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Sex determination systems as the interface between male-killing bacteria and their hosts

Arthropods host a range of sex-ratio-distorting selfish elements, including diverse maternally inherited endosymbionts that solely kill infected males. Male-killing heritable microbes are common, reach high frequency, but until recently have been poorly understood in terms of the host–microbe intera...

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Detalles Bibliográficos
Autores principales: Hornett, Emily A., Kageyama, Daisuke, Hurst, Gregory D. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9005997/
https://www.ncbi.nlm.nih.gov/pubmed/35414231
http://dx.doi.org/10.1098/rspb.2021.2781
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author Hornett, Emily A.
Kageyama, Daisuke
Hurst, Gregory D. D.
author_facet Hornett, Emily A.
Kageyama, Daisuke
Hurst, Gregory D. D.
author_sort Hornett, Emily A.
collection PubMed
description Arthropods host a range of sex-ratio-distorting selfish elements, including diverse maternally inherited endosymbionts that solely kill infected males. Male-killing heritable microbes are common, reach high frequency, but until recently have been poorly understood in terms of the host–microbe interaction. Additionally, while male killing should generate strong selection for host resistance, evidence of this has been scant. The interface of the microbe with host sex determination is integral to the understanding of how death is sex limited and how hosts can evolve evasion of male killing. We first review current knowledge of the mechanisms diverse endosymbionts use to induce male-specific death. We then examine recent evidence that these agents do produce intense selection for host nuclear suppressor elements. We argue, from our understanding of male-killing mechanisms, that suppression will commonly involve evolution of the host sex determination pathways and that the host's response to male-killing microbes thus represents an unrecognized driver of the diversity of arthropod sex determination. Further work is required to identify the genes and mechanisms responsible for male-killing suppression, which will both determine the components of sex determination (or other) systems associated with suppressor evolution, and allow insight into the mechanism of male killing itself.
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spelling pubmed-90059972022-04-20 Sex determination systems as the interface between male-killing bacteria and their hosts Hornett, Emily A. Kageyama, Daisuke Hurst, Gregory D. D. Proc Biol Sci Special Feature Arthropods host a range of sex-ratio-distorting selfish elements, including diverse maternally inherited endosymbionts that solely kill infected males. Male-killing heritable microbes are common, reach high frequency, but until recently have been poorly understood in terms of the host–microbe interaction. Additionally, while male killing should generate strong selection for host resistance, evidence of this has been scant. The interface of the microbe with host sex determination is integral to the understanding of how death is sex limited and how hosts can evolve evasion of male killing. We first review current knowledge of the mechanisms diverse endosymbionts use to induce male-specific death. We then examine recent evidence that these agents do produce intense selection for host nuclear suppressor elements. We argue, from our understanding of male-killing mechanisms, that suppression will commonly involve evolution of the host sex determination pathways and that the host's response to male-killing microbes thus represents an unrecognized driver of the diversity of arthropod sex determination. Further work is required to identify the genes and mechanisms responsible for male-killing suppression, which will both determine the components of sex determination (or other) systems associated with suppressor evolution, and allow insight into the mechanism of male killing itself. The Royal Society 2022-04-13 2022-04-13 /pmc/articles/PMC9005997/ /pubmed/35414231 http://dx.doi.org/10.1098/rspb.2021.2781 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Special Feature
Hornett, Emily A.
Kageyama, Daisuke
Hurst, Gregory D. D.
Sex determination systems as the interface between male-killing bacteria and their hosts
title Sex determination systems as the interface between male-killing bacteria and their hosts
title_full Sex determination systems as the interface between male-killing bacteria and their hosts
title_fullStr Sex determination systems as the interface between male-killing bacteria and their hosts
title_full_unstemmed Sex determination systems as the interface between male-killing bacteria and their hosts
title_short Sex determination systems as the interface between male-killing bacteria and their hosts
title_sort sex determination systems as the interface between male-killing bacteria and their hosts
topic Special Feature
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9005997/
https://www.ncbi.nlm.nih.gov/pubmed/35414231
http://dx.doi.org/10.1098/rspb.2021.2781
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