Domka Joanna, Lee Jintae, Wood Thomas K
Artie McFerrin Department of Chemical Engineering, 220 Jack E. Brown Building, Texas A&M University, College Station, TX 77843-3122, USA.
Appl Environ Microbiol. 2006 Apr;72(4):2449-59. doi: 10.1128/AEM.72.4.2449-2459.2006.
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 < or = 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 < or = 0.05) in LB, and YceP repressed motility sevenfold (P < or = 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."
我们之前发现,yliH和yceP在大肠杆菌生物膜中被诱导表达(D. Ren、L. A. Bedzyk、S. M. Thomas、R. W. Ye和T. K. Wood,《应用微生物学与生物技术》64:515 - 524,2004年)。在此,研究表明,在含极少葡萄糖的连续流培养室中,缺失yceP(b1060)和yliH(b0836)会通过增加生物膜量(240至290倍)、表面覆盖率(16至31倍)和平均厚度(2800倍)来增强生物膜形成。为确定生物膜形成增加的遗传基础,我们检测了在富含葡萄糖的培养基中,这两个突变体相对于野生型菌株在生物膜中的差异基因表达谱,发现有372至882个基因被诱导,76至337个基因被持续抑制超过2倍(P≤0.05)。这两个突变体生物膜形成的增加与应激反应相关基因(8至64个基因)的差异表达有关,包括rpoS和sdiA。更重要的是,42至130个与自诱导物2细胞信号传导相关的基因也有差异表达,包括gadAB和flgBCEGHIJLMN,以及通过吲哚的信号传导,因为有17至26个与吲哚相关的基因有差异表达,包括phoAER、gltBD、mtr(编码吲哚转运蛋白)和acrEF(编码吲哚输出蛋白)。在添加0.2%葡萄糖的LB培养基(LB glu)中,yliH和yceP突变体生物膜形成增加是由于两个突变体胞外和胞内吲哚浓度均降低(50至140倍),向培养物中添加吲哚可恢复野生型生物膜表型;因此,吲哚可抑制生物膜。此外,两个突变体都通过群体感应调节生物膜,因为在复杂培养基中生长(最显著的是在稳定期)时,缺失yliH或yceP会使胞外自诱导物2浓度增加50倍。这两种蛋白质都参与运动性调节,因为YliH(127个氨基酸)和YceP(84个氨基酸)在LB中使运动性降低2至7倍(P≤0.05),而YceP在LB glu中使运动性降低7倍(P≤0.05)。yceP突变体中运动性增强是由于鞭毛和运动性基因座的转录增加,包括fliC、motA和qseB(3至86倍)。基于“通过信号分泌调节生物膜”这一表述,我们为这两个基因座提出了新名称:yliH为bssR,yceP为bssS。