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中国牡蛎对灿烂弧菌胞外产物的感应模式和抗毒反应。

The sensing pattern and antitoxic response of Crassostrea gigas against extracellular products of Vibrio splendidus.

机构信息

Liaoning Key Laboratory of Marine Animal Immunology, Dalian Ocean University, Dalian, 116023, China; Functional Laboratory of Marine Fisheries Science and Food Production Process, Qingdao National Laboratory for Marine Science and Technology, Qingdao, 266200, China; Liaoning Key Laboratory of Marine Animal Immunology and Disease Control, Dalian Ocean University, Dalian, 116023, China.

Liaoning Key Laboratory of Marine Animal Immunology, Dalian Ocean University, Dalian, 116023, China; Liaoning Key Laboratory of Marine Animal Immunology and Disease Control, Dalian Ocean University, Dalian, 116023, China.

出版信息

Dev Comp Immunol. 2020 Jan;102:103467. doi: 10.1016/j.dci.2019.103467. Epub 2019 Aug 16.

Abstract

Serious juvenile oyster disease induced by pathogenic Vibrio splendidus has resulted in tremendous economic loss, but the molecular mechanisms underlying this killing mechanism remain unclear. The resistance of adult oyster to V. splendidus or its virulence factors might provide a possible access to cognize the interaction between pathogen and host. In the present study, the extracellular products (ECP) from less virulent V. splendidus JZ6 were injected into adult Pacific oyster Crassostrea gigas, and the cellular and humoral immune response induced by ECP were investigated. The phagocytosis rate of hemocytes was significantly up-regulated (30.57%) at 6 h after ECP injection compared with that (21%) of control groups. And significantly high level of ROS production was also observed from 3 h to 12 h in ECP-injected oysters, concomitant with increased apoptosis rate of hemocytes (16.4% in ECP-injected group, p < 0.01) compared with control group (6.7%). By RT-PCR analysis, the expression level of antioxidant CgSOD in hemocytes significantly increased to 6.41-fold of that in control groups (p < 0.01) at 12 h post ECP injection. The expression levels of anti-toxic metalloprotease inhibitors CgTIMP629 and CgTIMP628 were also significantly up-regulated at the early (3-6 h) and late (6-24 h) stage of immune response, respectively. Moreover, after the ECP were incubated with serum proteins isolated from the ECP-injected oysters in vitro, the metalloprotease activity of ECP significantly declined by 21.39%, and less degraded serum proteins were detected by SDS-PAGE. When the primarily cultured hemocytes were stimulated with heat-inactivated ECP or fragments derived from ECP-degraded serum proteins, the expressions of CgTIMP629 (13.64 and 7.03-fold of that in saline group, respectively, p < 0.01) and CgTIMP628 (5.07 and 6.08-fold of that in saline group, respectively, p < 0.01) in hemocytes were all significantly induced. All the results indicated that the adult oysters could launch phagocytosis, antioxidant and anti-toxic response to resist the virulence of ECP, possibly by sensing heterologous ECP and ECP-induced endogenous alarm signals. These results provided a possible clue for the resistance mechanism of adult oysters towards the ECP of less virulent V. splendidus, which might be valuable for exploring strategies for the control of oyster disease.

摘要

由致病性灿烂弧菌引起的严重幼蚝病导致了巨大的经济损失,但这种杀伤机制的分子机制尚不清楚。成蚝对灿烂弧菌或其毒力因子的抗性可能为认识病原体与宿主之间的相互作用提供了一个可能的途径。本研究中,将致病性较弱的灿烂弧菌 JZ6 的胞外产物(ECP)注入太平洋牡蛎成体中,研究 ECP 诱导的细胞和体液免疫反应。与对照组(21%)相比,ECP 注射后 6 小时血细胞的吞噬率显著升高(30.57%)。在 ECP 注射的牡蛎中,还观察到从 3 小时到 12 小时 ROS 产生水平显著升高,同时血细胞凋亡率也显著升高(ECP 注射组为 16.4%,p<0.01)与对照组(6.7%)相比。通过 RT-PCR 分析,ECP 注射后 12 小时,血细胞中抗氧化酶 CgSOD 的表达水平显著增加到对照组的 6.41 倍(p<0.01)。抗毒金属蛋白酶抑制剂 CgTIMP629 和 CgTIMP628 的表达水平也分别在免疫反应的早期(3-6 小时)和晚期(6-24 小时)显著上调。此外,当 ECP 与从 ECP 注射牡蛎中分离的血清蛋白在体外孵育时,ECP 的金属蛋白酶活性显著下降了 21.39%,并且通过 SDS-PAGE 检测到较少的降解血清蛋白。当用热灭活的 ECP 或源自 ECP 降解的血清蛋白片段刺激原代培养的血细胞时,CgTIMP629(分别为盐水组的 13.64 和 7.03 倍,p<0.01)和 CgTIMP628(分别为盐水组的 5.07 和 6.08 倍,p<0.01)在血细胞中的表达均显著诱导。所有结果表明,成蚝可以通过感应异源 ECP 和 ECP 诱导的内源性警报信号,发动吞噬、抗氧化和抗毒反应来抵抗 ECP 的毒力。这些结果为成蚝对致病性较弱的灿烂弧菌 ECP 的抗性机制提供了一个可能的线索,这可能有助于探索控制牡蛎疾病的策略。

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