Search

The tremendous expansion of Chinese abalone production has not been without challenges such as low salinity stress, which may occur during severe summer rainstorms and typhoon events. Interspecific hybrids have, however, been of great use to the aquaculture industry in withstanding environmental stresses. This study adopted the non-invasive method of measuring heart rate to monitor the cardiac performance of the Pacific abalone and two of its interspecific hybrids during the incidence of continuous salinity decrease. The results showed that low salinity significantly influences the heart rate of abalone. Fluctuation in the abalone’s heartbeat suggests a pattern with three phases and two breakpoints of salinity (BOS1 and BOS2). BOS1 represents an isosmotic point, and BOS2 represents lethal salinity. We argue that relatively lower BOS suggests better tolerance to low salinity, and long-term exposure to salinities around BOS2 could be detrimental to all three species. The hybrid H. discus hannai ♀ x H. fulgens ♂ (DF) recorded the lowest BOS1 and BOS2, which was also significantly different (P = 0.01) from DD at BOS1, suggesting a better tolerance potential for low salinities than the other species. Altogether, our data establish species-specific BOS and reveal the cardiac mechanism by which abalone responds to low salinity. The results confirm that the non-invasive heart rate detection method could likewise be adopted to define critical salinities for abalone, and hybridization could be a potential method to breed the more stress-resilient aquatic animals.

Background Transcriptome sequencing is an effective tool to reveal the essential genes and pathways underlying countless biotic and abiotic stress adaptation mechanisms. Although severely challenged by diverse environmental conditions, the Pacific abalone Haliotis discus hannai remains a high-value aquaculture mollusk and a Chinese predominantly cultured abalone species. Salinity is one of such environmental factors whose fluctuation could significantly affect the abalone’s cellular and molecular immune responses and result in high mortality and reduced growth rate during prolonged exposure. Meanwhile, hybrids have shown superiority in tolerating diverse environmental stresses over their purebred counterparts and have gained admiration in the Chinese abalone aquaculture industry. The objective of this study was to investigate the molecular and cellular mechanisms of low salinity adaptation in abalone. Therefore, this study used transcriptome analysis of the gill tissues and flow cytometric analysis of hemolymph of H. discus hannai (DD) and interspecific hybrid H. discus hannai ♀ x H. fulgens ♂ (DF) during low salinity exposure. Also, the survival and growth rate of the species under various salinities were assessed. Results The transcriptome data revealed that the differentially expressed genes (DEGs) were significantly enriched on the fluid shear stress and atherosclerosis (FSS) pathway. Meanwhile, the expression profiles of some essential genes involved in this pathway suggest that abalone significantly up-regulated calmodulin-4 (CaM-4) and heat-shock protein90 (HSP90), and significantly down-regulated tumor necrosis factor (TNF), bone morphogenetic protein-4 (BMP-4), and nuclear factor kappa B (NF-kB). Also, the hybrid DF showed significantly higher and sustained expression of CaM and HSP90, significantly higher phagocytosis, significantly lower hemocyte mortality, and significantly higher survival at low salinity, suggesting a more active molecular and hemocyte-mediated immune response and a more efficient capacity to tolerate low salinity than DD. Conclusions Our study argues that the abalone CaM gene might be necessary to maintain ion equilibrium while HSP90 can offset the adverse changes caused by low salinity, thereby preventing damage to gill epithelial cells (ECs). The data reveal a potential molecular mechanism by which abalone responds to low salinity and confirms that hybridization could be a method for breeding more stress-resilient aquatic species.

The nautilus, commonly known as a "living fossil," is endangered and may be at risk of extinction. The lack of genomic information hinders a thorough understanding of the biology and evolution of nautilus, which can shed light on the conservation of this endangered species. Here, we report the first high-quality chromosome-level genome assembly of Nautilus pompilius. The assembled genome size comprised 785.15 Mb. Comparative genomic analyses indicated that transposable elements (TEs) and large-scale genome reorganizations may have driven lineage-specific evolution in the cephalopods. Remarkably, evolving conserved genes and recent TE insertion activities were identified in N. pompilius, and we speculate that these findings reflect the strong adaptability and high survival of the nautilus. Besides, we also identified gene families that are potentially responsible for specific adaptation and evolution events. Our study provides unprecedented insights into the specialized biology and evolution of the N. pompilius, and the results serve as an important resource for future conservation genomics of the nautilus and its closely related species.