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首页> 外文期刊>Canadian journal of microbiology >Isolation of an Escherichia coli strain mutant unable to form biofilm on polystyrene and to adhere to human pneumocyte cells: involvement of tryptophanase
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Isolation of an Escherichia coli strain mutant unable to form biofilm on polystyrene and to adhere to human pneumocyte cells: involvement of tryptophanase

机译:大肠杆菌菌株突变体的分离,该突变体无法在聚苯乙烯上形成生物膜并不能粘附于人的肺细胞:色氨酸酶的参与

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Escherichia coli adherence to biotic and abiotic surfaces constitutes the first step of infection by promoting colonization and biofilm formation. The aim of this study was to gain a better understanding of the relationship between E. coli adherence to different biotic surfaces and biofilm formation on abiotic surfaces. We isolated mutants defective in A549 pneumocyte cells adherence, fibronectin adherence, and biofilm formation by random transposition mutagenesis and sequential passages over A549 cell monolayers. Among the 97 mutants tested, 80 were decreased in biofilm formation, 8 were decreased in A549 cells adherence, 7 were decreased in their adherence to fibronectin, and 17 had no perturbations in either of the three phenotypes. We observed a correlation between adherence to fibronectin or A549 cells and biofilm formation, indicating that biotic adhesive factors are involved in biofilm formation by E. coli. Molecular analysis of the mutants revealed that a transposon insertion in the tnaA gene encoding for tryptophanase was associated with a decrease in both A549 cells adherence and biofilm formation by E. coli. The complementation of the tnaA mutant with plasmid-located wild-type tnaA restored the tryptophanase activity, epithelial cells adherence, and biofilm formation on polystyrene. The possible mechanism of tryptophanase involvement in E. coli adherence and biofilm formation is discussed.
机译:大肠杆菌对生物和非生物表面的粘附是通过促进定殖和生物膜形成而构成感染的第一步。这项研究的目的是为了更好地理解大肠杆菌对不同生物表面的粘附与非生物表面生物膜形成之间的关系。我们通过随机换位诱变和在A549细胞单层上连续传代,分离了A549肺细胞粘附,纤连蛋白粘附和生物膜形成缺陷的突变体。在测试的97个突变体中,有80个生物膜形成减少,8个A549细胞粘附减少,7个对纤连蛋白的粘附减少,并且17个在这三个表型中都没有扰动。我们观察到对纤连蛋白或A549细胞的粘附与生物膜形成之间的相关性,表明生物粘附因子参与大肠杆菌的生物膜形成。突变体的分子分析表明,转座子在编码色氨酸酶的tnaA基因中的插入与大肠杆菌对A549细胞粘附和生物膜形成的减少有关。 tnaA突变体与质粒定位的野生型tnaA的互补恢复了色氨酸酶活性,上皮细胞粘附以及在聚苯乙烯上的生物膜形成。色氨酸酶参与大肠杆菌粘附和生物膜形成的可能机制进行了讨论。

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