Lipoteichoic Acid from Lacticaseibacillus rhamnosus GG as a Novel Intracanal Medicament Targeting Enterococcus faecalis Biofilm Formation.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-01 Epub Date: 2024-09-30 DOI:10.1007/s12275-024-00165-6
Ji-Young Yoon, Somin Park, Dongwook Lee, Ok-Jin Park, WooCheol Lee, Seung Hyun Han
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Abstract

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.

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将鼠李糖乳杆菌 GG 的脂联乳酸作为针对粪肠球菌生物膜形成的新型肛内药物
对安全有效的牙髓治疗药物的需求与日俱增,以控制造成根尖牙周炎的粪肠球菌生物膜。最近,乳酸菌科细菌的脂联乳酸(LTA)被证明对多种口腔病原体具有抗生物膜作用。初步实验表明,在鼠李糖乳杆菌 GG、干酪乳杆菌和嗜酸乳杆菌等三种乳杆菌科细菌的 LTA 中,从鼠李糖乳杆菌 GG(Lgg.LTA)中纯化的 LTA 对粪大肠杆菌生物膜最有效。因此,在本研究中,我们研究了 Lgg.LTA 作为一种根管内药物用于受粪大肠杆菌感染的人类根管的潜力。从拔出的人类牙齿上制备了 28 个牙本质圆柱体,在这些圆柱体中形成了两周大的粪大肠杆菌生物膜,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了根管内形成的细菌和生物膜。通过培养和计数,对根管内药物处理后剩余的粪大肠杆菌细胞进行了统计。在应用于根管内生物膜时,Lgg.LTA 与 CH 一样有效地抑制了粪大肠杆菌生物膜的形成,而 SDW 和 NMP 的效果甚微。此外,Lgg.LTA 还能减少牙本质小管内的活菌和死菌,这表明根管内再感染的可能性很小。总之,Lgg.LTA 在根管内的应用有效地抑制了粪大肠杆菌生物膜的形成,这意味着 Lgg.LTA 可用作一种新型的根管治疗药物。
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CiteScore
7.20
自引率
4.30%
发文量
567
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