Center of Excellence for Molecular Biology and Genomic of Shrimp, Department of Biochemistry, Faculty of Science, Chulalongkorn University, 254 Phaya Thai Rd, Wang Mai, Pathum Wan, Bangkok, 10330, Thailand.
Center of Excellence for Shrimp Molecular Biology and Biotechnology (Centex Shrimp), Faculty of Science, Mahidol University, 272 Rama VI, Road, Thung Phaya Thai, Ratchathewi, Bangkok, 10400, Thailand.
Fish Shellfish Immunol. 2023 Sep;140:108976. doi: 10.1016/j.fsi.2023.108976. Epub 2023 Jul 26.
Enterocytozoon hepatopenaei (EHP) is a microsporidian parasite that infects shrimp hepatopancreas, causing growth retardation and disease susceptibility. Knowledge of the host-pathogen molecular mechanisms is essential to understanding the microsporidian pathogenesis. Turtle-like protein (TLP) is part of the immunoglobulin superfamily of proteins, which is widely distributed in the animal kingdom. TLP has multiple functions, such as cell surface receptors and cell adhesion molecules. The spore wall proteins (SWPs) of microsporidia are involved in the infection mechanisms. Some SWPs are responsible for spore adherence, which is part of the activation and host cell invasion processes. Previous studies showed that TLP from silkworms (Bombyx mori) interacted with SWP26, contributing to the infectivity of Nosema bombycis to its host. In this study, we identified and characterized for the first time, the Litopenaeus vannamei TLP gene (LvTLP), which encodes an 827-aa protein (92.4 kDa) composed of five immunoglobulin domains, two fibronectin type III domains, and a transmembrane region. The LvTLP transcript was expressed in all tested tissues and upregulated in the hepatopancreas at 1 and 7 days post-cohabitation (dpc) and at 9 dpc in hemocytes. To identify the LvTLP binding counterpart, recombinant (r)LvTLP and recombinant (r)EhSWP1 were produced in Escherichia coli. Coimmunoprecipitation and enzyme-linked immunosorbent assays demonstrated that rLvTLP interacted with rEhSWP with high affinity (K = 1.20 × 10 M). In EHP-infected hepatopancreases, LvTLP was clustered and co-localized with some of the developing EHP plasmodia. Furthermore, LvTLP gene silencing reduced the EHP copy numbers compared with those of the control group, suggesting the critical role of LvTLP in EHP infection. These results provide insight into the molecular mechanisms of the host-pathogen interactions during EHP infection.
对虾微孢子虫(EHP)是一种感染虾肝胰腺的微孢子虫寄生虫,可导致生长迟缓和易感性疾病。了解宿主-病原体的分子机制对于理解微孢子虫的发病机制至关重要。龟形蛋白(TLP)是免疫球蛋白超家族蛋白的一部分,广泛分布于动物界。TLP 具有多种功能,例如细胞表面受体和细胞黏附分子。微孢子虫的孢子壁蛋白(SWP)参与感染机制。一些 SWP 负责孢子附着,这是激活和宿主细胞入侵过程的一部分。先前的研究表明,家蚕(Bombyx mori)的 TLP 与 SWP26 相互作用,有助于 Nosema bombycis 对其宿主的感染力。在本研究中,我们首次鉴定和表征了凡纳滨对虾 TLP 基因(LvTLP),该基因编码一个由五个免疫球蛋白结构域、两个纤维连接蛋白 III 结构域和一个跨膜区组成的 827-氨基酸蛋白(92.4 kDa)。LvTLP 转录本在所有测试的组织中表达,并在共培养后 1 和 7 天(dpc)以及在血细胞中 9 dpc 时在肝胰腺中上调。为了鉴定 LvTLP 的结合对应物,在大肠杆菌中生产了重组(r)LvTLP 和重组(r)EhSWP1。共免疫沉淀和酶联免疫吸附试验表明,rLvTLP 与 rEhSWP 具有高亲和力(K = 1.20 × 10 M)相互作用。在感染对虾微孢子虫的肝胰腺中,LvTLP 与一些正在发育的对虾微孢子虫 plasmodia 聚集并共定位。此外,与对照组相比,LvTLP 基因沉默降低了对虾微孢子虫的拷贝数,表明 LvTLP 在对虾微孢子虫感染中起关键作用。这些结果为对虾微孢子虫感染过程中宿主-病原体相互作用的分子机制提供了新的见解。