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Effects of a major deletion in the SARS-CoV-2 genome on the severity of infection and the inflammatory response: an observational cohort study

BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants with a 382-nucleotide deletion (∆382) in the open reading frame 8 (ORF8) region of the genome have been detected in Singapore and other countries. We investigated the effect of this deletion on the clinical features of...

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Autores principales: Young, Barnaby E, Fong, Siew-Wai, Chan, Yi-Hao, Mak, Tze-Minn, Ang, Li Wei, Anderson, Danielle E, Lee, Cheryl Yi-Pin, Amrun, Siti Naqiah, Lee, Bernett, Goh, Yun Shan, Su, Yvonne C F, Wei, Wycliffe E, Kalimuddin, Shirin, Chai, Louis Yi Ann, Pada, Surinder, Tan, Seow Yen, Sun, Louisa, Parthasarathy, Purnima, Chen, Yuan Yi Constance, Barkham, Timothy, Lin, Raymond Tzer Pin, Maurer-Stroh, Sebastian, Leo, Yee-Sin, Wang, Lin-Fa, Renia, Laurent, Lee, Vernon J, Smith, Gavin J D, Lye, David Chien, Ng, Lisa F P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434477/
https://www.ncbi.nlm.nih.gov/pubmed/32822564
http://dx.doi.org/10.1016/S0140-6736(20)31757-8
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author Young, Barnaby E
Fong, Siew-Wai
Chan, Yi-Hao
Mak, Tze-Minn
Ang, Li Wei
Anderson, Danielle E
Lee, Cheryl Yi-Pin
Amrun, Siti Naqiah
Lee, Bernett
Goh, Yun Shan
Su, Yvonne C F
Wei, Wycliffe E
Kalimuddin, Shirin
Chai, Louis Yi Ann
Pada, Surinder
Tan, Seow Yen
Sun, Louisa
Parthasarathy, Purnima
Chen, Yuan Yi Constance
Barkham, Timothy
Lin, Raymond Tzer Pin
Maurer-Stroh, Sebastian
Leo, Yee-Sin
Wang, Lin-Fa
Renia, Laurent
Lee, Vernon J
Smith, Gavin J D
Lye, David Chien
Ng, Lisa F P
author_facet Young, Barnaby E
Fong, Siew-Wai
Chan, Yi-Hao
Mak, Tze-Minn
Ang, Li Wei
Anderson, Danielle E
Lee, Cheryl Yi-Pin
Amrun, Siti Naqiah
Lee, Bernett
Goh, Yun Shan
Su, Yvonne C F
Wei, Wycliffe E
Kalimuddin, Shirin
Chai, Louis Yi Ann
Pada, Surinder
Tan, Seow Yen
Sun, Louisa
Parthasarathy, Purnima
Chen, Yuan Yi Constance
Barkham, Timothy
Lin, Raymond Tzer Pin
Maurer-Stroh, Sebastian
Leo, Yee-Sin
Wang, Lin-Fa
Renia, Laurent
Lee, Vernon J
Smith, Gavin J D
Lye, David Chien
Ng, Lisa F P
author_sort Young, Barnaby E
collection PubMed
description BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants with a 382-nucleotide deletion (∆382) in the open reading frame 8 (ORF8) region of the genome have been detected in Singapore and other countries. We investigated the effect of this deletion on the clinical features of infection. METHODS: We retrospectively identified patients who had been screened for the ∆382 variant and recruited to the PROTECT study—a prospective observational cohort study conducted at seven public hospitals in Singapore. We collected clinical, laboratory, and radiological data from patients' electronic medical records and serial blood and respiratory samples taken during hospitalisation and after discharge. Individuals infected with the ∆382 variant were compared with those infected with wild-type SARS-CoV-2. Exact logistic regression was used to examine the association between the infection groups and the development of hypoxia requiring supplemental oxygen (an indicator of severe COVID-19, the primary endpoint). Follow-up for the study's primary endpoint is completed. FINDINGS: Between Jan 22 and March 21, 2020, 278 patients with PCR-confirmed SARS-CoV-2 infection were screened for the ∆382 deletion and 131 were enrolled onto the study, of whom 92 (70%) were infected with the wild-type virus, ten (8%) had a mix of wild-type and ∆382-variant viruses, and 29 (22%) had only the ∆382 variant. Development of hypoxia requiring supplemental oxygen was less frequent in the ∆382 variant group (0 [0%] of 29 patients) than in the wild-type only group (26 [28%] of 92; absolute difference 28% [95% CI 14–28]). After adjusting for age and presence of comorbidities, infection with the ∆382 variant only was associated with lower odds of developing hypoxia requiring supplemental oxygen (adjusted odds ratio 0·07 [95% CI 0·00–0·48]) compared with infection with wild-type virus only. INTERPRETATION: The ∆382 variant of SARS-CoV-2 seems to be associated with a milder infection. The observed clinical effects of deletions in ORF8 could have implications for the development of treatments and vaccines. FUNDING: National Medical Research Council Singapore.
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spelling pubmed-74344772020-08-19 Effects of a major deletion in the SARS-CoV-2 genome on the severity of infection and the inflammatory response: an observational cohort study Young, Barnaby E Fong, Siew-Wai Chan, Yi-Hao Mak, Tze-Minn Ang, Li Wei Anderson, Danielle E Lee, Cheryl Yi-Pin Amrun, Siti Naqiah Lee, Bernett Goh, Yun Shan Su, Yvonne C F Wei, Wycliffe E Kalimuddin, Shirin Chai, Louis Yi Ann Pada, Surinder Tan, Seow Yen Sun, Louisa Parthasarathy, Purnima Chen, Yuan Yi Constance Barkham, Timothy Lin, Raymond Tzer Pin Maurer-Stroh, Sebastian Leo, Yee-Sin Wang, Lin-Fa Renia, Laurent Lee, Vernon J Smith, Gavin J D Lye, David Chien Ng, Lisa F P Lancet Article BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants with a 382-nucleotide deletion (∆382) in the open reading frame 8 (ORF8) region of the genome have been detected in Singapore and other countries. We investigated the effect of this deletion on the clinical features of infection. METHODS: We retrospectively identified patients who had been screened for the ∆382 variant and recruited to the PROTECT study—a prospective observational cohort study conducted at seven public hospitals in Singapore. We collected clinical, laboratory, and radiological data from patients' electronic medical records and serial blood and respiratory samples taken during hospitalisation and after discharge. Individuals infected with the ∆382 variant were compared with those infected with wild-type SARS-CoV-2. Exact logistic regression was used to examine the association between the infection groups and the development of hypoxia requiring supplemental oxygen (an indicator of severe COVID-19, the primary endpoint). Follow-up for the study's primary endpoint is completed. FINDINGS: Between Jan 22 and March 21, 2020, 278 patients with PCR-confirmed SARS-CoV-2 infection were screened for the ∆382 deletion and 131 were enrolled onto the study, of whom 92 (70%) were infected with the wild-type virus, ten (8%) had a mix of wild-type and ∆382-variant viruses, and 29 (22%) had only the ∆382 variant. Development of hypoxia requiring supplemental oxygen was less frequent in the ∆382 variant group (0 [0%] of 29 patients) than in the wild-type only group (26 [28%] of 92; absolute difference 28% [95% CI 14–28]). After adjusting for age and presence of comorbidities, infection with the ∆382 variant only was associated with lower odds of developing hypoxia requiring supplemental oxygen (adjusted odds ratio 0·07 [95% CI 0·00–0·48]) compared with infection with wild-type virus only. INTERPRETATION: The ∆382 variant of SARS-CoV-2 seems to be associated with a milder infection. The observed clinical effects of deletions in ORF8 could have implications for the development of treatments and vaccines. FUNDING: National Medical Research Council Singapore. Elsevier Ltd. 2020 2020-08-18 /pmc/articles/PMC7434477/ /pubmed/32822564 http://dx.doi.org/10.1016/S0140-6736(20)31757-8 Text en © 2020 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
Young, Barnaby E
Fong, Siew-Wai
Chan, Yi-Hao
Mak, Tze-Minn
Ang, Li Wei
Anderson, Danielle E
Lee, Cheryl Yi-Pin
Amrun, Siti Naqiah
Lee, Bernett
Goh, Yun Shan
Su, Yvonne C F
Wei, Wycliffe E
Kalimuddin, Shirin
Chai, Louis Yi Ann
Pada, Surinder
Tan, Seow Yen
Sun, Louisa
Parthasarathy, Purnima
Chen, Yuan Yi Constance
Barkham, Timothy
Lin, Raymond Tzer Pin
Maurer-Stroh, Sebastian
Leo, Yee-Sin
Wang, Lin-Fa
Renia, Laurent
Lee, Vernon J
Smith, Gavin J D
Lye, David Chien
Ng, Lisa F P
Effects of a major deletion in the SARS-CoV-2 genome on the severity of infection and the inflammatory response: an observational cohort study
title Effects of a major deletion in the SARS-CoV-2 genome on the severity of infection and the inflammatory response: an observational cohort study
title_full Effects of a major deletion in the SARS-CoV-2 genome on the severity of infection and the inflammatory response: an observational cohort study
title_fullStr Effects of a major deletion in the SARS-CoV-2 genome on the severity of infection and the inflammatory response: an observational cohort study
title_full_unstemmed Effects of a major deletion in the SARS-CoV-2 genome on the severity of infection and the inflammatory response: an observational cohort study
title_short Effects of a major deletion in the SARS-CoV-2 genome on the severity of infection and the inflammatory response: an observational cohort study
title_sort effects of a major deletion in the sars-cov-2 genome on the severity of infection and the inflammatory response: an observational cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434477/
https://www.ncbi.nlm.nih.gov/pubmed/32822564
http://dx.doi.org/10.1016/S0140-6736(20)31757-8
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