author><author xml:id="author-0001"><persName><forename type="first">Kawaoka</forename><surname>Yoshihiro</surname></persName><affiliation>Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, Memphis, Tennessee U.S.A.</affiliation></author><author xml:id="author-0002"><persName><forename type="first">Roger</forename><surname>Miller</surname></persName><affiliation>Hepatitis Section, Laboratory of Infectious Disease, NIAID, Bethesda, MarylandUSA</affiliation></author><author xml:id="author-0003"><persName><forename type="first">Robert G.</forename><surname>Webster</surname></persName><affiliation>Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, Memphis, Tennessee U.S.A.</affiliation></author><author xml:id="author-0004"><persName><forename type="first">Brian</forename><surname>Murphy</surname></persName><affiliation>Respiratory Laboratory of Infectious Disease, NIAID, Bethesda, MarylandUSA</affiliation></author><idno type="istex">5174CC987A39013BB6ADFFBCD08CABDFC01216C1</idno><idno type="ark">ark:/67375/6H6-VVKR89MJ-M</idno><idno type="DOI">10.1016/0168-1702(89)90006-3</idno><idno type="PII">0168-1702(89)90006-3</idno></analytic><monogr><title level="j">Virus Research</title><title level="j" type="abbrev">VIRUS</title><idno type="pISSN">0168-1702</idno><idno type="PII">S0168-1702(00)X0099-8</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1989"></date><biblScope unit="volume">14</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="257">257</biblScope><biblScope unit="page" to="269">269</biblScope></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1989</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Abstract: The avian influenza A/Mallard/NY/6750/78 virus is currently being evaluated as a donor of attenuating genes in the construction of live avian-human influenza A reassortant virus vaccines for use in humans. We determined the nucleotide sequences of the three polymerase gene segments of this virus. This completes the nucleotide sequence of the six transferrable genes of the avian donor virus. Comparison of the nucleotide and deduced amino acid sequences of the non-glycoprotein genes of the avian A/Mallard/78 virus with representative avian and human influenza A viruses suggests that the PB1 gene of H2N2 subtype human influenza A viruses may have been derived from a non-human, possibly avian influenza A virus by genetic reassortment. In addition, several regions of conserved amino acids with potential functional significance were identified in the deduced amino acid sequences of the polymerase proteins.</p></abstract><textClass><keywords scheme="keyword"><list><head>Keywords</head><item><term>Influenza A virus</term></item><item><term>Polymerase gene sequence</term></item><item><term>Influenza vaccine</term></item><item><term>Influenza virus evolution</term></item><item><term>Avian influenza A virus</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="1989-08-11">Modified</change><change when="1989">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-VVKR89MJ-M/fulltext.txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier, elements deleted: tail"><istex:xmlDeclaration>version="1.0" encoding="utf-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 4.5.2//EN//XML" URI="art452.dtd" name="istex:docType"></istex:docType><istex:document><converted-article version="4.5.2" docsubtype="fla"><item-info><jid>VIRUS</jid><aid>89900063</aid><ce:pii>0168-1702(89)90006-3</ce:pii><ce:doi>10.1016/0168-1702(89)90006-3</ce:doi><ce:copyright type="unknown" year="1989"></ce:copyright></item-info><head><ce:title>Nucleotide sequence of the avian influenza A/Mallard/NY/6750/78 virus polymerase genes</ce:title><ce:author-group><ce:author><ce:given-name>John</ce:given-name><ce:surname>Treanor</ce:surname><ce:cross-ref refid="COR1"><ce:sup>∗</ce:sup></ce:cross-ref><ce:cross-ref refid="AFF1"><ce:sup>1</ce:sup></ce:cross-ref></ce:author><ce:author><ce:surname>Yoshihiro</ce:surname><ce:given-name>Kawaoka</ce:given-name><ce:cross-ref refid="AFF3"><ce:sup>3</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>Roger</ce:given-name><ce:surname>Miller</ce:surname><ce:cross-ref refid="AFF2"><ce:sup>2</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>Robert G.</ce:given-name><ce:surname>Webster</ce:surname><ce:cross-ref refid="AFF3"><ce:sup>3</ce:sup></ce:cross-ref></ce:author><ce:author><ce:given-name>Brian</ce:given-name><ce:surname>Murphy</ce:surname><ce:cross-ref refid="AFF1"><ce:sup>1</ce:sup></ce:cross-ref></ce:author><ce:affiliation id="AFF1"><ce:label>1</ce:label><ce:textfn>Respiratory Laboratory of Infectious Disease, NIAID, Bethesda, MarylandUSA</ce:textfn></ce:affiliation><ce:affiliation id="AFF2"><ce:label>2</ce:label><ce:textfn>Hepatitis Section, Laboratory of Infectious Disease, NIAID, Bethesda, MarylandUSA</ce:textfn></ce:affiliation><ce:affiliation id="AFF3"><ce:label>3</ce:label><ce:textfn>Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, Memphis, Tennessee U.S.A.</ce:textfn></ce:affiliation><ce:correspondence id="COR1"><ce:label>∗</ce:label><ce:text>Correspondence to: J. Treanor, Respiratory Section, Laboratory, of Infectious Disease, NIAID, Bethesda, Maryland U.S.A..</ce:text></ce:correspondence></ce:author-group><ce:date-received day="9" month="5" year="1989"></ce:date-received><ce:date-revised day="11" month="8" year="1989"></ce:date-revised><ce:date-accepted day="11" month="8" year="1989"></ce:date-accepted><ce:abstract><ce:section-title>Abstract</ce:section-title><ce:abstract-sec><ce:simple-para>The avian influenza A/Mallard/NY/6750/78 virus is currently being evaluated as a donor of attenuating genes in the construction of live avian-human influenza A reassortant virus vaccines for use in humans. We determined the nucleotide sequences of the three polymerase gene segments of this virus. This completes the nucleotide sequence of the six transferrable genes of the avian donor virus. Comparison of the nucleotide and deduced amino acid sequences of the non-glycoprotein genes of the avian A/Mallard/78 virus with representative avian and human influenza A viruses suggests that the PB1 gene of H2N2 subtype human influenza A viruses may have been derived from a non-human, possibly avian influenza A virus by genetic reassortment. In addition, several regions of conserved amino acids with potential functional significance were identified in the deduced amino acid sequences of the polymerase proteins.</ce:simple-para></ce:abstract-sec></ce:abstract><ce:keywords><ce:section-title>Keywords</ce:section-title><ce:keyword><ce:text>Influenza A virus</ce:text></ce:keyword><ce:keyword><ce:text>Polymerase gene sequence</ce:text></ce:keyword><ce:keyword><ce:text>Influenza vaccine</ce:text></ce:keyword><ce:keyword><ce:text>Influenza virus evolution</ce:text></ce:keyword><ce:keyword><ce:text>Avian influenza A virus</ce:text></ce:keyword></ce:keywords></head></converted-article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo><title>Nucleotide sequence of the avian influenza A/Mallard/NY/6750/78 virus polymerase genes</title></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>Nucleotide sequence of the avian influenza A/Mallard/NY/6750/78 virus polymerase genes</title></titleInfo><name type="personal"><namePart type="given">John</namePart><namePart type="family">Treanor</namePart><affiliation>Respiratory Laboratory of Infectious Disease, NIAID, Bethesda, MarylandUSA</affiliation><description>Correspondence to: J. Treanor, Respiratory Section, Laboratory, of Infectious Disease, NIAID, Bethesda, Maryland U.S.A..</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Kawaoka</namePart><namePart type="family">Yoshihiro</namePart><affiliation>Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, Memphis, Tennessee U.S.A.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Roger</namePart><namePart type="family">Miller</namePart><affiliation>Hepatitis Section, Laboratory of Infectious Disease, NIAID, Bethesda, MarylandUSA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Robert G.</namePart><namePart type="family">Webster</namePart><affiliation>Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, Memphis, Tennessee U.S.A.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Brian</namePart><namePart type="family">Murphy</namePart><affiliation>Respiratory Laboratory of Infectious Disease, NIAID, Bethesda, MarylandUSA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Full-length article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1989</dateIssued><dateModified encoding="w3cdtf">1989-08-11</dateModified><copyrightDate encoding="w3cdtf">1989</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><abstract lang="en">Abstract: The avian influenza A/Mallard/NY/6750/78 virus is currently being evaluated as a donor of attenuating genes in the construction of live avian-human influenza A reassortant virus vaccines for use in humans. We determined the nucleotide sequences of the three polymerase gene segments of this virus. This completes the nucleotide sequence of the six transferrable genes of the avian donor virus. Comparison of the nucleotide and deduced amino acid sequences of the non-glycoprotein genes of the avian A/Mallard/78 virus with representative avian and human influenza A viruses suggests that the PB1 gene of H2N2 subtype human influenza A viruses may have been derived from a non-human, possibly avian influenza A virus by genetic reassortment. In addition, several regions of conserved amino acids with potential functional significance were identified in the deduced amino acid sequences of the polymerase proteins.</abstract><subject><genre>Keywords</genre><topic>Influenza A virus</topic><topic>Polymerase gene sequence</topic><topic>Influenza vaccine</topic><topic>Influenza virus evolution</topic><topic>Avian influenza A virus</topic></subject><relatedItem type="host"><titleInfo><title>Virus Research</title></titleInfo><titleInfo type="abbreviated"><title>VIRUS</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><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1989</dateIssued></originInfo><identifier type="ISSN">0168-1702</identifier><identifier type="PII">S0168-1702(00)X0099-8</identifier><part><date>1989</date><detail type="volume"><number>14</number><caption>vol.</caption></detail><detail type="issue"><number>3</number><caption>no.</caption></detail><extent unit="issue-pages"><start>189</start><end>272</end></extent><extent unit="pages"><start>257</start><end>269</end></extent></part></relatedItem><identifier type="istex">5174CC987A39013BB6ADFFBCD08CABDFC01216C1</identifier><identifier type="ark">ark:/67375/6H6-VVKR89MJ-M</identifier><identifier type="DOI">10.1016/0168-1702(89)90006-3</identifier><identifier type="PII">0168-1702(89)90006-3</identifier><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-HKKZVM7B-M">elsevier</recordContentSource></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-VVKR89MJ-M/record.json</uri></json:item></metadata></istex></record>Pour manipuler ce document sous Unix (Dilib)
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