Viviparity and habitat restrictions may influence the evolution of male reproductive genes in tsetse fly (Glossina) species.

Glossina Habitat Male accessory gland genes Selective pressure Testis genes Viviparity

Journal

BMC biology
ISSN: 1741-7007
Titre abrégé: BMC Biol
Pays: England
ID NLM: 101190720

Informations de publication

Date de publication:
23 09 2021
Historique:
received: 28 04 2021
accepted: 06 09 2021
entrez: 24 9 2021
pubmed: 25 9 2021
medline: 2 2 2022
Statut: epublish

Résumé

Glossina species (tsetse flies), the sole vectors of African trypanosomes, maintained along their long evolutionary history a unique reproductive strategy, adenotrophic viviparity. Viviparity reduces their reproductive rate and, as such, imposes strong selective pressures on males for reproductive success. These species live in sub-Saharan Africa, where the distributions of the main sub-genera Fusca, Morsitans, and Palpalis are restricted to forest, savannah, and riverine habitats, respectively. Here we aim at identifying the evolutionary patterns of the male reproductive genes of six species belonging to these three main sub-genera. We then interpreted the different patterns we found across the species in the light of viviparity and the specific habitat restrictions, which are known to shape reproductive behavior. We used a comparative genomic approach to build consensus evolutionary trees that portray the selective pressure acting on the male reproductive genes in these lineages. Such trees reflect the long and divergent demographic history that led to an allopatric distribution of the Fusca, Morsitans, and Palpalis species groups. A dataset of over 1700 male reproductive genes remained conserved over the long evolutionary time scale (estimated at 26.7 million years) across the genomes of the six species. We suggest that this conservation may result from strong functional selective pressure on the male imposed by viviparity. It is noteworthy that more than half of these conserved genes are novel sequences that are unique to the Glossina genus and are candidates for selection in the different lineages. Tsetse flies represent a model to interpret the evolution and differentiation of male reproductive biology under different, but complementary, perspectives. In the light of viviparity, we must take into account that these genes are constrained by a post-fertilization arena for genomic conflicts created by viviparity and absent in ovipositing species. This constraint implies a continuous antagonistic co-evolution between the parental genomes, thus accelerating inter-population post-zygotic isolation and, ultimately, favoring speciation. Ecological restrictions that affect reproductive behavior may further shape such antagonistic co-evolution.

Sections du résumé

BACKGROUND
Glossina species (tsetse flies), the sole vectors of African trypanosomes, maintained along their long evolutionary history a unique reproductive strategy, adenotrophic viviparity. Viviparity reduces their reproductive rate and, as such, imposes strong selective pressures on males for reproductive success. These species live in sub-Saharan Africa, where the distributions of the main sub-genera Fusca, Morsitans, and Palpalis are restricted to forest, savannah, and riverine habitats, respectively. Here we aim at identifying the evolutionary patterns of the male reproductive genes of six species belonging to these three main sub-genera. We then interpreted the different patterns we found across the species in the light of viviparity and the specific habitat restrictions, which are known to shape reproductive behavior.
RESULTS
We used a comparative genomic approach to build consensus evolutionary trees that portray the selective pressure acting on the male reproductive genes in these lineages. Such trees reflect the long and divergent demographic history that led to an allopatric distribution of the Fusca, Morsitans, and Palpalis species groups. A dataset of over 1700 male reproductive genes remained conserved over the long evolutionary time scale (estimated at 26.7 million years) across the genomes of the six species. We suggest that this conservation may result from strong functional selective pressure on the male imposed by viviparity. It is noteworthy that more than half of these conserved genes are novel sequences that are unique to the Glossina genus and are candidates for selection in the different lineages.
CONCLUSIONS
Tsetse flies represent a model to interpret the evolution and differentiation of male reproductive biology under different, but complementary, perspectives. In the light of viviparity, we must take into account that these genes are constrained by a post-fertilization arena for genomic conflicts created by viviparity and absent in ovipositing species. This constraint implies a continuous antagonistic co-evolution between the parental genomes, thus accelerating inter-population post-zygotic isolation and, ultimately, favoring speciation. Ecological restrictions that affect reproductive behavior may further shape such antagonistic co-evolution.

Identifiants

pubmed: 34556101
doi: 10.1186/s12915-021-01148-4
pii: 10.1186/s12915-021-01148-4
pmc: PMC8461966
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

211

Subventions

Organisme : NIAID NIH HHS
ID : R21 AI109263
Pays : United States
Organisme : NIH HHS
ID : AI128523
Pays : United States
Organisme : FIC NIH HHS
ID : D43 TW007391
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI128523
Pays : United States
Organisme : NIH HHS
ID : AI109263-01
Pays : United States

Informations de copyright

© 2021. The Author(s).

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Auteurs

Grazia Savini (G)

Department of Biology and Biotechnology, University of Pavia, Pavia, Italy.

Francesca Scolari (F)

Department of Biology and Biotechnology, University of Pavia, Pavia, Italy.
Institute of Molecular Genetics IGM-CNR "Luigi Luca Cavalli-Sforza", Pavia, Italy.

Lino Ometto (L)

Department of Biology and Biotechnology, University of Pavia, Pavia, Italy.

Omar Rota-Stabelli (O)

Research and Innovation Centre, Fondazione Edmund Mach (FEM), San Michele all'Adige, Italy.
Center Agriculture Food Environment (C3A), University of Trento, Trento, Italy.

Davide Carraretto (D)

Department of Biology and Biotechnology, University of Pavia, Pavia, Italy.

Ludvik M Gomulski (LM)

Department of Biology and Biotechnology, University of Pavia, Pavia, Italy.

Giuliano Gasperi (G)

Department of Biology and Biotechnology, University of Pavia, Pavia, Italy.

Adly M M Abd-Alla (AMM)

Insect Pest Control Laboratory, Joint FAO/IAEA Programme of Nuclear Techniques in Food & Agriculture, Vienna, Vienna, Austria. A.M.M.Abd-Alla@iaea.org.

Serap Aksoy (S)

Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.

Geoffrey M Attardo (GM)

Department of Entomology and Nematology, University of California, Davis, Davis, CA, USA.

Anna R Malacrida (AR)

Department of Biology and Biotechnology, University of Pavia, Pavia, Italy. malacrid@unipv.it.

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