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Molecular epidemiology, evolution and phylogeny of SARS coronavirus

Shortly after its emergence in southern China in 2002/2003, Severe Acute Respiratory Syndrome coronavirus (SARS-CoV) was confirmed to be the cause of SARS. Subsequently, SARS-related CoVs (SARSr-CoVs) were found in palm civets from live animal markets in Guangdong and in various horseshoe bat specie...

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Autores principales: Luk, Hayes K.H., Li, Xin, Fung, Joshua, Lau, Susanna K.P., Woo, Patrick C.Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106202/
https://www.ncbi.nlm.nih.gov/pubmed/30844511
http://dx.doi.org/10.1016/j.meegid.2019.03.001
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author Luk, Hayes K.H.
Li, Xin
Fung, Joshua
Lau, Susanna K.P.
Woo, Patrick C.Y.
author_facet Luk, Hayes K.H.
Li, Xin
Fung, Joshua
Lau, Susanna K.P.
Woo, Patrick C.Y.
author_sort Luk, Hayes K.H.
collection PubMed
description Shortly after its emergence in southern China in 2002/2003, Severe Acute Respiratory Syndrome coronavirus (SARS-CoV) was confirmed to be the cause of SARS. Subsequently, SARS-related CoVs (SARSr-CoVs) were found in palm civets from live animal markets in Guangdong and in various horseshoe bat species, which were believed to be the ultimate reservoir of SARSr-CoV. Till November 2018, 339 SARSr-CoV genomes have been sequenced, including 274 from human, 18 from civets and 47 from bats [mostly from Chinese horseshoe bats (Rhinolophus sinicus), n = 30; and greater horseshoe bats (Rhinolophus ferrumequinum), n = 9]. The human SARS-CoVs and civet SARSr-CoVs were collected in 2003/2004, while bat SARSr-CoVs were continuously isolated in the past 13 years even after the cessation of the SARS epidemic. SARSr-CoVs belong to the subgenus Sarbecovirus (previously lineage B) of genus Betacoronavirus and occupy a unique phylogenetic position. Overall, it is observed that the SARSr-CoV genomes from bats in Yunnan province of China possess the highest nucleotide identity to those from civets. It is evident from both multiple alignment and phylogenetic analyses that some genes of a particular SARSr-CoV from bats may possess higher while other genes possess much lower nucleotide identity to the corresponding genes of SARSr-CoV from human/civets, resulting in the shift of phylogenetic position in different phylogenetic trees. Our current model on the origin of SARS is that the human SARS-CoV that caused the epidemic in 2002/2003 was probably a result of multiple recombination events from a number of SARSr-CoV ancestors in different horseshoe bat species.
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spelling pubmed-71062022020-03-31 Molecular epidemiology, evolution and phylogeny of SARS coronavirus Luk, Hayes K.H. Li, Xin Fung, Joshua Lau, Susanna K.P. Woo, Patrick C.Y. Infect Genet Evol Review Shortly after its emergence in southern China in 2002/2003, Severe Acute Respiratory Syndrome coronavirus (SARS-CoV) was confirmed to be the cause of SARS. Subsequently, SARS-related CoVs (SARSr-CoVs) were found in palm civets from live animal markets in Guangdong and in various horseshoe bat species, which were believed to be the ultimate reservoir of SARSr-CoV. Till November 2018, 339 SARSr-CoV genomes have been sequenced, including 274 from human, 18 from civets and 47 from bats [mostly from Chinese horseshoe bats (Rhinolophus sinicus), n = 30; and greater horseshoe bats (Rhinolophus ferrumequinum), n = 9]. The human SARS-CoVs and civet SARSr-CoVs were collected in 2003/2004, while bat SARSr-CoVs were continuously isolated in the past 13 years even after the cessation of the SARS epidemic. SARSr-CoVs belong to the subgenus Sarbecovirus (previously lineage B) of genus Betacoronavirus and occupy a unique phylogenetic position. Overall, it is observed that the SARSr-CoV genomes from bats in Yunnan province of China possess the highest nucleotide identity to those from civets. It is evident from both multiple alignment and phylogenetic analyses that some genes of a particular SARSr-CoV from bats may possess higher while other genes possess much lower nucleotide identity to the corresponding genes of SARSr-CoV from human/civets, resulting in the shift of phylogenetic position in different phylogenetic trees. Our current model on the origin of SARS is that the human SARS-CoV that caused the epidemic in 2002/2003 was probably a result of multiple recombination events from a number of SARSr-CoV ancestors in different horseshoe bat species. Published by Elsevier B.V. 2019-07 2019-03-04 /pmc/articles/PMC7106202/ /pubmed/30844511 http://dx.doi.org/10.1016/j.meegid.2019.03.001 Text en © 2019 Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Review
Luk, Hayes K.H.
Li, Xin
Fung, Joshua
Lau, Susanna K.P.
Woo, Patrick C.Y.
Molecular epidemiology, evolution and phylogeny of SARS coronavirus
title Molecular epidemiology, evolution and phylogeny of SARS coronavirus
title_full Molecular epidemiology, evolution and phylogeny of SARS coronavirus
title_fullStr Molecular epidemiology, evolution and phylogeny of SARS coronavirus
title_full_unstemmed Molecular epidemiology, evolution and phylogeny of SARS coronavirus
title_short Molecular epidemiology, evolution and phylogeny of SARS coronavirus
title_sort molecular epidemiology, evolution and phylogeny of sars coronavirus
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106202/
https://www.ncbi.nlm.nih.gov/pubmed/30844511
http://dx.doi.org/10.1016/j.meegid.2019.03.001
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