Aias Meral, Azrad Maya, Saad Gewa, Leshem Tamar, Hamo Zohar, Rahmoun Layan Abu, Peretz Avi
Azrieli Faculty of Medicine, Bar Ilan University, Safed 1311502, Israel.
The Clinical Microbiology Laboratory, Tzafon Medical Center, Poriya 1528001, Israel.
J Microbiol Methods. 2023 Mar;206:106692. doi: 10.1016/j.mimet.2023.106692. Epub 2023 Feb 20.
Clostridioides difficile infection develops following ingestion of virulent stains by a susceptible host. Once germinated, toxins TcdA and TcdB, and in some of the strains binary toxin, are secreted, eliciting disease. Bile acids play a significant role in the process of spore germination and outgrowth, with cholate and its derivative enhancing colony formation, while chenodeoxycholate inhibit germination and outgrowth. This work investigated bile acids' impact on spore germination, toxin levels and biofilm formation in various strain types (STs). Thirty C. difficile isolates (A B CDT) of different STs were exposed to increasing concentrations of the bile acids, cholic acid (CA), taurocholic acid (TCA) and chenodeoxycholic acid (CDCA). Following treatments, spore germination was determined. Toxin concentrations were semi-quantified using the C. Diff Tox A/B II™ kit. Biofilm formation was detected by the microplate assay with crystal violet. SYTO® 9 and propidium iodide staining were used for live and dead cell detection, respectively, inside the biofilm. Toxins levels were increased by 1.5-28-fold in response to CA and by 1.5-20-fold in response to TCA, and decreased by 1-37-fold due to CDCA exposure. CA had a concentration-dependent effect on biofilm formation, with the low concentration (0.1%) inducing- and the higher concentrations inhibiting biofilm formation, while CDCA significantly reduced biofilm production at all concentrations. There were no differences in the bile acids effects on different STs. Further investigation might identify a specific bile acids' combination with inhibitory effects on C. difficile toxin and biofilm production, which could modulate toxin formation to reduce the likelihood of developing CDI.
艰难梭菌感染是由易感宿主摄入有毒菌株后引发的。一旦芽孢萌发,毒素TcdA和TcdB,以及某些菌株中的二元毒素就会分泌出来,引发疾病。胆汁酸在芽孢萌发和生长过程中起着重要作用,胆酸盐及其衍生物可促进菌落形成,而鹅去氧胆酸盐则抑制萌发和生长。这项研究调查了胆汁酸对不同菌株类型(STs)芽孢萌发、毒素水平和生物膜形成的影响。将30株不同STs的艰难梭菌分离株(A B CDT)暴露于浓度不断增加的胆汁酸、胆酸(CA)、牛磺胆酸(TCA)和鹅去氧胆酸(CDCA)中。处理后,测定芽孢萌发情况。使用艰难梭菌毒素A/B II™试剂盒对毒素浓度进行半定量。通过结晶紫微孔板试验检测生物膜形成。分别使用SYTO® 9和碘化丙啶染色来检测生物膜内的活细胞和死细胞。CA使毒素水平升高了1.5至28倍,TCA使毒素水平升高了1.5至20倍,而CDCA暴露则使毒素水平降低了1至37倍。CA对生物膜形成具有浓度依赖性影响,低浓度(0.1%)诱导生物膜形成,高浓度则抑制生物膜形成,而CDCA在所有浓度下均显著降低生物膜产生。胆汁酸对不同STs的影响没有差异。进一步的研究可能会确定一种对艰难梭菌毒素和生物膜产生具有抑制作用的特定胆汁酸组合,这可能会调节毒素形成,以降低发生艰难梭菌感染(CDI)的可能性。