Motegi Mizuho, Takagi Yuzo, Yonezawa Hideo, Hanada Nobuhiro, Terajima Jun, Watanabe Haruo, Senpuku Hidenobu
Department of Bacteriology, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8640, Japan.
Appl Environ Microbiol. 2006 Sep;72(9):6277-87. doi: 10.1128/AEM.00614-06.
Streptococcus mutans, the major pathogen responsible for dental caries in humans, is a biofilm-forming bacterium. In the present study, 17 different pulsed-field gel electrophoresis patterns of genomic DNA were identified in S. mutans organisms isolated clinically from whole saliva. The S. mutans isolates showed different abilities to form biofilms on polystyrene surfaces in semidefined minimal medium cultures. Following cultivation in a flow cell system in tryptic soy broth with 0.25% sucrose and staining using a BacLight LIVE/DEAD system, two strains, designated FSC-3 and FSC-4, showed the greatest and least, respectively, levels of biofilm formation when examined with confocal laser scanning microscopy. Further, image analyses of spatial distribution and architecture were performed to quantify the merged green (live cells) and red (dead cells) light. The light intensity of the FSC-3 biofilm was greater than that of the FSC-4 biofilm in the bottom area but not in the top area. S. mutans whole-genome array results showed that approximately 3.8% of the genes were differentially expressed in the two strains, of which approximately 2.2%, including bacitracin transport ATP-binding protein gene glrA and a BLpL-like putative immunity protein gene, were activated in FSC-3. In addition, about 1.6% of the genes, including those associated with phosphotransferase system genes, were repressed. Analyses of the glrA-deficient strains and reverse transcription-PCR confirmed the role of the gene in biofilm formation. Differential assessment of biofilm-associated genes in clinical strains may provide useful information for understanding the morphological development of streptococcal biofilm, as well as for colonization of S. mutans.
变形链球菌是导致人类龋齿的主要病原体,是一种能形成生物膜的细菌。在本研究中,从全唾液临床分离出的变形链球菌菌株中鉴定出17种不同的基因组DNA脉冲场凝胶电泳图谱。在半限定基本培养基培养物中,变形链球菌分离株在聚苯乙烯表面形成生物膜的能力不同。在含有0.25%蔗糖的胰蛋白胨大豆肉汤的流动细胞系统中培养后,使用BacLight LIVE/DEAD系统进行染色,用共聚焦激光扫描显微镜检查时,命名为FSC-3和FSC-4的两株菌株分别表现出最强和最弱的生物膜形成水平。此外,进行了空间分布和结构的图像分析,以量化合并的绿色(活细胞)和红色(死细胞)光。FSC-3生物膜在底部区域的光强度大于FSC-4生物膜,但在顶部区域则不然。变形链球菌全基因组芯片结果显示,两株菌株中约3.8%的基因表达存在差异,其中约2.2%,包括杆菌肽转运ATP结合蛋白基因glrA和一个BLpL样推定免疫蛋白基因,在FSC-3中被激活。此外,约1.6%的基因,包括那些与磷酸转移酶系统基因相关的基因,被抑制。对glrA缺陷菌株的分析和逆转录PCR证实了该基因在生物膜形成中的作用。对临床菌株中生物膜相关基因的差异评估可能为理解链球菌生物膜的形态发育以及变形链球菌的定植提供有用信息。