De Arpan, Liao Sumei, Bitoun Jacob P, Roth Randy, Beatty Wandy L, Wu Hui, Wen Zezhang T
Department of Comprehensive Dentistry and Biomaterials, Louisiana State University Health Sciences Center, New Orleans, Louisiana, USA.
Center of Oral and Craniofacial Biology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, USA.
Appl Environ Microbiol. 2017 Aug 17;83(17). doi: 10.1128/AEM.00928-17. Print 2017 Sep 1.
is known to possess rhamnose-glucose polysaccharide (RGP), a major cell wall antigen. strains deficient in , encoding the first enzyme of the RGP biosynthesis pathway, were constructed by allelic exchange. The deficiency had no effect on growth rate but caused major defects in cell division and altered cell morphology. Unlike the coccoid wild type, the mutant existed primarily in chains of swollen, "squarish" dividing cells. Deficiency of also causes significant reduction in biofilm formation ( < 0.01). Double and triple mutants with deficiency in and/or , genes coding for the LytR-CpsA-Psr family proteins BrpA and Psr, which were previously shown to play important roles in cell envelope biogenesis, were constructed using the mutant. There were no major differences in growth rates between the wild-type strain and the and double mutants, but the growth rate of the triple mutant was reduced drastically ( < 0.001). Under transmission electron microscopy, both double mutants resembled the mutant, while the triple mutant existed as giant cells with multiple asymmetric septa. When analyzed by immunoblotting, the mutant displayed major reductions in cell wall antigens compared to the wild type, while little or no signal was detected with the double and triple mutants and the and single mutants. These results suggest that RgpG in plays a critical role in cell division and biofilm formation and that BrpA and Psr may be responsible for attachment of cell wall antigens to the cell envelope., a major etiological agent of human dental caries, produces rhamnose-glucose polysaccharide (RGP) as the major cell wall antigen. This study provides direct evidence that deficiency of RgpG, the first enzyme of the RGP biosynthesis pathway, caused major defects in cell division and morphology and reduced biofilm formation by , indicative of a significant role of RGP in cell division and biofilm formation in These results are novel not only in , but also other streptococci that produce RGP. This study also shows that the LytR-CpsA-Psr family proteins BrpA and Psr in are involved in attachment of RGP and probably other cell wall glycopolymers to the peptidoglycan. In addition, the results also suggest that BrpA and Psr may play a direct role in cell division and biofilm formation in This study reveals new potential targets to develop anticaries therapeutics.
已知其具有鼠李糖 - 葡萄糖多糖(RGP),这是一种主要的细胞壁抗原。通过等位基因交换构建了编码RGP生物合成途径第一种酶的基因缺失菌株。该基因缺失对生长速率没有影响,但在细胞分裂方面导致了严重缺陷并改变了细胞形态。与球状野生型不同,该突变体主要以肿胀的“方形”正在分裂的细胞链形式存在。该基因的缺失还导致生物膜形成显著减少(P < 0.01)。利用该突变体构建了与编码LytR - CpsA - Psr家族蛋白BrpA和Psr的基因缺失的双突变体和三突变体,先前已表明这些蛋白在细胞壁生物合成中起重要作用。野生型菌株与该基因和另一个基因缺失的双突变体之间的生长速率没有重大差异,但该基因三突变体的生长速率急剧降低(P < 0.001)。在透射电子显微镜下,两个双突变体都类似于该基因缺失的突变体,而三突变体以具有多个不对称隔膜的巨型细胞形式存在。通过免疫印迹分析,与野生型相比,该基因缺失的突变体在细胞壁抗原方面表现出显著减少,而双突变体、三突变体以及另一个基因缺失的单突变体几乎检测不到信号或没有信号。这些结果表明,该基因中的RgpG在细胞分裂和生物膜形成中起关键作用,并且BrpA和Psr可能负责细胞壁抗原与细胞壁的附着。变形链球菌是人类龋齿的主要病原体,产生鼠李糖 - 葡萄糖多糖(RGP)作为主要的细胞壁抗原。本研究提供了直接证据,即RGP生物合成途径的第一种酶RgpG的缺失导致了变形链球菌在细胞分裂和形态方面的严重缺陷以及生物膜形成减少,这表明RGP在变形链球菌的细胞分裂和生物膜形成中起重要作用。这些结果不仅在变形链球菌中是新颖的,在其他产生RGP的链球菌中也是如此。本研究还表明,变形链球菌中的LytR - CpsA - Psr家族蛋白BrpA和Psr参与RGP以及可能其他细胞壁糖聚合物与肽聚糖的附着。此外,结果还表明BrpA和Psr可能在变形链球菌的细胞分裂和生物膜形成中起直接作用。本研究揭示了开发抗龋治疗药物的新潜在靶点。