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Mosaic evolution of the severe acute respiratory syndrome coronavirus

Identifieur interne : 000071 ( PascalFrancis/Curation ); précédent : 000070; suivant : 000072

Mosaic evolution of the severe acute respiratory syndrome coronavirus

Auteurs : John Stavrinides [Canada] ; David S. Guttman [Canada]

Source :

RBID : Pascal:04-0196351

Descripteurs français

English descriptors

Abstract

Severe acute respiratory syndrome (SARS) is a deadly form of pneumonia caused by a novel coronavirus, a viral family responsible for mild respiratory tract infections in a wide variety of animals including humans, pigs, cows, mice, cats, and birds. Analyses to date have been unable to identify the precise origin of the SARS coronavirus. We used Bayesian, neighbor-joining, and split decomposition phylogenetic techniques on the SARS virus replicase, surface spike, matrix, and nucleocapsid proteins to reveal the evolutionary origin of this recently emerging infectious agent. The analyses support a mammalian-like origin for the replicase protein, an avian-like origin for the matrix and nucleocapsid proteins, and a mammalian-avian mosaic origin for the host-determining spike protein. A bootscan recombination analysis of the spike gene revealed high nucleotide identity between the SARS virus and a feline infectious peritonitis virus throughout the gene, except for a 200-base-pair region of high identity to an avian sequence. These data support the phylogenetic analyses and suggest a possible past recombination event between mammalian-like and avian-like parent viruses. This event occurred near a region that has been implicated to be the human receptor binding site and may have been directly responsible for the switch of host of the SARS coronavirus from animals to humans.
pA  
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A03   1    @0 J. virol.
A05       @2 78
A06       @2 1
A08 01  1  ENG  @1 Mosaic evolution of the severe acute respiratory syndrome coronavirus
A11 01  1    @1 STAVRINIDES (John)
A11 02  1    @1 GUTTMAN (David S.)
A14 01      @1 Department of Botany, University of Toronto @2 Toronto, Ontario M5S 3B2 @3 CAN @Z 1 aut. @Z 2 aut.
A20       @1 76-82
A21       @1 2004
A23 01      @0 ENG
A43 01      @1 INIST @2 13592 @5 354000113543630080
A44       @0 0000 @1 © 2004 INIST-CNRS. All rights reserved.
A45       @0 40 ref.
A47 01  1    @0 04-0196351
A60       @1 P
A61       @0 A
A64 01  1    @0 Journal of virology
A66 01      @0 USA
C01 01    ENG  @0 Severe acute respiratory syndrome (SARS) is a deadly form of pneumonia caused by a novel coronavirus, a viral family responsible for mild respiratory tract infections in a wide variety of animals including humans, pigs, cows, mice, cats, and birds. Analyses to date have been unable to identify the precise origin of the SARS coronavirus. We used Bayesian, neighbor-joining, and split decomposition phylogenetic techniques on the SARS virus replicase, surface spike, matrix, and nucleocapsid proteins to reveal the evolutionary origin of this recently emerging infectious agent. The analyses support a mammalian-like origin for the replicase protein, an avian-like origin for the matrix and nucleocapsid proteins, and a mammalian-avian mosaic origin for the host-determining spike protein. A bootscan recombination analysis of the spike gene revealed high nucleotide identity between the SARS virus and a feline infectious peritonitis virus throughout the gene, except for a 200-base-pair region of high identity to an avian sequence. These data support the phylogenetic analyses and suggest a possible past recombination event between mammalian-like and avian-like parent viruses. This event occurred near a region that has been implicated to be the human receptor binding site and may have been directly responsible for the switch of host of the SARS coronavirus from animals to humans.
C02 01  X    @0 002A05C10
C03 01  X  FRE  @0 Coronavirus @2 NW @5 01
C03 01  X  ENG  @0 Coronavirus @2 NW @5 01
C03 01  X  SPA  @0 Coronavirus @2 NW @5 01
C03 02  X  FRE  @0 Evolution @5 05
C03 02  X  ENG  @0 Evolution @5 05
C03 02  X  SPA  @0 Evolución @5 05
C03 03  X  FRE  @0 Microbiologie @5 06
C03 03  X  ENG  @0 Microbiology @5 06
C03 03  X  SPA  @0 Microbiología @5 06
C03 04  X  FRE  @0 Virologie @5 07
C03 04  X  ENG  @0 Virology @5 07
C03 04  X  SPA  @0 Virología @5 07
C03 05  X  FRE  @0 Syndrome respiratoire aigu sévère @2 NM @5 14
C03 05  X  ENG  @0 Severe acute respiratory syndrome @2 NM @5 14
C03 05  X  SPA  @0 Síndrome respiratorio agudo severo @2 NM @5 14
C07 01  X  FRE  @0 Coronaviridae @2 NW
C07 01  X  ENG  @0 Coronaviridae @2 NW
C07 01  X  SPA  @0 Coronaviridae @2 NW
C07 02  X  FRE  @0 Nidovirales @2 NW
C07 02  X  ENG  @0 Nidovirales @2 NW
C07 02  X  SPA  @0 Nidovirales @2 NW
C07 03  X  FRE  @0 Virus @2 NW
C07 03  X  ENG  @0 Virus @2 NW
C07 03  X  SPA  @0 Virus @2 NW
C07 04  X  FRE  @0 Virose @2 NM
C07 04  X  ENG  @0 Viral disease @2 NM
C07 04  X  SPA  @0 Virosis @2 NM
C07 05  X  FRE  @0 Infection @2 NM
C07 05  X  ENG  @0 Infection @2 NM
C07 05  X  SPA  @0 Infección @2 NM
C07 06  X  FRE  @0 Appareil respiratoire pathologie @5 19
C07 06  X  ENG  @0 Respiratory disease @5 19
C07 06  X  SPA  @0 Aparato respiratorio patología @5 19
C07 07  X  FRE  @0 Poumon pathologie @5 20
C07 07  X  ENG  @0 Lung disease @5 20
C07 07  X  SPA  @0 Pulmón patología @5 20
N21       @1 131
N82       @1 OTO

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Pascal:04-0196351

Le document en format XML

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