Feature Selection Methods for Identifying Genetic Determinants of Host Species in RNA Viruses
Identifieur interne : 001938 ( Main/Curation ); précédent : 001937; suivant : 001939Feature Selection Methods for Identifying Genetic Determinants of Host Species in RNA Viruses
Auteurs : Ricardo Aguas ; Neil M. FergusonSource :
- PLoS Computational Biology [ 1553-734X ] ; 2013.
Descripteurs français
- KwdFr :
- Algorithmes, Analyse en composantes principales, Animaux, Biologie informatique (), Chiroptera (virologie), Gènes viraux (génétique), Humains, Intelligence artificielle, Interactions hôte-pathogène (génétique), Maladies virales (virologie), Phénotype, Protéines virales (), Protéines virales (génétique), Protéines virales (métabolisme), Récepteurs de surface cellulaire (), Récepteurs de surface cellulaire (génétique), Récepteurs de surface cellulaire (métabolisme), Sites de fixation, Virus à ARN (génétique), Zoonoses, Évolution moléculaire.
- MESH :
- génétique : Gènes viraux, Interactions hôte-pathogène, Protéines virales, Récepteurs de surface cellulaire, Virus à ARN.
- métabolisme : Protéines virales, Récepteurs de surface cellulaire.
- virologie : Chiroptera, Maladies virales.
- Algorithmes, Analyse en composantes principales, Animaux, Biologie informatique, Humains, Intelligence artificielle, Phénotype, Protéines virales, Récepteurs de surface cellulaire, Sites de fixation, Zoonoses, Évolution moléculaire.
English descriptors
- KwdEn :
- Algorithms, Animals, Artificial Intelligence, Binding Sites, Chiroptera (virology), Computational Biology (methods), Evolution, Molecular, Genes, Viral (genetics), Host-Pathogen Interactions (genetics), Humans, Phenotype, Principal Component Analysis, RNA Viruses (genetics), Receptors, Cell Surface (chemistry), Receptors, Cell Surface (genetics), Receptors, Cell Surface (metabolism), Viral Proteins (chemistry), Viral Proteins (genetics), Viral Proteins (metabolism), Virus Diseases (virology), Zoonoses.
- MESH :
- chemical , chemistry : Receptors, Cell Surface, Viral Proteins.
- genetics : Genes, Viral, Host-Pathogen Interactions, RNA Viruses, Receptors, Cell Surface, Viral Proteins.
- chemical , metabolism : Receptors, Cell Surface, Viral Proteins.
- methods : Computational Biology.
- virology : Chiroptera, Virus Diseases.
- Algorithms, Animals, Artificial Intelligence, Binding Sites, Evolution, Molecular, Humans, Phenotype, Principal Component Analysis, Zoonoses.
Abstract
Despite environmental, social and ecological dependencies, emergence of zoonotic viruses in human populations is clearly also affected by genetic factors which determine cross-species transmission potential. RNA viruses pose an interesting case study given their mutation rates are orders of magnitude higher than any other pathogen – as reflected by the recent emergence of SARS and Influenza for example. Here, we show how feature selection techniques can be used to reliably classify viral sequences by host species, and to identify the crucial minority of host-specific sites in pathogen genomic data. The variability in alleles at those sites can be translated into prediction probabilities that a particular pathogen isolate is adapted to a given host. We illustrate the power of these methods by: 1) identifying the sites explaining SARS coronavirus differences between human, bat and palm civet samples; 2) showing how cross species jumps of rabies virus among bat populations can be readily identified; and 3)
Url:
DOI: 10.1371/journal.pcbi.1003254
PubMed: 24130470
PubMed Central: 3794897
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PMC:3794897Le document en format XML
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<front><div type="abstract" xml:lang="en"><p>Despite environmental, social and ecological dependencies, emergence of zoonotic viruses in human populations is clearly also affected by genetic factors which determine cross-species transmission potential. RNA viruses pose an interesting case study given their mutation rates are orders of magnitude higher than any other pathogen – as reflected by the recent emergence of SARS and Influenza for example. Here, we show how feature selection techniques can be used to reliably classify viral sequences by host species, and to identify the crucial minority of host-specific sites in pathogen genomic data. The variability in alleles at those sites can be translated into prediction probabilities that a particular pathogen isolate is adapted to a given host. We illustrate the power of these methods by: 1) identifying the sites explaining SARS coronavirus differences between human, bat and palm civet samples; 2) showing how cross species jumps of rabies virus among bat populations can be readily identified; and 3) <italic>de novo</italic>
identification of likely functional influenza host discriminant markers.</p>
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