4.7 Article

Proteomic Changes Associated With Sperm Fertilizing Ability in Meat-Type Roosters

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2021.655866

Keywords

sperm; chicken; proteomic; fertility; semen

Funding

  1. French National Infrastructure of Research CRB anim - Investissements d'avenir [ANR-11-INBS-0003]
  2. French National Institute of Agronomic and Environmental Research (INRAe)
  3. European Regional Development Fund (ERDF)
  4. Conseil Regional du Centre
  5. French National Institute of Health and Medical Research (Inserm)

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Using two complementary proteomic methods, this study identified 57 differentially abundant proteins in fertile and subfertile rooster sperm. These proteins are involved in various molecular pathways such as flagellum integrity and movement, mitochondrial functions, sperm maturation, storage in female tract, and oocyte-sperm interaction. The data provides new insights into the complexity of male fertility in chickens and suggests the use of a combination of markers for predicting male fertility.
The molecular basis of male fertility remains unclear, especially in chickens, where decades of genetic selection increased male fertility variability as a side effect. As transcription and translation are highly limited in sperm, proteins are key molecules defining their functionality, making proteomic approaches one of the most adequate methods to investigate sperm capacity. In this context, it is interesting to combine complementary proteomic approaches to maximize the identification of proteins related to sperm-fertilizing ability. In the present study, we aimed at identifying proteins related to fertility in meat-type roosters, showing fertility variability. Fertile roosters (fertility rates higher than 70% after artificial insemination) differed from subfertile roosters (fertility rates lower than 40%) in their sperm mass motility. Fertile and subfertile sperm protein contents were compared using two complementary label-free quantitative proteomic methods: Intact Cell MALDI-TOF-Mass Spectrometry and GeLC-MS/MS. Combining the two strategies, 57 proteins were identified as differentially abundant. Most of them were described for the first time as differentially abundant according to fertility in this species. These proteins were involved in various molecular pathways including flagellum integrity and movement, mitochondrial functions, sperm maturation, and storage in female tract as well as oocyte-sperm interaction. Collectively, our data improved our understanding of chicken sperm biology by revealing new actors involved in the complexity of male fertility that depends on multiple cell functions to reach optimal rates. This explains the inability of reductionist in vitro fertility testing in predicting male fertility and suggests that the use of a combination of markers is a promising approach.

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