Non-random reassortment in human influenza A viruses.
Identifieur interne : 000268 ( PubMed/Curation ); précédent : 000267; suivant : 000269Non-random reassortment in human influenza A viruses.
Auteurs : Raul Rabadan [États-Unis] ; Arnold J. Levine ; Michael KrasnitzSource :
- Influenza and other respiratory viruses [ 1750-2659 ] ; 2008.
Descripteurs français
- KwdFr :
- Bases de données d'acides nucléiques, Biologie informatique, Grippe humaine (virologie), Humains, Nouvelle-Zélande, Sous-type H3N2 du virus de la grippe A (génétique), Sous-type H3N2 du virus de la grippe A (isolement et purification), Virus recombinants (génétique), Virus recombinants (isolement et purification), État de New York.
- MESH :
- génétique : Sous-type H3N2 du virus de la grippe A, Virus recombinants.
- isolement et purification : Sous-type H3N2 du virus de la grippe A, Virus recombinants.
- virologie : Grippe humaine.
- Bases de données d'acides nucléiques, Biologie informatique, Humains, Nouvelle-Zélande, État de New York.
- Wicri :
- geographic : Nouvelle-Zélande.
English descriptors
- KwdEn :
- MESH :
- geographic : New York, New Zealand.
- genetics : Influenza A Virus, H3N2 Subtype, Reassortant Viruses.
- isolation & purification : Influenza A Virus, H3N2 Subtype, Reassortant Viruses.
- virology : Influenza, Human.
- Computational Biology, Databases, Nucleic Acid, Humans.
Abstract
The influenza A virus has two basic modes of evolution. Because of a high error rate in the process of replication by RNA polymerase, the viral genome drifts via accumulated mutations. The second mode of evolution is termed a shift, which results from the reassortment of the eight segments of this virus. When two different influenza viruses co-infect the same host cell, new virions can be released that contain segments from both parental strains. This type of shift has been the source of at least two of the influenza pandemics in the 20th century (H2N2 in 1957 and H3N2 in 1968).
DOI: 10.1111/j.1750-2659.2007.00030.x
PubMed: 19453489
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pubmed:19453489Le document en format XML
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<author><name sortKey="Rabadan, Raul" sort="Rabadan, Raul" uniqKey="Rabadan R" first="Raul" last="Rabadan">Raul Rabadan</name>
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<term>Databases, Nucleic Acid</term>
<term>Humans</term>
<term>Influenza A Virus, H3N2 Subtype (genetics)</term>
<term>Influenza A Virus, H3N2 Subtype (isolation & purification)</term>
<term>Influenza, Human (virology)</term>
<term>New York</term>
<term>New Zealand</term>
<term>Reassortant Viruses (genetics)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Bases de données d'acides nucléiques</term>
<term>Biologie informatique</term>
<term>Grippe humaine (virologie)</term>
<term>Humains</term>
<term>Nouvelle-Zélande</term>
<term>Sous-type H3N2 du virus de la grippe A (génétique)</term>
<term>Sous-type H3N2 du virus de la grippe A (isolement et purification)</term>
<term>Virus recombinants (génétique)</term>
<term>Virus recombinants (isolement et purification)</term>
<term>État de New York</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Influenza A Virus, H3N2 Subtype</term>
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<keywords scheme="MESH" qualifier="isolation & purification" xml:lang="en"><term>Influenza A Virus, H3N2 Subtype</term>
<term>Reassortant Viruses</term>
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<keywords scheme="MESH" qualifier="isolement et purification" xml:lang="fr"><term>Sous-type H3N2 du virus de la grippe A</term>
<term>Virus recombinants</term>
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<keywords scheme="MESH" qualifier="virologie" xml:lang="fr"><term>Grippe humaine</term>
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<keywords scheme="MESH" qualifier="virology" xml:lang="en"><term>Influenza, Human</term>
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<term>Nouvelle-Zélande</term>
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<front><div type="abstract" xml:lang="en">The influenza A virus has two basic modes of evolution. Because of a high error rate in the process of replication by RNA polymerase, the viral genome drifts via accumulated mutations. The second mode of evolution is termed a shift, which results from the reassortment of the eight segments of this virus. When two different influenza viruses co-infect the same host cell, new virions can be released that contain segments from both parental strains. This type of shift has been the source of at least two of the influenza pandemics in the 20th century (H2N2 in 1957 and H3N2 in 1968).</div>
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<Title>Influenza and other respiratory viruses</Title>
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<ArticleTitle>Non-random reassortment in human influenza A viruses.</ArticleTitle>
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<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">The influenza A virus has two basic modes of evolution. Because of a high error rate in the process of replication by RNA polymerase, the viral genome drifts via accumulated mutations. The second mode of evolution is termed a shift, which results from the reassortment of the eight segments of this virus. When two different influenza viruses co-infect the same host cell, new virions can be released that contain segments from both parental strains. This type of shift has been the source of at least two of the influenza pandemics in the 20th century (H2N2 in 1957 and H3N2 in 1968).</AbstractText>
<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">The methods to measure these genetic shifts have not yet provided a quantitative answer to questions such as: what is the rate of genetic reassortment during a local epidemic? Are all possible reassortments equally likely or are there preferred patterns?</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">To answer these questions and provide a quantitative way to measure genetic shifts, a new method for detecting reassortments from nucleotide sequence data was created that does not rely upon phylogenetic analysis. Two different sequence databases were used: human H3N2 viruses isolated in New York State between 1995 and 2006, and human H3N2 viruses isolated in New Zealand between 2000 and 2005.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Using this new method, we were able to reproduce all the reassortments found in earlier works, as well as detect, with very high confidence, many reassortments that were not detected by previous authors. We obtain a lower bound on the reassortment rate of 2-3 events per year, and find a clear preference for reassortments involving only one segment, most often hemagglutinin or neuraminidase. At a lower frequency several segments appear to reassort in vivo in defined groups as has been suggested previously in vitro.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Our results strongly suggest that the patterns of reassortment in the viral population are not random. Deciphering these patterns can be a useful tool in attempting to understand and predict possible influenza pandemics.</AbstractText>
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