Jiangsu Key Laboratory for Aquatic Crustacean Diseases, College of Marine Science and Engineering, Nanjing Normal University, 2 Xuelin Road, Nanjing, 210023, China.
Freshwater Fisheries Research Institute of Jiangsu Province, Nanjing, 210017, China.
Fish Shellfish Immunol. 2024 Nov;154:109879. doi: 10.1016/j.fsi.2024.109879. Epub 2024 Sep 5.
Spiroplasma eriocheiris is a kind of intracellular pathogen without cell wall and the causative agent of Chinese mitten crab Eriocheir sinensis "tremor disease", which causes significant economic losses in the crustacean aquaculture. However, little is known about the intracellular transport of this pathogen and host innate immune response to this pathogen. Rab GTPases are key regulators for endocytosis and intracellular pathogen trafficking. In this study, we showed that S. eriocheiris infection upregulated the transcription of Rab7 through the downregulation of miR-131-3p. Subsequently, both hemocytes transfected with miR-131-3p mimics and hemocytes derived from Rab7 knockdown crabs exhibited reduced phagocytic activities and increased susceptibility to S. eriocheiris infection. Additionally, Rab7 could interact with the cell shape-determining protein MreB3 of S. eriocheiris, and its overexpression promoted S. eriocheiris internalization and fusion with lysosomes, thereby limiting S. eriocheiris replication in Drosophila S2 cells. Overall, these results demonstrated that Rab7 facilitated host cell phagocytosis and interacted with MreB3 of S. eriocheiris to prevent S. eriocheiris infection. Moreover, miR-131-3p was identified as a negative regulator of this process through its targeting of Rab7. Therefore, targeting miR-131-3p might be an effective strategy for controlling S. eriocheiris in crab aquaculture.
中华绒螯蟹“颤抖病”的病原体螺原体(Spiroplasma eriocheiris)是一种缺乏细胞壁的细胞内病原体,会给甲壳类水产养殖业造成重大经济损失。然而,人们对该病原体的细胞内运输以及宿主先天免疫反应对此病原体的作用机制知之甚少。Rab GTPases 是内吞作用和细胞内病原体运输的关键调节因子。在本研究中,我们发现 S. eriocheiris 感染通过下调 miR-131-3p 而上调 Rab7 的转录。随后,转染了 miR-131-3p 模拟物的血细胞和 Rab7 敲低蟹的血细胞表现出吞噬活性降低和对 S. eriocheiris 感染的易感性增加。此外,Rab7 可以与 S. eriocheiris 的细胞形态决定蛋白 MreB3 相互作用,其过表达促进 S. eriocheiris 的内化和与溶酶体融合,从而限制 S. eriocheiris 在果蝇 S2 细胞中的复制。总体而言,这些结果表明 Rab7 促进了宿主细胞的吞噬作用,并与 S. eriocheiris 的 MreB3 相互作用,从而防止 S. eriocheiris 感染。此外,miR-131-3p 通过靶向 Rab7 被鉴定为该过程的负调节剂。因此,靶向 miR-131-3p 可能是控制蟹类水产养殖中 S. eriocheiris 的有效策略。