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Ⅰ型和Ⅲ型菌毛在肺炎克雷伯菌生物膜形成中的作用。

Role of type 1 and type 3 fimbriae in Klebsiella pneumoniae biofilm formation.

机构信息

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

出版信息

BMC Microbiol. 2010 Jun 23;10:179. doi: 10.1186/1471-2180-10-179.

Abstract

BACKGROUND

Klebsiella pneumoniae is an important gram-negative opportunistic pathogen causing primarily urinary tract infections, respiratory infections, and bacteraemia. The ability of bacteria to form biofilms on medical devices, e.g. catheters, has a major role in development of many nosocomial infections. Most clinical K. pneumoniae isolates express two types of fimbrial adhesins, type 1 fimbriae and type 3 fimbriae. In this study, we characterized the role of type 1 and type 3 fimbriae in K. pneumoniae biofilm formation.

RESULTS

Isogenic fimbriae mutants of the clinical K. pneumoniae isolate C3091 were constructed, and their ability to form biofilm was investigated in a flow cell system by confocal scanning laser microscopy. The wild type strain was found to form characteristic biofilm and development of K. pneumoniae biofilm occurred primarily by clonal growth, not by recruitment of planktonic cells. Type 1 fimbriae did not influence biofilm formation and the expression of type 1 fimbriae was found to be down-regulated in biofilm forming cells. In contrast, expression of type 3 fimbriae was found to strongly promote biofilm formation.

CONCLUSION

By use of well defined isogenic mutants we found that type 3 fimbriae, but not type 1 fimbriae, strongly promote biofilm formation in K. pneumoniae C3091. As the vast majority of clinical K. pneumoniae isolates express type 3 fimbriae, this fimbrial adhesin may play a significant role in development of catheter associated K. pneumoniae infections.

摘要

背景

肺炎克雷伯菌是一种重要的革兰氏阴性机会致病菌,主要引起尿路感染、呼吸道感染和菌血症。细菌在医疗器械(如导管)上形成生物膜的能力在许多医院获得性感染的发展中起着重要作用。大多数临床肺炎克雷伯菌分离株表达两种类型的菌毛粘附素,即 1 型菌毛和 3 型菌毛。在本研究中,我们研究了 1 型和 3 型菌毛在肺炎克雷伯菌生物膜形成中的作用。

结果

构建了临床肺炎克雷伯菌分离株 C3091 的同源菌毛突变体,并通过共聚焦扫描激光显微镜在流动细胞系统中研究了它们形成生物膜的能力。野生型菌株形成特征性生物膜,肺炎克雷伯菌生物膜的发展主要通过克隆生长,而不是浮游细胞的募集。1 型菌毛不影响生物膜形成,并且发现 1 型菌毛的表达在生物膜形成细胞中被下调。相比之下,3 型菌毛的表达被发现强烈促进生物膜形成。

结论

通过使用定义明确的同源突变体,我们发现 3 型菌毛而不是 1 型菌毛强烈促进肺炎克雷伯菌 C3091 的生物膜形成。由于绝大多数临床肺炎克雷伯菌分离株表达 3 型菌毛,因此这种菌毛粘附素可能在导管相关肺炎克雷伯菌感染的发展中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4cfb/2911432/58ba2bbd9e5a/1471-2180-10-179-1.jpg

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