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The spread of incompatibility-inducing parasites in sub-divided host populations

BACKGROUND: Maternally transmitted symbionts have evolved a variety of ways to promote their spread through host populations. One strategy is to hamper the reproduction of uninfected females by a mechanism called cytoplasmic incompatibility (CI). CI occurs in crosses between infected males and uninf...

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Autores principales: Reuter, Max, Lehmann, Laurent, Guillaume, Frédéric
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2396168/
https://www.ncbi.nlm.nih.gov/pubmed/18460188
http://dx.doi.org/10.1186/1471-2148-8-134
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author Reuter, Max
Lehmann, Laurent
Guillaume, Frédéric
author_facet Reuter, Max
Lehmann, Laurent
Guillaume, Frédéric
author_sort Reuter, Max
collection PubMed
description BACKGROUND: Maternally transmitted symbionts have evolved a variety of ways to promote their spread through host populations. One strategy is to hamper the reproduction of uninfected females by a mechanism called cytoplasmic incompatibility (CI). CI occurs in crosses between infected males and uninfected females and leads to partial to near-complete infertility. CI-infections are under positive frequency-dependent selection and require genetic drift to overcome the range of low frequencies where they are counter-selected. Given the importance of drift, population sub-division would be expected to facilitate the spread of CI. Nevertheless, a previous model concluded that variance in infection between competing groups of breeding individuals impedes the spread of CI. RESULTS: In this paper we derive a model on the spread of CI-infections in populations composed of demes linked by restricted migration. Our model shows that population sub-division facilitates the invasion of CI. While host philopatry (low migration) favours the spread of infection, deme size has a non-monotonous effect, with CI-invasion being most likely at intermediate deme size. Individual-based simulations confirm these predictions and show that high levels of local drift speed up invasion but prevent high levels of prevalence across the entire population. Additional simulations with sex-specific migration rates further show that low migration rates of both sexes are required to facilitate the spread of CI. CONCLUSION: Our analyses show that population structure facilitates the invasion of CI-infections. Since some level of sub-division is likely to occur in most natural populations, our results help to explain the high incidence of CI-infections across species of arthropods. Furthermore, our work has important implications for the use of CI-systems in order to genetically modify natural populations of disease vectors.
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spelling pubmed-23961682008-05-28 The spread of incompatibility-inducing parasites in sub-divided host populations Reuter, Max Lehmann, Laurent Guillaume, Frédéric BMC Evol Biol Research Article BACKGROUND: Maternally transmitted symbionts have evolved a variety of ways to promote their spread through host populations. One strategy is to hamper the reproduction of uninfected females by a mechanism called cytoplasmic incompatibility (CI). CI occurs in crosses between infected males and uninfected females and leads to partial to near-complete infertility. CI-infections are under positive frequency-dependent selection and require genetic drift to overcome the range of low frequencies where they are counter-selected. Given the importance of drift, population sub-division would be expected to facilitate the spread of CI. Nevertheless, a previous model concluded that variance in infection between competing groups of breeding individuals impedes the spread of CI. RESULTS: In this paper we derive a model on the spread of CI-infections in populations composed of demes linked by restricted migration. Our model shows that population sub-division facilitates the invasion of CI. While host philopatry (low migration) favours the spread of infection, deme size has a non-monotonous effect, with CI-invasion being most likely at intermediate deme size. Individual-based simulations confirm these predictions and show that high levels of local drift speed up invasion but prevent high levels of prevalence across the entire population. Additional simulations with sex-specific migration rates further show that low migration rates of both sexes are required to facilitate the spread of CI. CONCLUSION: Our analyses show that population structure facilitates the invasion of CI-infections. Since some level of sub-division is likely to occur in most natural populations, our results help to explain the high incidence of CI-infections across species of arthropods. Furthermore, our work has important implications for the use of CI-systems in order to genetically modify natural populations of disease vectors. BioMed Central 2008-05-06 /pmc/articles/PMC2396168/ /pubmed/18460188 http://dx.doi.org/10.1186/1471-2148-8-134 Text en Copyright ©2008 Reuter et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Reuter, Max
Lehmann, Laurent
Guillaume, Frédéric
The spread of incompatibility-inducing parasites in sub-divided host populations
title The spread of incompatibility-inducing parasites in sub-divided host populations
title_full The spread of incompatibility-inducing parasites in sub-divided host populations
title_fullStr The spread of incompatibility-inducing parasites in sub-divided host populations
title_full_unstemmed The spread of incompatibility-inducing parasites in sub-divided host populations
title_short The spread of incompatibility-inducing parasites in sub-divided host populations
title_sort spread of incompatibility-inducing parasites in sub-divided host populations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2396168/
https://www.ncbi.nlm.nih.gov/pubmed/18460188
http://dx.doi.org/10.1186/1471-2148-8-134
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