Etifa Perezimor, Rodríguez César, Harmanus Céline, Sanders Ingrid M J G, Sidorov Igor A, Mohammed Olufunmilayo A, Savage Emily, Timms Andrew R, Freeman Jane, Smits Wiep Klaas, Wilcox Mark H, Baines Simon D
Department of Food and Nutritional Sciences, School of Chemistry, Food and Pharmacy, Reading RG6 6DZ, UK.
Facultad de Microbiología & CIET, Universidad de Costa Rica, San Pedro 11501-2060, Costa Rica.
Antibiotics (Basel). 2023 Feb 22;12(3):435. doi: 10.3390/antibiotics12030435.
infection (CDI) remains a significant healthcare burden. Non-toxigenic (NTCD) strains have shown a benefit in preventing porcine enteritis and in human recurrent CDI. In this study, we evaluated the efficacy of metronidazole-resistant NTCD-E4 in preventing CDI facilitated by a range of antimicrobials in an in vitro human gut model. NTCD-E4 spores (at a dose of 10) were instilled 7 days before a clinical ribotype (RT) 027 (at the same dose) strain (210). In separate experiments, four different antimicrobials were used to perturb gut microbiotas; bacterial populations and cytotoxin production were determined using viable counting and Vero cell cytotoxicity, respectively. RT027 and NTCD-E4 proliferated in the in vitro model when inoculated singly, with RT027 demonstrating high-level cytotoxin (3-5-log-relative units) production. In experiments where the gut model was pre-inoculated with NTCD-E4, RT027 was remained quiescent and failed to produce cytotoxins. NTCD-E4 showed mutations in and a gene homologous to CD196-1331, previously linked to medium-dependent metronidazole resistance, but lacked other metronidazole resistance determinants. This study showed that RT027 was unable to elicit simulated infection in the presence of NTCD-E4 following stimulation by four different antimicrobials. These data complement animal and clinical studies in suggesting NTCD offer prophylactic potential in the management of human CDI.
艰难梭菌感染(CDI)仍然是一个重大的医疗负担。非产毒(NTCD)菌株已显示出在预防猪肠炎和人类复发性CDI方面的益处。在本研究中,我们在体外人肠道模型中评估了耐甲硝唑的NTCD-E4在预防由一系列抗菌药物促成的CDI方面的疗效。在临床核糖体分型(RT)027(相同剂量)菌株(210)接种前7天,滴注NTCD-E4孢子(剂量为10)。在单独的实验中,使用四种不同的抗菌药物扰乱肠道微生物群;分别使用活菌计数和Vero细胞细胞毒性测定细菌种群和细胞毒素产生情况。单独接种时,RT027和NTCD-E4在体外模型中增殖,RT027显示出高水平的细胞毒素(3 - 5对数相对单位)产生。在肠道模型预先接种NTCD-E4的实验中,RT027保持静止,未产生细胞毒素。NTCD-E4在与CD196 - 1331同源的基因中显示出突变,该基因先前与培养基依赖性甲硝唑耐药性有关,但缺乏其他甲硝唑耐药决定因素。本研究表明,在四种不同抗菌药物刺激后,存在NTCD-E4时,RT027无法引发模拟感染。这些数据补充了动物和临床研究,表明NTCD在人类CDI的管理中具有预防潜力。