Kuchma Sherry L, Connolly John P, O'Toole George A
Department of Microbiology and Immunology, Dartmouth Medical School, North College St., Hanover, NH 03755, USA.
J Bacteriol. 2005 Feb;187(4):1441-54. doi: 10.1128/JB.187.4.1441-1454.2005.
Biofilms are structured communities found associated with a wide range of surfaces. Here we report the identification of a three-component regulatory system required for biofilm maturation by Pseudomonas aeruginosa strain PA14. A transposon mutation that altered biofilm formation in a 96-well dish assay originally defined this locus, which is comprised of genes for a putative sensor histidine kinase and two response regulators and has been designated sadARS. Nonpolar mutations in any of the sadARS genes result in biofilms with an altered mature structure but do not confer defects in growth or early biofilm formation, swimming, or twitching motility. After 2 days of growth under flowing conditions, biofilms formed by the mutants are indistinguishable from those formed by the wild-type (WT) strain. However, by 5 days, mutant biofilms appear to be more homogeneous than the WT in that they fail to form large and distinct macrocolonies and show a drastic reduction in water channels. We propose that the sadARS three-component system is required for later events in biofilm formation on an abiotic surface. Semiquantitative reverse transcription-PCR analysis showed that there is no detectable change in expression of the sadARS genes when cells are grown in a planktonic culture versus a biofilm, indicating that this locus is not itself induced during or in response to biofilm formation. DNA microarray studies were used to identify downstream targets of the SadARS system. Among the genes regulated by the SadARS system are those required for type III secretion. Mutations in type III secretion genes result in strains with enhanced biofilm formation. We propose a possible mechanism for the role that the SadARS system plays in biofilm formation.
生物膜是与多种表面相关的结构化群落。在此,我们报告了对铜绿假单胞菌PA14菌株生物膜成熟所需的一个三组分调节系统的鉴定。最初在96孔板试验中改变生物膜形成的一个转座子突变定义了这个位点,它由一个推定的传感器组氨酸激酶和两个反应调节因子的基因组成,并被命名为sadARS。sadARS基因中任何一个的非极性突变都会导致生物膜的成熟结构发生改变,但不会在生长、早期生物膜形成、游动或摆动运动方面产生缺陷。在流动条件下生长2天后,突变体形成的生物膜与野生型(WT)菌株形成的生物膜无法区分。然而,到第5天时,突变体生物膜似乎比WT更均匀,因为它们无法形成大的、明显的大菌落,并且水通道显著减少。我们提出,sadARS三组分系统是在非生物表面上生物膜形成后期事件所必需的。半定量逆转录 - PCR分析表明,当细胞在浮游培养物中生长与在生物膜中生长时,sadARS基因的表达没有可检测到的变化,这表明该位点本身在生物膜形成过程中或对生物膜形成的反应中不会被诱导。DNA微阵列研究用于鉴定SadARS系统的下游靶点。SadARS系统调节的基因中包括III型分泌所需的基因。III型分泌基因的突变导致生物膜形成增强的菌株。我们提出了SadARS系统在生物膜形成中所起作用的一种可能机制。