Center of Excellence for Molecular Biology and Genomics of Shrimp, Department of Biochemistry, Faculty of Science, Chulalongkorn University, Bangkok, Thailand.
Aquatic Molecular Genetics and Biotechnology Research Team, National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency (NSTDA), Pathumthani, Thailand.
PLoS Pathog. 2024 Apr 29;20(4):e1012199. doi: 10.1371/journal.ppat.1012199. eCollection 2024 Apr.
The microsporidian Enterocytozoon hepatopenaei (EHP) is a fungi-related, spore-forming parasite. EHP infection causes growth retardation and size variation in shrimp, resulting in severe economic losses. Studies on shrimp immune response have shown that several antimicrobial peptides (AMPs) were upregulated upon EHP infection. Among those highly upregulated AMPs is c-type lysozyme (LvLyz-c). However, the immune signaling pathway responsible for LvLyz-c production in shrimp as well as its function against the EHP infection are still poorly understood. Here, we characterized major shrimp immune signaling pathways and found that Toll and JAK/STAT pathways were up-regulated upon EHP infection. Knocking down of a Domeless (DOME) receptor in the JAK/STAT pathways resulted in a significant reduction of the LvLyz-c and the elevation of EHP copy number. We further elucidated the function of LvLyz-c by heterologously expressing a recombinant LvLyz-c (rLvLyz-c) in an Escherichia coli. rLvLyz-c exhibited antibacterial activity against several bacteria such as Bacillus subtilis and Vibrio parahaemolyticus. Interestingly, we found an antifungal activity of rLvLyz-c against Candida albican, which led us to further investigate the effects of rLvLyz-c on EHP spores. Incubation of the EHP spores with rLvLyz-c followed by a chitin staining showed that the signals were dramatically decreased in a dose-dependent manner, suggesting that rLvLyz-c possibly digest a chitin coat on the EHP spores. Transmission electron microscopy analysis revealed that an endospore layer, which is composed mainly of chitin, was digested by rLvLyz-c. Lastly, we observed that EHP spores that were treated with rLvLyz-c showed a significant reduction of the spore germination rate. We hypothesize that thinning of the endospore of EHP would result in altered permeability, hence affecting spore germination. This work provides insights into shrimp immune signaling pathways responsible for LvLyz-c production and its anti-EHP property. This knowledge will serve as important foundations for developing EHP control strategies.
微孢子虫 Enterocytozoon hepatopenaei (EHP) 是一种真菌相关的孢子形成寄生虫。EHP 感染会导致虾生长迟缓和大小变化,造成严重的经济损失。对虾免疫反应的研究表明,EHP 感染会上调几种抗菌肽 (AMP)。在这些高度上调的 AMP 中,有一种是 c 型溶菌酶 (LvLyz-c)。然而,负责虾中 LvLyz-c 产生的免疫信号通路及其对 EHP 感染的作用仍知之甚少。在这里,我们对主要的虾免疫信号通路进行了表征,发现 Toll 和 JAK/STAT 通路在 EHP 感染后被上调。JAK/STAT 通路中 Domeless (DOME) 受体的敲低导致 LvLyz-c 的显著减少和 EHP 拷贝数的升高。我们通过在大肠杆菌中异源表达重组 LvLyz-c (rLvLyz-c) 进一步阐明了 LvLyz-c 的功能。rLvLyz-c 对枯草芽孢杆菌和副溶血弧菌等几种细菌表现出抗菌活性。有趣的是,我们发现 rLvLyz-c 对白色念珠菌具有抗真菌活性,这促使我们进一步研究 rLvLyz-c 对 EHP 孢子的影响。用 rLvLyz-c 孵育 EHP 孢子,然后用几丁质染色,结果显示信号呈剂量依赖性显著减少,这表明 rLvLyz-c 可能消化了 EHP 孢子的几丁质外壳。透射电子显微镜分析显示,rLvLyz-c 消化了主要由几丁质组成的内孢子层。最后,我们观察到用 rLvLyz-c 处理的 EHP 孢子的孢子萌发率显著降低。我们假设 EHP 的内孢子变薄会导致渗透性改变,从而影响孢子萌发。这项工作为虾中负责 LvLyz-c 产生的免疫信号通路及其抗 EHP 特性提供了新的认识。这些知识将为开发 EHP 控制策略提供重要基础。