Piscon Bar, Fichtman Boris, Harel Amnon, Adler Amos, Rahav Galia, Gal-Mor Ohad
The Infectious Diseases Research Laboratory, Sheba Medical Center, Ramat-Gan, Israel.
Department of Clinical Microbiology and Immunology, Tel Aviv University, Tel Aviv, Israel.
Front Cell Infect Microbiol. 2025 Mar 20;15:1550545. doi: 10.3389/fcimb.2025.1550545. eCollection 2025.
Glycocholic acid (GCA) is a steroid acid and one of the main glycine-conjugated bile components in mammalian bile, which is involved in the emulsification and absorption of fats and sterols. It is long-known that the amphipathic nature of bile acids enables them to interact with the lipid membrane of Gram-positive bacteria and act as potent antimicrobial compounds. Nevertheless, Gram-negative Enterobacteriaceae species inhabiting the intestinal tract of mammals are considered to be more bile-resistant compared to Gram-positive bacteria and are thought to tolerate high bile concentrations.
Here, we show that 1-2% of GCA inhibit the growth of Enterobacteriaceae species, including , . spp., spp., and spp. during their late logarithmic phase in liquid culture, but not in solid media. Despite their lipopolysaccharide membrane layer, we demonstrate that, in liquid, GCA increases permeability, changes the surface of the Enterobacteriaceae membrane, and compromises its integrity. These changes result in leakage of cytoplasmic proteins and enhancement of their susceptibility to antibiotics. Moreover, GCA significantly reduces bacterial motility, the frequency of bacterial conjugation and horizontal acquisition of antibiotic resistance genes. These phenotypes are associated with repression of flagellin () transcription and a sharp decrease in the occurrence of conjugative pili in the presence of glycocholic acid, respectively.
Overall, these findings broaden the current understanding about bile resistance of Gram-negative bacteria and suggest that GCA can be used to inhibit bacterial growth, augment the activity of antimicrobial compounds and diminish acquisition and dissemination of antibiotic resistance genes by conjugation.
甘氨胆酸(GCA)是一种类固醇酸,是哺乳动物胆汁中主要的甘氨酸共轭胆汁成分之一,参与脂肪和固醇的乳化与吸收。长期以来已知胆汁酸的两亲性使其能够与革兰氏阳性菌的脂质膜相互作用,并作为有效的抗菌化合物发挥作用。然而,与革兰氏阳性菌相比,栖息于哺乳动物肠道的革兰氏阴性肠杆菌科细菌被认为对胆汁具有更强的抗性,并且被认为能够耐受高胆汁浓度。
在此,我们表明1 - 2%的GCA可抑制肠杆菌科细菌的生长,包括在液体培养的对数后期阶段的 、 、 属和 属细菌,但在固体培养基中则不然。尽管它们有脂多糖膜层,但我们证明,在液体中,GCA会增加通透性,改变肠杆菌科细菌膜的表面,并损害其完整性。这些变化导致细胞质蛋白泄漏,并增强它们对抗生素的敏感性。此外,GCA显著降低细菌的运动性、细菌接合频率以及抗生素抗性基因的水平获得。这些表型分别与鞭毛蛋白()转录的抑制以及在甘氨胆酸存在下接合菌毛出现频率的急剧下降有关。
总体而言,这些发现拓宽了当前对革兰氏阴性菌胆汁抗性的认识,并表明GCA可用于抑制细菌生长、增强抗菌化合物的活性以及减少通过接合作用获得和传播抗生素抗性基因。