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Rv0494蛋白有助于分枝杆菌的持续生存。

Rv0494 Protein Contributes to Mycobacterial Persistence.

作者信息

Ji Lei, Jiang Tingting, Zhao Xin, Cai Damin, Hua Kouzhen, Du Peng, Chen Yuanyuan, Xie Jianping

机构信息

School of Basic Medical Sciences and Forensic Medicine, Hangzhou Medical College, Hangzhou, Zhejiang, People's Republic of China.

Department of International Registration, Ustar Biotechnologies (Hangzhou) Ltd, Hangzhou, Zhejiang, People's Republic of China.

出版信息

Infect Drug Resist. 2023 Jul 22;16:4755-4762. doi: 10.2147/IDR.S419914. eCollection 2023.

DOI:10.2147/IDR.S419914
PMID:37501888
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10370413/
Abstract

PURPOSE

Fatty acid metabolism plays an important role in the survival and pathogenesis of . During dormancy, lipids are considered to be the main source of energy. A previous study found that Rv0494 is a starvation-inducible, lipid-responsive transcriptional regulator. However, the role of Rv0494 in bacterial persister survival has not been studied.

METHODS

We constructed a deletion mutant strain of H37Rv and evaluated the susceptibility of the mutant strain to antibiotics using a persistence test.

RESULTS

We found that mutations in lead to survival defects of persisters, which reflected in increased sensitivity to isoniazid.

CONCLUSION

We conclude that Rv0494 is important for persister survival and may serve as a good target for developing new antibiotics that kill persister bacteria for improved treatment of persistent bacterial infections.

摘要

目的

脂肪酸代谢在……的存活和发病机制中起重要作用。在休眠期间,脂质被认为是主要能量来源。先前的一项研究发现,Rv0494是一种饥饿诱导型、脂质反应性转录调节因子。然而,Rv0494在细菌持留菌存活中的作用尚未得到研究。

方法

我们构建了H37Rv的缺失突变株,并使用持留菌测试评估突变株对抗生素的敏感性。

结果

我们发现……中的突变导致持留菌的存活缺陷,这表现为对异烟肼的敏感性增加。

结论

我们得出结论,Rv0494对持留菌的存活很重要,可能作为开发新型抗生素的良好靶点,这些抗生素可杀死持留菌,以改善对持续性细菌感染的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3381/10370413/67dbcb68c94a/IDR-16-4755-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3381/10370413/1dbe2a03e7e0/IDR-16-4755-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3381/10370413/7b3c9edf1e9f/IDR-16-4755-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3381/10370413/c1194724d9f4/IDR-16-4755-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3381/10370413/67dbcb68c94a/IDR-16-4755-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3381/10370413/1dbe2a03e7e0/IDR-16-4755-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3381/10370413/7b3c9edf1e9f/IDR-16-4755-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3381/10370413/c1194724d9f4/IDR-16-4755-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3381/10370413/67dbcb68c94a/IDR-16-4755-g0004.jpg

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2
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本文引用的文献

1
An evolutionary functional genomics approach identifies novel candidate regions involved in isoniazid resistance in Mycobacterium tuberculosis.一种进化功能基因组学方法鉴定了与结核分枝杆菌异烟肼耐药相关的新候选区域。
Commun Biol. 2021 Nov 24;4(1):1322. doi: 10.1038/s42003-021-02846-z.
2
Label-Free Comparative Proteomics of Differentially Expressed Protein in Rifampicin-Related Drug-Resistant Strains.利福平相关耐药菌株中差异表达蛋白质的无标记比较蛋白质组学
Pathogens. 2021 May 15;10(5):607. doi: 10.3390/pathogens10050607.
3
Loss of phenotypic inheritance associated with mutation leads to increased frequency of small, slow persisters in .
与 突变相关的表型遗传丧失导致 中较小、较慢的持久型细菌的频率增加。
Proc Natl Acad Sci U S A. 2020 Feb 25;117(8):4152-4157. doi: 10.1073/pnas.1914741117. Epub 2020 Feb 6.
4
Defining the Transcriptional and Post-transcriptional Landscapes of in Aerobic Growth and Hypoxia.定义有氧生长和缺氧条件下的转录和转录后景观。
Front Microbiol. 2019 Mar 26;10:591. doi: 10.3389/fmicb.2019.00591. eCollection 2019.
5
Mce2R/Rv0586 of Mycobacterium tuberculosis is the functional homologue of FadR.结核分枝杆菌的Mce2R/Rv0586是FadR的功能同源物。
Microbiology (Reading). 2018 Sep;164(9):1133-1145. doi: 10.1099/mic.0.000686. Epub 2018 Jul 11.
6
Dual-Reporter Mycobacteriophages (Φ2DRMs) Reveal Preexisting Mycobacterium tuberculosis Persistent Cells in Human Sputum.双报告基因分枝杆菌噬菌体(Φ2DRMs)揭示人痰液中预先存在的结核分枝杆菌持留菌。
mBio. 2016 Oct 25;7(5):e01023-16. doi: 10.1128/mBio.01023-16.
7
The DNA-binding network of Mycobacterium tuberculosis.结核分枝杆菌的DNA结合网络。
Nat Commun. 2015 Jan 12;6:5829. doi: 10.1038/ncomms6829.
8
Rv0494 is a starvation-inducible, auto-regulatory FadR-like regulator from Mycobacterium tuberculosis.Rv0494是一种来自结核分枝杆菌的饥饿诱导型、自我调节的类FadR调节因子。
Microbiology (Reading). 2015 Mar;161(Pt 3):463-76. doi: 10.1099/mic.0.000017. Epub 2014 Dec 19.
9
Specialized transduction designed for precise high-throughput unmarked deletions in Mycobacterium tuberculosis.专为结核分枝杆菌精确高通量无标记缺失设计的特异性转导。
mBio. 2014 Jun 3;5(3):e01245-14. doi: 10.1128/mBio.01245-14.
10
Trans-translation mediates tolerance to multiple antibiotics and stresses in Escherichia coli.转译介导大肠杆菌对多种抗生素和应激的耐受。
J Antimicrob Chemother. 2013 Nov;68(11):2477-81. doi: 10.1093/jac/dkt231. Epub 2013 Jun 27.