Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Agricultural University, Tai'an, China.
College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, China.
Front Immunol. 2019 Dec 11;10:2834. doi: 10.3389/fimmu.2019.02834. eCollection 2019.
Enterotoxigenic (ETEC) that expresses F4ac fimbriae is the major pathogenic microorganism responsible for bacterial diarrhea in neonatal piglets. The susceptibility of piglets to ETEC F4ac is determined by a specific receptor on the small intestinal epithelium surface. We performed an iTRAQ-labeled quantitative proteome analysis using a case-control design in which susceptible and resistant full-sib piglets were compared for the protein expression levels. Two thousand two hundred forty-nine proteins were identified, of which 245 were differentially expressed (fold change > 1.5, FDR-adjusted < 0.05). The differentially expressed proteins fell into four functional classes: (I) cellular adhesion and binding, (II) metabolic process, (III) apoptosis and proliferation, and (IV) immune response. The integrin signaling pathway merited particular interest based on a pathway analysis using statistical overexpression and enrichment tests. Genomic locations of the integrin family genes were determined based on the most recent porcine genome sequence assembly (Sscrofa11.1). Only one gene, , which encodes the integrin β5 subunit that assorts with the αv subunit to generate integrin αvβ5, was located within the SSC13q41 region between 13:133161078 and 13:139609422, where strong associations of markers with the ETEC F4ac susceptibility were found in our previous GWAS results. To identify whether integrin αvβ5 is the ETEC F4acR, we established an experimental model for bacterial adhesion using IPEC-J2 cells. Then, the gene was knocked out in IPEC-J2 cell lines using CRISPR/Cas9, resulting in a biallelic deletion cell line (). Disruption of significantly reduced ETEC F4ac adhesion to porcine intestinal epithelial cells. In contrast, overexpression of significantly enhanced the adhesion. A GST pull-down assay with purified FaeG and ITGB5 also showed that FaeG binds directly to ITGB5. Together, the results suggested that is a key factor affecting the susceptibility of piglets to ETEC F4ac.
产肠毒素性大肠杆菌(ETEC)表达 F4ac 菌毛,是导致新生仔猪细菌性腹泻的主要致病微生物。仔猪对 ETEC F4ac 的易感性由小肠上皮表面的特定受体决定。我们采用病例对照设计进行 iTRAQ 标记定量蛋白质组分析,比较了易感和抗性全同胞仔猪的蛋白质表达水平。鉴定出 2249 种蛋白质,其中 245 种差异表达(倍数变化>1.5,FDR 调整<0.05)。差异表达的蛋白质分为四个功能类别:(I)细胞黏附和结合,(II)代谢过程,(III)凋亡和增殖,以及(IV)免疫反应。基于统计过表达和富集测试的通路分析,整合素信号通路特别值得关注。根据最近的猪基因组序列组装(Sscrofa11.1),确定了整合素家族基因的基因组位置。只有一个基因,编码整合素β5 亚基,该亚基与αv 亚基一起生成整合素αvβ5,位于 13:133161078 和 13:139609422 之间的 SSC13q41 区域内,在我们之前的 GWAS 结果中,该区域的标记与 ETEC F4ac 易感性有很强的关联。为了确定整合素αvβ5是否是 ETEC F4acR,我们使用 IPEC-J2 细胞建立了细菌黏附的实验模型。然后,使用 CRISPR/Cas9 敲除了 IPEC-J2 细胞系中的 基因,导致等位基因缺失的细胞系()。 基因的破坏显著降低了 ETEC F4ac 对猪肠上皮细胞的黏附。相反,过表达 显著增强了黏附。用纯化的 FaeG 和 ITGB5 进行 GST 下拉测定也表明 FaeG 直接与 ITGB5 结合。总之,结果表明 是影响仔猪对 ETEC F4ac 易感性的关键因素。