Infectious Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Yusong, Daejeon, 34141, Republic of Korea.
Nat Commun. 2024 Jul 6;15(1):5683. doi: 10.1038/s41467-024-50116-3.
Bacteria within mature biofilms are highly resistant to antibiotics than planktonic cells. Oxygen limitation contributes to antibiotic resistance in mature biofilms. Nitric oxide (NO) induces biofilm dispersal; however, low NO levels stimulate biofilm formation, an underexplored process. Here, we introduce a mechanism of anaerobic biofilm formation by investigating the antibiofilm activity of tyrosol, a component in wine. Tyrosol inhibits E. coli and Pseudomonas aeruginosa biofilm formation by enhancing NO production. YbfA is identified as a target of tyrosol and its downstream targets are sequentially determined. YbfA activates YfeR, which then suppresses the anaerobic regulator FNR. This suppression leads to decreased NO production, elevated bis-(3'-5')-cyclic dimeric GMP levels, and finally stimulates anaerobic biofilm formation in the mature stage. Blocking YbfA with tyrosol treatment renders biofilm cells as susceptible to antibiotics as planktonic cells. Thus, this study presents YbfA as a promising antibiofilm target to address antibiotic resistance posed by biofilm-forming bacteria, with tyrosol acting as an inhibitor.
成熟生物膜中的细菌对抗生素的抵抗力比浮游细胞高。氧气限制导致成熟生物膜中的抗生素耐药性。一氧化氮 (NO) 诱导生物膜分散;然而,低水平的 NO 刺激生物膜形成,这是一个尚未充分探索的过程。在这里,我们通过研究葡萄酒中的一种成分——酪醇,介绍了一种厌氧生物膜形成的机制。酪醇通过增强 NO 产生来抑制大肠杆菌和铜绿假单胞菌的生物膜形成。鉴定出 YbfA 是酪醇的靶标,并且其下游靶标是依次确定的。YbfA 激活 YfeR,然后抑制厌氧调节剂 FNR。这种抑制导致 NO 产生减少、双-(3'-5')-环二核苷酸 GMP 水平升高,最终刺激成熟阶段的厌氧生物膜形成。用酪醇处理阻断 YbfA 使生物膜细胞对浮游细胞一样容易受到抗生素的影响。因此,这项研究提出 YbfA 是一个有前途的抗生物膜靶标,可以解决由形成生物膜的细菌引起的抗生素耐药性问题,而酪醇则作为抑制剂发挥作用。