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Evolutionary history and introduction of SARS-CoV-2 Alpha VOC/B.1.1.7 in Pakistan through international travelers

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants continue to emerge, and their identification is important for the public health response to coronavirus disease 2019 (COVID-19). Genomic sequencing provides robust information but may not always be accessible, and therefore, mutat...

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Autores principales: Nasir, Asghar, Bukhari, Ali Raza, Trovão, Nídia S, Thielen, Peter M, Kanji, Akbar, Mahmood, Syed Faisal, Ghanchi, Najia Karim, Ansar, Zeeshan, Merritt, Brian, Mehoke, Thomas, Razzak, Safina Abdul, Syed, Muhammed Asif, Shaikh, Suhail Raza, Wassan, Mansoor, Aamir, Uzma Bashir, Baele, Guy, Rasmussen, Zeba, Spiro, David, Hasan, Rumina, Hasan, Zahra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021734/
https://www.ncbi.nlm.nih.gov/pubmed/35462736
http://dx.doi.org/10.1093/ve/veac020
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author Nasir, Asghar
Bukhari, Ali Raza
Trovão, Nídia S
Thielen, Peter M
Kanji, Akbar
Mahmood, Syed Faisal
Ghanchi, Najia Karim
Ansar, Zeeshan
Merritt, Brian
Mehoke, Thomas
Razzak, Safina Abdul
Syed, Muhammed Asif
Shaikh, Suhail Raza
Wassan, Mansoor
Aamir, Uzma Bashir
Baele, Guy
Rasmussen, Zeba
Spiro, David
Hasan, Rumina
Hasan, Zahra
author_facet Nasir, Asghar
Bukhari, Ali Raza
Trovão, Nídia S
Thielen, Peter M
Kanji, Akbar
Mahmood, Syed Faisal
Ghanchi, Najia Karim
Ansar, Zeeshan
Merritt, Brian
Mehoke, Thomas
Razzak, Safina Abdul
Syed, Muhammed Asif
Shaikh, Suhail Raza
Wassan, Mansoor
Aamir, Uzma Bashir
Baele, Guy
Rasmussen, Zeba
Spiro, David
Hasan, Rumina
Hasan, Zahra
author_sort Nasir, Asghar
collection PubMed
description Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants continue to emerge, and their identification is important for the public health response to coronavirus disease 2019 (COVID-19). Genomic sequencing provides robust information but may not always be accessible, and therefore, mutation-based polymerase chain reaction (PCR) approaches can be used for rapid identification of known variants. International travelers arriving in Karachi between December 2020 and February 2021 were tested for SARS-CoV-2 by PCR. A subset of positive samples was tested for S-gene target failure (SGTF) on TaqPathTM COVID-19 (Thermo Fisher Scientific) and for mutations using the GSD NovaType SARS-CoV-2 (Eurofins Technologies) assays. Sequencing was conducted on the MinION platform (Oxford Nanopore Technologies). Bayesian phylogeographic inference was performed integrating the patients’ travel history information. Of the thirty-five COVID-19 cases screened, thirteen had isolates with SGTF. The travelers transmitted infection to sixty-eight contact cases. The B.1.1.7 lineage was confirmed through sequencing and PCR. The phylogenetic analysis of sequence data available for six cases included four B.1.1.7 strains and one B.1.36 and B.1.1.212 lineage isolate. Phylogeographic modeling estimated at least three independent B.1.1.7 introductions into Karachi, Pakistan, originating from the UK. B.1.1.212 and B.1.36 were inferred to be introduced either from the UK or the travelers’ layover location. We report the introduction of SARS-CoV-2 B.1.1.7 and other lineages in Pakistan by international travelers arriving via different flight routes. This highlights SARS-CoV-2 transmission through travel, importance of testing, and quarantine post-travel to prevent transmission of new strains, as well as recording detailed patients’ metadata. Such results help inform policies on restricting travel from destinations where new highly transmissible variants have emerged.
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spelling pubmed-90217342022-04-21 Evolutionary history and introduction of SARS-CoV-2 Alpha VOC/B.1.1.7 in Pakistan through international travelers Nasir, Asghar Bukhari, Ali Raza Trovão, Nídia S Thielen, Peter M Kanji, Akbar Mahmood, Syed Faisal Ghanchi, Najia Karim Ansar, Zeeshan Merritt, Brian Mehoke, Thomas Razzak, Safina Abdul Syed, Muhammed Asif Shaikh, Suhail Raza Wassan, Mansoor Aamir, Uzma Bashir Baele, Guy Rasmussen, Zeba Spiro, David Hasan, Rumina Hasan, Zahra Virus Evol Research Article Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants continue to emerge, and their identification is important for the public health response to coronavirus disease 2019 (COVID-19). Genomic sequencing provides robust information but may not always be accessible, and therefore, mutation-based polymerase chain reaction (PCR) approaches can be used for rapid identification of known variants. International travelers arriving in Karachi between December 2020 and February 2021 were tested for SARS-CoV-2 by PCR. A subset of positive samples was tested for S-gene target failure (SGTF) on TaqPathTM COVID-19 (Thermo Fisher Scientific) and for mutations using the GSD NovaType SARS-CoV-2 (Eurofins Technologies) assays. Sequencing was conducted on the MinION platform (Oxford Nanopore Technologies). Bayesian phylogeographic inference was performed integrating the patients’ travel history information. Of the thirty-five COVID-19 cases screened, thirteen had isolates with SGTF. The travelers transmitted infection to sixty-eight contact cases. The B.1.1.7 lineage was confirmed through sequencing and PCR. The phylogenetic analysis of sequence data available for six cases included four B.1.1.7 strains and one B.1.36 and B.1.1.212 lineage isolate. Phylogeographic modeling estimated at least three independent B.1.1.7 introductions into Karachi, Pakistan, originating from the UK. B.1.1.212 and B.1.36 were inferred to be introduced either from the UK or the travelers’ layover location. We report the introduction of SARS-CoV-2 B.1.1.7 and other lineages in Pakistan by international travelers arriving via different flight routes. This highlights SARS-CoV-2 transmission through travel, importance of testing, and quarantine post-travel to prevent transmission of new strains, as well as recording detailed patients’ metadata. Such results help inform policies on restricting travel from destinations where new highly transmissible variants have emerged. Oxford University Press 2022-03-17 /pmc/articles/PMC9021734/ /pubmed/35462736 http://dx.doi.org/10.1093/ve/veac020 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Nasir, Asghar
Bukhari, Ali Raza
Trovão, Nídia S
Thielen, Peter M
Kanji, Akbar
Mahmood, Syed Faisal
Ghanchi, Najia Karim
Ansar, Zeeshan
Merritt, Brian
Mehoke, Thomas
Razzak, Safina Abdul
Syed, Muhammed Asif
Shaikh, Suhail Raza
Wassan, Mansoor
Aamir, Uzma Bashir
Baele, Guy
Rasmussen, Zeba
Spiro, David
Hasan, Rumina
Hasan, Zahra
Evolutionary history and introduction of SARS-CoV-2 Alpha VOC/B.1.1.7 in Pakistan through international travelers
title Evolutionary history and introduction of SARS-CoV-2 Alpha VOC/B.1.1.7 in Pakistan through international travelers
title_full Evolutionary history and introduction of SARS-CoV-2 Alpha VOC/B.1.1.7 in Pakistan through international travelers
title_fullStr Evolutionary history and introduction of SARS-CoV-2 Alpha VOC/B.1.1.7 in Pakistan through international travelers
title_full_unstemmed Evolutionary history and introduction of SARS-CoV-2 Alpha VOC/B.1.1.7 in Pakistan through international travelers
title_short Evolutionary history and introduction of SARS-CoV-2 Alpha VOC/B.1.1.7 in Pakistan through international travelers
title_sort evolutionary history and introduction of sars-cov-2 alpha voc/b.1.1.7 in pakistan through international travelers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021734/
https://www.ncbi.nlm.nih.gov/pubmed/35462736
http://dx.doi.org/10.1093/ve/veac020
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