INRA, UMR1319 Micalis, F-78350 Jouy-en-Josas, France;
Mol Cell Proteomics. 2013 Dec;12(12):3935-47. doi: 10.1074/mcp.M113.029066. Epub 2013 Sep 3.
Surface proteins of Gram-positive bacteria play crucial roles in bacterial adhesion to host tissues. Regarding commensal or probiotic bacteria, adhesion to intestinal mucosa may promote their persistence in the gastro-intestinal tract and their beneficial effects to the host. In this study, seven Lactococcus lactis strains exhibiting variable surface physico-chemical properties were compared for their adhesion to Caco-2 intestinal epithelial cells. In this test, only one vegetal isolate TIL448 expressed a high-adhesion phenotype. A nonadhesive derivative was obtained by plasmid curing from TIL448, indicating that the adhesion determinants were plasmid-encoded. Surface-exposed proteins in TIL448 were analyzed by a proteomic approach consisting in shaving of the bacterial surface with trypsin and analysis of the released peptides by LC-MS/MS. As the TIL448 complete genome sequence was not available, the tryptic peptides were identified by a mass matching approach against a database including all Lactococcus protein sequences and the sequences deduced from partial DNA sequences of the TIL448 plasmids. Two surface proteins, encoded by plasmids in TIL448, were identified as candidate adhesins, the first one displaying pilin characteristics and the second one containing two mucus-binding domains. Inactivation of the pilin gene abolished adhesion to Caco-2 cells whereas inactivation of the mucus-binding protein gene had no effect on adhesion. The pilin gene is located inside a cluster of four genes encoding two other pilin-like proteins and one class-C sortase. Synthesis of pili was confirmed by immunoblotting detection of high molecular weight forms of pilins associated to the cell wall as well as by electron and atomic force microscopy observations. As a conclusion, surface proteome analysis allowed us to detect pilins at the surface of L. lactis TIL448. Moreover we showed that pili appendages are formed and involved in adhesion to Caco-2 intestinal epithelial cells.
革兰氏阳性菌的表面蛋白在细菌与宿主组织的黏附中起着至关重要的作用。对于共生菌或益生菌而言,黏附于肠道黏膜有助于其在胃肠道中持续存在,并对宿主产生有益作用。在本研究中,我们比较了 7 株具有不同表面物理化学特性的乳球菌(Lactococcus lactis)菌株对 Caco-2 肠上皮细胞的黏附能力。在该试验中,只有一株植物分离株 TIL448 表现出高黏附表型。通过质粒消除,从 TIL448 中获得了一个非黏附衍生物,表明黏附决定簇是质粒编码的。通过一种蛋白质组学方法分析 TIL448 的表面暴露蛋白,该方法包括用胰蛋白酶刮削细菌表面,并通过 LC-MS/MS 分析释放的肽。由于 TIL448 的完整基因组序列不可用,因此通过质量匹配方法将胰蛋白酶肽与包括所有乳球菌蛋白序列和 TIL448 质粒部分 DNA 序列推导的序列的数据库进行匹配来鉴定。在 TIL448 中发现两个表面蛋白,由质粒编码,被鉴定为候选黏附素,第一个具有菌毛特征,第二个包含两个黏液结合结构域。pil 基因失活后,对 Caco-2 细胞的黏附能力丧失,而黏液结合蛋白基因失活后对黏附能力没有影响。pil 基因位于四个基因簇内,该基因簇编码另外两个菌毛样蛋白和一个 C 类分类酶。通过免疫印迹检测与细胞壁结合的高分子量形式的菌毛以及电子和原子力显微镜观察,证实了菌毛的合成。综上所述,表面蛋白质组分析使我们能够检测到 L. lactis TIL448 表面的菌毛。此外,我们表明,菌毛附属物的形成并参与了与 Caco-2 肠上皮细胞的黏附。