Department of Conservative Dentistry, and DRI, School of Dentistry, Seoul National University, Seoul, 03080, Republic of Korea.
Department of Conservative Dentistry, Seoul National University Bundang Hospital, Seongnam, 13620, Republic of Korea.
J Microbiol. 2024 Oct;62(10):897-905. doi: 10.1007/s12275-024-00165-6. Epub 2024 Sep 30.
The demand for safe and effective endodontic medicaments to control Enterococcus faecalis biofilms, a contributor to apical periodontitis, is increasing. Recently, lipoteichoic acid (LTA) of family Lactobacillaceae has been shown to have anti-biofilm effects against various oral pathogens. Preliminary experiments showed that LTA purified from Lacticaseibacillus rhamnosus GG (Lgg.LTA) was the most effective against E. faecalis biofilms among LTAs from three Lactobacillaceae including L. rhamnosus GG, Lacticaseibacillus casei, and Lactobacillus acidophilus. Therefore, in this study, we investigated the potential of Lgg.LTA as an intracanal medicament in human root canals infected with E. faecalis. Twenty eight dentinal cylinders were prepared from extracted human teeth, where two-week-old E. faecalis biofilms were formed followed by intracanal treatment with sterile distilled water (SDW), N-2 methyl pyrrolidone (NMP), calcium hydroxide (CH), or Lgg.LTA. Bacteria and biofilms that formed in the root canals were analyzed by scanning electron microscopy and confocal laser scanning microscopy. The remaining E. faecalis cells in the root canals after intracanal medicament treatment were enumerated by culturing and counting. When applied to intracanal biofilms, Lgg.LTA effectively inhibited E. faecalis biofilm formation as much as CH, while SDW and NMP had little effect. Furthermore, Lgg.LTA reduced both live and dead bacteria within the dentinal tubules, indicating the possibility of minimal re-infection in the root canals. Collectively, intracanal application of Lgg.LTA effectively inhibited E. faecalis biofilm formation, implying that Lgg.LTA can be used as a novel endodontic medicament.
目前,人们对安全有效的根管内药物的需求不断增加,以控制粪肠球菌生物膜,粪肠球菌是根尖周炎的主要致病菌之一。最近,乳杆菌科的脂磷壁酸(LTA)已被证明具有抗多种口腔病原体生物膜的作用。初步实验表明,从乳双歧杆菌 GG(Lgg.LTA)中纯化的 LTA 对粪肠球菌生物膜的抑制作用最强,而来自乳杆菌 GG、干酪乳杆菌和嗜酸乳杆菌的三种乳杆菌科的 LTA 中抑制作用最强。因此,本研究旨在探讨 Lgg.LTA 作为一种根管内药物应用于感染粪肠球菌的人根管的潜力。从拔除的人类牙齿中制备了 28 个牙本质圆柱体,其中培养两周形成粪肠球菌生物膜,然后用无菌蒸馏水(SDW)、N-2 甲基吡咯烷酮(NMP)、氢氧化钙(CH)或 Lgg.LTA 进行根管内处理。通过扫描电子显微镜和共聚焦激光扫描显微镜分析根管内的细菌和生物膜。通过培养和计数,分析根管内药物处理后残留的粪肠球菌细胞。当应用于根管内生物膜时,Lgg.LTA 与 CH 一样有效地抑制粪肠球菌生物膜的形成,而 SDW 和 NMP 几乎没有作用。此外,Lgg.LTA 减少了牙本质小管内的活细菌和死细菌,表明根管内再次感染的可能性较小。总之,Lgg.LTA 根管内应用能有效抑制粪肠球菌生物膜的形成,提示 Lgg.LTA 可作为一种新型的根管内药物。