Department of Biology and Guangdong Provincial Key Laboratory of Marine Biotechnology, Shantou University , Shantou, China.
STU-UMT Joint Shellfish Research Laboratory, Shantou University , Shantou, China.
Virulence. 2021 Dec;12(1):481-492. doi: 10.1080/21505594.2021.1872171.
Acute hepatopancreatic necrosis disease (AHPND) is a major debilitating disease that causes massive shrimp death resulting in substantial economic losses in shrimp aquaculture. The Pir toxin proteins secreted by a unique strain of play an essential role in the pathogenesis of AHPND. At present, most studies on the effects of Pir toxin proteins in shrimp focus on digestive tissues or organs such as hepatopancreas, stomach, etc., with none on the immune organs. In the present study, two recombinant Pir toxin proteins (rPirA and rPirB) of were expressed with rPirB shown to enter shrimp hemocytes. Employing pull-down and LC-MS/MS analysis, GST-rPirB was found to interact with 13 proteins in hemocytes, including histone H3 and histone H4 and among which histone H4 had the highest protein score. Further analysis using GST pull-down and Far-Western blot analysis revealed that rPirB could interact with histone H4. In addition, using the purified nucleosome protein from S2 cells, it was found that PirB protein could specifically bind to histones. When flow cytometry was applied, it was observed that the interaction between PirB and histones in shrimp hemocytes induces apoptosis, which results in the dephosphorylation of Serine 10 in histone H3. Collectively, the current study shows that in addition to its effect on the digestive tract of shrimp, the PirB toxin protein interacts with histones to affect the phosphorylation of histone H3-S10, thereby inducing apoptosis.
急性肝胰腺坏死病 (AHPND) 是一种严重的致残性疾病,可导致大量虾类死亡,给虾类养殖业造成重大经济损失。一种独特菌株分泌的 Pir 毒素蛋白在 AHPND 的发病机制中发挥着重要作用。目前,关于 Pir 毒素蛋白在虾类中的作用的大多数研究都集中在消化组织或器官上,如肝胰腺、胃等,而对免疫器官的研究则很少。在本研究中,表达了两种重组 Pir 毒素蛋白(rPirA 和 rPirB),结果显示 rPirB 进入了虾的血细胞。采用下拉和 LC-MS/MS 分析,发现 GST-rPirB 与血细胞中的 13 种蛋白质相互作用,包括组蛋白 H3 和组蛋白 H4,其中组蛋白 H4 的蛋白评分最高。进一步采用 GST 下拉和 Far-Western blot 分析表明,rPirB 可以与组蛋白 H4 相互作用。此外,利用 S2 细胞提取的纯化核小体蛋白,发现 PirB 蛋白可以特异性结合组蛋白。当应用流式细胞术时,观察到 PirB 与虾血细胞中组蛋白的相互作用诱导细胞凋亡,导致组蛋白 H3 的丝氨酸 10 去磷酸化。综上所述,本研究表明,除了对虾类消化道的影响外,PirB 毒素蛋白还与组蛋白相互作用,影响组蛋白 H3-S10 的磷酸化,从而诱导细胞凋亡。