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QseC 除了依赖 AI-2 的机制外,还控制了无定型流感嗜血杆菌生物膜的形成。

QseC controls biofilm formation of non-typeable Haemophilus influenzae in addition to an AI-2-dependent mechanism.

机构信息

Medical Microbiology, Department of Laboratory Medicine Malmö, Lund University, Skåne University Hospital, Malmö, Sweden.

出版信息

Int J Med Microbiol. 2012 Nov;302(6):261-9. doi: 10.1016/j.ijmm.2012.07.013. Epub 2012 Sep 4.

Abstract

Non-typeable Haemophilus influenzae (NTHi) is a common pathogen associated with diseases such as acute otitis media or exacerbations in patients with chronic obstructive pulmonary disease. The biofilm-forming capability substantially contributes to the persistence of NTHi. However, the regulation of biofilm formation is not completely understood. Quorum sensing regulated by autoinducer-2 produced by luxS is until now the only described regulatory mechanism. In this study, we show that the two-component signalling system QseB/C is involved in the biofilm formation of NTHi in vitro. An isogenic NTHi mutant of qseC (Hi3655KR2) showed a significant decrease in biofilm formation under static and semi-static conditions as assessed by crystal violet staining. In addition, under constant flow conditions, Hi3655KR2 formed less biofilm after 48 h. The biofilm defects were irrespective of autoinducer-2 levels. Hence, here we suggest for the first time a regulatory circuit in NTHi, which controls biofilm formation by mechanisms other than or in addition to luxS-dependent factors.

摘要

无乳链球菌(NTHi)是一种常见的病原体,与急性中耳炎或慢性阻塞性肺疾病患者的恶化等疾病有关。生物膜形成能力对 NTHi 的持续存在有很大贡献。然而,生物膜形成的调节机制尚不完全清楚。目前为止,群体感应调节系统由 luxS 产生的自动诱导物-2 调节是唯一描述的调节机制。在这项研究中,我们表明,双组分信号系统 QseB/C 参与了 NTHi 的体外生物膜形成。通过结晶紫染色评估,qseC 的同源缺失突变体(Hi3655KR2)在静态和半静态条件下的生物膜形成显著减少。此外,在恒定流速条件下,Hi3655KR2 在 48 小时后形成的生物膜较少。生物膜缺陷与自动诱导物-2 水平无关。因此,我们首次提出了一种 NTHi 的调控回路,该回路通过 luxS 依赖性因子以外或除此之外的机制来控制生物膜的形成。

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