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利用fosmid文库筛选参与肺炎克雷伯菌生物膜形成的基因。

Screening for genes involved in Klebsiella pneumoniae biofilm formation using a fosmid library.

作者信息

Stahlhut Steen G, Schroll Casper, Harmsen Morten, Struve Carsten, Krogfelt Karen A

机构信息

Department of Microbiological Surveillance and Research, Statens Serum Institut, Copenhagen S, Denmark.

出版信息

FEMS Immunol Med Microbiol. 2010 Aug;59(3):521-4. doi: 10.1111/j.1574-695X.2010.00685.x. Epub 2010 Apr 14.

Abstract

Klebsiella pneumoniae is a well-known opportunistic pathogen, often causing catheter-associated urinary tract infections. Biofilm formation on the catheter surfaces is an important step in the development of these infections. To identify the genes involved in the ability of K. pneumoniae to form a biofilm on abiotic surfaces, a novel strategy was used. A clone library was constructed by cloning the entire K. pneumoniae genome of the clinical isolate C3091 into a fosmid vector and the clone library was expressed in Escherichia coli. A total of 1152 clones were screened for enhanced biofilm formation compared with the E. coli parent strain using a biofilm microtiter plate assay. Nine clones with significantly enhanced biofilm formation were identified, subjected to random Tn5 transposon mutagenesis, screened for biofilm deficiency and the biofilm-promoting genes identified. Five of the clones contained the type 3 fimbriae gene cluster, a well-known K. pneumoniae virulence factor and biofilm promoter. Thus, the effectiveness of our approach was confirmed. Furthermore, genes encoding cell surface proteins and proteins involved in metabolism, none of them previously associated with biofilm formation in K. pneumoniae, were identified by our screening method. In conclusion, the use of fosmid libraries is an effective high throughput screening method to identify the genes involved in biofilm formation.

摘要

肺炎克雷伯菌是一种著名的机会致病菌,常引起导管相关的尿路感染。在导管表面形成生物膜是这些感染发展过程中的重要一步。为了鉴定参与肺炎克雷伯菌在非生物表面形成生物膜能力的基因,采用了一种新策略。通过将临床分离株C3091的整个肺炎克雷伯菌基因组克隆到一个fosmid载体中构建克隆文库,并在大肠杆菌中表达该克隆文库。使用生物膜微量滴定板分析法,与大肠杆菌亲本菌株相比,共筛选了1152个克隆以寻找增强的生物膜形成。鉴定出9个生物膜形成显著增强的克隆,对其进行随机Tn5转座子诱变,筛选生物膜缺陷并鉴定生物膜促进基因。其中5个克隆含有3型菌毛基因簇,这是一种著名的肺炎克雷伯菌毒力因子和生物膜促进因子。因此,证实了我们方法的有效性。此外,通过我们的筛选方法鉴定出了编码细胞表面蛋白和参与代谢的蛋白的基因,这些基因以前均未与肺炎克雷伯菌的生物膜形成相关联。总之,使用fosmid文库是鉴定参与生物膜形成基因的一种有效的高通量筛选方法。

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