Cargando…

Novel genetic sex markers reveal unexpected lack of, and similar susceptibility to, sex reversal in free‐living common toads in both natural and anthropogenic habitats

Anthropogenic environmental changes are affecting biodiversity and microevolution worldwide. Ectothermic vertebrates are especially vulnerable because environmental changes can disrupt their sexual development and cause sex reversal, a mismatch between genetic and phenotypic sex. This can potentiall...

Descripción completa

Detalles Bibliográficos
Autores principales: Nemesházi, Edina, Sramkó, Gábor, Laczkó, Levente, Balogh, Emese, Szatmári, Lajos, Vili, Nóra, Ujhegyi, Nikolett, Üveges, Bálint, Bókony, Veronika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544883/
https://www.ncbi.nlm.nih.gov/pubmed/35146823
http://dx.doi.org/10.1111/mec.16388
_version_ 1784804697249415168
author Nemesházi, Edina
Sramkó, Gábor
Laczkó, Levente
Balogh, Emese
Szatmári, Lajos
Vili, Nóra
Ujhegyi, Nikolett
Üveges, Bálint
Bókony, Veronika
author_facet Nemesházi, Edina
Sramkó, Gábor
Laczkó, Levente
Balogh, Emese
Szatmári, Lajos
Vili, Nóra
Ujhegyi, Nikolett
Üveges, Bálint
Bókony, Veronika
author_sort Nemesházi, Edina
collection PubMed
description Anthropogenic environmental changes are affecting biodiversity and microevolution worldwide. Ectothermic vertebrates are especially vulnerable because environmental changes can disrupt their sexual development and cause sex reversal, a mismatch between genetic and phenotypic sex. This can potentially lead to sex‐ratio distortion and population decline. Despite these implications, there is scarce empirical knowledge on the incidence of sex reversal in nature. Populations in anthropogenic environments may be exposed to sex‐reversing stimuli more frequently, which may lead to higher sex‐reversal rate or, alternatively, these populations may adapt to resist sex reversal. We developed PCR‐based genetic sex markers for the common toad (Bufo bufo) to assess the prevalence of sex reversal in wild populations living in natural, agricultural and urban habitats, and the susceptibility of the same populations to two ubiquitous oestrogenic pollutants in a common garden experiment. We found negligible sex‐reversal frequency in free‐living adults despite the presence of various endocrine‐disrupting pollutants in their breeding ponds. Individuals from different habitat types showed similar susceptibility to sex reversal in the laboratory: all genetic males developed female phenotype when exposed to 1 µg L(−1) 17α‐ethinylestradiol (EE2) during larval development, whereas no sex reversal occurred in response to 1 ng L(−1) EE2 and a glyphosate‐based herbicide with 3 µg L(−1) or 3 mg L(−1) glyphosate. The latter results do not support that populations in anthropogenic habitats would have either increased propensity for or higher tolerance to chemically induced sex reversal. Thus, the extremely low sex‐reversal frequency in wild toads compared to other ectothermic vertebrates studied before might indicate idiosyncratic, potentially species‐specific resistance to sex reversal.
format Online
Article
Text
id pubmed-9544883
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-95448832022-10-14 Novel genetic sex markers reveal unexpected lack of, and similar susceptibility to, sex reversal in free‐living common toads in both natural and anthropogenic habitats Nemesházi, Edina Sramkó, Gábor Laczkó, Levente Balogh, Emese Szatmári, Lajos Vili, Nóra Ujhegyi, Nikolett Üveges, Bálint Bókony, Veronika Mol Ecol ORIGINAL ARTICLES Anthropogenic environmental changes are affecting biodiversity and microevolution worldwide. Ectothermic vertebrates are especially vulnerable because environmental changes can disrupt their sexual development and cause sex reversal, a mismatch between genetic and phenotypic sex. This can potentially lead to sex‐ratio distortion and population decline. Despite these implications, there is scarce empirical knowledge on the incidence of sex reversal in nature. Populations in anthropogenic environments may be exposed to sex‐reversing stimuli more frequently, which may lead to higher sex‐reversal rate or, alternatively, these populations may adapt to resist sex reversal. We developed PCR‐based genetic sex markers for the common toad (Bufo bufo) to assess the prevalence of sex reversal in wild populations living in natural, agricultural and urban habitats, and the susceptibility of the same populations to two ubiquitous oestrogenic pollutants in a common garden experiment. We found negligible sex‐reversal frequency in free‐living adults despite the presence of various endocrine‐disrupting pollutants in their breeding ponds. Individuals from different habitat types showed similar susceptibility to sex reversal in the laboratory: all genetic males developed female phenotype when exposed to 1 µg L(−1) 17α‐ethinylestradiol (EE2) during larval development, whereas no sex reversal occurred in response to 1 ng L(−1) EE2 and a glyphosate‐based herbicide with 3 µg L(−1) or 3 mg L(−1) glyphosate. The latter results do not support that populations in anthropogenic habitats would have either increased propensity for or higher tolerance to chemically induced sex reversal. Thus, the extremely low sex‐reversal frequency in wild toads compared to other ectothermic vertebrates studied before might indicate idiosyncratic, potentially species‐specific resistance to sex reversal. John Wiley and Sons Inc. 2022-02-24 2022-04 /pmc/articles/PMC9544883/ /pubmed/35146823 http://dx.doi.org/10.1111/mec.16388 Text en © 2022 The Authors. Molecular Ecology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle ORIGINAL ARTICLES
Nemesházi, Edina
Sramkó, Gábor
Laczkó, Levente
Balogh, Emese
Szatmári, Lajos
Vili, Nóra
Ujhegyi, Nikolett
Üveges, Bálint
Bókony, Veronika
Novel genetic sex markers reveal unexpected lack of, and similar susceptibility to, sex reversal in free‐living common toads in both natural and anthropogenic habitats
title Novel genetic sex markers reveal unexpected lack of, and similar susceptibility to, sex reversal in free‐living common toads in both natural and anthropogenic habitats
title_full Novel genetic sex markers reveal unexpected lack of, and similar susceptibility to, sex reversal in free‐living common toads in both natural and anthropogenic habitats
title_fullStr Novel genetic sex markers reveal unexpected lack of, and similar susceptibility to, sex reversal in free‐living common toads in both natural and anthropogenic habitats
title_full_unstemmed Novel genetic sex markers reveal unexpected lack of, and similar susceptibility to, sex reversal in free‐living common toads in both natural and anthropogenic habitats
title_short Novel genetic sex markers reveal unexpected lack of, and similar susceptibility to, sex reversal in free‐living common toads in both natural and anthropogenic habitats
title_sort novel genetic sex markers reveal unexpected lack of, and similar susceptibility to, sex reversal in free‐living common toads in both natural and anthropogenic habitats
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544883/
https://www.ncbi.nlm.nih.gov/pubmed/35146823
http://dx.doi.org/10.1111/mec.16388
work_keys_str_mv AT nemeshaziedina novelgeneticsexmarkersrevealunexpectedlackofandsimilarsusceptibilitytosexreversalinfreelivingcommontoadsinbothnaturalandanthropogenichabitats
AT sramkogabor novelgeneticsexmarkersrevealunexpectedlackofandsimilarsusceptibilitytosexreversalinfreelivingcommontoadsinbothnaturalandanthropogenichabitats
AT laczkolevente novelgeneticsexmarkersrevealunexpectedlackofandsimilarsusceptibilitytosexreversalinfreelivingcommontoadsinbothnaturalandanthropogenichabitats
AT baloghemese novelgeneticsexmarkersrevealunexpectedlackofandsimilarsusceptibilitytosexreversalinfreelivingcommontoadsinbothnaturalandanthropogenichabitats
AT szatmarilajos novelgeneticsexmarkersrevealunexpectedlackofandsimilarsusceptibilitytosexreversalinfreelivingcommontoadsinbothnaturalandanthropogenichabitats
AT vilinora novelgeneticsexmarkersrevealunexpectedlackofandsimilarsusceptibilitytosexreversalinfreelivingcommontoadsinbothnaturalandanthropogenichabitats
AT ujhegyinikolett novelgeneticsexmarkersrevealunexpectedlackofandsimilarsusceptibilitytosexreversalinfreelivingcommontoadsinbothnaturalandanthropogenichabitats
AT uvegesbalint novelgeneticsexmarkersrevealunexpectedlackofandsimilarsusceptibilitytosexreversalinfreelivingcommontoadsinbothnaturalandanthropogenichabitats
AT bokonyveronika novelgeneticsexmarkersrevealunexpectedlackofandsimilarsusceptibilitytosexreversalinfreelivingcommontoadsinbothnaturalandanthropogenichabitats