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本文引用的文献

1
Pyrazinoic Acid Inhibits Mycobacterial Coenzyme A Biosynthesis by Binding to Aspartate Decarboxylase PanD.吡嗪酸通过与天冬氨酸脱羧酶PanD结合抑制分枝杆菌辅酶A的生物合成。
ACS Infect Dis. 2017 Nov 10;3(11):807-819. doi: 10.1021/acsinfecdis.7b00079. Epub 2017 Oct 18.
2
Anti-tubercular Activity of Pyrazinamide is Independent of trans-Translation and RpsA.吡嗪酰胺的抗结核活性不依赖于反翻译和 RpsA。
Sci Rep. 2017 Jul 21;7(1):6135. doi: 10.1038/s41598-017-06415-5.
3
Non- Gene-Mutated but Pyrazinamide-Resistant Mycobacterium tuberculosis: Why Is That?非基因变异但对吡嗪酰胺耐药的结核分枝杆菌:原因何在?
J Clin Microbiol. 2017 Jun;55(6):1920-1927. doi: 10.1128/JCM.02532-16. Epub 2017 Apr 12.
4
Mutation in clpC1 encoding an ATP-dependent ATPase involved in protein degradation is associated with pyrazinamide resistance in Mycobacterium tuberculosis.编码参与蛋白质降解的ATP依赖性ATP酶的clpC1基因突变与结核分枝杆菌对吡嗪酰胺的耐药性有关。
Emerg Microbes Infect. 2017 Feb 15;6(2):e8. doi: 10.1038/emi.2017.1.
5
Biosynthesis and Regulation of Sulfomenaquinone, a Metabolite Associated with Virulence in Mycobacterium tuberculosis.结核分枝杆菌中与毒力相关的代谢产物硫代甲萘醌的生物合成与调控
ACS Infect Dis. 2016 Nov 11;2(11):800-806. doi: 10.1021/acsinfecdis.6b00106. Epub 2016 Aug 15.
6
Missense Mutations in the Unfoldase ClpC1 of the Caseinolytic Protease Complex Are Associated with Pyrazinamide Resistance in Mycobacterium tuberculosis.酪蛋白水解蛋白酶复合体的解折叠酶ClpC1中的错义突变与结核分枝杆菌对吡嗪酰胺的耐药性相关。
Antimicrob Agents Chemother. 2017 Jan 24;61(2). doi: 10.1128/AAC.02342-16. Print 2017 Feb.
7
Pyrazinamide Resistance Is Caused by Two Distinct Mechanisms: Prevention of Coenzyme A Depletion and Loss of Virulence Factor Synthesis.吡嗪酰胺耐药性由两种不同机制引起:防止辅酶A耗竭和毒力因子合成丧失。
ACS Infect Dis. 2016 Sep 9;2(9):616-626. doi: 10.1021/acsinfecdis.6b00070. Epub 2016 Aug 8.
8
Mycobacterial Metabolic Syndrome: LprG and Rv1410 Regulate Triacylglyceride Levels, Growth Rate and Virulence in Mycobacterium tuberculosis.分枝杆菌代谢综合征:LprG和Rv1410调节结核分枝杆菌中的甘油三酯水平、生长速率和毒力。
PLoS Pathog. 2016 Jan 11;12(1):e1005351. doi: 10.1371/journal.ppat.1005351. eCollection 2016 Jan.
9
Aspartate decarboxylase (PanD) as a new target of pyrazinamide in Mycobacterium tuberculosis.天冬氨酸脱羧酶(PanD)作为结核分枝杆菌中吡嗪酰胺的新靶点。
Emerg Microbes Infect. 2014 Aug;3(8):e58. doi: 10.1038/emi.2014.61. Epub 2014 Aug 13.
10
Mutations in panD encoding aspartate decarboxylase are associated with pyrazinamide resistance in Mycobacterium tuberculosis.编码天冬氨酸脱羧酶的panD基因突变与结核分枝杆菌对吡嗪酰胺的耐药性相关。
Emerg Microbes Infect. 2013 Jun;2(6):e34. doi: 10.1038/emi.2013.38. Epub 2013 Jun 12.

鉴定与结核分枝杆菌吡嗪酸/吡嗪酰胺耐药相关的 LprG () 、 、 、 、 和 中的新型突变。

Identification of Novel Mutations in LprG (), , , , , and Associated with Pyrazinoic Acid/Pyrazinamide Resistance in Mycobacterium tuberculosis.

机构信息

Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland, USA.

Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.

出版信息

Antimicrob Agents Chemother. 2018 Jun 26;62(7). doi: 10.1128/AAC.00430-18. Print 2018 Jul.

DOI:10.1128/AAC.00430-18
PMID:29686155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6021685/
Abstract

Despite progress, the mechanisms of action and resistance of pyrazinamide (PZA) are not well understood. We characterized 109 mutants resistant to pyrazinoic acid (POA), the active form of PZA, and found that while most ( = 101 [93%]) mutants had mutations and 4 (4%) had mutations (S91G), new mutations in () and ( = 4 [4%]), , , , and (cytochrome P450 128) were identified, shedding new light on the mechanisms of action and resistance of PZA in .

摘要

尽管取得了进展,但吡嗪酰胺(PZA)的作用机制和耐药机制仍不清楚。我们对 109 株耐吡嗪酸(POA)的突变体进行了特征描述,POA 是 PZA 的活性形式,结果发现,虽然大多数(=101 [93%])突变株具有 突变,而 4 株(4%)具有 突变(S91G),但在 (=4 [4%])中发现了新的突变, (细胞色素 P450 128),这为 PZA 在结核分枝杆菌中的作用机制和耐药机制提供了新的认识。