Brown Carla L, Smith Karen, Wall Daniel M, Walker Daniel
Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Inflamm Bowel Dis. 2015 Oct;21(10):2372-82. doi: 10.1097/MIB.0000000000000488.
Crohn's disease (CD) is associated with bacterial dysbiosis that frequently includes colonization by adherent-invasive Escherichia coli (AIEC). AIEC are adept at forming biofilms and are able to invade host cells and stimulate the production of proinflammatory cytokines. The use of traditional antibiotics for the treatment of CD shows limited efficacy. In this study, we investigate the use of species-specific antibiotics termed colicins for treatment of CD-associated AIEC.
Colicin activity was tested against a range of AIEC isolates growing in the planktonic and biofilm mode of growth. Colicins were also tested against AIEC bacteria associated with T84 intestinal epithelial cells and surviving inside RAW264.7 macrophages using adhesion assays and gentamicin protection assay, respectively. Uptake of colicins into eukaryotic cells was visualized using confocal microscopy. The effect of colicin treatment on the production of proinflammatory cytokine tumor necrosis factor alpha by macrophages was assessed by an enzyme-linked immunosorbent assay.
Colicins show potent activity against AIEC bacteria growing as biofilms when delivered either as a purified protein or through a colicin-producing bacterial strain. In addition, colicins E1 and E9 are able to kill cell-associated and intracellular AIEC, but do not show toxicity toward macrophage cells or stimulate the production of proinflammatory cytokines. Colicin killing of intracellular bacteria occurs after entry of colicin protein into AIEC-infected macrophage compartments by actin-mediated endocytosis.
Our results demonstrate the potential of colicins as highly selective probiotic therapeutics for the eradication of E. coli from the gastrointestinal tract of patients with CD.
克罗恩病(CD)与细菌生态失调有关,这种失调通常包括由粘附侵袭性大肠杆菌(AIEC)定植。AIEC擅长形成生物膜,能够侵入宿主细胞并刺激促炎细胞因子的产生。使用传统抗生素治疗CD疗效有限。在本研究中,我们调查了使用称为大肠杆菌素的种特异性抗生素治疗与CD相关的AIEC的情况。
测试了大肠杆菌素对一系列以浮游和生物膜生长模式生长的AIEC分离株的活性。还分别使用粘附试验和庆大霉素保护试验,测试了大肠杆菌素对与T84肠上皮细胞相关并在RAW264.7巨噬细胞内存活的AIEC细菌的作用。使用共聚焦显微镜观察大肠杆菌素进入真核细胞的情况。通过酶联免疫吸附试验评估大肠杆菌素处理对巨噬细胞促炎细胞因子肿瘤坏死因子α产生的影响。
当以纯化蛋白形式或通过产生大肠杆菌素的菌株递送时,大肠杆菌素对以生物膜形式生长的AIEC细菌显示出强大的活性。此外,大肠杆菌素E1和E9能够杀死与细胞相关的和细胞内的AIEC,但对巨噬细胞没有毒性,也不会刺激促炎细胞因子的产生。大肠杆菌素对细胞内细菌的杀伤作用发生在大肠杆菌素蛋白通过肌动蛋白介导的内吞作用进入AIEC感染的巨噬细胞区室之后。
我们的结果证明了大肠杆菌素作为高度选择性益生菌疗法从CD患者胃肠道根除大肠杆菌的潜力。