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Comparative full-length genome sequence analysis of 14 SARS coronavirus isolates and common mutations associated with putative origins of infection

BACKGROUND: The cause of severe acute respiratory syndrome (SARS) has been identified as a new coronavirus. Whole genome sequence analysis of various isolates might provide an indication of potential strain differences of this new virus. Moreover, mutation analysis will help to develop effective vac...

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Autores principales: Ruan, Yijun, Wei, Chia Lin, Ling, Ai Ee, Vega, Vinsensius B, Thoreau, Herve, Se Thoe, Su Yun, Chia, Jer-Ming, Ng, Patrick, Chiu, Kuo Ping, Lim, Landri, Zhang, Tao, Chan, Kwai Peng, Lin Ean, Lynette Oon, Ng, Mah Lee, Leo, Sin Yee, Ng, Lisa FP, Ren, Ee Chee, Stanton, Lawrence W, Long, Philip M, Liu, Edison T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140172/
https://www.ncbi.nlm.nih.gov/pubmed/12781537
http://dx.doi.org/10.1016/S0140-6736(03)13414-9
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author Ruan, Yijun
Wei, Chia Lin
Ling, Ai Ee
Vega, Vinsensius B
Thoreau, Herve
Se Thoe, Su Yun
Chia, Jer-Ming
Ng, Patrick
Chiu, Kuo Ping
Lim, Landri
Zhang, Tao
Chan, Kwai Peng
Lin Ean, Lynette Oon
Ng, Mah Lee
Leo, Sin Yee
Ng, Lisa FP
Ren, Ee Chee
Stanton, Lawrence W
Long, Philip M
Liu, Edison T
author_facet Ruan, Yijun
Wei, Chia Lin
Ling, Ai Ee
Vega, Vinsensius B
Thoreau, Herve
Se Thoe, Su Yun
Chia, Jer-Ming
Ng, Patrick
Chiu, Kuo Ping
Lim, Landri
Zhang, Tao
Chan, Kwai Peng
Lin Ean, Lynette Oon
Ng, Mah Lee
Leo, Sin Yee
Ng, Lisa FP
Ren, Ee Chee
Stanton, Lawrence W
Long, Philip M
Liu, Edison T
author_sort Ruan, Yijun
collection PubMed
description BACKGROUND: The cause of severe acute respiratory syndrome (SARS) has been identified as a new coronavirus. Whole genome sequence analysis of various isolates might provide an indication of potential strain differences of this new virus. Moreover, mutation analysis will help to develop effective vaccines. METHODS: We sequenced the entire SARS viral genome of cultured isolates from the index case (SIN2500) presenting in Singapore, from three primary contacts (SIN2774, SIN2748, and SIN2677), and one secondary contact (SIN2679). These sequences were compared with the isolates from Canada (TOR2), Hong Kong (CUHK-W1 and HKU39849), Hanoi (URBANI), Guangzhou (GZ01), and Beijing (BJ01, BJ02, BJ03, BJ04). FINDINGS: We identified 129 sequence variations among the 14 isolates, with 16 recurrent variant sequences. Common variant sequences at four loci define two distinct genotypes of the SARS virus. One genotype was linked with infections originating in Hotel M in Hong Kong, the second contained isolates from Hong Kong, Guangzhou, and Beijing with no association with Hotel M (p<0.0001). Moreover, other common sequence variants further distinguished the geographical origins of the isolates, especially between Singapore and Beijing. INTERPRETATION: Despite the recent onset of the SARS epidemic, genetic signatures are emerging that partition the worldwide SARS viral isolates into groups on the basis of contact source history and geography. These signatures can be used to trace sources of infection. In addition, a common variant associated with a non-conservative aminoacid change in the S1 region of the spike protein, suggests that immunological pressures might be starting to influence the evolution of the SARS virus in human populations. Published online May 9, 2003 http://image.thelancet.com/extras/03art4454web.pdf
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spelling pubmed-71401722020-04-08 Comparative full-length genome sequence analysis of 14 SARS coronavirus isolates and common mutations associated with putative origins of infection Ruan, Yijun Wei, Chia Lin Ling, Ai Ee Vega, Vinsensius B Thoreau, Herve Se Thoe, Su Yun Chia, Jer-Ming Ng, Patrick Chiu, Kuo Ping Lim, Landri Zhang, Tao Chan, Kwai Peng Lin Ean, Lynette Oon Ng, Mah Lee Leo, Sin Yee Ng, Lisa FP Ren, Ee Chee Stanton, Lawrence W Long, Philip M Liu, Edison T Lancet Article BACKGROUND: The cause of severe acute respiratory syndrome (SARS) has been identified as a new coronavirus. Whole genome sequence analysis of various isolates might provide an indication of potential strain differences of this new virus. Moreover, mutation analysis will help to develop effective vaccines. METHODS: We sequenced the entire SARS viral genome of cultured isolates from the index case (SIN2500) presenting in Singapore, from three primary contacts (SIN2774, SIN2748, and SIN2677), and one secondary contact (SIN2679). These sequences were compared with the isolates from Canada (TOR2), Hong Kong (CUHK-W1 and HKU39849), Hanoi (URBANI), Guangzhou (GZ01), and Beijing (BJ01, BJ02, BJ03, BJ04). FINDINGS: We identified 129 sequence variations among the 14 isolates, with 16 recurrent variant sequences. Common variant sequences at four loci define two distinct genotypes of the SARS virus. One genotype was linked with infections originating in Hotel M in Hong Kong, the second contained isolates from Hong Kong, Guangzhou, and Beijing with no association with Hotel M (p<0.0001). Moreover, other common sequence variants further distinguished the geographical origins of the isolates, especially between Singapore and Beijing. INTERPRETATION: Despite the recent onset of the SARS epidemic, genetic signatures are emerging that partition the worldwide SARS viral isolates into groups on the basis of contact source history and geography. These signatures can be used to trace sources of infection. In addition, a common variant associated with a non-conservative aminoacid change in the S1 region of the spike protein, suggests that immunological pressures might be starting to influence the evolution of the SARS virus in human populations. Published online May 9, 2003 http://image.thelancet.com/extras/03art4454web.pdf Elsevier Ltd. 2003-05-24 2003-05-22 /pmc/articles/PMC7140172/ /pubmed/12781537 http://dx.doi.org/10.1016/S0140-6736(03)13414-9 Text en Copyright © 2003 Elsevier Ltd. All rights reserved. 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 Article
Ruan, Yijun
Wei, Chia Lin
Ling, Ai Ee
Vega, Vinsensius B
Thoreau, Herve
Se Thoe, Su Yun
Chia, Jer-Ming
Ng, Patrick
Chiu, Kuo Ping
Lim, Landri
Zhang, Tao
Chan, Kwai Peng
Lin Ean, Lynette Oon
Ng, Mah Lee
Leo, Sin Yee
Ng, Lisa FP
Ren, Ee Chee
Stanton, Lawrence W
Long, Philip M
Liu, Edison T
Comparative full-length genome sequence analysis of 14 SARS coronavirus isolates and common mutations associated with putative origins of infection
title Comparative full-length genome sequence analysis of 14 SARS coronavirus isolates and common mutations associated with putative origins of infection
title_full Comparative full-length genome sequence analysis of 14 SARS coronavirus isolates and common mutations associated with putative origins of infection
title_fullStr Comparative full-length genome sequence analysis of 14 SARS coronavirus isolates and common mutations associated with putative origins of infection
title_full_unstemmed Comparative full-length genome sequence analysis of 14 SARS coronavirus isolates and common mutations associated with putative origins of infection
title_short Comparative full-length genome sequence analysis of 14 SARS coronavirus isolates and common mutations associated with putative origins of infection
title_sort comparative full-length genome sequence analysis of 14 sars coronavirus isolates and common mutations associated with putative origins of infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140172/
https://www.ncbi.nlm.nih.gov/pubmed/12781537
http://dx.doi.org/10.1016/S0140-6736(03)13414-9
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