Blanco-Romero Esther, Garrido-Sanz Daniel, Durán David, Rybtke Morten, Tolker-Nielsen Tim, Redondo-Nieto Miguel, Rivilla Rafael, Martín Marta
Departamento de Biología, Facultad de Ciencias, Universidad Autónoma de Madrid, Madrid, Spain.
Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland.
Front Microbiol. 2024 Jan 25;15:1341728. doi: 10.3389/fmicb.2024.1341728. eCollection 2024.
Regulating the transition of bacteria from motile to sessile lifestyles is crucial for their ability to compete effectively in the rhizosphere environment. are known to rely on extracellular matrix (ECM) components for microcolony and biofilm formation, allowing them to adapt to a sessile lifestyle. F113 possesses eight gene clusters responsible for the production of ECM components. These gene clusters are tightly regulated by AmrZ, a major transcriptional regulator that influences the cellular levels of c-di-GMP. The AmrZ-mediated transcriptional regulation of ECM components is primarily mediated by the signaling molecule c-di-GMP and the flagella master regulator FleQ. To investigate the functional role of these ECM components in F113, we performed phenotypic analyses using mutants in genes encoding these ECM components. These analyses included assessments of colony morphology, dye-staining, static attachment to abiotic surfaces, dynamic biofilm formation on abiotic surfaces, swimming motility, and competitive colonization assays of the rhizosphere. Our results revealed that alginate and PNAG polysaccharides, along with PsmE and the fimbrial low molecular weight protein/tight adherence (Flp/Tad) pilus, are the major ECM components contributing to biofilm formation. Additionally, we found that the majority of these components and MapA are needed for a competitive colonization of the rhizosphere in F113.
调控细菌从游动生活方式向固着生活方式的转变,对于它们在根际环境中有效竞争的能力至关重要。已知细菌依靠细胞外基质(ECM)成分进行微菌落和生物膜的形成,从而使其适应固着生活方式。F113拥有八个负责产生ECM成分的基因簇。这些基因簇受到AmrZ的严格调控,AmrZ是一种主要的转录调节因子,会影响细胞内c-di-GMP的水平。AmrZ介导的ECM成分转录调控主要由信号分子c-di-GMP和鞭毛主调节因子FleQ介导。为了研究这些ECM成分在F113中的功能作用,我们使用编码这些ECM成分的基因突变体进行了表型分析。这些分析包括菌落形态评估、染料染色、对非生物表面的静态附着、在非生物表面上的动态生物膜形成、游动性以及根际竞争定殖试验。我们的结果表明,藻酸盐和PNAG多糖,以及PsmE和菌毛低分子量蛋白/紧密黏附(Flp/Tad)菌毛,是促成生物膜形成的主要ECM成分。此外,我们发现F113在根际的竞争定殖需要这些成分中的大多数以及MapA。