Yu Feifei, Chen Jiayu, Lin Jinji, Zhong Zhiming, Lu Yishan, Zeng Xiangrong, Lei Xiaoya
College of Fishery, Guangdong Ocean University, Zhanjiang, Guangdong, 524088, China; Academician Joint Laboratory of Germplasm Resource Exploitation, Utilization and Health Assessment for Aquatic Animal, Guangdong Ocean University, Zhanjiang, Guangdong, 524088, China.
College of Fishery, Guangdong Ocean University, Zhanjiang, Guangdong, 524088, China.
Fish Shellfish Immunol. 2023 Mar;134:108591. doi: 10.1016/j.fsi.2023.108591. Epub 2023 Feb 4.
Vibrio parahaemolyticus (V. parahaemolyticus) is a salt-loving gram-negative bacterium, and is the leading cause of mortality in cultured shellfish in recent years. Toll-like Receptor 4 (TLR4) is a classical pattern recognition receptor (PRRs) that recognizes pathogen-associated molecular patterns (PAMPs) of pathogenic microorganism and activates the immune response. However, the function and signal pathway of TLR4 in oyster are still unknown. In this study, a new TLR4 gene was identified from the Crassostrea hongkongensis (C. hongkongensis). The ChTLR4 contained an open reading frame of 2643 bp, encoding 880 amino acids with seven leucine-rich repeat (LRR) domains and a Toll/IL-1R (TIR) domain. The ChTLR4 shared the highest sequence identity (83.0%) with TLR4 of Crassostrea gigas. Tissue expression analysis revealed that ChTLR4 showed the highest constitutive expression in the gill and hepatopancreas, and was significantly upregulated in immune tissues post V. parahaemolyticus infection, especially in gill and hemocytes. Moreover, TLR4 silencing significantly inhibited the immune-enzyme activities, including SOD, CAT, ACP, AKP in gill and LZM in hemolymph supernatant, and increased MDA content in hemolymph supernatant. Meanwhile, the antimicrobial activities of the hemolymph supernatant were also significantly inhibited by TLR4 silencing. These data demonstrated that the ChTLR4 involved in innate immune response of C. hongkongensis against V. parahaemolyticus challenge. Finally, qRT-PCR analysis showed that ChTLR4 silencing clearly inhibited the expression of genes in TLR4-MyD88 pathway, indicating that MyD88-dependent pathway played a crucial role in ChTLR4-mediated immune response against V. parahaemolyticus.
副溶血性弧菌是一种嗜盐革兰氏阴性菌,是近年来养殖贝类死亡的主要原因。Toll样受体4(TLR4)是一种经典的模式识别受体(PRRs),可识别病原微生物的病原体相关分子模式(PAMPs)并激活免疫反应。然而,TLR4在牡蛎中的功能和信号通路仍不清楚。在本研究中,从香港牡蛎中鉴定出一个新的TLR4基因。ChTLR4包含一个2643 bp的开放阅读框,编码880个氨基酸,具有七个富含亮氨酸重复序列(LRR)结构域和一个Toll/IL-1R(TIR)结构域。ChTLR4与太平洋牡蛎的TLR4序列同一性最高(83.0%)。组织表达分析表明,ChTLR4在鳃和肝胰腺中组成性表达最高,在副溶血性弧菌感染后免疫组织中显著上调,尤其是在鳃和血细胞中。此外,TLR4沉默显著抑制了免疫酶活性,包括鳃中的超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、酸性磷酸酶(ACP)、碱性磷酸酶(AKP)以及血淋巴上清液中的溶菌酶(LZM),并增加了血淋巴上清液中的丙二醛(MDA)含量。同时,TLR4沉默也显著抑制了血淋巴上清液的抗菌活性。这些数据表明,ChTLR4参与了香港牡蛎对副溶血性弧菌攻击的先天免疫反应。最后,实时定量聚合酶链反应(qRT-PCR)分析表明,ChTLR4沉默明显抑制了TLR4-MyD88途径中基因的表达,表明MyD88依赖途径在ChTLR4介导的抗副溶血性弧菌免疫反应中起关键作用。