Institut für Mikrobiologie und Tierseuchen, Freie Universität Berlin, Philippstr, 13, 10115 Berlin, Germany.
Gut Pathog. 2009 Dec 10;1(1):22. doi: 10.1186/1757-4749-1-22.
The ability to adhere to host surfaces is by far the most vital step in the successful colonization by microbial pathogens. Colonization begins with the attachment of the bacterium to receptors expressed by cells forming the lining of the mucosa. Long hair like extracellular appendages called fimbriae, produced by most Gram-negative pathogens, mediate specific attachment to the epithelial cell surface. Associated with the fimbriae is a protein called an adhesin, which directs high-affinity binding to specific cell surface components. In the last couple of years, an enormous amount of research has been undertaken that deals with understanding how bacterial pathogens adhere to host cells. E. coli in all probability is one of the best studied free-living organisms. A group of E. coli called Extraintestinal pathogenic E. coli (ExPEC) including both human and animal pathogens like Uropathogenic E. coli (UPEC), Newborn meningitic E. coli (NMEC) and Avian pathogenic E. coli (APEC), have been found to harbour many fimbriae including Type 1 fimbriae, P fimbriae, curli fibres, S fimbriae, F1C fimbriae, Dr fimbriae, afimbrial adhesins, temperature-sensitive haemagglutinin and many novel adhesin gene clusters that have not yet been characterized. Each of these adhesins is unique due to the recognition of an adhesin-specific receptor, though as a group these adhesins share common genomic organization. A newly identified putative adhesin temporarily termed ExPEC Adhesin I, encoded by gene yqi, has been recently found to play a significant role in the pathogenesis of APEC infection, thus making it an interesting candidate for future research. The aim of this review is to describe the role of ExPEC adhesins during extraintestinal infections known till date, and to suggest the idea of investigating their potential role in the colonization of the host gut which is said to be a reservoir for ExPEC.
到目前为止,微生物病原体成功定殖宿主的最重要步骤是能够附着在宿主表面。定殖始于细菌附着在构成黏膜衬里的细胞表达的受体上。大多数革兰氏阴性病原体产生的长毛发状细胞外附属物称为菌毛,介导与上皮细胞表面的特异性附着。与菌毛相关的是一种称为黏附素的蛋白质,它指导与特定细胞表面成分的高亲和力结合。在过去的几年中,已经进行了大量的研究来了解细菌病原体如何附着在宿主细胞上。大肠杆菌很可能是研究最多的自由生活生物之一。一组称为肠外致病性大肠杆菌(ExPEC)的大肠杆菌,包括人类和动物病原体,如尿路致病性大肠杆菌(UPEC)、新生脑膜炎大肠杆菌(NMEC)和禽致病性大肠杆菌(APEC),被发现拥有许多菌毛,包括 1 型菌毛、P 菌毛、卷曲菌纤维、S 菌毛、F1C 菌毛、Dr 菌毛、无菌毛黏附素、温度敏感血凝素和许多尚未被表征的新型黏附素基因簇。由于识别特定黏附素的受体,每种黏附素都是独特的,尽管作为一组,这些黏附素具有共同的基因组组织。最近发现一种新鉴定的假定黏附素,暂时称为 ExPEC 黏附素 I,由基因 yqi 编码,在 APEC 感染的发病机制中发挥重要作用,因此成为未来研究的有趣候选者。本文综述的目的是描述 ExPEC 黏附素在迄今为止已知的肠外感染中的作用,并提出研究其在宿主肠道定植中潜在作用的想法,因为据说宿主肠道是 ExPEC 的储存库。