Molecular basis of the short- and long-term osmoregulation capability in the euryhaline unicellular eukaryote Paramecium calkinsi

assembled high-quality genome, comparative genomic analysis across 17 species revealed an expansion of osmoregulatory genes, identifying 195 expanded gene families implicated in oxidoreductase activity, ion binding, and transmembrane transport. Transcriptomic analysis under varying salinity treatments revealed distinct molecular foundations that underpin transient and sustained adaptation to hyperosmotic and hypoosmotic stress. Under hyperosmotic conditions, cells exhibit a rapid activation of the membrane transport system in the short term, whereas long-term adaptation features enhanced ribosome biogenesis, chromatin remodeling, activation of transport systems, and metabolic downregulation to optimize energy use. For hypoosmotic stress, short-term adaptation is characterized by specific hydrolysis of intracellular substances, while long-term adaptation involves sustained oxidoreductase activation and enhanced vesicular/proton transport to maintain oxidative balance and cellular homeostasis. Moreover, we found that genes involved in signaling, transport, and protein stability pathways exhibit high rates of alternative splicing, suggesting a potential role of mRNA splicing in osmoregulation. Our findings provide molecular insights into osmoregulation in unicellular eukaryotes, highlighting their unique genetic responses to transient and sustained salinity stress and offering a valuable starting point for future functional studies.IMPORTANCEEuryhaline species exhibit significant adaptability to different salinities. This study elucidates how a single-celled euryhaline eukaryote navigates both transient and sustained salinity shifts at the molecular level. Comparative genomic analysis revealed that this organism expanded 195 gene families involved in ion transport and stress response. Transcriptomic analysis revealed distinct molecular foundations that underpin its transient and sustained adaptation to salinity stress. For high salinity, it transiently activates membrane transport systems, while long-term adaptation focuses on reprogramming metabolism to optimize energy use. In response to low salinity, the short-term response involves hydrolyzing intracellular materials, followed by the long-term activation of protective mechanisms. Additionally, alternative splicing fine-tunes genes involved in signaling and transport. These findings reveal unique genetic and cellular adaptation to salinity fluctuations in unicellular eukaryotes and establish a valuable resource for future functional investigations.