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Genomic epidemiology of syphilis reveals independent emergence of macrolide resistance across multiple circulating lineages
Syphilis is a sexually transmitted infection caused by Treponema pallidum subspecies pallidum and may lead to severe complications. Recent years have seen striking increases in syphilis in many countries. Previous analyses have suggested one lineage of syphilis, SS14, may have expanded recently, ind...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646400/ https://www.ncbi.nlm.nih.gov/pubmed/31332179 http://dx.doi.org/10.1038/s41467-019-11216-7 |
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author | Beale, Mathew A. Marks, Michael Sahi, Sharon K. Tantalo, Lauren C. Nori, Achyuta V. French, Patrick Lukehart, Sheila A. Marra, Christina M. Thomson, Nicholas R. |
author_facet | Beale, Mathew A. Marks, Michael Sahi, Sharon K. Tantalo, Lauren C. Nori, Achyuta V. French, Patrick Lukehart, Sheila A. Marra, Christina M. Thomson, Nicholas R. |
author_sort | Beale, Mathew A. |
collection | PubMed |
description | Syphilis is a sexually transmitted infection caused by Treponema pallidum subspecies pallidum and may lead to severe complications. Recent years have seen striking increases in syphilis in many countries. Previous analyses have suggested one lineage of syphilis, SS14, may have expanded recently, indicating emergence of a single pandemic azithromycin-resistant cluster. Here we use direct sequencing of T. pallidum combined with phylogenomic analyses to show that both SS14- and Nichols-lineages are simultaneously circulating in clinically relevant populations in multiple countries. We correlate the appearance of genotypic macrolide resistance with multiple independently evolved SS14 sub-lineages and show that genotypically resistant and sensitive sub-lineages are spreading contemporaneously. These findings inform our understanding of the current syphilis epidemic by demonstrating how macrolide resistance evolves in Treponema subspecies and provide a warning on broader issues of antimicrobial resistance. |
format | Online Article Text |
id | pubmed-6646400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66464002019-07-24 Genomic epidemiology of syphilis reveals independent emergence of macrolide resistance across multiple circulating lineages Beale, Mathew A. Marks, Michael Sahi, Sharon K. Tantalo, Lauren C. Nori, Achyuta V. French, Patrick Lukehart, Sheila A. Marra, Christina M. Thomson, Nicholas R. Nat Commun Article Syphilis is a sexually transmitted infection caused by Treponema pallidum subspecies pallidum and may lead to severe complications. Recent years have seen striking increases in syphilis in many countries. Previous analyses have suggested one lineage of syphilis, SS14, may have expanded recently, indicating emergence of a single pandemic azithromycin-resistant cluster. Here we use direct sequencing of T. pallidum combined with phylogenomic analyses to show that both SS14- and Nichols-lineages are simultaneously circulating in clinically relevant populations in multiple countries. We correlate the appearance of genotypic macrolide resistance with multiple independently evolved SS14 sub-lineages and show that genotypically resistant and sensitive sub-lineages are spreading contemporaneously. These findings inform our understanding of the current syphilis epidemic by demonstrating how macrolide resistance evolves in Treponema subspecies and provide a warning on broader issues of antimicrobial resistance. Nature Publishing Group UK 2019-07-22 /pmc/articles/PMC6646400/ /pubmed/31332179 http://dx.doi.org/10.1038/s41467-019-11216-7 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Beale, Mathew A. Marks, Michael Sahi, Sharon K. Tantalo, Lauren C. Nori, Achyuta V. French, Patrick Lukehart, Sheila A. Marra, Christina M. Thomson, Nicholas R. Genomic epidemiology of syphilis reveals independent emergence of macrolide resistance across multiple circulating lineages |
title | Genomic epidemiology of syphilis reveals independent emergence of macrolide resistance across multiple circulating lineages |
title_full | Genomic epidemiology of syphilis reveals independent emergence of macrolide resistance across multiple circulating lineages |
title_fullStr | Genomic epidemiology of syphilis reveals independent emergence of macrolide resistance across multiple circulating lineages |
title_full_unstemmed | Genomic epidemiology of syphilis reveals independent emergence of macrolide resistance across multiple circulating lineages |
title_short | Genomic epidemiology of syphilis reveals independent emergence of macrolide resistance across multiple circulating lineages |
title_sort | genomic epidemiology of syphilis reveals independent emergence of macrolide resistance across multiple circulating lineages |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646400/ https://www.ncbi.nlm.nih.gov/pubmed/31332179 http://dx.doi.org/10.1038/s41467-019-11216-7 |
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