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The evolution of cytoplasmic incompatibility types: integrating segregation, inbreeding and outbreeding
Jan Engelstädter1, Sylvain Charlat, Andrew Pomiankowski
1Department of Biology, University College, The Galton Laboratories, London NW1 2HE, United Kingdom. j.engelstaedter@ucl.ac.uk
Insights
Cytoplasmic incompatibility (CI) arises from maternally inherited bacteria. Evolution of new CI types is hindered by inbreeding but facilitated by outbreeding, impacting bacterial strain coexistence.
Area of Science:
- Evolutionary biology
- Microbial genetics
Background:
- Cytoplasmic incompatibility (CI) is a reproductive barrier caused by maternally inherited bacteria like Wolbachia and Cardinium.
- CI typically manifests as reduced offspring viability in crosses between infected males and uninfected females.
- Incompatibility also occurs between individuals carrying different bacterial strains, complicating CI evolution.
Purpose of the Study:
- To model the evolutionary processes driving the emergence of new cytoplasmic incompatibility (CI) types.
- To investigate the impact of bacterial strain segregation and diverse breeding systems on CI evolution.
Main Methods:
- Development of a theoretical model incorporating bacterial strain segregation during maternal transmission.
- Analysis of a spectrum of breeding systems, from inbreeding to outbreeding.
Main Results:
- Bacterial strain segregation makes the co-evolution of new CI types with pre-existing ones unlikely.
- Inbreeding significantly impedes the evolution of novel CI types.
- Outbreeding substantially facilitates the emergence of new CI types.
Conclusions:
- The study provides insights into the evolutionary pathways of cytoplasmic incompatibility.
- Outbreeding systems are more conducive to the diversification of CI.
- The model offers a hypothesis for the evolutionary origins of CI.
Abstract:
Cytoplasmic incompatibility (CI) is a reproductive incompatibility induced by maternally transmitted bacteria of the genera Wolbachia and Cardinium. In the simplest form of CI, offspring from infected males and uninfected females suffer from increased mortality. However, it has been noted that crosses between males and females carrying different strains of infection are often also incompatible. The evolutionary processes leading to the emergence of new CI-compatibility types are still not resolved. Here, we develop a model that extends previous theoretical approaches by including segregation of bacterial strains during transmission as well as a continuum of breeding systems ranging from inbreeding (complete sib mating) to outbreeding (complete sib-mating avoidance). Our results demonstrate that (1) with segregation of strains, evolution is unlikely to lead to new CI types that co-occur as a double infection with the preexisting one, (2) inbreeding substantially hampers the evolution of new CI types, and (3) outbreeding facilitates the evolution of new CI types. Our model also provides a hypothesis on the evolutionary origin of CI.
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