Martino P Di, Fursy R, Bret L, Sundararaju B, Phillips R S
Equipe de Recherche sur les Relations Matrice Extracellulaire-Cellules, Université de Cergy-Pontoise, Pontoise, France.
Can J Microbiol. 2003 Jul;49(7):443-9. doi: 10.1139/w03-056.
We demonstrated previously that genetic inactivation of tryptophanase is responsible for a dramatic decrease in biofilm formation in the laboratory strain Escherichia coli S17-1. In the present study, we tested whether the biochemical inhibition of tryptophanase, with the competitive inhibitor oxindolyl-L-alanine, could affect polystyrene colonization by E. coli and other indole-producing bacteria. Oxindolyl-L-alanine inhibits, in a dose-dependent manner, indole production and biofilm formation by strain S17-1 grown in Luria-Bertani (LB) medium. Supplementation with indole at physiologically relevant concentrations restores biofilm formation by strain S17-1 in the presence of oxindolyl-L-alanine and by mutant strain E. coli 3714 (S17-1 tnaA::Tn5) in LB medium. Oxindolyl-L-alanine also inhibits the adherence of S17-1 cells to polystyrene for a 3-h incubation time, but mutant strain 3714 cells are unaffected. At 0.5 mg/mL, oxindolyl-L-alanine exhibits inhibitory activity against biofilm formation in LB medium and in synthetic urine for several clinical isolates of E. coli, Klebsiella oxytoca, Citrobacter koseri, Providencia stuartii, and Morganella morganii but has no affect on indole-negative Klebsiella pneumoniae strains. In conclusion, these data suggest that indole, produced by the action of tryptophanase, is involved in polystyrene colonization by several indole-producing bacterial species. Indole may act as a signalling molecule to regulate the expression of adhesion and biofilm-promoting factors.
我们之前证明,色氨酸酶的基因失活是实验室菌株大肠杆菌S17-1生物膜形成显著减少的原因。在本研究中,我们测试了用竞争性抑制剂氧化吲哚基-L-丙氨酸对色氨酸酶进行生化抑制是否会影响大肠杆菌和其他产吲哚细菌在聚苯乙烯上的定殖。氧化吲哚基-L-丙氨酸以剂量依赖的方式抑制在Luria-Bertani(LB)培养基中生长的S17-1菌株的吲哚产生和生物膜形成。在存在氧化吲哚基-L-丙氨酸的情况下,用生理相关浓度的吲哚补充可恢复S17-1菌株的生物膜形成,以及突变菌株大肠杆菌3714(S17-1 tnaA::Tn5)在LB培养基中的生物膜形成。氧化吲哚基-L-丙氨酸在3小时的孵育时间内也抑制S17-1细胞对聚苯乙烯的粘附,但突变菌株3714细胞不受影响。在0.5 mg/mL时,氧化吲哚基-L-丙氨酸对几种大肠杆菌、产酸克雷伯菌、科氏柠檬酸杆菌、斯氏普罗威登斯菌和摩根氏摩根菌的临床分离株在LB培养基和合成尿液中的生物膜形成具有抑制活性,但对吲哚阴性的肺炎克雷伯菌菌株没有影响。总之,这些数据表明,由色氨酸酶作用产生的吲哚参与了几种产吲哚细菌物种在聚苯乙烯上的定殖。吲哚可能作为一种信号分子来调节粘附和生物膜促进因子的表达。