Cargando…
Contrasting within- and between-host immune selection shapes Neisseria Opa repertoires
Pathogen evolution is influenced strongly by the host immune response. Previous studies of the effects of herd immunity on the population structure of directly transmitted, short-lived pathogens have primarily focused on the impact of competition for hosts. In contrast, for long-lived infections lik...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894414/ https://www.ncbi.nlm.nih.gov/pubmed/25296566 http://dx.doi.org/10.1038/srep06554 |
_version_ | 1782435672436506624 |
---|---|
author | Watkins, Eleanor R. Grad, Yonatan H. Gupta, Sunetra Buckee, Caroline O. |
author_facet | Watkins, Eleanor R. Grad, Yonatan H. Gupta, Sunetra Buckee, Caroline O. |
author_sort | Watkins, Eleanor R. |
collection | PubMed |
description | Pathogen evolution is influenced strongly by the host immune response. Previous studies of the effects of herd immunity on the population structure of directly transmitted, short-lived pathogens have primarily focused on the impact of competition for hosts. In contrast, for long-lived infections like HIV, theoretical work has focused on the mechanisms promoting antigenic variation within the host. In reality, successful transmission requires that pathogens balance both within- and between-host immune selection. The Opa adhesins in the bacterial Neisseria genus provide a unique system to study the evolution of the same antigens across two major pathogens: while N. meningitidis is an airborne, respiratory pathogen colonising the nasopharynx relatively transiently, N. gonorrhoeae can cause sexually transmitted, long-lived infections. We use a simple mathematical model and genomic data to show that trade-offs between immune selection pressures within- and between-hosts can explain the contrasting Opa repertoires observed in meningococci and gonococci. |
format | Online Article Text |
id | pubmed-4894414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48944142016-06-10 Contrasting within- and between-host immune selection shapes Neisseria Opa repertoires Watkins, Eleanor R. Grad, Yonatan H. Gupta, Sunetra Buckee, Caroline O. Sci Rep Article Pathogen evolution is influenced strongly by the host immune response. Previous studies of the effects of herd immunity on the population structure of directly transmitted, short-lived pathogens have primarily focused on the impact of competition for hosts. In contrast, for long-lived infections like HIV, theoretical work has focused on the mechanisms promoting antigenic variation within the host. In reality, successful transmission requires that pathogens balance both within- and between-host immune selection. The Opa adhesins in the bacterial Neisseria genus provide a unique system to study the evolution of the same antigens across two major pathogens: while N. meningitidis is an airborne, respiratory pathogen colonising the nasopharynx relatively transiently, N. gonorrhoeae can cause sexually transmitted, long-lived infections. We use a simple mathematical model and genomic data to show that trade-offs between immune selection pressures within- and between-hosts can explain the contrasting Opa repertoires observed in meningococci and gonococci. Nature Publishing Group 2014-10-09 /pmc/articles/PMC4894414/ /pubmed/25296566 http://dx.doi.org/10.1038/srep06554 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Watkins, Eleanor R. Grad, Yonatan H. Gupta, Sunetra Buckee, Caroline O. Contrasting within- and between-host immune selection shapes Neisseria Opa repertoires |
title | Contrasting within- and between-host immune selection shapes Neisseria Opa repertoires |
title_full | Contrasting within- and between-host immune selection shapes Neisseria Opa repertoires |
title_fullStr | Contrasting within- and between-host immune selection shapes Neisseria Opa repertoires |
title_full_unstemmed | Contrasting within- and between-host immune selection shapes Neisseria Opa repertoires |
title_short | Contrasting within- and between-host immune selection shapes Neisseria Opa repertoires |
title_sort | contrasting within- and between-host immune selection shapes neisseria opa repertoires |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894414/ https://www.ncbi.nlm.nih.gov/pubmed/25296566 http://dx.doi.org/10.1038/srep06554 |
work_keys_str_mv | AT watkinseleanorr contrastingwithinandbetweenhostimmuneselectionshapesneisseriaoparepertoires AT gradyonatanh contrastingwithinandbetweenhostimmuneselectionshapesneisseriaoparepertoires AT guptasunetra contrastingwithinandbetweenhostimmuneselectionshapesneisseriaoparepertoires AT buckeecarolineo contrastingwithinandbetweenhostimmuneselectionshapesneisseriaoparepertoires |