Pappert Freya Adele, Wüst Vincent Alexander, Fontanes Eguiguren Carmen, Roth Olivia
Marine Evolutionary Biology, Zoological Institute, Christian-Albrechts-Universität Kiel, Kiel, Germany.
Evolutionary Ecology of Marine Fishes, Helmholtz-Centre for Ocean Research Kiel (GEOMAR), Kiel, Germany.
Mol Ecol. 2025 May;34(9):e17754. doi: 10.1111/mec.17754. Epub 2025 Apr 7.
Caloric restriction (CR) studies have traditionally focused on species with conventional reproductive roles, emphasising female's greater investment in costly gametes and parental care. While the divergent impact of CR on males and females is evident across species, the factors driving this variation, that is, resource allocation to reproductive elements as part of distinct life history strategies, remain unclear. To address this, we investigated the effects of CR on development, gene expression and intestinal microbiota in the lined seahorse Hippocampus erectus, a species with male pregnancy, where fathers invest in offspring through gestation. Juvenile seahorses were subjected to ad libitum (AL) or CR feeding for 5 months. CR stunted male growth and brood pouch development, reflecting the energy demands of this crucial parental care trait. However, condition index declined in CR females but not males, while ovarian weight remained unchanged. Transcriptome analysis demonstrated organ- and sex-specific responses to CR with distinct lipid and energy-related pathways activated in male and female livers, indicative of survival enhancement strategies. CR had minimal impact on genes associated with spermatogenesis, but downregulated lipid metabolic and inflammatory genes in ovaries, emphasising the importance of pre-copulatory resource allocation in female gametes. CR strongly shaped gut microbial composition, creating distinct communities from AL seahorses while also driving sex-specific taxonomic differences. Our research indicates that nutrient limitation's impact on males and females is influenced by their allocation of resources to reproduction and parental investment. We underscore the significance of studying species with diverse reproductive strategies, sex roles and life-history strategies.
传统上,热量限制(CR)研究主要集中在具有传统生殖角色的物种上,强调雌性在成本高昂的配子和亲代抚育方面投入更多。虽然CR对雄性和雌性的不同影响在不同物种中很明显,但驱动这种差异的因素,即作为不同生活史策略一部分对生殖要素的资源分配,仍不清楚。为了解决这个问题,我们研究了CR对雄性怀孕的直立海马发育、基因表达和肠道微生物群的影响,在这个物种中,雄性通过怀孕来投资后代。幼年海马接受自由采食(AL)或CR喂养5个月。CR阻碍了雄性的生长和育儿袋发育,反映了这种关键亲代抚育特征的能量需求。然而,CR组雌性的条件指数下降,而雄性没有,同时卵巢重量保持不变。转录组分析表明,CR对器官和性别有特异性反应,雄性和雌性肝脏中不同的脂质和能量相关途径被激活,这表明了生存增强策略。CR对与精子发生相关的基因影响最小,但下调了卵巢中的脂质代谢和炎症基因,强调了雌性配子交配前资源分配的重要性。CR强烈塑造了肠道微生物组成,与AL组海马形成了不同的群落,同时也导致了性别特异性的分类差异。我们的研究表明,营养限制对雄性和雌性的影响受到它们对生殖和亲代投资的资源分配的影响。我们强调研究具有不同生殖策略、性别角色和生活史策略的物种的重要性。