Cookson Adrian L, Cooley William A, Woodward Martin J
Department of Bacterial Diseases, Veterinary Laboratories Agency Weybridge, Addlestone, Surrey, UK.
Int J Med Microbiol. 2002 Sep;292(3-4):195-205. doi: 10.1078/1438-4221-00203.
Biofilm formation on abiotic surfaces may provide a source of microbial contamination and may also enhance microbial environmental survival. The role of fimbrial expression by Shiga toxin-producing Escherichia coli (STEC) in biofilm formation is poorly understood. This study aimed to investigate the role of STEC type 1 and curli fimbriae in adhesion to and biofilm formation on abiotic surfaces. None of 13 O157:H7 isolates expressed either fimbrial type whereas 11 of 13 and 5 of 13 non-O157 STEC elaborated type 1 fimbriae and curli fimbriae, respectively. Mutants made by allelic exchange of a diarrhoeal non-O157 STEC isolate, O128:H2 (E41509), unable to elaborate type 1 and curli fimbriae were made for adherence and biofilm assays. Elaboration of type 1 fimbriae was necessary for the adhesion to abiotic surfaces whereas curliation was associated with both adherence and subsequent biofilm formation. STEC O157:H7 adhered to thermanox and glass but poorly to polystyrene. Additionally, STEC O157:H7 failed to form biofilms. These data indicate that certain STEC isolates are able to form biofilms and that the elaboration of curli fimbriae may enhance biofilm formation leading to possible long-term survival and a potential source of human infection.
非生物表面上生物膜的形成可能会成为微生物污染的一个来源,还可能增强微生物在环境中的生存能力。产志贺毒素大肠杆菌(STEC)菌毛表达在生物膜形成中的作用目前了解甚少。本研究旨在调查STEC 1型菌毛和卷曲菌毛在非生物表面黏附和生物膜形成中的作用。13株O157:H7分离株均不表达这两种菌毛类型,而13株非O157 STEC中分别有11株和5株表达1型菌毛和卷曲菌毛。通过等位基因交换构建了一株腹泻性非O157 STEC分离株O128:H2(E41509)的突变体,该突变体无法表达1型菌毛和卷曲菌毛,用于黏附及生物膜测定。1型菌毛的表达对于非生物表面的黏附是必需的,而卷曲菌毛的形成与黏附及随后的生物膜形成均有关联。STEC O157:H7能黏附到聚四氟乙烯和玻璃上,但对聚苯乙烯的黏附性较差。此外,STEC O157:H7无法形成生物膜。这些数据表明,某些STEC分离株能够形成生物膜,卷曲菌毛的形成可能会增强生物膜形成,从而导致可能的长期生存及成为人类感染的一个潜在来源。