MDCK-SIAT1 cells show improved isolation rates for recent human influenza viruses compared to conventional MDCK cells.
Identifieur interne : 003871 ( Main/Exploration ); précédent : 003870; suivant : 003872MDCK-SIAT1 cells show improved isolation rates for recent human influenza viruses compared to conventional MDCK cells.
Auteurs : Ding Yuan Oh [Australie] ; Ian G. Barr ; Jenny A. Mosse ; Karen L. LaurieSource :
- Journal of clinical microbiology [ 1098-660X ] ; 2008.
Descripteurs français
- KwdFr :
- Analyse de séquence d'ADN (MeSH), Animaux (MeSH), Chiens (MeSH), Cochons d'Inde (MeSH), Culture virale (méthodes), Dindons (MeSH), Données de séquences moléculaires (MeSH), Grippe humaine (diagnostic), Humains (MeSH), Hémagglutination (MeSH), Hémagglutinines virales (génétique), Lignée cellulaire (MeSH), Mutation faux-sens (MeSH), Sous-type H1N1 du virus de la grippe A (isolement et purification), Sous-type H3N2 du virus de la grippe A (isolement et purification), Substitution d'acide aminé (génétique), Virus influenza B (isolement et purification), Érythrocytes (virologie).
- MESH :
- diagnostic : Grippe humaine.
- génétique : Hémagglutinines virales, Substitution d'acide aminé.
- isolement et purification : Sous-type H1N1 du virus de la grippe A, Sous-type H3N2 du virus de la grippe A, Virus influenza B.
- méthodes : Culture virale.
- virologie : Érythrocytes.
- Analyse de séquence d'ADN, Animaux, Chiens, Cochons d'Inde, Dindons, Données de séquences moléculaires, Humains, Hémagglutination, Lignée cellulaire, Mutation faux-sens.
English descriptors
- KwdEn :
- Amino Acid Substitution (genetics), Animals (MeSH), Cell Line (MeSH), Dogs (MeSH), Erythrocytes (virology), Guinea Pigs (MeSH), Hemagglutination (MeSH), Hemagglutinins, Viral (genetics), Humans (MeSH), Influenza A Virus, H1N1 Subtype (isolation & purification), Influenza A Virus, H3N2 Subtype (isolation & purification), Influenza B virus (isolation & purification), Influenza, Human (diagnosis), Molecular Sequence Data (MeSH), Mutation, Missense (MeSH), Sequence Analysis, DNA (MeSH), Turkeys (MeSH), Virus Cultivation (methods).
- MESH :
- chemical , genetics : Hemagglutinins, Viral.
- diagnosis : Influenza, Human.
- genetics : Amino Acid Substitution.
- isolation & purification : Influenza A Virus, H1N1 Subtype, Influenza A Virus, H3N2 Subtype, Influenza B virus.
- methods : Virus Cultivation.
- virology : Erythrocytes.
- Animals, Cell Line, Dogs, Guinea Pigs, Hemagglutination, Humans, Molecular Sequence Data, Mutation, Missense, Sequence Analysis, DNA, Turkeys.
Abstract
The ability to isolate and propagate influenza virus is an essential tool for the yearly surveillance of circulating virus strains and to ensure accurate clinical diagnosis for appropriate treatment. The suitability of MDCK-SIAT1 cells, engineered to express increased levels of alpha-2,6-linked sialic acid receptors, as an alternative to conventional MDCK cells for isolation of circulating influenza virus was assessed. A greater number of influenza A (H1N1 and H3N2) and B viruses from stored human clinical specimens collected between 2005 and 2007 were isolated following inoculation in MDCK-SIAT1 cells than in MDCK cells. In addition, a higher titer of virus was recovered following culture in MDCK-SIAT1 cells. All A(H1N1) viruses recovered from MDCK-SIAT1 cells were able to agglutinate both turkey and guinea pig red blood cells (RBC), while half of the A(H3N2) viruses recovered after passage in MDCK-SIAT1 cells lost the ability to agglutinate turkey RBC. Importantly, the HA-1 domain of the hemagglutinin gene was genetically stable after passaging in MDCK-SIAT1 cells, a feature not always seen following MDCK cell or embryonated chicken egg passage of human influenza virus. These data indicate that the MDCK-SIAT1 cell line is superior to conventional MDCK cells for isolation of human influenza virus from clinical specimens and may be used routinely for the isolation and propagation of current human influenza viruses for surveillance, diagnostic, and research purposes.
DOI: 10.1128/JCM.00398-08
PubMed: 18480230
PubMed Central: PMC2446904
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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The suitability of MDCK-SIAT1 cells, engineered to express increased levels of alpha-2,6-linked sialic acid receptors, as an alternative to conventional MDCK cells for isolation of circulating influenza virus was assessed. A greater number of influenza A (H1N1 and H3N2) and B viruses from stored human clinical specimens collected between 2005 and 2007 were isolated following inoculation in MDCK-SIAT1 cells than in MDCK cells. In addition, a higher titer of virus was recovered following culture in MDCK-SIAT1 cells. All A(H1N1) viruses recovered from MDCK-SIAT1 cells were able to agglutinate both turkey and guinea pig red blood cells (RBC), while half of the A(H3N2) viruses recovered after passage in MDCK-SIAT1 cells lost the ability to agglutinate turkey RBC. Importantly, the HA-1 domain of the hemagglutinin gene was genetically stable after passaging in MDCK-SIAT1 cells, a feature not always seen following MDCK cell or embryonated chicken egg passage of human influenza virus. These data indicate that the MDCK-SIAT1 cell line is superior to conventional MDCK cells for isolation of human influenza virus from clinical specimens and may be used routinely for the isolation and propagation of current human influenza viruses for surveillance, diagnostic, and research purposes.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">18480230</PMID><DateCompleted><Year>2008</Year><Month>08</Month><Day>12</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1098-660X</ISSN><JournalIssue CitedMedium="Internet"><Volume>46</Volume><Issue>7</Issue><PubDate><Year>2008</Year><Month>Jul</Month></PubDate></JournalIssue><Title>Journal of clinical microbiology</Title><ISOAbbreviation>J Clin Microbiol</ISOAbbreviation></Journal><ArticleTitle>MDCK-SIAT1 cells show improved isolation rates for recent human influenza viruses compared to conventional MDCK cells.</ArticleTitle><Pagination><MedlinePgn>2189-94</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1128/JCM.00398-08</ELocationID><Abstract><AbstractText>The ability to isolate and propagate influenza virus is an essential tool for the yearly surveillance of circulating virus strains and to ensure accurate clinical diagnosis for appropriate treatment. The suitability of MDCK-SIAT1 cells, engineered to express increased levels of alpha-2,6-linked sialic acid receptors, as an alternative to conventional MDCK cells for isolation of circulating influenza virus was assessed. A greater number of influenza A (H1N1 and H3N2) and B viruses from stored human clinical specimens collected between 2005 and 2007 were isolated following inoculation in MDCK-SIAT1 cells than in MDCK cells. In addition, a higher titer of virus was recovered following culture in MDCK-SIAT1 cells. All A(H1N1) viruses recovered from MDCK-SIAT1 cells were able to agglutinate both turkey and guinea pig red blood cells (RBC), while half of the A(H3N2) viruses recovered after passage in MDCK-SIAT1 cells lost the ability to agglutinate turkey RBC. Importantly, the HA-1 domain of the hemagglutinin gene was genetically stable after passaging in MDCK-SIAT1 cells, a feature not always seen following MDCK cell or embryonated chicken egg passage of human influenza virus. These data indicate that the MDCK-SIAT1 cell line is superior to conventional MDCK cells for isolation of human influenza virus from clinical specimens and may be used routinely for the isolation and propagation of current human influenza viruses for surveillance, diagnostic, and research purposes.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Oh</LastName><ForeName>Ding Yuan</ForeName><Initials>DY</Initials><AffiliationInfo><Affiliation>WHO Collaborating Centre for Reference and Research on Influenza, 45 Poplar Road, Parkville, Melbourne, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Barr</LastName><ForeName>Ian G</ForeName><Initials>IG</Initials></Author><Author ValidYN="Y"><LastName>Mosse</LastName><ForeName>Jenny A</ForeName><Initials>JA</Initials></Author><Author ValidYN="Y"><LastName>Laurie</LastName><ForeName>Karen L</ForeName><Initials>KL</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D003160">Comparative Study</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2008</Year><Month>05</Month><Day>14</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>J Clin Microbiol</MedlineTA><NlmUniqueID>7505564</NlmUniqueID><ISSNLinking>0095-1137</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D006389">Hemagglutinins, Viral</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C458881">hemagglutinin fusogenic peptide, influenza 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MajorTopicYN="Y">diagnosis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008969" MajorTopicYN="N">Molecular Sequence Data</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D020125" MajorTopicYN="N">Mutation, Missense</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D017422" MajorTopicYN="N">Sequence Analysis, DNA</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014422" MajorTopicYN="N">Turkeys</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014776" MajorTopicYN="N">Virus Cultivation</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2008</Year><Month>5</Month><Day>16</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2008</Year><Month>8</Month><Day>13</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate 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IdType="pubmed">2219728</ArticleId></ArticleIdList></Reference><Reference><Citation>Acta Histochem Suppl. 1990;40:35-8</Citation><ArticleIdList><ArticleId IdType="pubmed">2091044</ArticleId></ArticleIdList></Reference><Reference><Citation>J Gen Virol. 1991 Nov;72 ( Pt 11):2671-7</Citation><ArticleIdList><ArticleId IdType="pubmed">1940864</ArticleId></ArticleIdList></Reference><Reference><Citation>J Virol Methods. 1993 May;42(2-3):241-50</Citation><ArticleIdList><ArticleId IdType="pubmed">8390473</ArticleId></ArticleIdList></Reference><Reference><Citation>Virus Res. 1993 Aug;29(2):155-65</Citation><ArticleIdList><ArticleId IdType="pubmed">8212857</ArticleId></ArticleIdList></Reference><Reference><Citation>J Gen Virol. 1993 Nov;74 ( Pt 11):2513-8</Citation><ArticleIdList><ArticleId IdType="pubmed">8245870</ArticleId></ArticleIdList></Reference><Reference><Citation>J Infect Dis. 1995 Jul;172(1):250-3</Citation><ArticleIdList><ArticleId IdType="pubmed">7797924</ArticleId></ArticleIdList></Reference><Reference><Citation>J Virol. 1996 Aug;70(8):5519-24</Citation><ArticleIdList><ArticleId IdType="pubmed">8764064</ArticleId></ArticleIdList></Reference><Reference><Citation>Virology. 1983 Jun;127(2):361-73</Citation><ArticleIdList><ArticleId IdType="pubmed">6868370</ArticleId></ArticleIdList></Reference><Reference><Citation>Virology. 1985 May;143(1):166-74</Citation><ArticleIdList><ArticleId IdType="pubmed">4060580</ArticleId></ArticleIdList></Reference><Reference><Citation>Virology. 1987 Sep;160(1):31-7</Citation><ArticleIdList><ArticleId IdType="pubmed">3629978</ArticleId></ArticleIdList></Reference><Reference><Citation>Arch Virol. 1996;141(7):1349-55</Citation><ArticleIdList><ArticleId IdType="pubmed">8774693</ArticleId></ArticleIdList></Reference><Reference><Citation>Virology. 1997 Jan 20;227(2):493-9</Citation><ArticleIdList><ArticleId IdType="pubmed">9018149</ArticleId></ArticleIdList></Reference><Reference><Citation>J Virol. 1997 Apr;71(4):3357-62</Citation><ArticleIdList><ArticleId IdType="pubmed">9060710</ArticleId></ArticleIdList></Reference><Reference><Citation>J Gen Virol. 1998 Jun;79 ( Pt 6):1405-9</Citation><ArticleIdList><ArticleId IdType="pubmed">9634082</ArticleId></ArticleIdList></Reference><Reference><Citation>Virology. 1999 Jun 5;258(2):232-9</Citation><ArticleIdList><ArticleId IdType="pubmed">10366560</ArticleId></ArticleIdList></Reference><Reference><Citation>Virology. 1999 Sep 15;262(1):31-8</Citation><ArticleIdList><ArticleId IdType="pubmed">10489338</ArticleId></ArticleIdList></Reference><Reference><Citation>Dev Biol Stand. 1999;98:39-51; discussion 73-4</Citation><ArticleIdList><ArticleId IdType="pubmed">10494958</ArticleId></ArticleIdList></Reference><Reference><Citation>J Clin Microbiol. 2005 Aug;43(8):4139-46</Citation><ArticleIdList><ArticleId IdType="pubmed">16081961</ArticleId></ArticleIdList></Reference><Reference><Citation>Vaccine. 2005 Nov 16;23(46-47):5440-9</Citation><ArticleIdList><ArticleId IdType="pubmed">16168526</ArticleId></ArticleIdList></Reference><Reference><Citation>Nat Rev Drug Discov. 2006 Mar;5(3):183-4</Citation><ArticleIdList><ArticleId IdType="pubmed">16557657</ArticleId></ArticleIdList></Reference><Reference><Citation>Vaccine. 2007 Aug 10;25(32):6028-36</Citation><ArticleIdList><ArticleId IdType="pubmed">17614165</ArticleId></ArticleIdList></Reference><Reference><Citation>Virology. 2007 Sep 15;366(1):23-7</Citation><ArticleIdList><ArticleId IdType="pubmed">17651774</ArticleId></ArticleIdList></Reference><Reference><Citation>Vaccine. 2008 Jan 17;26(3):361-71</Citation><ArticleIdList><ArticleId IdType="pubmed">18079027</ArticleId></ArticleIdList></Reference><Reference><Citation>Curr Opin Mol Ther. 2008 Feb;10(1):56-61</Citation><ArticleIdList><ArticleId IdType="pubmed">18228182</ArticleId></ArticleIdList></Reference><Reference><Citation>J Virol. 2000 Sep;74(18):8502-12</Citation><ArticleIdList><ArticleId IdType="pubmed">10954551</ArticleId></ArticleIdList></Reference><Reference><Citation>Virology. 2000 Dec 20;278(2):587-96</Citation><ArticleIdList><ArticleId IdType="pubmed">11118381</ArticleId></ArticleIdList></Reference><Reference><Citation>J Virol. 2001 Oct;75(19):9517-25</Citation><ArticleIdList><ArticleId IdType="pubmed">11533214</ArticleId></ArticleIdList></Reference><Reference><Citation>Virology. 2001 Oct 10;289(1):74-85</Citation><ArticleIdList><ArticleId IdType="pubmed">11601919</ArticleId></ArticleIdList></Reference><Reference><Citation>Virology. 2003 Mar 1;307(1):90-7</Citation><ArticleIdList><ArticleId IdType="pubmed">12667817</ArticleId></ArticleIdList></Reference><Reference><Citation>J Virol. 2003 Aug;77(15):8418-25</Citation><ArticleIdList><ArticleId IdType="pubmed">12857911</ArticleId></ArticleIdList></Reference><Reference><Citation>J Med Virol. 2004 Oct;74(2):336-43</Citation><ArticleIdList><ArticleId IdType="pubmed">15332284</ArticleId></ArticleIdList></Reference><Reference><Citation>Appl Microbiol. 1968 Apr;16(4):588-94</Citation><ArticleIdList><ArticleId IdType="pubmed">5647517</ArticleId></ArticleIdList></Reference><Reference><Citation>Med Microbiol Immunol. 1975 Dec 30;162(1):23-7</Citation><ArticleIdList><ArticleId IdType="pubmed">1214707</ArticleId></ArticleIdList></Reference><Reference><Citation>Med Microbiol Immunol. 1975 Dec 30;162(1):9-14</Citation><ArticleIdList><ArticleId IdType="pubmed">1214709</ArticleId></ArticleIdList></Reference><Reference><Citation>J Clin Microbiol. 1979 Feb;9(2):175-9</Citation><ArticleIdList><ArticleId IdType="pubmed">219021</ArticleId></ArticleIdList></Reference><Reference><Citation>J Clin Microbiol. 1989 Mar;27(3):524-8</Citation><ArticleIdList><ArticleId IdType="pubmed">2715324</ArticleId></ArticleIdList></Reference></ReferenceList></PubmedData></pubmed><affiliations><list><country><li>Australie</li></country><region><li>Victoria (État)</li></region><settlement><li>Melbourne</li></settlement></list><tree><noCountry><name sortKey="Barr, Ian G" sort="Barr, Ian G" uniqKey="Barr I" first="Ian G" last="Barr">Ian G. Barr</name><name sortKey="Laurie, Karen L" sort="Laurie, Karen L" uniqKey="Laurie K" first="Karen L" last="Laurie">Karen L. Laurie</name><name sortKey="Mosse, Jenny A" sort="Mosse, Jenny A" uniqKey="Mosse J" first="Jenny A" last="Mosse">Jenny A. Mosse</name></noCountry><country name="Australie"><region name="Victoria (État)"><name sortKey="Oh, Ding Yuan" sort="Oh, Ding Yuan" uniqKey="Oh D" first="Ding Yuan" last="Oh">Ding Yuan Oh</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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