Microbiology and Immunology Department, Faculty of Pharmacy, Zagazig University, Zagazig, 44519, Egypt.
Microbiology and Biotechnology Department, Faculty of Pharmacy, Delta University for Science and Technology, Gamasa, 11152, Egypt.
J Antibiot (Tokyo). 2023 Apr;76(4):225-235. doi: 10.1038/s41429-023-00595-1. Epub 2023 Feb 1.
In a healthy gut microbiota, short chain fatty acids (SCFAs) are produced. The antibacterial action of SCFAs against intestinal pathogens makes them useful for ensuring the safety of food and human health. In this study, we aimed to assess the in vitro inhibitory activity of SCFAs, and to report, for the first time, their impact on the activity of new β-lactam/β-lactamase inhibitor combinations. The minimum inhibitory concentrations of acetic, propionic, and butyric acids were determined against E. coli clinical isolates recovered from gastrointestinal infections. Cefoperazone/sulbactam, ceftazidime/avibactam and cefepime/enmetazobactam are new β-lactam/β-lactamase inhibitor combinations that were studied for their combined therapeutic effects. Also, the effects of pH and concentration of SCFAs were evaluated on in vitro bacterial growth and expression of genes encoding for motility, adhesion, invasion, and biofilm formation. SCFAs were tested at concentrations of 12 mM at pH 7.4 (ileum-conditions), in addition to 60 mM and 123 mM, at pH 6.5 (colon-conditions). The tested SCFAs showed the same MIC (3750 μg ml ≃ 60 mM) against all isolates. Furthermore, the addition of SCFAs to the tested β-lactam/β-lactamase inhibitor combinations greatly restored the susceptibility of the isolates. SCFAs had significant effect on bacterial growth and virulence in a pH and concentration-dependent manner; low ileal concentration potentiated E. coli growth, while higher colonic concentration significantly suppressed growth and down-regulated the expression of virulence genes (fliC, ipaH, FimH, BssS). Therefore, the significant inhibitory effect of colonic SCFAs on β-lactam/β-lactamase inhibitor combinations might lead to the development of promising treatment strategies.
在健康的肠道微生物群中,会产生短链脂肪酸 (SCFA)。SCFA 对肠道病原体的抗菌作用使其可用于确保食品安全和人类健康。在这项研究中,我们旨在评估 SCFA 的体外抑制活性,并首次报告它们对新的β-内酰胺/β-内酰胺酶抑制剂组合活性的影响。测定了从胃肠道感染中回收的临床分离大肠杆菌对乙酸、丙酸和丁酸的最小抑菌浓度。头孢哌酮/舒巴坦、头孢他啶/阿维巴坦和头孢吡肟/恩他培南是新的β-内酰胺/β-内酰胺酶抑制剂组合,研究了它们的联合治疗效果。此外,还评估了 SCFA 的 pH 值和浓度对体外细菌生长和编码运动、粘附、侵袭和生物膜形成的基因表达的影响。在 pH 7.4(回肠条件)下测试了浓度为 12 mM 的 SCFA,此外还在 pH 6.5(结肠条件)下测试了 60 mM 和 123 mM 的 SCFA。测试的 SCFA 对所有分离株的 MIC 相同(3750μg/ml≈60mM)。此外,将 SCFA 添加到测试的β-内酰胺/β-内酰胺酶抑制剂组合中大大恢复了分离株的敏感性。SCFA 以 pH 和浓度依赖的方式对细菌生长和毒力有显著影响;低回肠浓度增强大肠杆菌的生长,而较高的结肠浓度则显著抑制生长并下调毒力基因(fliC、ipaH、FimH、BssS)的表达。因此,结肠 SCFA 对β-内酰胺/β-内酰胺酶抑制剂组合的显著抑制作用可能导致开发有前途的治疗策略。