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...

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Main Authors: Watkins, E, Grad, Y, Gupta, S, Buckee, C
Format: Journal article
Language:English
Published: Nature Publishing Group 2014
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author Watkins, E
Grad, Y
Gupta, S
Buckee, C
author_facet Watkins, E
Grad, Y
Gupta, S
Buckee, C
author_sort Watkins, E
collection OXFORD
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.
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spelling oxford-uuid:a85319a0-8b5d-4468-be64-f31520fdd6732022-03-27T03:00:38ZContrasting within- and between-host immune selection shapes Neisseria Opa repertoiresJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:a85319a0-8b5d-4468-be64-f31520fdd673EnglishSymplectic Elements at OxfordNature Publishing Group2014Watkins, EGrad, YGupta, SBuckee, CPathogen 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.
spellingShingle Watkins, E
Grad, Y
Gupta, S
Buckee, C
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
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