Filifactor alocis enhances survival of Porphyromonas gingivalis W83 in response to H2 O2 -induced stress.

IF 2.8 3区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Molecular Oral Microbiology Pub Date : 2024-02-01 Epub Date: 2023-12-01 DOI:10.1111/omi.12445
Arunima Mishra, Yuetan Dou, Charles Wang, Hansel M Fletcher
{"title":"Filifactor alocis enhances survival of Porphyromonas gingivalis W83 in response to H<sub>2</sub> O<sub>2</sub> -induced stress.","authors":"Arunima Mishra, Yuetan Dou, Charles Wang, Hansel M Fletcher","doi":"10.1111/omi.12445","DOIUrl":null,"url":null,"abstract":"<p><p>A dysbiotic microbial community whose members have specific/synergistic functions that are modulated by environmental conditions, can disturb homeostasis in the subgingival space leading to destructive inflammation, plays a role in the progression of periodontitis. Filifactor alocis, a gram-positive, anaerobic bacterium, is a newly recognized microbe that shows a strong correlation with periodontal disease. Our previous observations suggested F. alocis to be more resistant to oxidative stress compared to Porphyromonas gingivalis. The objective of this study is to further determine if F. alocis, because of its increased resistance to oxidative stress, can affect the survival of other 'established' periodontal pathogens under environmental stress conditions typical of the periodontal pocket. Here, we have shown that via their interaction, F. alocis protects P. gingivalis W83 under H<sub>2</sub> O<sub>2</sub> -induced oxidative stress conditions. Transcriptional profiling of the interaction of F. alocis and P. gingivalis in the presence of H<sub>2</sub> O<sub>2</sub> -induced stress revealed the modulation of several genes, including those with ABC transporter and other cellular functions. The ABC transporter operon (PG0682-PG0685) of P. gingivalis was not significant to its enhanced survival when cocultured with F. alocis under H<sub>2</sub> O<sub>2</sub> -induced oxidative stress. In F. alocis, one of the most highly up-regulated operons (FA0894-FA0897) is predicted to encode a putative manganese ABC transporter, which in other bacteria can play an essential role in oxidative stress protection. Collectively, the results may indicate that F. alocis could likely stabilize the microbial community in the inflammatory microenvironment of the periodontal pocket by reducing the oxidative environment. This strategy could be vital to the survival of other pathogens, such as P. gingivalis, and its ability to adapt and persist in the periodontal pocket.</p>","PeriodicalId":18815,"journal":{"name":"Molecular Oral Microbiology","volume":" ","pages":"12-26"},"PeriodicalIF":2.8000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10842171/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Oral Microbiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/omi.12445","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/12/1 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
引用次数: 0

Abstract

A dysbiotic microbial community whose members have specific/synergistic functions that are modulated by environmental conditions, can disturb homeostasis in the subgingival space leading to destructive inflammation, plays a role in the progression of periodontitis. Filifactor alocis, a gram-positive, anaerobic bacterium, is a newly recognized microbe that shows a strong correlation with periodontal disease. Our previous observations suggested F. alocis to be more resistant to oxidative stress compared to Porphyromonas gingivalis. The objective of this study is to further determine if F. alocis, because of its increased resistance to oxidative stress, can affect the survival of other 'established' periodontal pathogens under environmental stress conditions typical of the periodontal pocket. Here, we have shown that via their interaction, F. alocis protects P. gingivalis W83 under H2 O2 -induced oxidative stress conditions. Transcriptional profiling of the interaction of F. alocis and P. gingivalis in the presence of H2 O2 -induced stress revealed the modulation of several genes, including those with ABC transporter and other cellular functions. The ABC transporter operon (PG0682-PG0685) of P. gingivalis was not significant to its enhanced survival when cocultured with F. alocis under H2 O2 -induced oxidative stress. In F. alocis, one of the most highly up-regulated operons (FA0894-FA0897) is predicted to encode a putative manganese ABC transporter, which in other bacteria can play an essential role in oxidative stress protection. Collectively, the results may indicate that F. alocis could likely stabilize the microbial community in the inflammatory microenvironment of the periodontal pocket by reducing the oxidative environment. This strategy could be vital to the survival of other pathogens, such as P. gingivalis, and its ability to adapt and persist in the periodontal pocket.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
在h2o2诱导的应激下,丝状因子可提高牙龈卟啉单胞菌W83的存活率。
一个生态失调的微生物群落,其成员具有受环境条件调节的特定/协同功能,可以扰乱龈下空间的稳态,导致破坏性炎症,在牙周炎的进展中起作用。纤裂菌是一种革兰氏阳性的厌氧细菌,是一种新发现的与牙周病密切相关的微生物。我们之前的观察表明,与牙龈卟啉单胞菌相比,金黄色葡萄球菌对氧化应激的抵抗力更强。本研究的目的是进一步确定,在典型的牙周袋环境应激条件下,由于其对氧化应激的抵抗力增强,是否会影响其他“既定”牙周病原体的生存。在这里,我们已经证明,通过它们的相互作用,F. alocis在H2诱导的氧化应激条件下保护牙龈卟啉单胞菌W83。在h2o2诱导的应激条件下,F. alocis和P. gingivalis相互作用的转录谱揭示了几个基因的调节,包括ABC转运蛋白和其他细胞功能的基因。在h2o2诱导的氧化应激下,牙龈假单胞菌ABC转运体操纵子(PG0682-PG0685)对其存活率的提高无显著影响。在F. alocis中,一个高度上调的操作子(FA0894-FA0897)被预测编码一种推测的锰ABC转运蛋白,该转运蛋白在其他细菌中可以在氧化应激保护中发挥重要作用。综上所述,这些结果可能表明alocis可能通过减少氧化环境来稳定牙周袋炎症微环境中的微生物群落。这一策略可能对其他病原体的生存至关重要,例如牙龈卟啉卟啉菌,以及它在牙周袋中适应和持续存在的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
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.
期刊最新文献
NOD2 contributes to Parvimonas micra-induced bone resorption in diabetic rats with experimental periodontitis. The role of Fusobacterium nucleatum in cancer and its implications for clinical applications. Effect of toxins from different periodontitis-associated bacteria on human platelet function. High-throughput characterization of the influence of Streptococcus sanguinis genes on the interaction between Streptococcus sanguinis and Porphyromonas gingivalis. Effects of fluid shear stress on oral biofilm formation and composition and the transcriptional response of Streptococcus gordonii.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1