Serveur d'exploration MERS

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Molecular Evolution of Human Coronavirus Genomes

Identifieur interne : 001809 ( Ncbi/Merge ); précédent : 001808; suivant : 001810

Molecular Evolution of Human Coronavirus Genomes

Auteurs : Diego Forni [Italie] ; Rachele Cagliani [Italie] ; Mario Clerici [Italie] ; Manuela Sironi [Italie]

Source :

RBID : PMC:7111218

Descripteurs français

English descriptors

Abstract

Human coronaviruses (HCoVs), including SARS-CoV and MERS-CoV, are zoonotic pathogens that originated in wild animals. HCoVs have large genomes that encode a fixed array of structural and nonstructural components, as well as a variety of accessory proteins that differ in number and sequence even among closely related CoVs. Thus, in addition to recombination and mutation, HCoV genomes evolve through gene gains and losses. In this review we summarize recent findings on the molecular evolution of HCoV genomes, with special attention to recombination and adaptive events that generated new viral species and contributed to host shifts and to HCoV emergence.

Video Abstract


Url:
DOI: 10.1016/j.tim.2016.09.001
PubMed: 27743750
PubMed Central: 7111218

Links toward previous steps (curation, corpus...)


Links to Exploration step

PMC:7111218

Le document en format XML

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<p>Human coronaviruses (HCoVs), including SARS-CoV and MERS-CoV, are zoonotic pathogens that originated in wild animals. HCoVs have large genomes that encode a fixed array of structural and nonstructural components, as well as a variety of accessory proteins that differ in number and sequence even among closely related CoVs. Thus, in addition to recombination and mutation, HCoV genomes evolve through gene gains and losses. In this review we summarize recent findings on the molecular evolution of HCoV genomes, with special attention to recombination and adaptive events that generated new viral species and contributed to host shifts and to HCoV emergence.</p>
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<p>Human coronaviruses (HCoVs), including SARS-CoV and MERS-CoV, are zoonotic pathogens that originated in wild animals. HCoVs have large genomes that encode a fixed array of structural and nonstructural components, as well as a variety of accessory proteins that differ in number and sequence even among closely related CoVs. Thus, in addition to recombination and mutation, HCoV genomes evolve through gene gains and losses. In this review we summarize recent findings on the molecular evolution of HCoV genomes, with special attention to recombination and adaptive events that generated new viral species and contributed to host shifts and to HCoV emergence.</p>
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<title>Video Abstract</title>
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<title xml:lang="en">Molecular Evolution of Human Coronavirus Genomes.</title>
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<name sortKey="Forni, Diego" sort="Forni, Diego" uniqKey="Forni D" first="Diego" last="Forni">Diego Forni</name>
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<nlm:affiliation>Scientific Institute IRCCS E. MEDEA, Bioinformatics, Bosisio Parini, Italy.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Scientific Institute IRCCS E. MEDEA, Bioinformatics, Bosisio Parini</wicri:regionArea>
<wicri:noRegion>Bosisio Parini</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Cagliani, Rachele" sort="Cagliani, Rachele" uniqKey="Cagliani R" first="Rachele" last="Cagliani">Rachele Cagliani</name>
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<nlm:affiliation>Scientific Institute IRCCS E. MEDEA, Bioinformatics, Bosisio Parini, Italy.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Scientific Institute IRCCS E. MEDEA, Bioinformatics, Bosisio Parini</wicri:regionArea>
<wicri:noRegion>Bosisio Parini</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Clerici, Mario" sort="Clerici, Mario" uniqKey="Clerici M" first="Mario" last="Clerici">Mario Clerici</name>
<affiliation wicri:level="3">
<nlm:affiliation>Department of Physiopathology and Transplantation, University of Milan, Milan, Italy; Don C. Gnocchi Foundation ONLUS, IRCCS, Milan, Italy.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Department of Physiopathology and Transplantation, University of Milan, Milan, Italy; Don C. Gnocchi Foundation ONLUS, IRCCS, Milan</wicri:regionArea>
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<settlement type="city">Milan</settlement>
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<nlm:affiliation>Scientific Institute IRCCS E. MEDEA, Bioinformatics, Bosisio Parini, Italy. Electronic address: manuela.sironi@bp.lnf.it.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Scientific Institute IRCCS E. MEDEA, Bioinformatics, Bosisio Parini</wicri:regionArea>
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<nlm:affiliation>Scientific Institute IRCCS E. MEDEA, Bioinformatics, Bosisio Parini, Italy.</nlm:affiliation>
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<nlm:affiliation>Scientific Institute IRCCS E. MEDEA, Bioinformatics, Bosisio Parini, Italy.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Scientific Institute IRCCS E. MEDEA, Bioinformatics, Bosisio Parini</wicri:regionArea>
<wicri:noRegion>Bosisio Parini</wicri:noRegion>
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</author>
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<name sortKey="Clerici, Mario" sort="Clerici, Mario" uniqKey="Clerici M" first="Mario" last="Clerici">Mario Clerici</name>
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<nlm:affiliation>Department of Physiopathology and Transplantation, University of Milan, Milan, Italy; Don C. Gnocchi Foundation ONLUS, IRCCS, Milan, Italy.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Department of Physiopathology and Transplantation, University of Milan, Milan, Italy; Don C. Gnocchi Foundation ONLUS, IRCCS, Milan</wicri:regionArea>
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<settlement type="city">Milan</settlement>
<region nuts="2">Lombardie</region>
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<name sortKey="Sironi, Manuela" sort="Sironi, Manuela" uniqKey="Sironi M" first="Manuela" last="Sironi">Manuela Sironi</name>
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<nlm:affiliation>Scientific Institute IRCCS E. MEDEA, Bioinformatics, Bosisio Parini, Italy. Electronic address: manuela.sironi@bp.lnf.it.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Scientific Institute IRCCS E. MEDEA, Bioinformatics, Bosisio Parini</wicri:regionArea>
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</author>
</analytic>
<series>
<title level="j">Trends in microbiology</title>
<idno type="eISSN">1878-4380</idno>
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<date when="2017" type="published">2017</date>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Evolution, Molecular</term>
<term>Genome, Viral (genetics)</term>
<term>Hemagglutinins, Viral (genetics)</term>
<term>Hemagglutinins, Viral (metabolism)</term>
<term>Host Specificity (genetics)</term>
<term>Humans</term>
<term>Middle East Respiratory Syndrome Coronavirus (genetics)</term>
<term>Phosphoric Diester Hydrolases (genetics)</term>
<term>Phosphoric Diester Hydrolases (metabolism)</term>
<term>SARS Virus (genetics)</term>
<term>Viral Fusion Proteins (genetics)</term>
<term>Viral Fusion Proteins (metabolism)</term>
<term>Viral Regulatory and Accessory Proteins (genetics)</term>
<term>Viral Regulatory and Accessory Proteins (metabolism)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Coronavirus du syndrome respiratoire du Moyen-Orient (génétique)</term>
<term>Génome viral (génétique)</term>
<term>Humains</term>
<term>Hémagglutinines virales (génétique)</term>
<term>Hémagglutinines virales (métabolisme)</term>
<term>Phosphodiesterases (génétique)</term>
<term>Phosphodiesterases (métabolisme)</term>
<term>Protéines de fusion virale (génétique)</term>
<term>Protéines de fusion virale (métabolisme)</term>
<term>Protéines virales régulatrices ou accessoires (génétique)</term>
<term>Protéines virales régulatrices ou accessoires (métabolisme)</term>
<term>Spécificité d'hôte (génétique)</term>
<term>Virus du SRAS (génétique)</term>
<term>Évolution moléculaire</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Hemagglutinins, Viral</term>
<term>Phosphoric Diester Hydrolases</term>
<term>Viral Fusion Proteins</term>
<term>Viral Regulatory and Accessory Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Genome, Viral</term>
<term>Host Specificity</term>
<term>Middle East Respiratory Syndrome Coronavirus</term>
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Coronavirus du syndrome respiratoire du Moyen-Orient</term>
<term>Génome viral</term>
<term>Hémagglutinines virales</term>
<term>Phosphodiesterases</term>
<term>Protéines de fusion virale</term>
<term>Protéines virales régulatrices ou accessoires</term>
<term>Spécificité d'hôte</term>
<term>Virus du SRAS</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Hemagglutinins, Viral</term>
<term>Phosphoric Diester Hydrolases</term>
<term>Viral Fusion Proteins</term>
<term>Viral Regulatory and Accessory Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Hémagglutinines virales</term>
<term>Phosphodiesterases</term>
<term>Protéines de fusion virale</term>
<term>Protéines virales régulatrices ou accessoires</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Evolution, Molecular</term>
<term>Humans</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Humains</term>
<term>Évolution moléculaire</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Human coronaviruses (HCoVs), including SARS-CoV and MERS-CoV, are zoonotic pathogens that originated in wild animals. HCoVs have large genomes that encode a fixed array of structural and nonstructural components, as well as a variety of accessory proteins that differ in number and sequence even among closely related CoVs. Thus, in addition to recombination and mutation, HCoV genomes evolve through gene gains and losses. In this review we summarize recent findings on the molecular evolution of HCoV genomes, with special attention to recombination and adaptive events that generated new viral species and contributed to host shifts and to HCoV emergence. VIDEO ABSTRACT.</div>
</front>
</TEI>
</pubmed>
</double>
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