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Resurgence of Omicron BA.2 in SARS-CoV-2 infection-naive Hong Kong

Hong Kong experienced a surge of Omicron BA.2 infections in early 2022, resulting in one of the highest per-capita death rates of COVID-19. The outbreak occurred in a dense population with low immunity towards natural SARS-CoV-2 infection, high vaccine hesitancy in vulnerable populations, comprehens...

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Autores principales: Xie, Ruopeng, Edwards, Kimberly M., Adam, Dillon C., Leung, Kathy S. M., Tsang, Tim K., Gurung, Shreya, Xiong, Weijia, Wei, Xiaoman, Ng, Daisy Y. M., Liu, Gigi Y. Z., Krishnan, Pavithra, Chang, Lydia D. J., Cheng, Samuel M. S., Gu, Haogao, Siu, Gilman K. H., Wu, Joseph T., Leung, Gabriel M., Peiris, Malik, Cowling, Benjamin J., Poon, Leo L. M., Dhanasekaran, Vijaykrishna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10134727/
https://www.ncbi.nlm.nih.gov/pubmed/37105966
http://dx.doi.org/10.1038/s41467-023-38201-5
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author Xie, Ruopeng
Edwards, Kimberly M.
Adam, Dillon C.
Leung, Kathy S. M.
Tsang, Tim K.
Gurung, Shreya
Xiong, Weijia
Wei, Xiaoman
Ng, Daisy Y. M.
Liu, Gigi Y. Z.
Krishnan, Pavithra
Chang, Lydia D. J.
Cheng, Samuel M. S.
Gu, Haogao
Siu, Gilman K. H.
Wu, Joseph T.
Leung, Gabriel M.
Peiris, Malik
Cowling, Benjamin J.
Poon, Leo L. M.
Dhanasekaran, Vijaykrishna
author_facet Xie, Ruopeng
Edwards, Kimberly M.
Adam, Dillon C.
Leung, Kathy S. M.
Tsang, Tim K.
Gurung, Shreya
Xiong, Weijia
Wei, Xiaoman
Ng, Daisy Y. M.
Liu, Gigi Y. Z.
Krishnan, Pavithra
Chang, Lydia D. J.
Cheng, Samuel M. S.
Gu, Haogao
Siu, Gilman K. H.
Wu, Joseph T.
Leung, Gabriel M.
Peiris, Malik
Cowling, Benjamin J.
Poon, Leo L. M.
Dhanasekaran, Vijaykrishna
author_sort Xie, Ruopeng
collection PubMed
description Hong Kong experienced a surge of Omicron BA.2 infections in early 2022, resulting in one of the highest per-capita death rates of COVID-19. The outbreak occurred in a dense population with low immunity towards natural SARS-CoV-2 infection, high vaccine hesitancy in vulnerable populations, comprehensive disease surveillance and the capacity for stringent public health and social measures (PHSMs). By analyzing genome sequences and epidemiological data, we reconstructed the epidemic trajectory of BA.2 wave and found that the initial BA.2 community transmission emerged from cross-infection within hotel quarantine. The rapid implementation of PHSMs suppressed early epidemic growth but the effective reproduction number (R(e)) increased again during the Spring festival in early February and remained around 1 until early April. Independent estimates of point prevalence and incidence using phylodynamics also showed extensive superspreading at this time, which likely contributed to the rapid expansion of the epidemic. Discordant inferences based on genomic and epidemiological data underscore the need for research to improve near real-time epidemic growth estimates by combining multiple disparate data sources to better inform outbreak response policy.
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spelling pubmed-101347272023-04-28 Resurgence of Omicron BA.2 in SARS-CoV-2 infection-naive Hong Kong Xie, Ruopeng Edwards, Kimberly M. Adam, Dillon C. Leung, Kathy S. M. Tsang, Tim K. Gurung, Shreya Xiong, Weijia Wei, Xiaoman Ng, Daisy Y. M. Liu, Gigi Y. Z. Krishnan, Pavithra Chang, Lydia D. J. Cheng, Samuel M. S. Gu, Haogao Siu, Gilman K. H. Wu, Joseph T. Leung, Gabriel M. Peiris, Malik Cowling, Benjamin J. Poon, Leo L. M. Dhanasekaran, Vijaykrishna Nat Commun Article Hong Kong experienced a surge of Omicron BA.2 infections in early 2022, resulting in one of the highest per-capita death rates of COVID-19. The outbreak occurred in a dense population with low immunity towards natural SARS-CoV-2 infection, high vaccine hesitancy in vulnerable populations, comprehensive disease surveillance and the capacity for stringent public health and social measures (PHSMs). By analyzing genome sequences and epidemiological data, we reconstructed the epidemic trajectory of BA.2 wave and found that the initial BA.2 community transmission emerged from cross-infection within hotel quarantine. The rapid implementation of PHSMs suppressed early epidemic growth but the effective reproduction number (R(e)) increased again during the Spring festival in early February and remained around 1 until early April. Independent estimates of point prevalence and incidence using phylodynamics also showed extensive superspreading at this time, which likely contributed to the rapid expansion of the epidemic. Discordant inferences based on genomic and epidemiological data underscore the need for research to improve near real-time epidemic growth estimates by combining multiple disparate data sources to better inform outbreak response policy. Nature Publishing Group UK 2023-04-27 /pmc/articles/PMC10134727/ /pubmed/37105966 http://dx.doi.org/10.1038/s41467-023-38201-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Xie, Ruopeng
Edwards, Kimberly M.
Adam, Dillon C.
Leung, Kathy S. M.
Tsang, Tim K.
Gurung, Shreya
Xiong, Weijia
Wei, Xiaoman
Ng, Daisy Y. M.
Liu, Gigi Y. Z.
Krishnan, Pavithra
Chang, Lydia D. J.
Cheng, Samuel M. S.
Gu, Haogao
Siu, Gilman K. H.
Wu, Joseph T.
Leung, Gabriel M.
Peiris, Malik
Cowling, Benjamin J.
Poon, Leo L. M.
Dhanasekaran, Vijaykrishna
Resurgence of Omicron BA.2 in SARS-CoV-2 infection-naive Hong Kong
title Resurgence of Omicron BA.2 in SARS-CoV-2 infection-naive Hong Kong
title_full Resurgence of Omicron BA.2 in SARS-CoV-2 infection-naive Hong Kong
title_fullStr Resurgence of Omicron BA.2 in SARS-CoV-2 infection-naive Hong Kong
title_full_unstemmed Resurgence of Omicron BA.2 in SARS-CoV-2 infection-naive Hong Kong
title_short Resurgence of Omicron BA.2 in SARS-CoV-2 infection-naive Hong Kong
title_sort resurgence of omicron ba.2 in sars-cov-2 infection-naive hong kong
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10134727/
https://www.ncbi.nlm.nih.gov/pubmed/37105966
http://dx.doi.org/10.1038/s41467-023-38201-5
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