Key Laboratory for Sustainable Utilization of Marine Fisheries Resources, Ministry of Agriculture, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, China.
Key Laboratory for Sustainable Utilization of Marine Fisheries Resources, Ministry of Agriculture, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, China; Function Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China.
Gene. 2020 May 30;741:144523. doi: 10.1016/j.gene.2020.144523. Epub 2020 Mar 4.
Chitinases play an important role in many biological processes in crustaceans, including molting, digestion, and immunity. In order to further explore the immune defense mechanism of chitinase in Portunus trituberculatus, the PtCht-1 gene was cloned by RACE (rapid-amplification of cDNA ends). This cDNA with a full length of 1910 bp, and an ORF (open reading frame) 1749 bp, coded for 582 amino acid residues and was classified into P. trituberculatus chitinase GH18-group4. It had the typical structural characteristics of GH18 chitinase family. Real-time PCR was used to analyze the expression of PtCht-1 in different tissues, molting stages, after pathogen infection, and low salinity (11‰). PtCht-1 was expressed in all tissues, with the highest expression in the hepatopancreas. In the hepatopancreas of different molting stages, the expression level decreased successively during post-molt stages (A/B), pre-molt stage (D) and inter-molt stage (C). Under normal circumstances, after artificial infection with WSSV and Vibrio parahaemolyticus, the expression of PtCht-1 in hepatopancreas reached the maximum at 48 h, and in hemolymph at 72 h and 24 h, respectively. Overall PtCht-1 expression was up-regulated compared with the control group. Low salinity stress significantly inhibited the expression of PtCht-1, up to 42 folds. Under low salinity stress, the time when WSSV infection reached the peak was markedly delayed by at least 24 h. The results of this study indicate that PtCht-1, as an immune factor, is likely involved in pathogen defense of P. trituberculatus, the immune function of which may be inhibited to some extent after low salinity stress.
几丁质酶在甲壳动物的许多生物学过程中发挥着重要作用,包括蜕皮、消化和免疫。为了进一步探讨三疣梭子蟹几丁质酶的免疫防御机制,通过 RACE(快速扩增 cDNA 末端)克隆了 PtCht-1 基因。该 cDNA 全长 1910bp,开放阅读框(ORF)为 1749bp,编码 582 个氨基酸残基,归类为三疣梭子蟹几丁质酶 GH18-4 组。它具有 GH18 几丁质酶家族的典型结构特征。实时 PCR 用于分析 PtCht-1 在不同组织、蜕皮阶段、病原体感染后和低盐度(11‰)下的表达。PtCht-1 在所有组织中均有表达,在肝胰腺中表达量最高。在不同蜕皮阶段的肝胰腺中,蜕皮后阶段(A/B)、蜕皮前阶段(D)和蜕皮间阶段(C)的表达水平依次降低。在正常情况下,人工感染 WSSV 和副溶血弧菌后,肝胰腺中 PtCht-1 的表达在 48h 时达到最大值,在血淋巴中分别在 72h 和 24h 时达到最大值。总体而言,PtCht-1 的表达水平与对照组相比上调。低盐度胁迫显著抑制 PtCht-1 的表达,最高可达 42 倍。在低盐度胁迫下,WSSV 感染达到峰值的时间至少延迟了 24h。本研究结果表明,PtCht-1 作为一种免疫因子,可能参与了三疣梭子蟹的病原体防御,低盐度胁迫后其免疫功能可能受到一定程度的抑制。