Ruscitto Angela, Honma Kiyonobu, Veeramachineni Vamsee M, Nishikawa Kiyoshi, Stafford Graham P, Sharma Ashu
Department of Oral Biology, University at Buffalo, BuffaloNY, USA.
Department of Microbiology and Removable Prosthodontics, School of Dentistry, Aichi Gakuin UniversityNagoya, Japan.
Front Microbiol. 2017 Apr 12;8:648. doi: 10.3389/fmicb.2017.00648. eCollection 2017.
is a Gram-negative oral anaerobe associated with periodontitis. This bacterium is auxotrophic for the peptidoglycan amino sugar -acetylmuramic (MurNAc) and likely relies on scavenging peptidoglycan fragments (muropeptides) released by cohabiting bacteria during their cell wall recycling. Many Gram-negative bacteria utilize an inner membrane permease, AmpG, to transport peptidoglycan fragments into their cytoplasm. In the genome, the Tanf_08365 ORF has been identified as a homolog of AmpG permease. In order to confirm the functionality of Tanf_08365, a reporter system in an host was generated that could detect AmpG-dependent accumulation of cytosolic muropeptides via a muropeptide-inducible β-lactamase reporter gene. complementation of this reporter strain with a Tanf_08365 containing plasmid caused significant induction of β-lactamase activity compared to that with an empty plasmid control. These data indicated that Tanf_08365 acted as a functional muropeptide permease causing accumulation of muropeptides in and thus suggested that it is a permease involved in muropeptide scavenging in . Furthermore, we showed that the promoter regulating the expression of Tanf_08365 was activated significantly by a hybrid two-component system regulatory protein, GppX. We also showed that compared to the parental strain a mutant lacking GppX in which the expression of AmpG was reduced significantly attenuated in utilizing free muropeptides. In summary, we have uncovered the mechanism by which this nutritionally fastidious microbe accesses released muropeptides in its environment, opening up the possibility of targeting this activity to reduce its numbers in periodontitis patients with potential benefits in the treatment of disease.
是一种与牙周炎相关的革兰氏阴性口腔厌氧菌。这种细菌对肽聚糖氨基糖 - 乙酰胞壁酸(MurNAc)营养缺陷,可能依赖于清除同居细菌在细胞壁循环过程中释放的肽聚糖片段(胞壁肽)。许多革兰氏阴性细菌利用内膜通透酶AmpG将肽聚糖片段转运到细胞质中。在该基因组中,Tanf_08365开放阅读框已被鉴定为AmpG通透酶的同源物。为了确认Tanf_08365的功能,在宿主中构建了一个报告系统,该系统可以通过肽聚糖诱导型β-内酰胺酶报告基因检测胞质胞壁肽的AmpG依赖性积累。用含有Tanf_08365的质粒对该报告菌株进行互补,与空质粒对照相比,导致β-内酰胺酶活性显著诱导。这些数据表明Tanf_08365作为一种功能性胞壁肽通透酶,导致胞壁肽在(此处原文有缺失)中积累,因此表明它是一种参与(此处原文有缺失)中胞壁肽清除的通透酶。此外,我们表明调节Tanf_08365表达的启动子被一种混合双组分系统调节蛋白GppX显著激活。我们还表明,与亲本(此处原文有缺失)菌株相比,缺乏GppX的突变体中AmpG的表达显著降低,在利用游离胞壁肽方面减弱。总之,我们揭示了这种营养苛求微生物在其环境中获取释放的胞壁肽的机制,为靶向这种活性以减少牙周炎患者体内其数量从而可能有益于疾病治疗开辟了可能性。