Graduate School of Fisheries Science & Environmental Studies, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki, 852-8521, Japan.
Graduate School of Fisheries Science & Environmental Studies, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki, 852-8521, Japan; Faculty of Fisheries, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki, 852-8521, Japan.
Microb Pathog. 2023 Mar;176:105993. doi: 10.1016/j.micpath.2023.105993. Epub 2023 Jan 16.
Edwardsiella tarda is a causative pathogen of edwardsiellosis in fish. Our previous studies on high (NUF251) and low (NUF194) virulent strains of E. tarda demonstrated that NUF251 strain induced significantly higher levels of NO and TNF-α from fish and mouse macrophages than NUF194 strain. Subsequent studies suggested that a flagellin-like protein secreted from E. tarda might be a responsible factor for the macrophage-stimulating activities. To evaluate the activities of flagellins of E. tarda, in this study, the flagellin genes of NUF251 and NUF194 strains were isolated by PCR and cloned into pQE-30 and pCold I expression vectors, and then the recombinant flagellins of two strains were overexpressed in E. coli JM109 and pG-Tf/BL21, respectively. The molecular weight of the purified recombinant flagellins of NUF251 and NUF194 strains were estimated to be 45 kDa and 37 kDa, respectively on SDS-PAGE analysis. Referring the three-dimensional structure of Salmonella flagellin, which has been reported to have 4 domains (D0, D1, D2, and D3), high sequence homology between two flagellins of E. tarda was observed at conservative domain (D0 and D1) regions, whereas the sequences equivalent to D2 and D3 domains were different, and even equivalent to 57 amino acids were deleted in NUF194. Both recombinant flagellins induced NO production, mRNA expression level of inducible NO synthase (iNOS), and intercellular ROS production in mouse macrophage cell line RAW264.7 cells. Also, the secretion of TNF-α and its mRNA expression level were increased by treatment of both recombinant flagellins. These results indicate that the recombinant flagellins from different virulent E. tarda strains can stimulate macrophages with nearly equal levels as judged by the parameters tested, even though they are differences in the structure and molecular weight, suggesting that conservative D0 and D1 domains are sufficient structural elements for the recombinant flagellins to induce a certain level of macrophage-stimulation in vitro. Further studies are necessary focusing on the role of D2 and D3 domain regions of the recombinant flagellins as macrophage-stimulating agent as well as their influence on host immune system in vivo.
迟缓爱德华氏菌是鱼类爱德华氏菌病的病原体。我们之前的研究表明,高毒力(NUF251)和低毒力(NUF194)迟缓爱德华氏菌株均可诱导鱼类和鼠源巨噬细胞产生大量的一氧化氮(NO)和肿瘤坏死因子-α(TNF-α)。随后的研究表明,迟缓爱德华氏菌分泌的一种鞭毛样蛋白可能是刺激巨噬细胞的活性物质。为了评估迟缓爱德华氏菌鞭毛蛋白的活性,本研究通过 PCR 分别从 NUF251 和 NUF194 菌株中克隆出 flagellin 基因,并将其克隆到 pQE-30 和 pCold I 表达载体中,然后分别在大肠杆菌 JM109 和 pG-Tf/BL21 中过表达重组菌株的 flagellin。SDS-PAGE 分析结果显示,纯化的 NUF251 和 NUF194 菌株的重组 flagellin 的分子量分别约为 45 kDa 和 37 kDa。参照已报道的具有 4 个结构域(D0、D1、D2 和 D3)的沙门氏菌鞭毛蛋白的三维结构,迟缓爱德华氏菌的两种鞭毛蛋白在保守结构域(D0 和 D1)具有很高的序列同源性,而 D2 和 D3 结构域的序列则不同,甚至在 NUF194 中缺失了 57 个氨基酸。两种重组鞭毛蛋白均可诱导 RAW264.7 巨噬细胞产生一氧化氮(NO),诱导型一氧化氮合酶(iNOS)的 mRNA 表达水平以及细胞内活性氧(ROS)的产生,并且均可增加 TNF-α的分泌及其 mRNA 表达水平。这些结果表明,用不同毒力迟缓爱德华氏菌菌株的重组鞭毛蛋白刺激巨噬细胞,通过所测参数判断其具有相近的刺激效果,尽管它们在结构和分子量上存在差异,但这表明保守的 D0 和 D1 结构域是重组鞭毛蛋白在体外诱导一定水平的巨噬细胞刺激所必需的结构元件。进一步的研究需要集中在 D2 和 D3 结构域区域的重组鞭毛蛋白作为巨噬细胞刺激物的作用及其对体内宿主免疫系统的影响。