Department of Oral Biology, University of Florida, College of Dentistry, Gainesville, FL, USA.
Center for Oral Biology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Mol Oral Microbiol. 2018 Jun;33(3):257-269. doi: 10.1111/omi.12222. Epub 2018 Apr 17.
We report the whole genome sequence of the serotype e Cbm strain LAR01 of Streptococcus mutans, a dental pathogen frequently associated with extra-oral infections. The LAR01 genome is a single circular chromosome of 2.1 Mb with a GC content of 36.96%. The genome contains 15 phosphotransferase system gene clusters, seven cell wall-anchored (LPxTG) proteins, all genes required for the development of natural competence and genes coding for mutacins VI and K8. Interestingly, the cbm gene is genetically linked to a putative type VII secretion system that has been found in Mycobacteria and few other Gram-positive bacteria. When compared with the UA159 type strain, phenotypic characterization of LAR01 revealed increased biofilm formation in the presence of either glucose or sucrose but similar abilities to withstand acid and oxidative stresses. LAR01 was unable to inhibit the growth of Strpetococcus gordonii, which is consistent with the genomic data that indicate absence of mutacins that can kill mitis streptococci. On the other hand, LAR01 effectively inhibited growth of other S. mutans strains, suggesting that it may be specialized to outcompete strains from its own species. In vitro and in vivo studies using mutational and heterologous expression approaches revealed that Cbm is a virulence factor of S. mutans by mediating binding to extracellular matrix proteins and intracellular invasion. Collectively, the whole genome sequence analysis and phenotypic characterization of LAR01 provides new insights on the virulence properties of S. mutans and grants further opportunities to understand the genomic fluidity of this important human pathogen.
我们报告了口腔变形链球菌 e 型 Cbm 株 LAR01 的全基因组序列,该菌是一种与口腔外感染密切相关的口腔病原体。LAR01 基因组是一条 2.1Mb 的单链环状染色体,GC 含量为 36.96%。基因组包含 15 个磷酸转移酶系统基因簇、7 个细胞壁锚定(LPxTG)蛋白、天然感受态发育所需的所有基因以及编码 mutacins VI 和 K8 的基因。有趣的是,cbm 基因与一种假定的 VII 型分泌系统在分枝杆菌和少数其他革兰氏阳性菌中被发现存在遗传关联。与 UA159 标准株相比,LAR01 的表型特征研究表明,在存在葡萄糖或蔗糖的情况下,其生物膜形成能力增强,但对酸和氧化应激的耐受能力相似。LAR01 无法抑制链球菌的生长,这与基因组数据一致,表明缺乏能够杀死米氏链球菌的 mutacins。另一方面,LAR01 有效地抑制了其他 S. mutans 菌株的生长,表明它可能专门与来自其自身物种的菌株竞争。通过突变和异源表达方法的体外和体内研究表明,Cbm 通过介导与细胞外基质蛋白的结合和细胞内入侵,是 S. mutans 的一种毒力因子。总的来说,LAR01 的全基因组序列分析和表型特征为 S. mutans 的毒力特性提供了新的见解,并进一步为了解这种重要的人类病原体的基因组流动性提供了机会。