• 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

相似文献

1
Host-imposed manganese starvation of invading pathogens: two routes to the same destination.宿主对入侵病原体施加的锰饥饿:通往同一目的地的两条途径。
Biometals. 2015 Jun;28(3):509-19. doi: 10.1007/s10534-015-9850-z. Epub 2015 Apr 3.
2
Competition for Manganese at the Host-Pathogen Interface.宿主-病原体界面处的锰竞争。
Prog Mol Biol Transl Sci. 2016;142:1-25. doi: 10.1016/bs.pmbts.2016.05.002. Epub 2016 Jun 20.
3
A Manganese-independent Aldolase Enables Staphylococcus aureus To Resist Host-imposed Metal Starvation.一种锰非依赖性醛缩酶使金黄色葡萄球菌能够抵抗宿主施加的金属饥饿。
mBio. 2023 Feb 28;14(1):e0322322. doi: 10.1128/mbio.03223-22. Epub 2023 Jan 4.
4
Manganese acquisition and homeostasis at the host-pathogen interface.宿主-病原体界面的锰摄取和稳态。
Front Cell Infect Microbiol. 2013 Dec 5;3:91. doi: 10.3389/fcimb.2013.00091. eCollection 2013.
5
Manganese homeostasis and utilization in pathogenic bacteria.致病细菌中的锰稳态与利用
Mol Microbiol. 2015 Jul;97(2):216-28. doi: 10.1111/mmi.13034. Epub 2015 May 15.
6
Nutritional immunity beyond iron: a role for manganese and zinc.营养性免疫:锰和锌的作用不止于铁。
Curr Opin Chem Biol. 2010 Apr;14(2):218-24. doi: 10.1016/j.cbpa.2009.11.008. Epub 2009 Dec 16.
7
Manganese and microbial pathogenesis: sequestration by the Mammalian immune system and utilization by microorganisms.锰与微生物致病机制:被哺乳动物免疫系统隔离及被微生物利用
ACS Chem Biol. 2015 Mar 20;10(3):641-51. doi: 10.1021/cb500792b. Epub 2015 Jan 16.
8
The impact of metal availability on immune function during infection.金属元素可利用性对感染期间免疫功能的影响。
Trends Endocrinol Metab. 2021 Nov;32(11):916-928. doi: 10.1016/j.tem.2021.08.004. Epub 2021 Sep 3.
9
Multi-metal nutrient restriction and crosstalk in metallostasis systems in microbial pathogens.微生物病原体中金属稳态系统中的多金属营养限制和串扰。
Curr Opin Microbiol. 2020 Jun;55:17-25. doi: 10.1016/j.mib.2020.01.010. Epub 2020 Feb 12.
10
The role of metal ions in the virulence and viability of bacterial pathogens.金属离子在细菌病原体的毒力和生存能力中的作用。
Biochem Soc Trans. 2019 Feb 28;47(1):77-87. doi: 10.1042/BST20180275. Epub 2019 Jan 9.

引用本文的文献

1
Slc11 Synapomorphy: A Conserved 3D Framework Articulating Carrier Conformation Switch.Slc11 同源特征:一个保守的 3D 框架,连接载体构象开关。
Int J Mol Sci. 2023 Oct 11;24(20):15076. doi: 10.3390/ijms242015076.
2
TerC proteins function during protein secretion to metalate exoenzymes.TerC 蛋白在蛋白质分泌过程中发挥作用,以使外切酶金属化。
Nat Commun. 2023 Oct 4;14(1):6186. doi: 10.1038/s41467-023-41896-1.
3
The role of CopA in Streptococcus pyogenes copper homeostasis and virulence.CopA 在酿脓链球菌铜稳态和毒力中的作用。
J Inorg Biochem. 2023 Mar;240:112122. doi: 10.1016/j.jinorgbio.2023.112122. Epub 2023 Jan 6.
4
The structural basis of bacterial manganese import.细菌锰摄取的结构基础。
Sci Adv. 2021 Aug 6;7(32). doi: 10.1126/sciadv.abg3980. Print 2021 Aug.
5
Bioinformatic Mapping of Opine-Like Zincophore Biosynthesis in Bacteria.细菌中类冠瘿碱锌载体生物合成的生物信息学图谱分析
mSystems. 2020 Aug 18;5(4):e00554-20. doi: 10.1128/mSystems.00554-20.
6
Enterococcus faecalis Manganese Exporter MntE Alleviates Manganese Toxicity and Is Required for Mouse Gastrointestinal Colonization.粪肠球菌锰转运蛋白 MntE 缓解锰毒性并有助于其在小鼠胃肠道中的定植。
Infect Immun. 2020 May 20;88(6). doi: 10.1128/IAI.00058-20.
7
Further aspects of Toxoplasma gondii elimination in the presence of metals.在金属存在的情况下弓形虫消除的其他方面。
Parasitol Res. 2018 Apr;117(4):1245-1256. doi: 10.1007/s00436-018-5806-x. Epub 2018 Feb 18.
8
Eat Prey, Live: As a Model for Cell-Autonomous Defenses.捕食、生存:作为细胞自主防御的一种模式。
Front Immunol. 2018 Jan 4;8:1906. doi: 10.3389/fimmu.2017.01906. eCollection 2017.
9
Bacillus subtilis MntR coordinates the transcriptional regulation of manganese uptake and efflux systems.枯草芽孢杆菌MntR协调锰摄取和外排系统的转录调控。
Mol Microbiol. 2017 Jan;103(2):253-268. doi: 10.1111/mmi.13554. Epub 2016 Nov 2.

本文引用的文献

1
Zinc supplementation for the prevention of pneumonia in children aged 2 months to 59 months.补充锌剂预防2至59个月儿童肺炎
Cochrane Database Syst Rev. 2016 Dec 4;12(12):CD005978. doi: 10.1002/14651858.CD005978.pub3.
2
Crystal structure of a SLC11 (NRAMP) transporter reveals the basis for transition-metal ion transport.SLC11(NRAMP)转运蛋白的晶体结构揭示了过渡金属离子转运的基础。
Nat Struct Mol Biol. 2014 Nov;21(11):990-6. doi: 10.1038/nsmb.2904. Epub 2014 Oct 19.
3
Apo, Zn2+-bound and Mn2+-bound structures reveal ligand-binding properties of SitA from the pathogen Staphylococcus pseudintermedius.载脂蛋白、锌结合和锰结合结构揭示了病原体中间型葡萄球菌中 SitA 的配体结合特性。
Biosci Rep. 2014 Nov 24;34(6):e00154. doi: 10.1042/BSR20140088.
4
Extracellular zinc competitively inhibits manganese uptake and compromises oxidative stress management in Streptococcus pneumoniae.细胞外锌竞争性抑制肺炎链球菌对锰的摄取,并损害其氧化应激管理能力。
PLoS One. 2014 Feb 18;9(2):e89427. doi: 10.1371/journal.pone.0089427. eCollection 2014.
5
An antimicrobial role for zinc in innate immune defense against group A streptococcus.锌在先天免疫防御 A 组链球菌中的抗菌作用。
J Infect Dis. 2014 May 15;209(10):1500-8. doi: 10.1093/infdis/jiu053. Epub 2014 Jan 20.
6
AdcA and AdcAII employ distinct zinc acquisition mechanisms and contribute additively to zinc homeostasis in Streptococcus pneumoniae.AdcA和AdcAII采用不同的锌获取机制,并对肺炎链球菌的锌稳态起累加作用。
Mol Microbiol. 2014 Feb;91(4):834-51. doi: 10.1111/mmi.12504. Epub 2014 Jan 16.
7
Manganese acquisition and homeostasis at the host-pathogen interface.宿主-病原体界面的锰摄取和稳态。
Front Cell Infect Microbiol. 2013 Dec 5;3:91. doi: 10.3389/fcimb.2013.00091. eCollection 2013.
8
Identifying potential therapeutic targets of methicillin-resistant Staphylococcus aureus through in vivo proteomic analysis.通过体内蛋白质组学分析鉴定耐甲氧西林金黄色葡萄球菌的潜在治疗靶点。
J Infect Dis. 2014 May 15;209(10):1533-41. doi: 10.1093/infdis/jit662. Epub 2013 Nov 26.
9
Contributions of the S100A9 C-terminal tail to high-affinity Mn(II) chelation by the host-defense protein human calprotectin.宿主防御蛋白人钙卫蛋白通过 S100A9 C 端尾部对高亲和力 Mn(II)螯合的贡献。
J Am Chem Soc. 2013 Nov 27;135(47):17804-17. doi: 10.1021/ja407147d. Epub 2013 Nov 18.
10
Imperfect coordination chemistry facilitates metal ion release in the Psa permease.不完善的配位化学促进了 Psa 通透酶中金属离子的释放。
Nat Chem Biol. 2014 Jan;10(1):35-41. doi: 10.1038/nchembio.1382. Epub 2013 Nov 10.

宿主对入侵病原体施加的锰饥饿:通往同一目的地的两条途径。

Host-imposed manganese starvation of invading pathogens: two routes to the same destination.

作者信息

Morey Jacqueline R, McDevitt Christopher A, Kehl-Fie Thomas E

机构信息

Research Centre for Infectious Diseases, School of Molecular and Biomedical Science, University of Adelaide, Adelaide, SA, 5005, Australia.

出版信息

Biometals. 2015 Jun;28(3):509-19. doi: 10.1007/s10534-015-9850-z. Epub 2015 Apr 3.

DOI:10.1007/s10534-015-9850-z
PMID:25836716
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4430393/
Abstract

During infection invading pathogens must acquire all essential nutrients, including first row transition metals, from the host. To combat invaders, the host exploits this fact and restricts the availability of these nutrients using a defense mechanism known as nutritional immunity. While iron sequestration is the most well-known aspect of this defense, recent work has revealed that the host restricts the availability of other essential elements, notably manganese (Mn), during infection. Furthermore, these studies have revealed that the host utilizes multiple strategies that extend beyond metal sequestration to prevent bacteria from obtaining these metals. This review will discuss the mechanisms by which bacteria attempt to obtain the essential first row transition metal ion Mn during infection, and the approaches utilized by the host to prevent this occurrence. In addition, this review will discuss the impact of host-imposed Mn starvation on invading bacteria.

摘要

在感染过程中,入侵的病原体必须从宿主获取所有必需营养素,包括第一排过渡金属。为了对抗入侵者,宿主利用这一事实,并通过一种称为营养免疫的防御机制来限制这些营养素的可用性。虽然铁螯合是这种防御最广为人知的方面,但最近的研究表明,宿主在感染期间会限制其他必需元素的可用性,尤其是锰(Mn)。此外,这些研究还表明,宿主利用多种策略,不仅仅是金属螯合,来阻止细菌获取这些金属。本综述将讨论细菌在感染过程中试图获取必需的第一排过渡金属离子锰的机制,以及宿主用来防止这种情况发生的方法。此外,本综述还将讨论宿主施加的锰饥饿对入侵细菌的影响。