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Metabolic shift in the emergence of hyperinvasive pandemic meningococcal lineages
Hyperinvasive lineages of Neisseria meningitidis, which persist despite extensive horizontal genetic exchange, are a major cause of meningitis and septicaemia worldwide. Over the past 50 years one such lineage of meningococci, known as serogroup A, clonal complex 5 (A:cc5), has caused three successi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5282872/ https://www.ncbi.nlm.nih.gov/pubmed/28112239 http://dx.doi.org/10.1038/srep41126 |
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author | Watkins, Eleanor R. Maiden, Martin C. J. |
author_facet | Watkins, Eleanor R. Maiden, Martin C. J. |
author_sort | Watkins, Eleanor R. |
collection | PubMed |
description | Hyperinvasive lineages of Neisseria meningitidis, which persist despite extensive horizontal genetic exchange, are a major cause of meningitis and septicaemia worldwide. Over the past 50 years one such lineage of meningococci, known as serogroup A, clonal complex 5 (A:cc5), has caused three successive pandemics, including epidemics in sub-Saharan Africa. Although the principal antigens that invoke effective immunity have remained unchanged, distinct A:cc5 epidemic clones have nevertheless emerged. An analysis of whole genome sequence diversity among 153 A:cc5 isolates identified eleven genetic introgression events in the emergence of the epidemic clones, which primarily involved variants of core genes encoding metabolic processes. The acquired DNA was identical to that found over many years in other, unrelated, hyperinvasive meningococci, suggesting that the epidemic clones emerged by acquisition of pre-existing metabolic gene variants, rather than ‘virulence’ associated or antigen-encoding genes. This is consistent with mathematical models which predict the association of transmission fitness with the emergence and maintenance of virulence in recombining commensal organisms. |
format | Online Article Text |
id | pubmed-5282872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52828722017-02-03 Metabolic shift in the emergence of hyperinvasive pandemic meningococcal lineages Watkins, Eleanor R. Maiden, Martin C. J. Sci Rep Article Hyperinvasive lineages of Neisseria meningitidis, which persist despite extensive horizontal genetic exchange, are a major cause of meningitis and septicaemia worldwide. Over the past 50 years one such lineage of meningococci, known as serogroup A, clonal complex 5 (A:cc5), has caused three successive pandemics, including epidemics in sub-Saharan Africa. Although the principal antigens that invoke effective immunity have remained unchanged, distinct A:cc5 epidemic clones have nevertheless emerged. An analysis of whole genome sequence diversity among 153 A:cc5 isolates identified eleven genetic introgression events in the emergence of the epidemic clones, which primarily involved variants of core genes encoding metabolic processes. The acquired DNA was identical to that found over many years in other, unrelated, hyperinvasive meningococci, suggesting that the epidemic clones emerged by acquisition of pre-existing metabolic gene variants, rather than ‘virulence’ associated or antigen-encoding genes. This is consistent with mathematical models which predict the association of transmission fitness with the emergence and maintenance of virulence in recombining commensal organisms. Nature Publishing Group 2017-01-23 /pmc/articles/PMC5282872/ /pubmed/28112239 http://dx.doi.org/10.1038/srep41126 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Watkins, Eleanor R. Maiden, Martin C. J. Metabolic shift in the emergence of hyperinvasive pandemic meningococcal lineages |
title | Metabolic shift in the emergence of hyperinvasive pandemic meningococcal lineages |
title_full | Metabolic shift in the emergence of hyperinvasive pandemic meningococcal lineages |
title_fullStr | Metabolic shift in the emergence of hyperinvasive pandemic meningococcal lineages |
title_full_unstemmed | Metabolic shift in the emergence of hyperinvasive pandemic meningococcal lineages |
title_short | Metabolic shift in the emergence of hyperinvasive pandemic meningococcal lineages |
title_sort | metabolic shift in the emergence of hyperinvasive pandemic meningococcal lineages |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5282872/ https://www.ncbi.nlm.nih.gov/pubmed/28112239 http://dx.doi.org/10.1038/srep41126 |
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