核梭杆菌:适应有氧应激的策略。

IF 2.7 3区 生物学 Q3 MICROBIOLOGY
Alexandra K McGregor, Kirsten R Wolthers
{"title":"核梭杆菌:适应有氧应激的策略。","authors":"Alexandra K McGregor, Kirsten R Wolthers","doi":"10.1128/jb.00090-25","DOIUrl":null,"url":null,"abstract":"<p><p><i>Fusobacterium nucleatum</i>-a gram-negative anaerobe-is commensal to the oral cavity, where it plays an important role in the maturation of the oral biofilm. The bacterium is also an opportunistic pathogen, given its association with systemic infections and cancer progression. Although residing in largely anoxic microenvironments within the oral biofilm, <i>F. nucleatum</i> encounters oxygen (O₂) present in the circulating saliva and reactive oxygen species formed endogenously, by an activated immune system or neighboring oral commensal streptococci. This review explores the bacterium's adaptive mechanisms that enable survival under oxidative stress. We discuss how <i>F. nucleatum</i> mitigates oxidative damage and aerobic stress through common detoxifying and repair enzymes such as peroxiredoxins, methionine sulfoxide reductases, and rubrerythrin and through the activity of the recently identified multicomponent enzyme, termed butyryl-CoA oxygen oxidoreductase. Turnover by the latter enzyme enables <i>F. nucleatum</i> to exploit molecular oxygen for the conservation of energy. Additionally, we discuss how a two-component signal transduction system, ModRS, a global regulator of oxidative stress, functions in part to reprogram core metabolism to counterbalance the inactivation of a glycyl radical enzyme hypersensitive to O<sub>2</sub>. Our findings provide new insight into how <i>F. nucleatum</i> resists fluctuating dioxygen environments, shedding light on its persistence in extraoral sites and its potential role in disease progression.</p>","PeriodicalId":15107,"journal":{"name":"Journal of Bacteriology","volume":" ","pages":"e0009025"},"PeriodicalIF":2.7000,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"<i>Fusobacterium nucleatum</i>: strategies for adapting to aerobic stress.\",\"authors\":\"Alexandra K McGregor, Kirsten R Wolthers\",\"doi\":\"10.1128/jb.00090-25\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Fusobacterium nucleatum</i>-a gram-negative anaerobe-is commensal to the oral cavity, where it plays an important role in the maturation of the oral biofilm. The bacterium is also an opportunistic pathogen, given its association with systemic infections and cancer progression. Although residing in largely anoxic microenvironments within the oral biofilm, <i>F. nucleatum</i> encounters oxygen (O₂) present in the circulating saliva and reactive oxygen species formed endogenously, by an activated immune system or neighboring oral commensal streptococci. This review explores the bacterium's adaptive mechanisms that enable survival under oxidative stress. We discuss how <i>F. nucleatum</i> mitigates oxidative damage and aerobic stress through common detoxifying and repair enzymes such as peroxiredoxins, methionine sulfoxide reductases, and rubrerythrin and through the activity of the recently identified multicomponent enzyme, termed butyryl-CoA oxygen oxidoreductase. Turnover by the latter enzyme enables <i>F. nucleatum</i> to exploit molecular oxygen for the conservation of energy. Additionally, we discuss how a two-component signal transduction system, ModRS, a global regulator of oxidative stress, functions in part to reprogram core metabolism to counterbalance the inactivation of a glycyl radical enzyme hypersensitive to O<sub>2</sub>. Our findings provide new insight into how <i>F. nucleatum</i> resists fluctuating dioxygen environments, shedding light on its persistence in extraoral sites and its potential role in disease progression.</p>\",\"PeriodicalId\":15107,\"journal\":{\"name\":\"Journal of Bacteriology\",\"volume\":\" \",\"pages\":\"e0009025\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-06-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Bacteriology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1128/jb.00090-25\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bacteriology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/jb.00090-25","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

核梭杆菌是一种革兰氏阴性厌氧菌,与口腔共生,在口腔生物膜的成熟中起着重要作用。这种细菌也是一种机会性病原体,因为它与全身感染和癌症进展有关。虽然主要生活在口腔生物膜内的缺氧微环境中,但核梭菌会遇到循环唾液中存在的氧(O₂)和由激活的免疫系统或邻近的口腔共生链球菌内源性形成的活性氧。这篇综述探讨了细菌在氧化应激下存活的适应机制。我们讨论了核梭菌如何通过常见的解毒和修复酶,如过氧化物还毒素、蛋氨酸亚砜还原酶和红赤菊酯,以及最近发现的多组分酶,称为丁基辅酶a氧氧化还原酶的活性,来减轻氧化损伤和有氧应激。后一种酶的周转使核梭菌能够利用分子氧进行能量守恒。此外,我们还讨论了一个双组分信号转导系统,ModRS,一个氧化应激的全局调节剂,如何在一定程度上重新编程核心代谢,以抵消对氧过敏的甘酰自由基酶的失活。我们的研究结果为核梭菌如何抵抗波动的双氧环境提供了新的见解,揭示了其在口腔外部位的持久性及其在疾病进展中的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fusobacterium nucleatum: strategies for adapting to aerobic stress.

Fusobacterium nucleatum-a gram-negative anaerobe-is commensal to the oral cavity, where it plays an important role in the maturation of the oral biofilm. The bacterium is also an opportunistic pathogen, given its association with systemic infections and cancer progression. Although residing in largely anoxic microenvironments within the oral biofilm, F. nucleatum encounters oxygen (O₂) present in the circulating saliva and reactive oxygen species formed endogenously, by an activated immune system or neighboring oral commensal streptococci. This review explores the bacterium's adaptive mechanisms that enable survival under oxidative stress. We discuss how F. nucleatum mitigates oxidative damage and aerobic stress through common detoxifying and repair enzymes such as peroxiredoxins, methionine sulfoxide reductases, and rubrerythrin and through the activity of the recently identified multicomponent enzyme, termed butyryl-CoA oxygen oxidoreductase. Turnover by the latter enzyme enables F. nucleatum to exploit molecular oxygen for the conservation of energy. Additionally, we discuss how a two-component signal transduction system, ModRS, a global regulator of oxidative stress, functions in part to reprogram core metabolism to counterbalance the inactivation of a glycyl radical enzyme hypersensitive to O2. Our findings provide new insight into how F. nucleatum resists fluctuating dioxygen environments, shedding light on its persistence in extraoral sites and its potential role in disease progression.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Bacteriology
Journal of Bacteriology 生物-微生物学
CiteScore
6.10
自引率
9.40%
发文量
324
审稿时长
1.3 months
期刊介绍: The Journal of Bacteriology (JB) publishes research articles that probe fundamental processes in bacteria, archaea and their viruses, and the molecular mechanisms by which they interact with each other and with their hosts and their environments.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信