Evidence map›Paper›PMID 27829374›Full record

ArticleBMC evolutionary biology2016

The role of prezygotic isolation mechanisms in the divergence of two parasite species.

Tina Henrich, Martin Kalbe

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Article in BMC evolutionary biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Tina HenrichDepartment of Evolutionary Ecology, Max Planck Institute for Evolutionary, Biology, August-Thienemann-Strasse 2, 24306, Plön, Germany. henrich@evolbio.mpg.de.
Martin KalbeDepartment of Evolutionary Ecology, Max Planck Institute for Evolutionary, Biology, August-Thienemann-Strasse 2, 24306, Plön, Germany. kalbe@evolbio.mpg.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe formation of reproductive barriers in diverging lineages is a prerequisite to complete speciation according to the biological species concept. In parasites with complex life cycles, speciation may be driven by adaptation to different intermediate hosts, yet diverging lineages can still share the same definitive host where reproduction takes place. In these cases, prezygotic isolation mechanisms should evolve very early and be particularly strong, preventing costly unfavourable matings. In this study, we investigated the importance of prezygotic barriers to reproduction in two cestode species that diverged 20-25mya and show an extraordinary degree of specificity to different intermediate hosts. Both species share the same definitive hosts and hybridize in the laboratory. Yet, natural hybrids have so far not been detected.

methodsWe used a combination of different experiments to investigate the role of prezygotic barriers to reproduction in the speciation of these parasites. First, we investigated whether hybridization is possible under natural conditions by exposing lab-reared herring gulls (Larus argentatus, the definitive hosts) to both parasites of either sympatric or allopatric combinations. In a second experiment, we tested whether the parasites prefer conspecifics over parasites from a different species in dichotomous mate choice trials.

resultsOur results show that the two species hybridize under natural conditions with parasites originating either from sympatric or allopatric populations producing hybrid offspring. Surprisingly, the mate choice experiment indicated that both parasite species prefer mates of the different species to conspecifics.

conclusionsNeither fundamental constraints against hybridization in a natural host nor assortative mate choice sufficiently explain the persistent segregation of the two tapeworm species in nature. Hence, postzygotic ecological selection against hybrids is presumably the more important driving force limiting gene flow between the two parasite sister species.

Indexed as

Biological EvolutionReproductive IsolationAnimalsCharadriiformesGene FlowGenetic SpeciationHybridization, GeneticMating Preference, AnimalParasitesSympatryTime FactorsZygoteHybridizationMate choiceReproductive isolationSchistocephalus pungitiiSchistocephalus solidusSticklebacks

Identifiers

PMID27829374
PMCPMC5103353

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.