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Evolution of reproductive parasites with direct fitness benefits
Maternally inherited symbionts such as Wolbachia have long been seen mainly as reproductive parasites, with deleterious effects on host fitness. It is becoming clear, however, that, frequently, these symbionts also have beneficial effects on host fitness, either along with reproductive parasitism or...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836592/ https://www.ncbi.nlm.nih.gov/pubmed/29234159 http://dx.doi.org/10.1038/s41437-017-0022-5 |
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author | Zug, Roman Hammerstein, Peter |
author_facet | Zug, Roman Hammerstein, Peter |
author_sort | Zug, Roman |
collection | PubMed |
description | Maternally inherited symbionts such as Wolbachia have long been seen mainly as reproductive parasites, with deleterious effects on host fitness. It is becoming clear, however, that, frequently, these symbionts also have beneficial effects on host fitness, either along with reproductive parasitism or not. Using the examples of cytoplasmic incompatibility (CI) and male-killing (MK), we here analyze the effect of direct fitness benefits on the evolution of reproductive parasites. By means of a simple theoretical framework, we synthesize and extend earlier modeling approaches for CI and MK, which usually ignore fitness benefits. Moreover, our framework is not restricted to a particular mechanism underlying the fitness benefit (e.g., protection against pathogens). We derive invasion conditions and equilibrium frequencies for the different infection scenarios. Our results demonstrate the importance of a symbiont’s “effective fecundity” (i.e., the product of the relative fecundity of an infected female and her transmission efficiency) for a symbiont’s invasion success. In particular, we adopt the concept of effective fecundity to scenarios where CI and MK co-occur in one host population. We confirm that direct fitness benefits substantially facilitate the invasion and spread of infections (for example, by lowering or removing the invasion threshold) or even make invasion possible in the first place (for example, if reproductive parasitism is weak or absent). Finally, we discuss the role of direct fitness benefits in long-term evolutionary dynamics of reproductive phenotypes and highlight their potential to resolve genetic conflicts between maternally inherited symbionts and their hosts. |
format | Online Article Text |
id | pubmed-5836592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-58365922018-03-06 Evolution of reproductive parasites with direct fitness benefits Zug, Roman Hammerstein, Peter Heredity (Edinb) Article Maternally inherited symbionts such as Wolbachia have long been seen mainly as reproductive parasites, with deleterious effects on host fitness. It is becoming clear, however, that, frequently, these symbionts also have beneficial effects on host fitness, either along with reproductive parasitism or not. Using the examples of cytoplasmic incompatibility (CI) and male-killing (MK), we here analyze the effect of direct fitness benefits on the evolution of reproductive parasites. By means of a simple theoretical framework, we synthesize and extend earlier modeling approaches for CI and MK, which usually ignore fitness benefits. Moreover, our framework is not restricted to a particular mechanism underlying the fitness benefit (e.g., protection against pathogens). We derive invasion conditions and equilibrium frequencies for the different infection scenarios. Our results demonstrate the importance of a symbiont’s “effective fecundity” (i.e., the product of the relative fecundity of an infected female and her transmission efficiency) for a symbiont’s invasion success. In particular, we adopt the concept of effective fecundity to scenarios where CI and MK co-occur in one host population. We confirm that direct fitness benefits substantially facilitate the invasion and spread of infections (for example, by lowering or removing the invasion threshold) or even make invasion possible in the first place (for example, if reproductive parasitism is weak or absent). Finally, we discuss the role of direct fitness benefits in long-term evolutionary dynamics of reproductive phenotypes and highlight their potential to resolve genetic conflicts between maternally inherited symbionts and their hosts. Springer International Publishing 2017-12-13 2018-03 /pmc/articles/PMC5836592/ /pubmed/29234159 http://dx.doi.org/10.1038/s41437-017-0022-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License, which permits any non-commercial 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 license, and indicate if changes were made. If you remix, transform, or build upon this article or a part thereof, you must distribute your contributions under the same license as the original. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/. |
spellingShingle | Article Zug, Roman Hammerstein, Peter Evolution of reproductive parasites with direct fitness benefits |
title | Evolution of reproductive parasites with direct fitness benefits |
title_full | Evolution of reproductive parasites with direct fitness benefits |
title_fullStr | Evolution of reproductive parasites with direct fitness benefits |
title_full_unstemmed | Evolution of reproductive parasites with direct fitness benefits |
title_short | Evolution of reproductive parasites with direct fitness benefits |
title_sort | evolution of reproductive parasites with direct fitness benefits |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836592/ https://www.ncbi.nlm.nih.gov/pubmed/29234159 http://dx.doi.org/10.1038/s41437-017-0022-5 |
work_keys_str_mv | AT zugroman evolutionofreproductiveparasiteswithdirectfitnessbenefits AT hammersteinpeter evolutionofreproductiveparasiteswithdirectfitnessbenefits |