Struve Carsten, Bojer Martin, Krogfelt Karen Angeliki
Department of Bacteriology, Mycology and Parasitology, Statens Serum Institut, Copenhagen, Denmark.
Infect Immun. 2008 Sep;76(9):4055-65. doi: 10.1128/IAI.00494-08. Epub 2008 Jun 16.
Klebsiella pneumoniae is recognized as an important gram-negative opportunistic pathogen. The ability of bacteria to adhere to host structures is considered essential for the development of infections; however, few studies have examined the influence of adhesion factors on K. pneumoniae virulence. In this study, we cloned and characterized the type 1 fimbria gene cluster of a clinical K. pneumoniae isolate. Although this cluster was not identical to the Escherichia coli type 1 fimbria gene cluster, an overall high degree of structural resemblance was demonstrated. Unique to the K. pneumoniae fim gene cluster is the fimK gene, whose product contains an EAL domain, suggesting that it has a role in regulation of fimbrial expression. Like expression of type 1 fimbriae in E. coli, expression of type 1 fimbriae in K. pneumoniae was found to be phase variable, and an invertible DNA element (fim switch) was characterized. An isogenic type 1 fimbria mutant was constructed and used to evaluate the influence of type 1 fimbriae in different infection models. Type 1 fimbriae did not influence the ability of K. pneumoniae to colonize the intestine or infect the lungs, but they were determined to be a significant virulence factor in K. pneumoniae urinary tract infection. By use of a PCR-based assay, the orientation of the fim switch during colonization and infection was investigated and was found to be all "off" in the intestine and lungs but all "on" in the urinary tract. Our results suggest that during colonization and infection, there is pronounced selective pressure in different host environments for selection of either the type 1 fimbriated or nonfimbriated phenotype of K. pneumoniae.
肺炎克雷伯菌被认为是一种重要的革兰氏阴性机会致病菌。细菌黏附于宿主结构的能力被认为是感染发生的关键;然而,很少有研究探讨黏附因子对肺炎克雷伯菌毒力的影响。在本研究中,我们克隆并鉴定了一株临床肺炎克雷伯菌分离株的1型菌毛基因簇。尽管该基因簇与大肠杆菌的1型菌毛基因簇并不完全相同,但整体结构相似度较高。肺炎克雷伯菌菌毛基因簇特有的是fimK基因,其产物含有一个EAL结构域,表明它在菌毛表达调控中发挥作用。与大肠杆菌中1型菌毛的表达情况类似,肺炎克雷伯菌中1型菌毛的表达也具有相变特性,并且鉴定出了一个可逆DNA元件(菌毛开关)。构建了一个同基因的1型菌毛突变体,并用于评估1型菌毛在不同感染模型中的影响。1型菌毛不影响肺炎克雷伯菌在肠道定植或感染肺部的能力,但它们被确定为肺炎克雷伯菌尿路感染中的一个重要毒力因子。通过基于PCR的检测方法,研究了菌毛开关在定植和感染过程中的方向,发现其在肠道和肺部均为“关闭”状态,而在尿路中均为“开启”状态。我们的结果表明,在定植和感染过程中,不同宿主环境对肺炎克雷伯菌1型菌毛化或非菌毛化表型的选择存在明显的选择性压力。