a Department of Biosciences , Università degli Studi di Milano , Milan , Italy.
b Novo Nordisk Center for Biosustainabiliy , Technical University of Denmark , Kgs. Lyngby , Denmark.
Crit Rev Microbiol. 2018 Feb;44(1):1-30. doi: 10.1080/1040841X.2017.1303660. Epub 2017 May 9.
Escherichia coli can commonly be found, either as a commensal, probiotic or a pathogen, in the human gastrointestinal (GI) tract. Biofilm formation and its regulation is surprisingly variable, although distinct regulatory pattern of red, dry and rough (rdar) biofilm formation arise in certain pathovars and even clones. In the GI tract, environmental conditions, signals from the host and from commensal bacteria contribute to shape E. coli biofilm formation within the multi-faceted multicellular communities in a complex and integrated fashion. Although some major regulatory networks, adhesion factors and extracellular matrix components constituting E. coli biofilms have been recognized, these processes have mainly been characterized in vitro and in the context of interaction of E. coli strains with intestinal epithelial cells. However, direct observation of E. coli cells in situ, and the vast number of genes encoding surface appendages on the core or accessory genome of E. coli suggests the complexity of the biofilm process to be far from being fully understood. In this review, we summarize biofilm formation mechanisms of commensal, probiotic and pathogenic E. coli in the context of the gastrointestinal tract.
大肠杆菌通常可以在人类胃肠道(GI)中作为共生菌、益生菌或病原体存在。生物膜的形成及其调控是非常多变的,尽管某些病原菌甚至克隆中会出现红色、干燥和粗糙(rdar)生物膜形成的独特调控模式。在胃肠道中,环境条件、宿主和共生细菌的信号共同作用,以复杂和综合的方式塑造多细胞群落中的大肠杆菌生物膜形成。尽管已经识别出一些构成大肠杆菌生物膜的主要调控网络、粘附因子和细胞外基质成分,但这些过程主要是在体外和大肠杆菌菌株与肠道上皮细胞相互作用的背景下进行表征的。然而,直接观察原位大肠杆菌细胞以及核心或辅助基因组上编码表面附属物的大量基因表明,生物膜过程的复杂性远未被完全理解。在这篇综述中,我们总结了胃肠道中共生菌、益生菌和病原菌大肠杆菌的生物膜形成机制。