Fsr quorum sensing system modulates the temporal development of Enterococcus faecalis biofilm matrix

生物膜 群体感应 微生物学 粪肠球菌 明胶酶 毒力 细菌 生物 多糖 突变体 分泌物 胞外聚合物 化学 生物化学 基质金属蛋白酶 基因 金黄色葡萄球菌 遗传学
作者
Islam A. A. Ali,Christian Lévesque,Prasanna Neelakantan
出处
期刊:Molecular Oral Microbiology [Wiley]
卷期号:37 (1): 22-30 被引量:15
标识
DOI:10.1111/omi.12357
摘要

Quorum sensing (QS) is a cell-to-cell communication process that regulates major pathogenic attributes in bacteria including biofilm formation, secretion of virulence factors, and antimicrobial resistance. The two-component Fsr-QS system of the nosocomial pathogen Enterococcus faecalis controls the production of extracellular gelatinase that contributes to biofilm development by enhancing the release of nucleic acids into the biofilm matrix. However, the contribution of this system to the deposition of other biofilm matrix components such as polysaccharides and proteins remains unknown. Using wild type and mutant strains, we discovered that biofilm formation was attenuated by inactivation of the Fsr system or its downstream gelatinase production. Inactivation of the Fsr system caused a modest, yet significant reduction in biofilm metabolic activity without affecting cell counts. Inactivation of the QS-signal sensor FsrC and response regulator FsrA resulted in decreased extracellular polysaccharides and proteins in biofilms in a temporal manner. Irrespective of biofilm age, eDNA levels were reduced in the gelatinase mutant strain. Our results collectively suggest that the Fsr system contributes to the temporal deposition of polysaccharides and proteins into the extracellular polymeric matrix (EPS) of E. faecalis biofilm, without affecting bacterial viability. This understanding of the role of the Fsr-QS system in biofilm development may reveal a novel target to develop effective antibiofilm agents to tackle E. faecalis-mediated infections such as in dental root canals, heart valves, and surgical sites.

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