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Published on: March 15, 2018
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Lifetime inbreeding depression, purging, and mating system evolution in a simultaneous hermaphrodite tapeworm
Daniel P Benesh1, Friederike Weinreich, Martin Kalbe
1Department of Evolutionary Ecology, Max Planck Institute for Evolutionary Biology, August-Thienemann-Strasse 2, 24306 Plön, Germany. daniel.benesh@lifesci.ucsb.edu.
Evolution; International Journal of Organic Evolution
|March 12, 2014
Summary
Inbreeding depression (ID) severely impacts tapeworm fitness after self-fertilization, but purging of deleterious alleles occurs over generations. This suggests severe ID may prevent a complete shift to selfing in this parasite.
Area of Science:
- Evolutionary biology
- Genetics
- Parasitology
Background:
- Mating system evolution in simultaneous hermaphrodites is typically predicted to favor either outcrossing or self-fertilization based on inbreeding depression (ID) levels.
- However, many species exhibit a mixed mating system, with tapeworms like Schistocephalus solidus self-fertilizing some eggs despite experiencing ID.
- The evolutionary success of selfing depends on the fitness of selfed offspring and the capacity to purge genetic load.
Purpose of the Study:
- To investigate the fitness consequences of two consecutive generations of selfing in Schistocephalus solidus.
- To determine the extent of inbreeding depression and the potential for purging deleterious alleles in this parasitic tapeworm.
Main Methods:
- Breeding Schistocephalus solidus through two successive generations of self-fertilization.
- Measuring various fitness correlates across the entire life cycle for both selfed and outcrossed progeny.
- Quantifying inbreeding depression and estimating the load of lethal equivalents.
Main Results:
- One generation of selfing resulted in pronounced inbreeding depression, with selfed progeny exhibiting only 9% of the lifetime fitness of outcrossed controls, particularly affecting early-life traits.
- A second generation of selfing showed a significant reduction in ID across several traits, with a 48% decrease in the estimated load of lethal equivalents, indicating purging of deleterious recessive alleles.
- Despite purging, inbreeding depression remained substantial, suggesting it could impede a complete transition to self-fertilization.
Conclusions:
- Severe inbreeding depression, even with purging, likely prevents obligate selfing in Schistocephalus solidus.
- While purging of deleterious alleles occurs, the persistent high ID suggests limitations on the spread of self-fertilization.
- The possibility of undetected benefits of low-level selfing cannot be entirely ruled out.

