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Temporal dynamics and fatality of SARS‐CoV‐2 variants in Bangladesh

BACKGROUND AND AIMS: Since the beginning of the SARS‐CoV‐2 pandemic, multiple new variants have emerged posing an increased risk to global public health. This study aimed to investigate SARS‐CoV‐2 variants, their temporal dynamics, infection rate (IFR) and case fatality rate (CFR) in Bangladesh by a...

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Autores principales: Rahman, M. Shaminur, Hoque, M. Nazmul, Chowdhury, Susmita Roy, Siddique, Md. Moradul, Islam, Ovinu Kibria, Galib, Syed Md., Islam, Md. Tanvir, Hossain, M. Anwar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108430/
https://www.ncbi.nlm.nih.gov/pubmed/37077184
http://dx.doi.org/10.1002/hsr2.1209
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author Rahman, M. Shaminur
Hoque, M. Nazmul
Chowdhury, Susmita Roy
Siddique, Md. Moradul
Islam, Ovinu Kibria
Galib, Syed Md.
Islam, Md. Tanvir
Hossain, M. Anwar
author_facet Rahman, M. Shaminur
Hoque, M. Nazmul
Chowdhury, Susmita Roy
Siddique, Md. Moradul
Islam, Ovinu Kibria
Galib, Syed Md.
Islam, Md. Tanvir
Hossain, M. Anwar
author_sort Rahman, M. Shaminur
collection PubMed
description BACKGROUND AND AIMS: Since the beginning of the SARS‐CoV‐2 pandemic, multiple new variants have emerged posing an increased risk to global public health. This study aimed to investigate SARS‐CoV‐2 variants, their temporal dynamics, infection rate (IFR) and case fatality rate (CFR) in Bangladesh by analyzing the published genomes. METHODS: We retrieved 6610 complete whole genome sequences of the SARS‐CoV‐2 from the GISAID (Global Initiative on Sharing all Influenza Data) platform from March 2020 to October 2022, and performed different in‐silico bioinformatics analyses. The clade and Pango lineages were assigned by using Nextclade v2.8.1. SARS‐CoV‐2 infections and fatality data were collected from the Institute of Epidemiology Disease Control and Research (IEDCR), Bangladesh. The average IFR was calculated from the monthly COVID‐19 cases and population size while average CFR was calculated from the number of monthly deaths and number of confirmed COVID‐19 cases. RESULTS: SARS‐CoV‐2 first emerged in Bangladesh on March 3, 2020 and created three pandemic waves so far. The phylogenetic analysis revealed multiple introductions of SARS‐CoV‐2 variant(s) into Bangladesh with at least 22 Nextstrain clades and 107 Pangolin lineages with respect to the SARS‐CoV‐2 reference genome of Wuhan/Hu‐1/2019. The Delta variant was detected as the most predominant (48.06%) variant followed by Omicron (27.88%), Beta (7.65%), Alpha (1.56%), Eta (0.33%) and Gamma (0.03%) variant. The overall IFR and CFR from circulating variants were 13.59% and 1.45%, respectively. A time‐dependent monthly analysis showed significant variations in the IFR (p = 0.012, Kruskal–Wallis test) and CFR (p = 0.032, Kruskal–Wallis test) throughout the study period. We found the highest IFR (14.35%) in 2020 while Delta (20A) and Beta (20H) variants were circulating in Bangladesh. Remarkably, the highest CFR (1.91%) from SARS‐CoV‐2 variants was recorded in 2021. CONCLUSION: Our findings highlight the importance of genomic surveillance for careful monitoring of variants of concern emergence to interpret correctly their relative IFR and CFR, and thus, for implementation of strengthened public health and social measures to control the spread of the virus. Furthermore, the results of the present study may provide important context for sequence‐based inference in SARS‐CoV‐2 variant(s) evolution and clinical epidemiology beyond Bangladesh.
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spelling pubmed-101084302023-04-18 Temporal dynamics and fatality of SARS‐CoV‐2 variants in Bangladesh Rahman, M. Shaminur Hoque, M. Nazmul Chowdhury, Susmita Roy Siddique, Md. Moradul Islam, Ovinu Kibria Galib, Syed Md. Islam, Md. Tanvir Hossain, M. Anwar Health Sci Rep Original Research BACKGROUND AND AIMS: Since the beginning of the SARS‐CoV‐2 pandemic, multiple new variants have emerged posing an increased risk to global public health. This study aimed to investigate SARS‐CoV‐2 variants, their temporal dynamics, infection rate (IFR) and case fatality rate (CFR) in Bangladesh by analyzing the published genomes. METHODS: We retrieved 6610 complete whole genome sequences of the SARS‐CoV‐2 from the GISAID (Global Initiative on Sharing all Influenza Data) platform from March 2020 to October 2022, and performed different in‐silico bioinformatics analyses. The clade and Pango lineages were assigned by using Nextclade v2.8.1. SARS‐CoV‐2 infections and fatality data were collected from the Institute of Epidemiology Disease Control and Research (IEDCR), Bangladesh. The average IFR was calculated from the monthly COVID‐19 cases and population size while average CFR was calculated from the number of monthly deaths and number of confirmed COVID‐19 cases. RESULTS: SARS‐CoV‐2 first emerged in Bangladesh on March 3, 2020 and created three pandemic waves so far. The phylogenetic analysis revealed multiple introductions of SARS‐CoV‐2 variant(s) into Bangladesh with at least 22 Nextstrain clades and 107 Pangolin lineages with respect to the SARS‐CoV‐2 reference genome of Wuhan/Hu‐1/2019. The Delta variant was detected as the most predominant (48.06%) variant followed by Omicron (27.88%), Beta (7.65%), Alpha (1.56%), Eta (0.33%) and Gamma (0.03%) variant. The overall IFR and CFR from circulating variants were 13.59% and 1.45%, respectively. A time‐dependent monthly analysis showed significant variations in the IFR (p = 0.012, Kruskal–Wallis test) and CFR (p = 0.032, Kruskal–Wallis test) throughout the study period. We found the highest IFR (14.35%) in 2020 while Delta (20A) and Beta (20H) variants were circulating in Bangladesh. Remarkably, the highest CFR (1.91%) from SARS‐CoV‐2 variants was recorded in 2021. CONCLUSION: Our findings highlight the importance of genomic surveillance for careful monitoring of variants of concern emergence to interpret correctly their relative IFR and CFR, and thus, for implementation of strengthened public health and social measures to control the spread of the virus. Furthermore, the results of the present study may provide important context for sequence‐based inference in SARS‐CoV‐2 variant(s) evolution and clinical epidemiology beyond Bangladesh. John Wiley and Sons Inc. 2023-04-17 /pmc/articles/PMC10108430/ /pubmed/37077184 http://dx.doi.org/10.1002/hsr2.1209 Text en © 2023 The Authors. Health Science Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Rahman, M. Shaminur
Hoque, M. Nazmul
Chowdhury, Susmita Roy
Siddique, Md. Moradul
Islam, Ovinu Kibria
Galib, Syed Md.
Islam, Md. Tanvir
Hossain, M. Anwar
Temporal dynamics and fatality of SARS‐CoV‐2 variants in Bangladesh
title Temporal dynamics and fatality of SARS‐CoV‐2 variants in Bangladesh
title_full Temporal dynamics and fatality of SARS‐CoV‐2 variants in Bangladesh
title_fullStr Temporal dynamics and fatality of SARS‐CoV‐2 variants in Bangladesh
title_full_unstemmed Temporal dynamics and fatality of SARS‐CoV‐2 variants in Bangladesh
title_short Temporal dynamics and fatality of SARS‐CoV‐2 variants in Bangladesh
title_sort temporal dynamics and fatality of sars‐cov‐2 variants in bangladesh
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108430/
https://www.ncbi.nlm.nih.gov/pubmed/37077184
http://dx.doi.org/10.1002/hsr2.1209
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