Aqawi Muna, Sionov Ronit Vogt, Friedman Michael, Steinberg Doron
The Biofilm Research Laboratory, The Institute of Biomedical and Oral Research (IBOR), The Faculty of Dental Medicine, The Hebrew University of Jerusalem, Jerusalem 9112102, Israel.
The Institute of Drug Research, School of Pharmacy, The Hebrew University of Jerusalem, Jerusalem 9112102, Israel.
Biomedicines. 2023 Feb 22;11(3):668. doi: 10.3390/biomedicines11030668.
Bacteria can communicate through an intercellular signaling system referred to as quorum sensing (QS). The QS system involves the production of autoinducers that interact with their respective receptors, leading to the induction of specific signal transduction pathways. The QS systems of the oral cariogenic regulate the maturation of biofilms and affect its virulent properties. We have previously shown that the non-psychoactive compound cannabigerol (CBG) of the L. plant has anti-bacterial and anti-biofilm activities towards . Here we were interested in investigating the effect of the two QS systems ComCDE and LuxS on the susceptibility of to CBG and the anti-QS activities of CBG. This was assessed by using various and mutant strains and complementation with the respective autoinducers, competence stimulating peptide (CSP) and (S)-4,5-dihydroxy-2,3-pentandione (DPD, pre-AI-2). We found that knockout strains were more sensitive to the anti-bacterial actions of CBG compared to the WT strain. Exogenously added 21-CSP prevented the anti-bacterial actions caused by CBG on the , and mutants, while having no effect on the susceptibility of the WT and strains to CBG. Exogenously added DPD increased the susceptibility of WT and to CBG. Vice versa, CBG significantly reduced the 21-CSP-induced expression of genes and ComE-regulated genes and suppressed the expression of with concomitant reduction in AI-2 production. DPD induced the expression of genes and ComE-regulated genes, and this induction was repressed by CBG. 21-CSP alone had no significant effect on gene expression, while strains showed reduced AI-2 production. In conclusion, our study shows that the susceptibility of to CBG is affected by the ComCDE and LuxS QS pathways, and CBG is a potential anti-QS compound for . Additionally, we provide evidence for crosstalk between the ComCDE and LuxS QS systems.
细菌可通过一种称为群体感应(QS)的细胞间信号系统进行通讯。群体感应系统涉及自诱导物的产生,这些自诱导物与其各自的受体相互作用,从而导致特定信号转导途径的诱导。口腔致龋菌的群体感应系统调节生物膜的成熟并影响其毒力特性。我们之前已经表明,植物乳杆菌的非精神活性化合物大麻二酚(CBG)对[具体细菌名称未给出]具有抗菌和抗生物膜活性。在此,我们感兴趣的是研究两种群体感应系统ComCDE和LuxS对[具体细菌名称未给出]对CBG的敏感性的影响以及CBG的抗群体感应活性。这是通过使用各种[具体细菌名称未给出]和突变菌株,并与各自的自诱导物、感受态刺激肽(CSP)和(S)-4,5-二羟基-2,3-戊二酮(DPD,前体AI-2)互补来评估的。我们发现,与野生型菌株相比,[具体细菌名称未给出]敲除菌株对CBG的抗菌作用更敏感。外源添加的21-CSP可防止CBG对[具体细菌名称未给出]、[具体细菌名称未给出]和[具体细菌名称未给出]突变体产生的抗菌作用,而对野生型和[具体细菌名称未给出]菌株对CBG的敏感性没有影响。外源添加的DPD增加了野生型和[具体细菌名称未给出]对CBG的敏感性。反之,CBG显著降低了21-CSP诱导的[具体细菌名称未给出]基因和ComE调控基因的表达,并抑制了[具体细菌名称未给出]的表达,同时伴随着AI-2产量的降低。DPD诱导了[具体细菌名称未给出]基因和ComE调控基因的表达,而这种诱导被CBG抑制。单独的21-CSP对[具体细菌名称未给出]基因表达没有显著影响,而[具体细菌名称未给出]菌株显示AI-2产量降低。总之,我们的研究表明,[具体细菌名称未给出]对CBG的敏感性受ComCDE和LuxS群体感应途径的影响,并且CBG是[具体细菌名称未给出]的一种潜在抗群体感应化合物。此外,我们提供了ComCDE和LuxS群体感应系统之间存在串扰的证据。