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Distributed genotyping and clustering of Neisseria strains reveal continual emergence of epidemic meningococcus over a century
Core genome multilocus sequence typing (cgMLST) is commonly used to classify bacterial strains into different types, for taxonomical and epidemiological applications. However, cgMLST schemes require central databases for the nomenclature of new alleles and sequence types, which must be synchronized...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673917/ https://www.ncbi.nlm.nih.gov/pubmed/38001084 http://dx.doi.org/10.1038/s41467-023-43528-0 |
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author | Zhong, Ling Zhang, Menghan Sun, Libing Yang, Yu Wang, Bo Yang, Haibing Shen, Qiang Xia, Yu Cui, Jiarui Hang, Hui Ren, Yi Pang, Bo Deng, Xiangyu Zhan, Yahui Li, Heng Zhou, Zhemin |
author_facet | Zhong, Ling Zhang, Menghan Sun, Libing Yang, Yu Wang, Bo Yang, Haibing Shen, Qiang Xia, Yu Cui, Jiarui Hang, Hui Ren, Yi Pang, Bo Deng, Xiangyu Zhan, Yahui Li, Heng Zhou, Zhemin |
author_sort | Zhong, Ling |
collection | PubMed |
description | Core genome multilocus sequence typing (cgMLST) is commonly used to classify bacterial strains into different types, for taxonomical and epidemiological applications. However, cgMLST schemes require central databases for the nomenclature of new alleles and sequence types, which must be synchronized worldwide and involve increasingly intensive calculation and storage demands. Here, we describe a distributed cgMLST (dcgMLST) scheme that does not require a central database of allelic sequences and apply it to study evolutionary patterns of epidemic and endemic strains of the genus Neisseria. We classify 69,994 worldwide Neisseria strains into multi-level clusters that assign species, lineages, and local disease outbreaks. We divide Neisseria meningitidis into 168 endemic lineages and three epidemic lineages responsible for at least 9 epidemics in the past century. According to our analyses, the epidemic and endemic lineages experienced very different population dynamics in the past 100 years. Epidemic lineages repetitively emerged from endemic lineages, disseminated worldwide, and apparently disappeared rapidly afterward. We propose a stepwise model for the evolutionary trajectory of epidemic lineages in Neisseria, and expect that the development of similar dcgMLST schemes will facilitate epidemiological studies of other bacterial pathogens. |
format | Online Article Text |
id | pubmed-10673917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106739172023-11-24 Distributed genotyping and clustering of Neisseria strains reveal continual emergence of epidemic meningococcus over a century Zhong, Ling Zhang, Menghan Sun, Libing Yang, Yu Wang, Bo Yang, Haibing Shen, Qiang Xia, Yu Cui, Jiarui Hang, Hui Ren, Yi Pang, Bo Deng, Xiangyu Zhan, Yahui Li, Heng Zhou, Zhemin Nat Commun Article Core genome multilocus sequence typing (cgMLST) is commonly used to classify bacterial strains into different types, for taxonomical and epidemiological applications. However, cgMLST schemes require central databases for the nomenclature of new alleles and sequence types, which must be synchronized worldwide and involve increasingly intensive calculation and storage demands. Here, we describe a distributed cgMLST (dcgMLST) scheme that does not require a central database of allelic sequences and apply it to study evolutionary patterns of epidemic and endemic strains of the genus Neisseria. We classify 69,994 worldwide Neisseria strains into multi-level clusters that assign species, lineages, and local disease outbreaks. We divide Neisseria meningitidis into 168 endemic lineages and three epidemic lineages responsible for at least 9 epidemics in the past century. According to our analyses, the epidemic and endemic lineages experienced very different population dynamics in the past 100 years. Epidemic lineages repetitively emerged from endemic lineages, disseminated worldwide, and apparently disappeared rapidly afterward. We propose a stepwise model for the evolutionary trajectory of epidemic lineages in Neisseria, and expect that the development of similar dcgMLST schemes will facilitate epidemiological studies of other bacterial pathogens. Nature Publishing Group UK 2023-11-24 /pmc/articles/PMC10673917/ /pubmed/38001084 http://dx.doi.org/10.1038/s41467-023-43528-0 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhong, Ling Zhang, Menghan Sun, Libing Yang, Yu Wang, Bo Yang, Haibing Shen, Qiang Xia, Yu Cui, Jiarui Hang, Hui Ren, Yi Pang, Bo Deng, Xiangyu Zhan, Yahui Li, Heng Zhou, Zhemin Distributed genotyping and clustering of Neisseria strains reveal continual emergence of epidemic meningococcus over a century |
title | Distributed genotyping and clustering of Neisseria strains reveal continual emergence of epidemic meningococcus over a century |
title_full | Distributed genotyping and clustering of Neisseria strains reveal continual emergence of epidemic meningococcus over a century |
title_fullStr | Distributed genotyping and clustering of Neisseria strains reveal continual emergence of epidemic meningococcus over a century |
title_full_unstemmed | Distributed genotyping and clustering of Neisseria strains reveal continual emergence of epidemic meningococcus over a century |
title_short | Distributed genotyping and clustering of Neisseria strains reveal continual emergence of epidemic meningococcus over a century |
title_sort | distributed genotyping and clustering of neisseria strains reveal continual emergence of epidemic meningococcus over a century |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673917/ https://www.ncbi.nlm.nih.gov/pubmed/38001084 http://dx.doi.org/10.1038/s41467-023-43528-0 |
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