{"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}
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.
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.