Balestrino Damien, Ghigo Jean-Marc, Charbonnel Nicolas, Haagensen Janus A J, Forestier Christiane
Laboratoire de Bactériologie, Université d'Auvergne-Clermont1, Faculté de Pharmacie, Clermont-Ferrand, 63000 Clermont-Ferrand, France.
Environ Microbiol. 2008 Mar;10(3):685-701. doi: 10.1111/j.1462-2920.2007.01491.x.
The ability to form biofilm is seen as an increasingly important colonization strategy among both pathogenic and environmental Klebsiella pneumoniae strains. The aim of the present study was to identify abiotic surface colonization factors of K. pneumoniae using different models at different phases of biofilm development. A 2200 K. pneumoniae mutant library previously obtained by signature-tagged mutagenesis was screened in static and dynamic culture models to detect clones impaired at early and/or mature stages of biofilm formation. A total of 28 mutants were affected during late phases of biofilm formation, whereas 16 mutants displayed early adhesion defect. These mutants corresponded to genes involved in potential cellular and DNA metabolism pathways and to membrane transport functions. Eight mutants were deficient in capsule or LPS production. Gene disruption and microscopic analyses showed that LPS is involved in initial adhesion on both glass and polyvinyl-chloride and the capsule required for the appropriate initial coverage of substratum and the construction of mature biofilm architecture. These results give new insight into the bacterial factors sequentially associated with the ability to colonize an abiotic surface and reveal the dual roles played by surface exopolysaccharides during K. pneumoniae biofilm formation.
形成生物膜的能力在致病性和环境性肺炎克雷伯菌菌株中都被视为一种日益重要的定植策略。本研究的目的是使用生物膜发育不同阶段的不同模型来鉴定肺炎克雷伯菌的非生物表面定植因子。在静态和动态培养模型中筛选了先前通过签名标签诱变获得的2200个肺炎克雷伯菌突变体文库,以检测在生物膜形成早期和/或成熟阶段受损的克隆。共有28个突变体在生物膜形成后期受到影响,而16个突变体表现出早期黏附缺陷。这些突变体对应于参与潜在细胞和DNA代谢途径以及膜转运功能的基因。8个突变体在荚膜或脂多糖产生方面存在缺陷。基因破坏和显微镜分析表明,脂多糖参与了在玻璃和聚氯乙烯上的初始黏附,而荚膜对于适当的初始覆盖基质和构建成熟生物膜结构是必需的。这些结果为与非生物表面定植能力依次相关的细菌因子提供了新的见解,并揭示了表面胞外多糖在肺炎克雷伯菌生物膜形成过程中所起的双重作用。