Key Laboratory of Tropical Marine Ecosystem and Bioresource, Fourth Institute of Oceanography, Ministry of Natural Resources, Beihai, 536000, PR China.
Guangxi Key Laboratory of Marine Drugs, Institute of Marine Drugs, Guangxi University of Chinese Medicine, Nanning, 530200, PR China.
Fish Shellfish Immunol. 2023 Sep;140:108978. doi: 10.1016/j.fsi.2023.108978. Epub 2023 Aug 6.
Portunion is a rare endoparasitic isopod genus, recently observed inhabiting the hemocoel of the commercially important mud crab, Scylla paramamosain. For better understanding of the host-parasite interaction between S. paramamosain and Portunion sp., the metabolomic and transcriptomic changes in the hemolymph of the S. paramamosain were analyzed. We detected a total of 143 and 126 differentially accumulated metabolites in the positive and negative modes, respectively. Pathways related to amino acids and vitamin synthesis, such as Aminoacyl-tRNA biosynthesis, Tyrosine metabolism, Cysteine and methionine metabolism, Vitamin B6 metabolism, and Biotin metabolism were significantly enriched. Based on the transcriptomic data, a total of 942 differentially expressed genes were identified, of which 25 and 36 were significantly related to the immune system and metabolic pathways, respectively. Based on the metabolomic and transcriptomic data, 90 correlated metabolite-gene pairs were selected to build a regulatory network. Common significantly enriched pathways, including Starch and sucrose metabolism, Metabolism of xenobiotics by cytochrome P450, Aminoacyl-tRNA biosynthesis, Nitrogen metabolism, and Galactose metabolism were detected. On the basis of our analysis, the endoparasite Portunion sp. places a heavy metabolic burden on the host, particularly with respect to fundamental resources, such as amino acids, vitamins, carbohydrates, and lipids. In summary, these data provide an overview of the global metabolic and transcriptomic changes of the S. paramamosain resulting from Portunion sp. infection.
门蟹属是一种罕见的内寄生等足目动物,最近在商业上重要的锯缘青蟹(Scylla paramamosain)的血腔中发现了该属的内寄生现象。为了更好地了解锯缘青蟹与门蟹属之间的宿主-寄生虫相互作用,我们分析了锯缘青蟹血淋巴中的代谢组学和转录组学变化。我们在正离子模式和负离子模式下分别检测到了总共 143 种和 126 种差异积累代谢物。与氨基酸和维生素合成相关的途径,如氨酰-tRNA 生物合成、酪氨酸代谢、半胱氨酸和蛋氨酸代谢、维生素 B6 代谢和生物素代谢,显著富集。基于转录组数据,共鉴定出 942 个差异表达基因,其中与免疫系统和代谢途径显著相关的分别有 25 个和 36 个。基于代谢组学和转录组学数据,选择了 90 个相关的代谢物-基因对来构建调控网络。共同检测到常见的显著富集途径,包括淀粉和蔗糖代谢、细胞色素 P450 介导的外源物质代谢、氨酰-tRNA 生物合成、氮代谢和半乳糖代谢。基于我们的分析,内寄生的门蟹属给宿主带来了沉重的代谢负担,特别是在氨基酸、维生素、碳水化合物和脂质等基本资源方面。总之,这些数据提供了锯缘青蟹感染门蟹属后整体代谢和转录组变化的概述。