• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

2 型烟酰胺腺嘌呤二核苷酸脱氢酶是电子进入酿脓链球菌呼吸链的唯一入口,也是一个潜在的药物靶点。

Type 2 NADH Dehydrogenase Is the Only Point of Entry for Electrons into the Streptococcus agalactiae Respiratory Chain and Is a Potential Drug Target.

机构信息

Department of Biochemistry, University of Illinois, Urbana, Illinois, USA.

Micalis Institute, INRA, AgroParisTech, Université Paris-Saclay, Jouy-en-Josas, France.

出版信息

mBio. 2018 Jul 3;9(4):e01034-18. doi: 10.1128/mBio.01034-18.

DOI:10.1128/mBio.01034-18
PMID:29970468
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6030563/
Abstract

The opportunistic pathogen is the major cause of meningitis and sepsis in a newborn's first week, as well as a considerable cause of pneumonia, urinary tract infections, and sepsis in immunocompromised adults. This pathogen respires aerobically if heme and quinone are available in the environment, and a functional respiratory chain is required for full virulence. Remarkably, it is shown here that the entire respiratory chain of consists of only two enzymes, a type 2 NADH dehydrogenase (NDH-2) and a cytochrome oxygen reductase. There are no respiratory dehydrogenases other than NDH-2 to feed electrons into the respiratory chain, and there is only one respiratory oxygen reductase to reduce oxygen to water. Although grows well in by fermentative metabolism, it is shown here that the absence of NDH-2 results in attenuated virulence, as observed by reduced colonization in heart and kidney in a mouse model of systemic infection. The lack of NDH-2 in mammalian mitochondria and its important role for virulence suggest this enzyme may be a potential drug target. For this reason, in this study, NDH-2 was purified and biochemically characterized, and the isolated enzyme was used to screen for inhibitors from libraries of FDA-approved drugs. Zafirlukast was identified to successfully inhibit both NDH-2 activity and aerobic respiration in intact cells. This compound may be useful as a laboratory tool to inhibit respiration in and, since it has few side effects, it might be considered a lead compound for therapeutics development. is part of the human intestinal microbiota and is present in the vagina of ~30% of healthy women. Although a commensal, it is also the leading cause of septicemia and meningitis in neonates and immunocompromised adults. This organism can aerobically respire, but only using external sources of heme and quinone, required to have a functional electron transport chain. Although bacteria usually have a branched respiratory chain with multiple dehydrogenases and terminal oxygen reductases, here we establish that utilizes only one type 2 NADH dehydrogenase (NDH-2) and one cytochrome oxygen reductase to perform respiration. NADH-dependent respiration plays a critical role in the pathogen in maintaining NADH/NAD redox balance in the cell, optimizing ATP production, and tolerating oxygen. In summary, we demonstrate the essential role of NDH-2 in respiration and its contribution to virulence and propose it as a potential drug target.

摘要

机会性病原体是新生儿出生后第一周脑膜炎和败血症的主要病因,也是免疫功能低下成年人肺炎、尿路感染和败血症的重要病因。如果环境中存在血红素和醌,这种病原体就会进行需氧呼吸,并且需要功能性呼吸链才能充分发挥毒力。值得注意的是,这里显示 的整个呼吸链仅由两种酶组成,即一种类型 2 的 NADH 脱氢酶(NDH-2)和一种细胞色素 氧还原酶。除了 NDH-2 之外,没有其他呼吸脱氢酶将电子输入呼吸链,并且只有一种呼吸氧还原酶将氧气还原为水。尽管 通过发酵代谢在 中生长良好,但这里显示 NDH-2 的缺失会导致毒力减弱,如在系统性感染的小鼠模型中观察到心脏和肾脏的定植减少。哺乳动物线粒体中缺乏 NDH-2 及其对毒力的重要作用表明,该酶可能是一个潜在的药物靶点。出于这个原因,在这项研究中,NDH-2 被纯化并进行了生化表征,并用分离的酶从 FDA 批准药物的文库中筛选抑制剂。扎鲁司特被鉴定为可成功抑制完整细胞中的 NDH-2 活性和需氧呼吸。由于这种化合物副作用很少,因此它可能被认为是治疗开发的先导化合物,因此它可能是一种有用的实验室工具,可用于抑制 和 的呼吸。 是人类肠道微生物群的一部分,存在于约 30%健康女性的阴道中。尽管它是一种共生菌,但它也是新生儿和免疫功能低下成年人败血症和脑膜炎的主要原因。这种生物体可以需氧呼吸,但只能使用血红素和醌的外部来源,这是发挥功能电子传递链所必需的。尽管细菌通常具有分支呼吸链,具有多种脱氢酶和末端氧还原酶,但在这里我们确定 仅利用一种类型 2 的 NADH 脱氢酶(NDH-2)和一种细胞色素 氧还原酶进行呼吸。NADH 依赖性呼吸在病原体中发挥着至关重要的作用,可维持细胞内 NADH/NAD 氧化还原平衡,优化 ATP 产生,并耐受氧气。总之,我们证明了 NDH-2 在呼吸中的重要作用及其对 毒力的贡献,并提出将其作为潜在的药物靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/0bc8ee00e525/mbo0041839590007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/93d0040dbc2d/mbo0041839590001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/3eebbb5a31d4/mbo0041839590002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/689589d3868d/mbo0041839590003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/33de49edac8c/mbo0041839590004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/49b754e98c12/mbo0041839590005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/3a7aba3ed2b4/mbo0041839590006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/0bc8ee00e525/mbo0041839590007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/93d0040dbc2d/mbo0041839590001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/3eebbb5a31d4/mbo0041839590002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/689589d3868d/mbo0041839590003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/33de49edac8c/mbo0041839590004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/49b754e98c12/mbo0041839590005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/3a7aba3ed2b4/mbo0041839590006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80a3/6030563/0bc8ee00e525/mbo0041839590007.jpg

相似文献

1
Type 2 NADH Dehydrogenase Is the Only Point of Entry for Electrons into the Streptococcus agalactiae Respiratory Chain and Is a Potential Drug Target.2 型烟酰胺腺嘌呤二核苷酸脱氢酶是电子进入酿脓链球菌呼吸链的唯一入口,也是一个潜在的药物靶点。
mBio. 2018 Jul 3;9(4):e01034-18. doi: 10.1128/mBio.01034-18.
2
Glutathione Synthesis Contributes to Virulence of in a Murine Model of Sepsis.谷胱甘肽合成有助于 在脓毒症小鼠模型中的毒力。
J Bacteriol. 2019 Sep 20;201(20). doi: 10.1128/JB.00367-19. Print 2019 Oct 15.
3
The global motion affecting electron transfer in Plasmodium falciparum type II NADH dehydrogenases: a novel non-competitive mechanism for quinoline ketone derivative inhibitors.全球运动影响恶性疟原虫 II 型 NADH 脱氢酶中的电子转移:一种新型的喹啉酮衍生物抑制剂的非竞争性机制。
Phys Chem Chem Phys. 2019 Aug 21;21(33):18105-18118. doi: 10.1039/c9cp02645b.
4
The Auxiliary NADH Dehydrogenase Plays a Crucial Role in Redox Homeostasis of Nicotinamide Cofactors in the Absence of the Periplasmic Oxidation System in Gluconobacter oxydans NBRC3293.在缺少谷氨酸氧化醋酸杆菌 NBRC3293 周质氧化系统的情况下,辅助 NADH 脱氢酶在烟酰胺辅酶的氧化还原平衡中发挥关键作用。
Appl Environ Microbiol. 2021 Jan 4;87(2). doi: 10.1128/AEM.02155-20.
5
Characterization of the type 2 NADH:menaquinone oxidoreductases from Staphylococcus aureus and the bactericidal action of phenothiazines.金黄色葡萄球菌2型NADH:甲萘醌氧化还原酶的特性及吩噻嗪类药物的杀菌作用
Biochim Biophys Acta. 2014 Jul;1837(7):954-63. doi: 10.1016/j.bbabio.2014.03.017. Epub 2014 Apr 5.
6
Roles of environmental heme, and menaquinone, in streptococcus agalactiae.环境血红素和甲萘醌在无乳链球菌中的作用。
Biometals. 2006 Apr;19(2):205-10. doi: 10.1007/s10534-005-5419-6.
7
Shewanella oneidensis MR-1 Utilizes both Sodium- and Proton-Pumping NADH Dehydrogenases during Aerobic Growth.希瓦氏菌属(Shewanella oneidensis)MR-1 在好氧生长过程中同时利用钠离子和质子泵 NADH 脱氢酶。
Appl Environ Microbiol. 2018 May 31;84(12). doi: 10.1128/AEM.00415-18. Print 2018 Jun 15.
8
Electron transfer ability from NADH to menaquinone and from NADPH to oxygen of type II NADH dehydrogenase of Corynebacterium glutamicum.谷氨酸棒杆菌II型NADH脱氢酶从NADH到甲基萘醌以及从NADPH到氧的电子传递能力。
Biosci Biotechnol Biochem. 2005 Jan;69(1):149-59. doi: 10.1271/bbb.69.149.
9
The two alternative NADH:quinone oxidoreductases from : two players with different molecular and cellular roles.来自[具体来源未给出]的两种交替型NADH:醌氧化还原酶:具有不同分子和细胞作用的两个参与者。
Microbiol Spectr. 2024 Aug 6;12(8):e0415223. doi: 10.1128/spectrum.04152-23. Epub 2024 Jul 16.
10
Synthetic lethality of NADH dehydrogenases is due to impaired NADH oxidation.NADH脱氢酶的合成致死性是由于NADH氧化受损。
bioRxiv. 2023 Apr 10:2023.04.10.536268. doi: 10.1101/2023.04.10.536268.

引用本文的文献

1
Gum Acacia-Dexamethasone Combination Attenuates Sepsis-Induced Acute Kidney Injury in Rats via Targeting SIRT1-HMGB1 Signaling Pathway and Preserving Mitochondrial Integrity.阿拉伯胶-地塞米松联合用药通过靶向SIRT1-HMGB1信号通路并维持线粒体完整性减轻大鼠脓毒症诱导的急性肾损伤。
Pharmaceuticals (Basel). 2025 Aug 5;18(8):1164. doi: 10.3390/ph18081164.
2
Interplay of niche and respiratory network in shaping bacterial colonization.生态位与呼吸网络在塑造细菌定殖过程中的相互作用。
J Biol Chem. 2025 Jan;301(1):108052. doi: 10.1016/j.jbc.2024.108052. Epub 2024 Dec 9.
3
The respiratory chain of in urine-like conditions: critical roles of NDH-2 and -terminal oxidases.

本文引用的文献

1
Crystal structure of type II NADH:quinone oxidoreductase from Caldalkalibacillus thermarum with an improved resolution of 2.15 Å.来自嗜热钙碱杆菌的II型NADH:醌氧化还原酶的晶体结构,分辨率提高到2.15 Å。
Acta Crystallogr F Struct Biol Commun. 2017 Oct 1;73(Pt 10):541-549. doi: 10.1107/S2053230X17013073. Epub 2017 Sep 23.
2
Acid Stress Response Mechanisms of Group B Streptococci.B 群链球菌的酸应激反应机制。
Front Cell Infect Microbiol. 2017 Sep 7;7:395. doi: 10.3389/fcimb.2017.00395. eCollection 2017.
3
Target Elucidation by Cocrystal Structures of NADH-Ubiquinone Oxidoreductase of Plasmodium falciparum (PfNDH2) with Small Molecule To Eliminate Drug-Resistant Malaria.
尿液样条件下的呼吸链:NDH-2和末端氧化酶的关键作用
Front Microbiol. 2024 Nov 6;15:1479714. doi: 10.3389/fmicb.2024.1479714. eCollection 2024.
4
Modifications of the respiratory chain of Bacillus licheniformis as an alkalophilic and cyanide-degrading microorganism.地衣芽孢杆菌作为嗜碱且能降解氰化物的微生物,其呼吸链的修饰。
J Bioenerg Biomembr. 2024 Dec;56(6):591-605. doi: 10.1007/s10863-024-10041-y. Epub 2024 Nov 5.
5
Chemically Mediated Artificial Electron Transport Chain.化学介导的人工电子传递链
ACS Cent Sci. 2024 Apr 10;10(6):1148-1155. doi: 10.1021/acscentsci.4c00165. eCollection 2024 Jun 26.
6
Myricetin Acts as an Inhibitor of Type II NADH Dehydrogenase from .杨梅素作为. 型 NADH 脱氢酶的抑制剂
Molecules. 2024 May 16;29(10):2354. doi: 10.3390/molecules29102354.
7
requires DHNA-dependent intracellular redox homeostasis facilitated by Ndh2 for survival and virulence.需要 Ndh2 依赖的 DHNA 依赖性细胞内氧化还原稳态来维持生存和毒力。
Infect Immun. 2023 Oct 17;91(10):e0002223. doi: 10.1128/iai.00022-23. Epub 2023 Sep 27.
8
requires DHNA-dependent intracellular redox homeostasis facilitated by Ndh2 for survival and virulence.需要由Ndh2促进的依赖于DHNA的细胞内氧化还原稳态以实现生存和毒力。
bioRxiv. 2023 Jan 14:2023.01.13.524026. doi: 10.1101/2023.01.13.524026.
9
requires cellular respiration for NAD regeneration and pathogenesis.需要细胞呼吸来进行 NAD 再生和发病机制。
Elife. 2022 Apr 5;11:e75424. doi: 10.7554/eLife.75424.
10
type II dehydrogenase is essential for parasite viability irrespective of the presence of an active complex I.Ⅱ型脱氢酶对于寄生虫的生存是必需的,无论是否存在活性复合物 I。
Proc Natl Acad Sci U S A. 2021 Oct 19;118(42). doi: 10.1073/pnas.2103803118.
通过恶性疟原虫NADH-泛醌氧化还原酶(PfNDH2)与小分子的共晶结构阐明靶点以消除耐药性疟疾
J Med Chem. 2017 Mar 9;60(5):1994-2005. doi: 10.1021/acs.jmedchem.6b01733. Epub 2017 Feb 22.
4
Visualization of the role of host heme on the virulence of the heme auxotroph Streptococcus agalactiae.宿主血红素对血红素营养缺陷型酿脓链球菌毒力作用的可视化。
Sci Rep. 2017 Jan 16;7:40435. doi: 10.1038/srep40435.
5
In vitro activity of the antiasthmatic drug zafirlukast against the oral pathogens Porphyromonas gingivalis and Streptococcus mutans.抗哮喘药物扎鲁司特对口腔病原菌牙龈卟啉单胞菌和变形链球菌的体外活性。
FEMS Microbiol Lett. 2017 Jan 1;364(2). doi: 10.1093/femsle/fnx005.
6
A partial metabolic pathway enables group b streptococcus to overcome quinone deficiency in a host bacterial community.一条部分代谢途径使B族链球菌能够克服宿主细菌群落中的醌缺乏问题。
Mol Microbiol. 2016 Oct;102(1):81-91. doi: 10.1111/mmi.13447. Epub 2016 Jul 8.
7
Oxidant Mechanisms in Renal Injury and Disease.肾脏损伤与疾病中的氧化机制
Antioxid Redox Signal. 2016 Jul 20;25(3):119-46. doi: 10.1089/ars.2016.6665. Epub 2016 Apr 26.
8
Streptococcal toxins: role in pathogenesis and disease.链球菌毒素:在发病机制和疾病中的作用
Cell Microbiol. 2015 Dec;17(12):1721-41. doi: 10.1111/cmi.12531. Epub 2015 Nov 17.
9
Mechanisms of group A Streptococcus resistance to reactive oxygen species.A 群链球菌对活性氧的耐药机制。
FEMS Microbiol Rev. 2015 Jul;39(4):488-508. doi: 10.1093/femsre/fuu009. Epub 2015 Feb 10.
10
Energetics of pathogenic bacteria and opportunities for drug development.病原菌的能量学与药物研发机遇
Adv Microb Physiol. 2014;65:1-62. doi: 10.1016/bs.ampbs.2014.08.001. Epub 2014 Nov 4.