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Genomic Tracking of SARS-CoV-2 Variants in Myanmar

In December 2019, the COVID-19 disease started in Wuhan, China. The WHO declared a pandemic on 12 March 2020, and the disease started in Myanmar on 23 March 2020. In December 2020, different variants were brought worldwide, threatening global health. To counter those threats, Myanmar started the COV...

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Autores principales: Oo, Khine Zaw, Htun, Zaw Win, Aung, Nay Myo, Win, Ko Ko, Linn, Kyaw Zawl, Htoo, Sett Paing, Aung, Phyo Kyaw, Oo, Thet Wai, Zaw, Myo Thiha, Ko, Linn Yuzana, Tun, Kyaw Myo, Myint, Kyee, Lwin, Ko Ko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9862072/
https://www.ncbi.nlm.nih.gov/pubmed/36679850
http://dx.doi.org/10.3390/vaccines11010006
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author Oo, Khine Zaw
Htun, Zaw Win
Aung, Nay Myo
Win, Ko Ko
Linn, Kyaw Zawl
Htoo, Sett Paing
Aung, Phyo Kyaw
Oo, Thet Wai
Zaw, Myo Thiha
Ko, Linn Yuzana
Tun, Kyaw Myo
Myint, Kyee
Lwin, Ko Ko
author_facet Oo, Khine Zaw
Htun, Zaw Win
Aung, Nay Myo
Win, Ko Ko
Linn, Kyaw Zawl
Htoo, Sett Paing
Aung, Phyo Kyaw
Oo, Thet Wai
Zaw, Myo Thiha
Ko, Linn Yuzana
Tun, Kyaw Myo
Myint, Kyee
Lwin, Ko Ko
author_sort Oo, Khine Zaw
collection PubMed
description In December 2019, the COVID-19 disease started in Wuhan, China. The WHO declared a pandemic on 12 March 2020, and the disease started in Myanmar on 23 March 2020. In December 2020, different variants were brought worldwide, threatening global health. To counter those threats, Myanmar started the COVID-19 variant surveillance program in late 2020. Whole genome sequencing was done six times between January 2021 and March 2022. Among them, 83 samples with a PCR threshold cycle of less than 25 were chosen. Then, we used MiSeq FGx for sequencing and Illumina DRAGEN COVIDSeq pipeline, command line interface, GISAID, and MEGA version 7 for data analysis. In January 2021, no variant was detected. The second run, during the rise of cases in June 2021, showed Alpha, Delta, and Kappa variants. The third and the fourth runs in August and December showed only a Delta variant. Omicron and Delta variants were detected during the fifth run in January 2022. The sixth run in March 2022 showed only Omicron BA.2. Amino acid mutation at the receptor binding domain of Spike glycoprotein started since the second run coupling with high transmission, recurrence, and vaccine escape. We also found the mutation at the primer targets used in current RT-PCR platforms, but there was no mutation at the existing antiviral drug targets. The occurrence of multiple variants and mutations claimed vigilance at ports of entry and preparedness for effective control measures. Genomic surveillance with the observation of evolutionary data is required to predict imminent threats of the current disease and diagnose emerging infectious diseases.
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spelling pubmed-98620722023-01-22 Genomic Tracking of SARS-CoV-2 Variants in Myanmar Oo, Khine Zaw Htun, Zaw Win Aung, Nay Myo Win, Ko Ko Linn, Kyaw Zawl Htoo, Sett Paing Aung, Phyo Kyaw Oo, Thet Wai Zaw, Myo Thiha Ko, Linn Yuzana Tun, Kyaw Myo Myint, Kyee Lwin, Ko Ko Vaccines (Basel) Article In December 2019, the COVID-19 disease started in Wuhan, China. The WHO declared a pandemic on 12 March 2020, and the disease started in Myanmar on 23 March 2020. In December 2020, different variants were brought worldwide, threatening global health. To counter those threats, Myanmar started the COVID-19 variant surveillance program in late 2020. Whole genome sequencing was done six times between January 2021 and March 2022. Among them, 83 samples with a PCR threshold cycle of less than 25 were chosen. Then, we used MiSeq FGx for sequencing and Illumina DRAGEN COVIDSeq pipeline, command line interface, GISAID, and MEGA version 7 for data analysis. In January 2021, no variant was detected. The second run, during the rise of cases in June 2021, showed Alpha, Delta, and Kappa variants. The third and the fourth runs in August and December showed only a Delta variant. Omicron and Delta variants were detected during the fifth run in January 2022. The sixth run in March 2022 showed only Omicron BA.2. Amino acid mutation at the receptor binding domain of Spike glycoprotein started since the second run coupling with high transmission, recurrence, and vaccine escape. We also found the mutation at the primer targets used in current RT-PCR platforms, but there was no mutation at the existing antiviral drug targets. The occurrence of multiple variants and mutations claimed vigilance at ports of entry and preparedness for effective control measures. Genomic surveillance with the observation of evolutionary data is required to predict imminent threats of the current disease and diagnose emerging infectious diseases. MDPI 2022-12-20 /pmc/articles/PMC9862072/ /pubmed/36679850 http://dx.doi.org/10.3390/vaccines11010006 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Oo, Khine Zaw
Htun, Zaw Win
Aung, Nay Myo
Win, Ko Ko
Linn, Kyaw Zawl
Htoo, Sett Paing
Aung, Phyo Kyaw
Oo, Thet Wai
Zaw, Myo Thiha
Ko, Linn Yuzana
Tun, Kyaw Myo
Myint, Kyee
Lwin, Ko Ko
Genomic Tracking of SARS-CoV-2 Variants in Myanmar
title Genomic Tracking of SARS-CoV-2 Variants in Myanmar
title_full Genomic Tracking of SARS-CoV-2 Variants in Myanmar
title_fullStr Genomic Tracking of SARS-CoV-2 Variants in Myanmar
title_full_unstemmed Genomic Tracking of SARS-CoV-2 Variants in Myanmar
title_short Genomic Tracking of SARS-CoV-2 Variants in Myanmar
title_sort genomic tracking of sars-cov-2 variants in myanmar
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9862072/
https://www.ncbi.nlm.nih.gov/pubmed/36679850
http://dx.doi.org/10.3390/vaccines11010006
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