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D-精氨酸对牙龈卟啉单胞菌生物膜的影响。

Effects of D-arginine on Porphyromonas gingivalis biofilm.

作者信息

Li Yu-Yang, Li Bao-Sheng, Liu Wei-Wei, Cai Qing, Wang Hao-Yang, Liu Yan-Qun, Liu Yu-Jie, Meng Wei-Yan

机构信息

Department of Dental Implantology, School and Hospital of Stomatology, Jilin University.

Jilin Provincial Key Laboratory of Tooth Development and Bone Remodeling.

出版信息

J Oral Sci. 2020;62(1):57-61. doi: 10.2334/josnusd.19-0075.

Abstract

Porphyromonas gingivalis (P. gingivalis) is one of the major pathogenic bacteria of periodontitis or peri-implantitis. P. gingivalis tends to attach to the implant's neck with the formation of biofilm, leading to peri-implantitis. d-arginine has been shown to have a potential antimicrobial role. In this study, P. gingivalis was cultured in Brain Heart Infusion broth together with d-arginine. After 3 days (inhibition) or 6 days (dissociation), these were characterized using crystal violet (CV) staining for the biofilm, extracellular polysaccharide (EPS) production from the biofilm, and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay for biofilm activation. Furthermore, the P. gingivalis biofilm was observed by scanning electron microscopy (SEM). d-arginine effectively reduced biomass accumulation and promoted dissociation at concentrations of ≥50 mM and 100 mM, respectively. Through CV staining, d-arginine concentrations of EPS production from the biofilm for inhibition and dissociation effects was ≥50 mM and 100 mM, respectively. In addition, d-arginine affected biofilm activation for the corresponding concentrations: ≥60 mM for inhibition and ≥90 mM for dispersal. Under SEM observation, d-arginine changed the P. gingivalis biofilm structure in relatively high concentrations for inhibition or dissociation, respectively. The authors concluded that d-arginine could inhibit the formation of P. gingivalis biofilm and promote the dissociation of P. gingivalis biofilm.

摘要

牙龈卟啉单胞菌是牙周炎或种植体周围炎的主要致病菌之一。牙龈卟啉单胞菌倾向于附着在种植体颈部并形成生物膜,导致种植体周围炎。已证明d -精氨酸具有潜在的抗菌作用。在本研究中,牙龈卟啉单胞菌与d -精氨酸一起在脑心浸液肉汤中培养。3天(抑制)或6天(解离)后,使用结晶紫(CV)染色检测生物膜、生物膜产生的细胞外多糖(EPS)以及用于生物膜活性检测的3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑(MTT)法对其进行表征。此外,通过扫描电子显微镜(SEM)观察牙龈卟啉单胞菌生物膜。d -精氨酸分别在≥50 mM和100 mM的浓度下有效减少生物量积累并促进解离。通过CV染色,生物膜产生EPS的d -精氨酸抑制和解离效应浓度分别为≥50 mM和100 mM。此外,d -精氨酸对相应浓度的生物膜活性有影响:抑制作用≥60 mM,分散作用≥90 mM。在SEM观察下,d -精氨酸在相对较高浓度下分别改变牙龈卟啉单胞菌生物膜结构以产生抑制或解离作用。作者得出结论,d -精氨酸可抑制牙龈卟啉单胞菌生物膜的形成并促进牙龈卟啉单胞菌生物膜的解离。

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