F C Nichols1, K Rojanasomsith. 1. Department of Oral Health and Diagnostic Sciences, University of Connecticut School of Dental Medicine, Farmington, CT, USA. nichols@nso.uchc.edu
Abstract
BACKGROUND/AIM: Porphyromonas gingivalis synthesizes several classes of dihydroceramides and at least one of these lipid classes promotes proinflammatory secretory reactions in gingival fibroblasts as well as alters fibroblast morphology in culture. The purpose of this investigation was to determine whether the dihydroceramide lipids of P. gingivalis are recovered in lipid extracts of subgingival plaque, diseased teeth, and diseased gingival tissue samples. METHODS: Lipids were extracted from P. gingivalis, subgingival plaque, subgingival calculus, teeth laden with gross accumulations of subgingival calculus, and gingival tissue samples obtained from chronic severe periodontitis sites. Lipid samples were analyzed by gas chromatography-mass spectrometry as trimethylsilyl derivatives or by electrospray-mass spectrometry as underivatized products. High-performance liquid chromatography fractions of P. gingivalis lipids and gingival tissue lipids were also analyzed by electrospray-mass spectrometry analysis. RESULTS: P. gingivalis phosphorylated dihydroceramides were recovered in lipid extracts of subgingival plaque, subgingival calculus, calculus contaminated teeth, and diseased gingival tissue samples. However, the distribution of phosphorylated dihydroceramides varied between these samples. CONCLUSION: Subgingival plaque, subgingival calculus, diseased teeth, and gingival tissue are contaminated with phosphorylated dihydroceramides produced by P. gingivalis. The previously reported biological activity of these substances together with the recovery of these lipids at periodontal disease sites argues strongly for their classification as virulence factors in promoting chronic inflammatory periodontal disease.
BACKGROUND/AIM: Porphyromonas gingivalis synthesizes several classes of dihydroceramides and at least one of these lipid classes promotes proinflammatory secretory reactions in gingival fibroblasts as well as alters fibroblast morphology in culture. The purpose of this investigation was to determine whether the dihydroceramide lipids of P. gingivalis are recovered in lipid extracts of subgingival plaque, diseased teeth, and diseased gingival tissue samples. METHODS:Lipids were extracted from P. gingivalis, subgingival plaque, subgingival calculus, teeth laden with gross accumulations of subgingival calculus, and gingival tissue samples obtained from chronic severe periodontitis sites. Lipid samples were analyzed by gas chromatography-mass spectrometry as trimethylsilyl derivatives or by electrospray-mass spectrometry as underivatized products. High-performance liquid chromatography fractions of P. gingivalislipids and gingival tissue lipids were also analyzed by electrospray-mass spectrometry analysis. RESULTS:P. gingivalis phosphorylated dihydroceramides were recovered in lipid extracts of subgingival plaque, subgingival calculus, calculus contaminated teeth, and diseased gingival tissue samples. However, the distribution of phosphorylated dihydroceramides varied between these samples. CONCLUSION: Subgingival plaque, subgingival calculus, diseased teeth, and gingival tissue are contaminated with phosphorylated dihydroceramides produced by P. gingivalis. The previously reported biological activity of these substances together with the recovery of these lipids at periodontal disease sites argues strongly for their classification as virulence factors in promoting chronic inflammatory periodontal disease.
Authors: Christopher S Mirucki; Mehran Abedi; Jin Jiang; Qiang Zhu; Yu-Hsiung Wang; Kamran E Safavi; Robert B Clark; Frank C Nichols Journal: J Endod Date: 2014-04-13 Impact factor: 4.171
Authors: Frank C Nichols; Robert B Clark; Yaling Liu; Anthony A Provatas; Christopher J Dietz; Qiang Zhu; Yu-Hsiung Wang; Michael B Smith Journal: Infect Immun Date: 2020-03-23 Impact factor: 3.441
Authors: Robert B Clark; Jorge L Cervantes; Mark W Maciejewski; Vahid Farrokhi; Reza Nemati; Xudong Yao; Emily Anstadt; Mai Fujiwara; Kyle T Wright; Caroline Riddle; Carson J La Vake; Juan C Salazar; Sydney Finegold; Frank C Nichols Journal: Infect Immun Date: 2013-07-08 Impact factor: 3.441
Authors: Yu-Hsiung Wang; Jin Jiang; Qiang Zhu; Amer Z AlAnezi; Robert B Clark; Xi Jiang; David W Rowe; Frank C Nichols Journal: Infect Immun Date: 2010-06-28 Impact factor: 3.441