The ancient and helical architecture of Elasmobranchii&apos

[EN] Subclass Elasmobranchii belongs to an old evolutionary class of Chondrichthyes that diverged 450 mya, presenting a wide diversity of reproductive strategies while preserving the ancient mode of internal fertilization. Despite such evolutionary success, many species in this group are at serious...

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Detalles Bibliográficos
Autores: Boryshpolets, Sergii, Dzyuba, Borys, García-Salinas, Pablo, Bloomfield-Gadêlha, Hermes, Sotnikov, Anatoliy, Gallego Albiach, Victor|||0000-0002-9733-0625, Asturiano, Juan F.|||0000-0002-6441-5294
Tipo de recurso: artículo
Fecha de publicación:2025
País:España
Institución:Universitat Politècnica de València (UPV)
Repositorio:RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
Idioma:inglés
OAI Identifier:oai:riunet.upv.es:10251/230577
Acceso en línea:https://riunet.upv.es/handle/10251/230577
Access Level:acceso abierto
Palabra clave:Elasmobranchii
Spermatozoa motility
Helical sperm morphology
Viscosity effects
Spermatozeugmata
Reproductive evolution
14.- Conservar y utilizar de forma sostenible los océanos, mares y recursos marinos para lograr el desarrollo sostenible
Descripción
Sumario:[EN] Subclass Elasmobranchii belongs to an old evolutionary class of Chondrichthyes that diverged 450 mya, presenting a wide diversity of reproductive strategies while preserving the ancient mode of internal fertilization. Despite such evolutionary success, many species in this group are at serious risk of extinction. Understanding the principles of sperm progressive motility and physiology of such an ancient group of vertebrates is crucial for advancing future assisted reproductive techniques to safeguard this species and for deepening our understanding of the evolution of reproduction. Elasmobranchii species possess big spermatozoa (compared to bony fishes) with an elongated helical head and tail similar to one currently existing (but later diverged) in birds, reptiles, and amphibians, which can be considered an evolutionary ancient. These structures may be associated with the necessity to penetrate viscous ovarian fluid or the jelly layer of eggs, suggesting environmental viscosity as the driving pressure shaping large-sized sperm heads into helical shapes through evolution. We observed spermatozoa motility with high-speed video microscopy to capture sperm and flagellar motion in three Elasmobranchii species: the freshwater ray Potamotrygon motoro, the marine skate Raja asterias and the shark Scyliorhinus canicula. We investigated the effect of viscosity on spermatozoa motility parameters and its ability to break free from spermatozeugmata, move progressively, and perform directional changes. After 20 min of observation, the spermatozeugmata conserved their structure in a low viscosity media of 1000 mOsm/kg osmolality. In comparison, no remaining structure of spermatozeugmata could be found in high-viscosity media with 2% methylcellulose (MC) in all three species due to progressive spermatozoa motion. We find that spermatozoa's unique helical head-to-flagellum architecture is specific to promote locomotion in high-viscosity fluid; they cannot move progressively in low viscosity. The highest velocity for shark sperm was observed at 0.75% MC and 1% MC for ray and skate sperm. Viscosity stabilizes the flagellar propagation, producing rotational forces and allowing the helical head to "screw" into the media. Our observations suggest that the surrounding viscosity is critical to allowing spermatozoa progressive motility and enabling spermatozoa to control direction via newly observed head buckling in high viscosity. As such, the viscosity may be a key element controlling and regulating sperm performance and navigation during fertilization in the Elasmobranchii species.