Luo Yu, Van Nguyen Ut, de la Fe Rodriguez Pedro Y, Devriendt Bert, Cox Eric
Laboratory of Veterinary Immunology, Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, Ghent, Belgium.
Department of Veterinary Medicine and Zootechnics, Universidad Central "Marta Abreu" de Las Villas, Carretera a Camajuani km 5½, 54830, Santa Clara, Villa Clara, Cuba.
Vet Res. 2015 Oct 21;46:121. doi: 10.1186/s13567-015-0264-2.
Enterotoxigenic Escherichia coli (ETEC) are an important cause of post-weaning diarrhea (PWD) in piglets. Porcine-specific ETEC strains possess different fimbrial subtypes of which F4 fimbriae are the most frequently associated with ETEC-induced diarrhea in piglets. These F4 fimbriae are potent oral immunogens that induce protective F4-specific IgA antibody secreting cells at intestinal tissues. Recently, T-helper 17 (Th17) cells have been implicated in the protection of the host against extracellular pathogens. However, it remains unknown if Th17 effector responses are needed to clear ETEC infections. In the present study, we aimed to elucidate if ETEC elicits a Th17 response in piglets and if F4 fimbriae trigger a similar response. F4(+) ETEC infection upregulated IL-17A, IL-17F, IL-21 and IL-23p19, but not IL-12 and IFN-γ mRNA expression in the systemic and mucosal immune system. Similarly, oral immunization with F4 fimbriae triggered a Th17 signature evidenced by an upregulated mRNA expression of IL-17F, RORγt, IL-23p19 and IL-21 in the peripheral blood mononuclear cells (PBMCs). Intriguingly, IL-17A mRNA levels were unaltered. To further evaluate this difference between systemic and mucosal immune responses, we assayed the cytokine mRNA profile of F4 fimbriae stimulated PBMCs. F4 fimbriae induced IL-17A, IL-17F, IL-22 and IL-23p19, but downregulated IL-17B mRNA expression. Altogether, these data indicate a Th17 dominated response upon oral immunization with F4 fimbriae and F4(+) ETEC infection. Our work also highlights that IL-17B and IL-17F participate in the immune response to protect the host against F4(+) ETEC infection and could aid in the design of future ETEC vaccines.
产肠毒素大肠杆菌(ETEC)是仔猪断奶后腹泻(PWD)的重要病因。猪特异性ETEC菌株具有不同的菌毛亚型,其中F4菌毛与仔猪ETEC诱导的腹泻最为相关。这些F4菌毛是强效口服免疫原,可在肠道组织诱导产生保护性F4特异性IgA抗体分泌细胞。最近,辅助性T细胞17(Th17)细胞被认为在宿主抵御细胞外病原体方面发挥作用。然而,清除ETEC感染是否需要Th17效应反应仍不清楚。在本研究中,我们旨在阐明ETEC是否在仔猪中引发Th17反应,以及F4菌毛是否引发类似反应。F4(+) ETEC感染上调了全身和黏膜免疫系统中IL-17A、IL-17F、IL-21和IL-23p19的表达,但未上调IL-12和IFN-γ的mRNA表达。同样,用F4菌毛进行口服免疫引发了Th17特征,表现为外周血单核细胞(PBMC)中IL-17F、RORγt、IL-23p19和IL-21的mRNA表达上调。有趣的是,IL-17A的mRNA水平未改变。为了进一步评估全身和黏膜免疫反应之间的这种差异,我们检测了F4菌毛刺激的PBMC的细胞因子mRNA谱。F4菌毛诱导了IL-17A、IL-17F、IL-22和IL-23p19的表达,但下调了IL-17B的mRNA表达。总之,这些数据表明在用F4菌毛进行口服免疫和F4(+) ETEC感染后,存在以Th17为主导的反应。我们的工作还强调,IL-17B和IL-17F参与免疫反应以保护宿主抵御F4(+) ETEC感染,并有助于未来ETEC疫苗的设计。