FluShuffle and FluResort: new algorithms to identify reassorted strains of the influenza virus by mass spectrometry
Identifieur interne : 000A56 ( Main/Exploration ); précédent : 000A55; suivant : 000A57FluShuffle and FluResort: new algorithms to identify reassorted strains of the influenza virus by mass spectrometry
Auteurs : Aaron Tl Lun [Australie] ; Jason Wh Wong [Australie] ; Kevin M. Downard [Australie]Source :
- BMC Bioinformatics [ 1471-2105 ] ; 2012.
Abstract
Influenza is one of the oldest and deadliest infectious diseases known to man. Reassorted strains of the virus pose the greatest risk to both human and animal health and have been associated with all pandemics of the past century, with the possible exception of the 1918 pandemic, resulting in tens of millions of deaths. We have developed and tested new computer algorithms, FluShuffle and FluResort, which enable reassorted viruses to be identified by the most rapid and direct means possible. These algorithms enable reassorted influenza, and other, viruses to be rapidly identified to allow prevention strategies and treatments to be more efficiently implemented.
The FluShuffle and FluResort algorithms were tested with both experimental and simulated mass spectra of whole virus digests. FluShuffle considers different combinations of viral protein identities that match the mass spectral data using a Gibbs sampling algorithm employing a mixed protein Markov chain Monte Carlo (MCMC) method. FluResort utilizes those identities to calculate the weighted distance of each across two or more different phylogenetic trees constructed through viral protein sequence alignments. Each weighted mean distance value is normalized by conversion to a Z-score to establish a reassorted strain.
The new FluShuffle and FluResort algorithms can correctly identify the origins of influenza viral proteins and the number of reassortment events required to produce the strains from the high resolution mass spectral data of whole virus proteolytic digestions. This has been demonstrated in the case of constructed vaccine strains as well as common human seasonal strains of the virus. The algorithms significantly improve the capability of the proteotyping approach to identify reassorted viruses that pose the greatest pandemic risk.
Url:
DOI: 10.1186/1471-2105-13-208
PubMed: 22906155
PubMed Central: 3505172
Affiliations:
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Downard</name><affiliation wicri:level="4"><nlm:aff id="I1">School of Molecular Bioscience G-08, The University of Sydney, Sydney, NSW, 2006, Australia</nlm:aff><country xml:lang="fr">Australie</country><wicri:regionArea>School of Molecular Bioscience G-08, The University of Sydney, Sydney, NSW, 2006</wicri:regionArea><orgName type="university">Université de Sydney</orgName><placeName><settlement type="city">Sydney</settlement><region type="état">Nouvelle-Galles du Sud</region></placeName></affiliation></author></analytic><series><title level="j">BMC Bioinformatics</title><idno type="eISSN">1471-2105</idno><imprint><date when="2012">2012</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec><title>Background</title><p>Influenza is one of the oldest and deadliest infectious diseases known to man. Reassorted strains of the virus pose the greatest risk to both human and animal health and have been associated with all pandemics of the past century, with the possible exception of the 1918 pandemic, resulting in tens of millions of deaths. We have developed and tested new computer algorithms, FluShuffle and FluResort, which enable reassorted viruses to be identified by the most rapid and direct means possible. These algorithms enable reassorted influenza, and other, viruses to be rapidly identified to allow prevention strategies and treatments to be more efficiently implemented.</p></sec><sec><title>Results</title><p>The FluShuffle and FluResort algorithms were tested with both experimental and simulated mass spectra of whole virus digests. FluShuffle considers different combinations of viral protein identities that match the mass spectral data using a Gibbs sampling algorithm employing a mixed protein Markov chain Monte Carlo (MCMC) method. FluResort utilizes those identities to calculate the weighted distance of each across two or more different phylogenetic trees constructed through viral protein sequence alignments. Each weighted mean distance value is normalized by conversion to a Z-score to establish a reassorted strain.</p></sec><sec><title>Conclusions</title><p>The new FluShuffle and FluResort algorithms can correctly identify the origins of influenza viral proteins and the number of reassortment events required to produce the strains from the high resolution mass spectral data of whole virus proteolytic digestions. This has been demonstrated in the case of constructed vaccine strains as well as common human seasonal strains of the virus. The algorithms significantly improve the capability of the proteotyping approach to identify reassorted viruses that pose the greatest pandemic risk.</p></sec></div></front><back><div1 type="bibliography"><listBibl><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Van Tam, J" uniqKey="Van Tam J">J Van-Tam</name></author><author><name sortKey="Sellwood, C" uniqKey="Sellwood C">C Sellwood</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Nelson, Mi" uniqKey="Nelson M">MI Nelson</name></author><author><name sortKey="Holmes, Ec" uniqKey="Holmes E">EC Holmes</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zambon, Mc" uniqKey="Zambon M">MC Zambon</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Nguyen Van Tam, Js" uniqKey="Nguyen Van Tam J">JS Nguyen-Van-Tam</name></author><author><name sortKey="Hampson, Aw" uniqKey="Hampson A">AW 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Downard</name><name sortKey="Wong, Jason Wh" sort="Wong, Jason Wh" uniqKey="Wong J" first="Jason Wh" last="Wong">Jason Wh Wong</name><name sortKey="Wong, Jason Wh" sort="Wong, Jason Wh" uniqKey="Wong J" first="Jason Wh" last="Wong">Jason Wh Wong</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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