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subsp. and Genes Code for Ferritins That Are Modulated by Iron Concentration.亚种以及由铁浓度调节的铁蛋白编码基因。
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Identification of a Mycobacterium tuberculosis gene cluster encoding the biosynthetic enzymes for assembly of the virulence-conferring siderophore mycobactin.鉴定一个编码用于组装赋予毒力的铁载体分枝杆菌素的生物合成酶的结核分枝杆菌基因簇。
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Proc Natl Acad Sci U S A. 2000 Feb 1;97(3):1252-7. doi: 10.1073/pnas.97.3.1252.

引用本文的文献

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Ferritin from Mycobacterium abscessus is involved in resistance to antibiotics and oxidative stress.分支杆菌属脓肿亚种的铁蛋白参与了对抗生素和氧化应激的耐药性。
Appl Microbiol Biotechnol. 2023 Apr;107(7-8):2577-2595. doi: 10.1007/s00253-023-12420-8. Epub 2023 Mar 2.
2
Targeting Siderophore-Mediated Iron Uptake in : A New Strategy to Limit the Virulence of Non-Tuberculous Mycobacteria.靶向铁载体介导的铁摄取:限制非结核分枝杆菌毒力的新策略
Pharmaceutics. 2023 Feb 2;15(2):502. doi: 10.3390/pharmaceutics15020502.

本文引用的文献

1
Mycobacterial siderophore: A review on chemistry and biology of siderophore and its potential as a target for tuberculosis.分枝杆菌的铁载体:铁载体化学与生物学及其作为结核病治疗靶点的潜力综述。
Eur J Med Chem. 2018 Sep 5;157:783-790. doi: 10.1016/j.ejmech.2018.08.030. Epub 2018 Aug 14.
2
subsp. and Genes Code for Ferritins That Are Modulated by Iron Concentration.亚种以及由铁浓度调节的铁蛋白编码基因。
Front Microbiol. 2018 Jun 1;9:1072. doi: 10.3389/fmicb.2018.01072. eCollection 2018.
3
Modulation of Macrophage Responses by CMX, a Fusion Protein Composed of Ag85c, MPT51, and HspX from .由来自……的Ag85c、MPT51和HspX组成的融合蛋白CMX对巨噬细胞反应的调节
Front Microbiol. 2017 Apr 12;8:623. doi: 10.3389/fmicb.2017.00623. eCollection 2017.
4
Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacterium.一种可在人际传播的多重耐药非结核分枝杆菌的出现与传播。
Science. 2016 Nov 11;354(6313):751-757. doi: 10.1126/science.aaf8156.
5
Iron Homeostasis in Mycobacterium tuberculosis: Mechanistic Insights into Siderophore-Mediated Iron Uptake.结核分枝杆菌中的铁稳态:对铁载体介导的铁摄取的机制性见解
J Bacteriol. 2016 Aug 25;198(18):2399-409. doi: 10.1128/JB.00359-16. Print 2016 Sep 15.
6
Mycobacterium abscessus Complex Infections in Humans.人类脓肿分枝杆菌复合群感染
Emerg Infect Dis. 2015 Sep;21(9):1638-46. doi: 10.3201/2109.141634.
7
Gallium Compounds Exhibit Potential as New Therapeutic Agents against Mycobacterium abscessus.镓化合物展现出作为抗脓肿分枝杆菌新治疗剂的潜力。
Antimicrob Agents Chemother. 2015 Aug;59(8):4826-34. doi: 10.1128/AAC.00331-15. Epub 2015 Jun 1.
8
Mycobacteria, metals, and the macrophage.分枝杆菌、金属与巨噬细胞。
Immunol Rev. 2015 Mar;264(1):249-63. doi: 10.1111/imr.12265.
9
Differential macrophage response to slow- and fast-growing pathogenic mycobacteria.巨噬细胞对生长缓慢和快速生长的致病性分枝杆菌的不同反应。
Biomed Res Int. 2014;2014:916521. doi: 10.1155/2014/916521. Epub 2014 May 18.
10
Transcriptional regulation of Mycobacterium tuberculosis hupB gene expression.结核分枝杆菌 hupB 基因表达的转录调控。
Microbiology (Reading). 2014 Aug;160(Pt 8):1637-1647. doi: 10.1099/mic.0.079640-0. Epub 2014 May 22.

来自亚种的基因与铁载体合成有关。

The Gene from subsp.  is Related to Siderophore Synthesis.

作者信息

de Oliveira Fábio Muniz, Corrêa Viviane Lopes Rocha, Corrêa André França, da Costa Adeliane Castro, Procopio Victor Oliveira, Junqueira-Kipnis Ana Paula, Kipnis André

机构信息

Tropical Institute of Pathology and Public Health, Federal University of Goiás, Rua 235 esquina com 1a avenida S/N, Setor Universitário, Goiânia, Goiás CEP 7405-050 Brazil.

出版信息

Indian J Microbiol. 2019 Jun;59(2):180-187. doi: 10.1007/s12088-019-00788-z. Epub 2019 Feb 27.

DOI:10.1007/s12088-019-00788-z
PMID:31031432
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6458192/
Abstract

Iron (Fe) homeostasis control is important for both pathogen and the host. During infection, the host reduces the access of microorganisms to iron, however, studies have shown that virulent pathogens are capable to sequester Fe from host proteins, and establish the infection. subsp. (Mycma), that is resistant to most drugs used against tuberculosis, was responsible for outbreaks around the world showing increased virulence when compared to other rapidly growing mycobacteria. The goal of this study was to determine whether Mycma produce siderophores and if the gene expression, a putative homolog of gene located in the gene cluster, is related to the synthesis of these molecules. For that, the effect of different iron concentrations on the growth of Mycma, the expression of gene, and the production of siderophores was evaluated in vitro and in vivo. It is shown that Mycma produce siderophores under iron deprivation conditions and gene expression was influenced by iron availability. The gene expression was also increased after macrophage or in vivo infection indicating that mycobactin synthesis by Mycma could participate in the Fe sequestration from the host during infection. In conclusion, we show that Mycma produces siderophores under iron deprivation conditions and that the gene is involved in this process, furthermore, this gene expression is induced during infection.

摘要

铁(Fe)稳态控制对病原体和宿主都很重要。在感染期间,宿主会减少微生物获取铁的机会,然而,研究表明,致病性病原体能够从宿主蛋白中螯合铁,并引发感染。 亚种(Mycma),对大多数用于治疗结核病的药物具有抗性,与其他快速生长的分枝杆菌相比,它在世界各地引发的疫情显示出更强的毒力。本研究的目的是确定Mycma是否产生铁载体,以及位于基因簇中的假定 基因同源物 基因的表达是否与这些分子的合成有关。为此,在体外和体内评估了不同铁浓度对Mycma生长、 基因表达和铁载体产生的影响。结果表明,Mycma在缺铁条件下产生铁载体,并且 基因表达受铁可用性的影响。巨噬细胞感染或体内感染后, 基因表达也会增加,这表明Mycma合成的分枝杆菌素可能参与感染期间从宿主中螯合铁的过程。总之,我们表明Mycma在缺铁条件下产生铁载体,并且 基因参与了这一过程,此外,该基因在感染期间被诱导表达。