Rapid strategy for screening by pyrosequencing of influenza virus reassortants--candidates for live attenuated vaccines.
Identifieur interne : 000104 ( PubMed/Curation ); précédent : 000103; suivant : 000105Rapid strategy for screening by pyrosequencing of influenza virus reassortants--candidates for live attenuated vaccines.
Auteurs : Svetlana V. Shcherbik [États-Unis] ; Nicholas C. Pearce [États-Unis] ; Marnie L. Levine [États-Unis] ; Alexander I. Klimov [États-Unis] ; Julie M. Villanueva [États-Unis] ; Tatiana L. Bousse [États-Unis]Source :
- PloS one [ 1932-6203 ] ; 2014.
Descripteurs français
- KwdFr :
- Humains, Sous-type H3N2 du virus de la grippe A (génétique), Sous-type H3N2 du virus de la grippe A (immunologie), Séquençage nucléotidique à haut débit, Vaccins antigrippaux (génétique), Vaccins antigrippaux (immunologie), Vaccins atténués (immunologie), Virus recombinants (génétique), Virus recombinants (immunologie).
- MESH :
English descriptors
- KwdEn :
- High-Throughput Nucleotide Sequencing, Humans, Influenza A Virus, H3N2 Subtype (genetics), Influenza A Virus, H3N2 Subtype (immunology), Influenza Vaccines (genetics), Influenza Vaccines (immunology), Reassortant Viruses (genetics), Reassortant Viruses (immunology), Vaccines, Attenuated (immunology).
- MESH :
- chemical , genetics : Influenza Vaccines.
- genetics : Influenza A Virus, H3N2 Subtype, Reassortant Viruses.
- immunology : Influenza A Virus, H3N2 Subtype, Influenza Vaccines, Reassortant Viruses, Vaccines, Attenuated.
- High-Throughput Nucleotide Sequencing, Humans.
Abstract
Live attenuated influenza vaccine viruses (LAIVs) can be generated by classical reassortment of gene segments between a cold adapted, temperature sensitive and attenuated Master Donor Virus (MDV) and a seasonal wild-type (wt) virus. The vaccine candidates contain hemagglutinin (HA) and neuraminidase (NA) genes derived from the circulating wt viruses and the remaining six genes derived from the MDV strains. Rapid, efficient selection of the viruses with 6∶2 genome compositions from the large number of genetically different viruses generated during reassortment is essential for the biannual production schedule of vaccine viruses.
DOI: 10.1371/journal.pone.0092580
PubMed: 24647786
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pubmed:24647786Le document en format XML
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<term>Influenza A Virus, H3N2 Subtype (immunology)</term>
<term>Influenza Vaccines (genetics)</term>
<term>Influenza Vaccines (immunology)</term>
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<term>Séquençage nucléotidique à haut débit</term>
<term>Vaccins antigrippaux (génétique)</term>
<term>Vaccins antigrippaux (immunologie)</term>
<term>Vaccins atténués (immunologie)</term>
<term>Virus recombinants (génétique)</term>
<term>Virus recombinants (immunologie)</term>
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<term>Vaccines, Attenuated</term>
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<front><div type="abstract" xml:lang="en">Live attenuated influenza vaccine viruses (LAIVs) can be generated by classical reassortment of gene segments between a cold adapted, temperature sensitive and attenuated Master Donor Virus (MDV) and a seasonal wild-type (wt) virus. The vaccine candidates contain hemagglutinin (HA) and neuraminidase (NA) genes derived from the circulating wt viruses and the remaining six genes derived from the MDV strains. Rapid, efficient selection of the viruses with 6∶2 genome compositions from the large number of genetically different viruses generated during reassortment is essential for the biannual production schedule of vaccine viruses.</div>
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<DateCompleted><Year>2014</Year>
<Month>11</Month>
<Day>12</Day>
</DateCompleted>
<DateRevised><Year>2018</Year>
<Month>11</Month>
<Day>13</Day>
</DateRevised>
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<ArticleTitle>Rapid strategy for screening by pyrosequencing of influenza virus reassortants--candidates for live attenuated vaccines.</ArticleTitle>
<Pagination><MedlinePgn>e92580</MedlinePgn>
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<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Live attenuated influenza vaccine viruses (LAIVs) can be generated by classical reassortment of gene segments between a cold adapted, temperature sensitive and attenuated Master Donor Virus (MDV) and a seasonal wild-type (wt) virus. The vaccine candidates contain hemagglutinin (HA) and neuraminidase (NA) genes derived from the circulating wt viruses and the remaining six genes derived from the MDV strains. Rapid, efficient selection of the viruses with 6∶2 genome compositions from the large number of genetically different viruses generated during reassortment is essential for the biannual production schedule of vaccine viruses.</AbstractText>
<AbstractText Label="METHODOLOGY/PRINCIPAL FINDINGS" NlmCategory="RESULTS">This manuscript describes a new approach for the genotypic analysis of LAIV reassortant virus clones based on pyrosequencing. LAIV candidate viruses were created by classical reassortment of seasonal influenza A (H3N2) (A/Victoria/361/2011, A/Ohio/02/2012, A/Texas/50/2012) or influenza A (H7N9) (A/Anhui/1/2013) wt viruses with the MDV A/Leningrad/134/17/57(H2N2). Using strain-specific pyrosequencing assays, mixed gene variations were detected in the allantoic progenies during the cloning procedure. The pyrosequencing analysis also allowed for estimation of the relative abundance of segment variants in mixed populations. This semi-quantitative approach was used for selecting specific clones for the subsequent cloning procedures.</AbstractText>
<AbstractText Label="CONCLUSIONS/SIGNIFICANCE" NlmCategory="CONCLUSIONS">The present study demonstrates that pyrosequencing analysis is a useful technique for rapid and reliable genotyping of reassortants and intermediate clones during the preparation of LAIV candidates, and can expedite the selection of vaccine virus candidates.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Shcherbik</LastName>
<ForeName>Svetlana V</ForeName>
<Initials>SV</Initials>
<AffiliationInfo><Affiliation>Virology, Surveillance and Diagnosis Branch, Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America; Battelle, Atlanta, Georgia, United States of America.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Pearce</LastName>
<ForeName>Nicholas C</ForeName>
<Initials>NC</Initials>
<AffiliationInfo><Affiliation>Virology, Surveillance and Diagnosis Branch, Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America; Battelle, Atlanta, Georgia, United States of America.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Levine</LastName>
<ForeName>Marnie L</ForeName>
<Initials>ML</Initials>
<AffiliationInfo><Affiliation>Virology, Surveillance and Diagnosis Branch, Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America; Battelle, Atlanta, Georgia, United States of America.</Affiliation>
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<Author ValidYN="Y"><LastName>Klimov</LastName>
<ForeName>Alexander I</ForeName>
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<AffiliationInfo><Affiliation>Virology, Surveillance and Diagnosis Branch, Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.</Affiliation>
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<ForeName>Julie M</ForeName>
<Initials>JM</Initials>
<AffiliationInfo><Affiliation>Virology, Surveillance and Diagnosis Branch, Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.</Affiliation>
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