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Paratype: a genotyping tool for Salmonella Paratyphi A reveals its global genomic diversity

Salmonella Paratyphi A, the primary etiology of paratyphoid, is estimated to cause 3.4 million infections annually, worldwide. With rising antimicrobial resistance and no licensed vaccines, genomic surveillance is key to track and monitor transmission, but there is currently no reliable genotyping f...

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Autores principales: Tanmoy, Arif M., Hooda, Yogesh, Sajib, Mohammad S. I., da Silva, Kesia E., Iqbal, Junaid, Qamar, Farah N., Luby, Stephen P., Dougan, Gordon, Dyson, Zoe A., Baker, Stephen, Garrett, Denise O., Andrews, Jason R., Saha, Samir K., Saha, Senjuti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782287/
https://www.ncbi.nlm.nih.gov/pubmed/36564386
http://dx.doi.org/10.1038/s41467-022-35587-6
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author Tanmoy, Arif M.
Hooda, Yogesh
Sajib, Mohammad S. I.
da Silva, Kesia E.
Iqbal, Junaid
Qamar, Farah N.
Luby, Stephen P.
Dougan, Gordon
Dyson, Zoe A.
Baker, Stephen
Garrett, Denise O.
Andrews, Jason R.
Saha, Samir K.
Saha, Senjuti
author_facet Tanmoy, Arif M.
Hooda, Yogesh
Sajib, Mohammad S. I.
da Silva, Kesia E.
Iqbal, Junaid
Qamar, Farah N.
Luby, Stephen P.
Dougan, Gordon
Dyson, Zoe A.
Baker, Stephen
Garrett, Denise O.
Andrews, Jason R.
Saha, Samir K.
Saha, Senjuti
author_sort Tanmoy, Arif M.
collection PubMed
description Salmonella Paratyphi A, the primary etiology of paratyphoid, is estimated to cause 3.4 million infections annually, worldwide. With rising antimicrobial resistance and no licensed vaccines, genomic surveillance is key to track and monitor transmission, but there is currently no reliable genotyping framework for this pathogen. Here, we sequence 817 isolates from South Asia and add 562 publicly available genomes to build a global database representing 37 countries, covering 1917–2019. We develop a single nucleotide polymorphism-based genotyping scheme, Paratype, that segregates Salmonella Paratyphi A population into three primary and nine secondary clades, and 18 genotypes. Each genotype is assigned a unique allele definition located on an essential gene. Using Paratype, we identify spatiotemporal genomic variation and antimicrobial resistance markers. We release Paratype as an open-access tool that can use raw read files from both Illumina and Nanopore platforms, and thus can assist surveillance studies tracking Salmonella Paratyphi A across the globe.
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spelling pubmed-97822872022-12-23 Paratype: a genotyping tool for Salmonella Paratyphi A reveals its global genomic diversity Tanmoy, Arif M. Hooda, Yogesh Sajib, Mohammad S. I. da Silva, Kesia E. Iqbal, Junaid Qamar, Farah N. Luby, Stephen P. Dougan, Gordon Dyson, Zoe A. Baker, Stephen Garrett, Denise O. Andrews, Jason R. Saha, Samir K. Saha, Senjuti Nat Commun Article Salmonella Paratyphi A, the primary etiology of paratyphoid, is estimated to cause 3.4 million infections annually, worldwide. With rising antimicrobial resistance and no licensed vaccines, genomic surveillance is key to track and monitor transmission, but there is currently no reliable genotyping framework for this pathogen. Here, we sequence 817 isolates from South Asia and add 562 publicly available genomes to build a global database representing 37 countries, covering 1917–2019. We develop a single nucleotide polymorphism-based genotyping scheme, Paratype, that segregates Salmonella Paratyphi A population into three primary and nine secondary clades, and 18 genotypes. Each genotype is assigned a unique allele definition located on an essential gene. Using Paratype, we identify spatiotemporal genomic variation and antimicrobial resistance markers. We release Paratype as an open-access tool that can use raw read files from both Illumina and Nanopore platforms, and thus can assist surveillance studies tracking Salmonella Paratyphi A across the globe. Nature Publishing Group UK 2022-12-23 /pmc/articles/PMC9782287/ /pubmed/36564386 http://dx.doi.org/10.1038/s41467-022-35587-6 Text en © The Author(s) 2022 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
Tanmoy, Arif M.
Hooda, Yogesh
Sajib, Mohammad S. I.
da Silva, Kesia E.
Iqbal, Junaid
Qamar, Farah N.
Luby, Stephen P.
Dougan, Gordon
Dyson, Zoe A.
Baker, Stephen
Garrett, Denise O.
Andrews, Jason R.
Saha, Samir K.
Saha, Senjuti
Paratype: a genotyping tool for Salmonella Paratyphi A reveals its global genomic diversity
title Paratype: a genotyping tool for Salmonella Paratyphi A reveals its global genomic diversity
title_full Paratype: a genotyping tool for Salmonella Paratyphi A reveals its global genomic diversity
title_fullStr Paratype: a genotyping tool for Salmonella Paratyphi A reveals its global genomic diversity
title_full_unstemmed Paratype: a genotyping tool for Salmonella Paratyphi A reveals its global genomic diversity
title_short Paratype: a genotyping tool for Salmonella Paratyphi A reveals its global genomic diversity
title_sort paratype: a genotyping tool for salmonella paratyphi a reveals its global genomic diversity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782287/
https://www.ncbi.nlm.nih.gov/pubmed/36564386
http://dx.doi.org/10.1038/s41467-022-35587-6
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