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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<term>Dogs (MeSH)</term>
<term>Erythrocytes (virology)</term>
<term>Guinea Pigs (MeSH)</term>
<term>Hemagglutination (MeSH)</term>
<term>Hemagglutinins, Viral (genetics)</term>
<term>Humans (MeSH)</term>
<term>Influenza A Virus, H1N1 Subtype (isolation & purification)</term>
<term>Influenza A Virus, H3N2 Subtype (isolation & purification)</term>
<term>Influenza B virus (isolation & purification)</term>
<term>Influenza, Human (diagnosis)</term>
<term>Molecular Sequence Data (MeSH)</term>
<term>Mutation, Missense (MeSH)</term>
<term>Sequence Analysis, DNA (MeSH)</term>
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<term>Virus Cultivation (methods)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Analyse de séquence d'ADN (MeSH)</term>
<term>Animaux (MeSH)</term>
<term>Chiens (MeSH)</term>
<term>Cochons d'Inde (MeSH)</term>
<term>Culture virale (méthodes)</term>
<term>Dindons (MeSH)</term>
<term>Données de séquences moléculaires (MeSH)</term>
<term>Grippe humaine (diagnostic)</term>
<term>Humains (MeSH)</term>
<term>Hémagglutination (MeSH)</term>
<term>Hémagglutinines virales (génétique)</term>
<term>Lignée cellulaire (MeSH)</term>
<term>Mutation faux-sens (MeSH)</term>
<term>Sous-type H1N1 du virus de la grippe A (isolement et purification)</term>
<term>Sous-type H3N2 du virus de la grippe A (isolement et purification)</term>
<term>Substitution d'acide aminé (génétique)</term>
<term>Virus influenza B (isolement et purification)</term>
<term>Érythrocytes (virologie)</term>
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<term>Substitution d'acide aminé</term>
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<term>Influenza A Virus, H3N2 Subtype</term>
<term>Influenza B virus</term>
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<keywords scheme="MESH" qualifier="isolement et purification" xml:lang="fr"><term>Sous-type H1N1 du virus de la grippe A</term>
<term>Sous-type H3N2 du virus de la grippe A</term>
<term>Virus influenza B</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Virus Cultivation</term>
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<keywords scheme="MESH" qualifier="méthodes" xml:lang="fr"><term>Culture virale</term>
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<keywords scheme="MESH" qualifier="virologie" xml:lang="fr"><term>Érythrocytes</term>
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<term>Dogs</term>
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<term>Molecular Sequence Data</term>
<term>Mutation, Missense</term>
<term>Sequence Analysis, DNA</term>
<term>Turkeys</term>
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<term>Chiens</term>
<term>Cochons d'Inde</term>
<term>Dindons</term>
<term>Données de séquences moléculaires</term>
<term>Humains</term>
<term>Hémagglutination</term>
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<front><div type="abstract" xml:lang="en">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.</div>
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<ArticleTitle>MDCK-SIAT1 cells show improved isolation rates for recent human influenza viruses compared to conventional MDCK cells.</ArticleTitle>
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<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>
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<AffiliationInfo><Affiliation>WHO Collaborating Centre for Reference and Research on Influenza, 45 Poplar Road, Parkville, Melbourne, Australia.</Affiliation>
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<Author ValidYN="Y"><LastName>Mosse</LastName>
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<MeshHeading><DescriptorName UI="D006168" MajorTopicYN="N">Guinea Pigs</DescriptorName>
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<MeshHeading><DescriptorName UI="D006384" MajorTopicYN="N">Hemagglutination</DescriptorName>
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<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
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<MeshHeading><DescriptorName UI="D053118" MajorTopicYN="N">Influenza A Virus, H1N1 Subtype</DescriptorName>
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<MeshHeading><DescriptorName UI="D014422" MajorTopicYN="N">Turkeys</DescriptorName>
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