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Sperm morphology and performance in relation to postmating prezygotic isolation in two recently diverged passerine species
Divergence in sperm phenotype and female reproductive environment may be a common source of postmating prezygotic (PMPZ) isolation between species. However, compared to other reproductive barriers it has received much less attention. In this study, we examined sperm morphology and velocity in two hy...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789955/ https://www.ncbi.nlm.nih.gov/pubmed/36566302 http://dx.doi.org/10.1038/s41598-022-26101-5 |
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author | Poignet, Manon Baránková, Lucie Reif, Jiří Stopka, Pavel Stopková, Romana Frolikova, Michaela Cramer, Emily R. A. Johnsen, Arild Kverek, Pavel Osiejuk, Tomasz S. Komrskova, Katerina Albrecht, Tomáš Reifová, Radka |
author_facet | Poignet, Manon Baránková, Lucie Reif, Jiří Stopka, Pavel Stopková, Romana Frolikova, Michaela Cramer, Emily R. A. Johnsen, Arild Kverek, Pavel Osiejuk, Tomasz S. Komrskova, Katerina Albrecht, Tomáš Reifová, Radka |
author_sort | Poignet, Manon |
collection | PubMed |
description | Divergence in sperm phenotype and female reproductive environment may be a common source of postmating prezygotic (PMPZ) isolation between species. However, compared to other reproductive barriers it has received much less attention. In this study, we examined sperm morphology and velocity in two hybridizing passerine species, the common nightingale (Luscinia megarhynchos) and thrush nightingale (L. luscinia). In addition, we for the first time characterized a passerine female reproductive tract fluid proteome. We demonstrate that spermatozoa of the common nightingale have significantly longer and wider midpiece (proximal part of the flagellum containing mitochondria) and longer tail compared to spermatozoa of thrush nightingale. On the other hand, they have significantly shorter and narrower acrosome. Importantly, these differences did not have any effect on sperm velocity. Furthermore, the fluid from the reproductive tract of common nightingale females did not differentially affect velocity of conspecific and heterospecific sperm. Our results indicate that the observed changes in the flagellum and acrosome size are unlikely to contribute to PMPZ isolation through differential sperm velocity of conspecific and heterospecific sperm in the female reproductive tract. However, they could affect other postcopulatory processes, which might be involved in PMPZ isolation, such as sperm storage, longevity or sperm-egg interaction. |
format | Online Article Text |
id | pubmed-9789955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97899552022-12-26 Sperm morphology and performance in relation to postmating prezygotic isolation in two recently diverged passerine species Poignet, Manon Baránková, Lucie Reif, Jiří Stopka, Pavel Stopková, Romana Frolikova, Michaela Cramer, Emily R. A. Johnsen, Arild Kverek, Pavel Osiejuk, Tomasz S. Komrskova, Katerina Albrecht, Tomáš Reifová, Radka Sci Rep Article Divergence in sperm phenotype and female reproductive environment may be a common source of postmating prezygotic (PMPZ) isolation between species. However, compared to other reproductive barriers it has received much less attention. In this study, we examined sperm morphology and velocity in two hybridizing passerine species, the common nightingale (Luscinia megarhynchos) and thrush nightingale (L. luscinia). In addition, we for the first time characterized a passerine female reproductive tract fluid proteome. We demonstrate that spermatozoa of the common nightingale have significantly longer and wider midpiece (proximal part of the flagellum containing mitochondria) and longer tail compared to spermatozoa of thrush nightingale. On the other hand, they have significantly shorter and narrower acrosome. Importantly, these differences did not have any effect on sperm velocity. Furthermore, the fluid from the reproductive tract of common nightingale females did not differentially affect velocity of conspecific and heterospecific sperm. Our results indicate that the observed changes in the flagellum and acrosome size are unlikely to contribute to PMPZ isolation through differential sperm velocity of conspecific and heterospecific sperm in the female reproductive tract. However, they could affect other postcopulatory processes, which might be involved in PMPZ isolation, such as sperm storage, longevity or sperm-egg interaction. Nature Publishing Group UK 2022-12-24 /pmc/articles/PMC9789955/ /pubmed/36566302 http://dx.doi.org/10.1038/s41598-022-26101-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Poignet, Manon Baránková, Lucie Reif, Jiří Stopka, Pavel Stopková, Romana Frolikova, Michaela Cramer, Emily R. A. Johnsen, Arild Kverek, Pavel Osiejuk, Tomasz S. Komrskova, Katerina Albrecht, Tomáš Reifová, Radka Sperm morphology and performance in relation to postmating prezygotic isolation in two recently diverged passerine species |
title | Sperm morphology and performance in relation to postmating prezygotic isolation in two recently diverged passerine species |
title_full | Sperm morphology and performance in relation to postmating prezygotic isolation in two recently diverged passerine species |
title_fullStr | Sperm morphology and performance in relation to postmating prezygotic isolation in two recently diverged passerine species |
title_full_unstemmed | Sperm morphology and performance in relation to postmating prezygotic isolation in two recently diverged passerine species |
title_short | Sperm morphology and performance in relation to postmating prezygotic isolation in two recently diverged passerine species |
title_sort | sperm morphology and performance in relation to postmating prezygotic isolation in two recently diverged passerine species |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789955/ https://www.ncbi.nlm.nih.gov/pubmed/36566302 http://dx.doi.org/10.1038/s41598-022-26101-5 |
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