Institut Pasteur, Genetics of Biofilms Laboratory, Paris, France.
Universite Paris Diderot, Bio Sorbonne Paris Cite, Paris, France.
J Bacteriol. 2019 Aug 22;201(18). doi: 10.1128/JB.00650-18. Print 2019 Sep 15.
is a prominent anaerobic member of the healthy human gut microbiota. While the majority of functional studies on addressed its impact on the immune system and the utilization of diet polysaccharides, biofilm capacity and its contribution to intestinal colonization are still poorly characterized. We tested the natural adhesion of 34 isolates and showed that although biofilm capacity is widespread among strains, this phenotype is masked or repressed in the widely used reference strain VPI 5482. Using transposon mutagenesis followed by a biofilm positive-selection procedure, we identified VPI 5482 mutants with increased biofilm capacity corresponding to an alteration in the C-terminal region of BT3147, encoded by the locus, which displays homology with Mfa-like type V pili found in many We show that BT3147 is exposed on the surface and that BT3147-dependent adhesion also requires BT3148, suggesting that BT3148 and BT3147 correspond to the anchor and stalk subunits of a new type V pilus involved in adhesion. This study therefore introduces as a model to study proteinaceous adhesins and biofilm-related phenotypes in this important intestinal symbiont. Although the gut anaerobe is a prominent member of the healthy human gut microbiota, little is known about its capacity to adhere to surfaces and form biofilms. Here, we identify that alteration of a surface-exposed protein corresponding to a type of pili found in many increases biofilm formation. This study lays the ground for establishing this bacterium as a model organism for and studies of biofilm-related phenotypes in gut anaerobes.
是健康人体肠道微生物群中的一种主要的厌氧成员。虽然关于 的功能研究主要集中在其对免疫系统的影响和对饮食多糖的利用上,但生物膜形成能力及其对肠道定植的贡献仍知之甚少。我们测试了 34 个分离株的自然粘附能力,并表明尽管生物膜形成能力在 菌株中广泛存在,但这种表型在广泛使用的参考菌株 VPI 5482 中被掩盖或抑制。使用转座子诱变,然后进行生物膜阳性选择程序,我们鉴定了具有增加的生物膜形成能力的 VPI 5482 突变体,这对应于 基因座编码的 BT3147 的 C 末端区域的改变,该区域与许多 中发现的 Mfa 样 V 型菌毛显示同源性。我们表明 BT3147 暴露在 表面上,并且 BT3147 依赖性粘附还需要 BT3148,这表明 BT3148 和 BT3147 对应于参与 粘附的新型 V 型菌毛的锚和柄亚基。因此,本研究将 引入作为研究这种重要肠道共生菌中蛋白粘附素和生物膜相关表型的模型。尽管肠道厌氧菌 是健康人体肠道微生物群中的主要成员,但对其粘附表面和形成生物膜的能力知之甚少。在这里,我们发现对应于许多 中发现的一种菌毛的表面暴露蛋白的改变增加了 生物膜形成。这项研究为建立这种细菌作为模型生物,用于 和肠道厌氧菌生物膜相关表型的研究奠定了基础。