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YliH (BssR) and YceP (BssS) Regulate Escherichia coli K-12 Biofilm Formation by Influencing Cell Signaling

机译:YliH(BssR)和YceP(BssS)通过影响细胞信号传导来调节大肠杆菌K-12生物膜的形成

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摘要

We previously discovered that yliH and yceP are induced in Escherichia coli biofilms (D. Ren, L. A. Bedzyk, S. M. Thomas, R. W. Ye, and T. K. Wood, Appl. Microbiol. Biotechnol. >64:515-524, 2004). Here, it is shown that deletion of yceP (b1060) and yliH (b0836) increases biofilm formation in continuous-flow chambers with minimal glucose medium by increasing biofilm mass (240- to 290-fold), surface coverage (16- to 31-fold), and mean thickness (2,800-fold). To determine the genetic basis of the increase in biofilm formation, we examined the differential gene expression profile in biofilms for both the mutants relative to the wild-type strain in rich medium with glucose and found that 372 to 882 genes were induced and that 76 to 337 were repressed consistently >2-fold (P ≤ 0.05). The increase in biofilm formation was related to differential expression of genes related to stress response (8 to 64 genes) for both mutants, including rpoS and sdiA. More importantly, 42 to 130 genes related to autoinducer 2 cell signaling were also differentially expressed, including gadAB and flgBCEGHIJLMN, as well as signaling through indole, since 17 to 26 indole-related genes were differentially expressed, including phoAER, gltBD, mtr (encodes protein for indole import), and acrEF (encodes proteins for indole export). Increased biofilm formation in the yliH and yceP mutants in LB supplemented with 0.2% glucose (LB glu) occurred through a reduction in extracellular and intracellular indole concentrations in both mutants (50- to 140-fold), and the addition of indole to the culture restored the wild-type biofilm phenotype; hence, indole represses biofilms. Additionally, both mutants regulate biofilms through quorum sensing, since deletion of either yliH or yceP increased extracellular autoinducer 2 concentrations 50-fold when grown in complex medium (most notably in the stationary phase). Both proteins are involved in motility regulation, since YliH (127 amino acids) and YceP (84 amino acids) repressed motility two to sevenfold (P ≤ 0.05) in LB, and YceP repressed motility sevenfold (P ≤ 0.05) in LB glu. Heightened motility in the yceP mutant occurred, due to increased transcription of the flagella and motility loci, including fliC, motA, and qseB (3- to 86-fold). We propose new names for these two loci: bssR for yliH and bssS for yceP, based on the phrase “regulator of biofilm through signal secretion.”
机译:我们先前发现yliH和yceP在大肠杆菌生物膜中被诱导(D. Ren,LA Bedzyk,SM Thomas,RW Ye和TK Wood,Appl。Microbiol。Biotechnol。> 64: 515-524, 2004)。在此显示,yceP(b1060)和yliH(b0836)的缺失通过增加生物膜质量(240-至290倍),表面覆盖率(16-31-倍)和平均厚度(2,800倍)。为了确定生物膜形成增加的遗传基础,我们检查了在富含葡萄糖的培养基中,与野生型菌株相关的两个突变体在生物膜中的差异基因表达谱,发现诱导了372至882个基因,其中76个337压抑持续> 2倍(P≤0.05)。生物膜形成的增加与两个突变体(包括rpoS和sdiA)与胁迫反应相关的基因(8至64个基因)的差异表达有关。更重要的是,与自动诱导物2细胞信号转导相关的42至130个基因也被差异表达,包括gadAB和flgBCEGHIJLMN,以及通过吲哚的信号转导,因为17至26个与吲哚相关的基因被差异表达,包括phoAER,gltBD,mtr(编码吲哚进口蛋白)和acrEF(编码吲哚出口蛋白)。补充了0.2%葡萄糖(LB glu)的LB中yliH和yceP突变体中生物膜形成的增加是通过两个突变体中细胞外和细胞内吲哚浓度的降低(50-至140倍)以及向培养物中添加吲哚而发生的。恢复了野生型生物膜表型;因此,吲哚抑制生物膜。此外,这两个突变体均通过群体感应来调节生物膜,因为在复杂培养基中生长时, yliH yceP 的缺失会增加细胞外自诱导因子2的浓度50倍(最显着的是在固定培养基中)相)。两种蛋白质都参与运动调节,因为YliH(127个氨基酸)和YceP(84个氨基酸)在LB中将运动抑制了2到7倍( P ≤0.05),而YceP将运动抑制了7倍( P ≤0.05)(LB glu)。由于鞭毛和运动位点包括 fliC motA qseB的转录增加,导致 yceP 突变体的运动性增强。 (3至86倍)。我们为这两个基因座提议新的名称: yliH bssR yceP bssS ,通过信号分泌调节生物膜。”

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