Reduced proinflammatory activity of outer membrane vesicles of Tannerella forsythia treated with quorum sensing inhibitors.

IF 2.8 3区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Sun-Jin An, Kyung-Won Ha, Hye-Kyoung Jun, Hyun Young Kim, Bong-Kyu Choi
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引用次数: 0

Abstract

Outer membrane vesicles (OMVs) of bacteria harbor physiologically active molecules, and quorum sensing inhibitors (QSIs) are expected to regulate bacterial virulence. In this study, we analyzed the proinflammatory activity of OMVs of the periodontal pathogen Tannerella forsythia treated with d-arabinose and d-galactose as QSIs, which inhibit the biofilm formation of periodontal pathogens and autoinducer 2 activity. Compared to OMVs of nontreated T. forsythia (TF OMVs), OMVs released from QSI-treated T. forsythia, designated TF ara-OMVs and TF gal-OMVs, showed reduced production of TNF-α, IL-1β, IL-6, and IL-8 in THP-1 monocytes through decreased activation of NF-κB/MAPKs. Using a human NF-κB reporter cell line and bone marrow-derived macrophages from TLR2-/- mice, TF ara-OMVs and TF gal-OMVs showed less activation of TLR2 than TF OMVs. These results demonstrated that QSIs provide a dual advantage against bacterial infection by inhibiting bacterial biofilm formation and generating OMVs with reduced proinflammatory activity.

群体感应抑制剂对单宁外膜囊泡促炎活性的影响。
细菌的外膜囊泡(omv)具有生理活性分子,而群体感应抑制剂(qsi)有望调节细菌的毒力。本研究分析了d-阿拉伯糖和d-半乳糖作为qsi处理的牙周病原菌连翘单宁菌omv的促炎活性,这两种qsi抑制了牙周病原菌生物膜的形成和自诱导剂2的活性。与未处理的连翘omv (TF omv)相比,qsi处理连翘释放的omv (TF ara- omv和TF gal- omv)通过降低NF-κB/MAPKs的激活,减少了THP-1单核细胞中TNF-α、IL-1β、IL-6和IL-8的产生。使用人NF-κ b报告细胞系和来自TLR2-/-小鼠的骨髓源性巨噬细胞,TF ara- omv和TF gal- omv显示TLR2的激活低于TF omv。这些结果表明,qsi通过抑制细菌生物膜的形成和产生促炎活性降低的omv,提供了对抗细菌感染的双重优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Oral Microbiology
Molecular Oral Microbiology DENTISTRY, ORAL SURGERY & MEDICINE-MICROBIOLOGY
CiteScore
6.50
自引率
5.40%
发文量
46
审稿时长
>12 weeks
期刊介绍: Molecular Oral Microbiology publishes high quality research papers and reviews on fundamental or applied molecular studies of microorganisms of the oral cavity and respiratory tract, host-microbe interactions, cellular microbiology, molecular ecology, and immunological studies of oral and respiratory tract infections. Papers describing work in virology, or in immunology unrelated to microbial colonization or infection, will not be acceptable. Studies of the prevalence of organisms or of antimicrobials agents also are not within the scope of the journal. The journal does not publish Short Communications or Letters to the Editor. Molecular Oral Microbiology is published bimonthly.
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