Suppr超能文献

替加环素对非结核分枝杆菌的药敏试验

Susceptibility Testing of Tedizolid against Nontuberculous Mycobacteria.

作者信息

Brown-Elliott Barbara A, Wallace Richard J

机构信息

The University of Texas Health Science Center at Tyler, Department of Microbiology, Tyler, Texas, USA

The University of Texas Health Science Center at Tyler, Department of Microbiology, Tyler, Texas, USA.

出版信息

J Clin Microbiol. 2017 Jun;55(6):1747-1754. doi: 10.1128/JCM.00274-17. Epub 2017 Mar 22.

Abstract

Tedizolid is a new oxazolidinone with improved and intracellular potency against , including multidrug-resistant strains, and some species of nontuberculous mycobacteria (NTM) compared with that of linezolid. Using the current Clinical and Laboratory Standards Institute (CLSI)-recommended method of broth microdilution, susceptibility testing of 170 isolates of rapidly growing mycobacteria showed equivalent or lower (1- to 8-fold) MIC and/or MIC values for tedizolid compared with that for linezolid. The tedizolid MIC values for 81 isolates of subsp. and 12 isolates of subsp. were 8 μg/ml and 4 μg/ml, respectively, compared with linezolid MIC values of 32 μg/ml for both. The MIC values for 20 isolates of were 2 μg/ml for tedizolid and 4 μg/ml for linezolid. Twenty-two isolates of had tedizolid and linezolid MICs of 2 μg/ml and 16 μg/ml, respectively. One hundred forty-two slowly growing NTM, including 7/7 , 7/7 , and 7/11 of other less commonly isolated species, had tedizolid MICs of ≤1 μg/ml and linezolid MICs of ≤4 μg/ml. One hundred isolates of complex and eight isolates had tedizolid MICs of 8 μg/ml and linezolid MICs 32 and 64 μg/ml, respectively. Nine isolates had MICs of 4 μg/ml and 16 μg/ml for tedizolid and linezolid, respectively. These findings demonstrate a greater potency of tedizolid than linezolid against NTM and suggest that an evaluation of tedizolid as a potential treatment agent for infections caused by selected NTM is warranted.

摘要

替加环素是一种新型恶唑烷酮类药物,与利奈唑胺相比,其对包括耐多药菌株在内的结核分枝杆菌以及一些非结核分枝杆菌(NTM)具有更高的体外和细胞内活性。采用当前临床和实验室标准协会(CLSI)推荐的肉汤微量稀释法,对170株快速生长分枝杆菌进行药敏试验,结果显示替加环素的最低抑菌浓度(MIC)和/或最低杀菌浓度(MBC)值与利奈唑胺相当或更低(低1至8倍)。81株脓肿分枝杆菌亚种和12株龟分枝杆菌亚种的替加环素MIC值分别为8μg/ml和4μg/ml,而两者的利奈唑胺MIC值均为32μg/ml。20株偶发分枝杆菌的替加环素MIC值为2μg/ml,利奈唑胺为4μg/ml。22株耻垢分枝杆菌的替加环素和利奈唑胺MIC值分别为2μg/ml和16μg/ml。142株缓慢生长的NTM,包括7/7株鸟分枝杆菌、7/7株胞内分枝杆菌以及7/11株其他较少见的菌种,替加环素MIC值≤1μg/ml,利奈唑胺MIC值≤4μg/ml。100株结核分枝杆菌复合群和8株堪萨斯分枝杆菌的替加环素MIC值为8μg/ml,利奈唑胺MIC值分别为32μg/ml和64μg/ml。9株海分枝杆菌的替加环素和利奈唑胺MIC值分别为4μg/ml和16μg/ml。这些结果表明,替加环素对NTM的抗菌活性比利奈唑胺更强,提示有必要评估替加环素作为某些NTM感染潜在治疗药物的可能性。

相似文献

1
Susceptibility Testing of Tedizolid against Nontuberculous Mycobacteria.
J Clin Microbiol. 2017 Jun;55(6):1747-1754. doi: 10.1128/JCM.00274-17. Epub 2017 Mar 22.
2
Susceptibility Testing of Tedizolid against Isolates of Nocardia.
Antimicrob Agents Chemother. 2017 Nov 22;61(12). doi: 10.1128/AAC.01537-17. Print 2017 Dec.
3
In Vitro Antimicrobial Susceptibility of Nontuberculous Mycobacteria in Iran.
Microb Drug Resist. 2016 Mar;22(2):172-8. doi: 10.1089/mdr.2015.0134. Epub 2015 Oct 15.
4
In vitro activities of the novel oxazolidinones DA-7867 and DA-7157 against rapidly and slowly growing mycobacteria.
Antimicrob Agents Chemother. 2006 Dec;50(12):4027-9. doi: 10.1128/AAC.00763-06. Epub 2006 Oct 2.
5
7
Susceptibility Testing of Omadacycline against Nontuberculous Mycobacteria.
Antimicrob Agents Chemother. 2021 Feb 17;65(3). doi: 10.1128/AAC.01947-20.
10
Susceptibility Testing of Eravacycline against Nontuberculous Mycobacteria.
Antimicrob Agents Chemother. 2022 Sep 20;66(9):e0068922. doi: 10.1128/aac.00689-22. Epub 2022 Aug 9.

引用本文的文献

1
The antimicrobial activity of linezolid against unconventional pathogens.
PeerJ. 2025 Feb 12;13:e18825. doi: 10.7717/peerj.18825. eCollection 2025.
2
Prevalence of in clinical and environmental isolates, a systematic review and meta-analysis.
Front Microbiol. 2024 Feb 19;15:1321273. doi: 10.3389/fmicb.2024.1321273. eCollection 2024.
3
Tackling Nontuberculous Mycobacteria by Repurposable Drugs and Potential Leads from Natural Products.
Curr Top Med Chem. 2024;24(15):1291-1326. doi: 10.2174/0115680266276938240108060247.
5
Non-tuberculous mycobacterial disease: progress and advances in the development of novel candidate and repurposed drugs.
Front Cell Infect Microbiol. 2023 Oct 2;13:1243457. doi: 10.3389/fcimb.2023.1243457. eCollection 2023.
6
Novel, sensitivity-based antibiotic regimen for multidrug-resistant infection following cosmetic surgery.
JAAD Case Rep. 2023 Apr 11;36:18-20. doi: 10.1016/j.jdcr.2023.02.029. eCollection 2023 Jun.
7
Antimicrobial Effect of Oxazolidinones and Its Synergistic Effect with Bedaquiline Against Complex.
Infect Drug Resist. 2023 Jan 14;16:279-287. doi: 10.2147/IDR.S395750. eCollection 2023.
8
Contemporary Pharmacotherapies for Nontuberculosis Mycobacterial Infections: A Narrative Review.
Infect Dis Ther. 2023 Feb;12(2):343-365. doi: 10.1007/s40121-022-00750-5. Epub 2023 Jan 7.
9
Variability of Complex Isolates Drug Susceptibility Testing by Broth Microdilution.
Antibiotics (Basel). 2022 Dec 4;11(12):1756. doi: 10.3390/antibiotics11121756.
10
In vitro Susceptibility of Nontuberculous Mycobacteria to Tedizolid.
Infect Drug Resist. 2022 Aug 25;15:4845-4852. doi: 10.2147/IDR.S362583. eCollection 2022.

本文引用的文献

1
Intracellular activity of tedizolid phosphate and ACH-702 versus Mycobacterium tuberculosis infected macrophages.
Ann Clin Microbiol Antimicrob. 2014 Apr 4;13:13. doi: 10.1186/1476-0711-13-13.
2
Tedizolid for the management of human infections: in vitro characteristics.
Clin Infect Dis. 2014 Jan;58 Suppl 1:S35-42. doi: 10.1093/cid/cit616.
3
7
Skin and soft tissue concentrations of tedizolid (formerly torezolid), a novel oxazolidinone, following a single oral dose in healthy volunteers.
Int J Antimicrob Agents. 2012 Jul;40(1):51-4. doi: 10.1016/j.ijantimicag.2012.03.006. Epub 2012 May 13.
8
Tedizolid (TR-701): a new oxazolidinone with enhanced potency.
Expert Opin Investig Drugs. 2012 Apr;21(4):515-22. doi: 10.1517/13543784.2012.660250. Epub 2012 Feb 13.
9
In vitro activity of tedizolid (TR-700) against linezolid-resistant staphylococci.
J Antimicrob Chemother. 2012 Jan;67(1):167-9. doi: 10.1093/jac/dkr403. Epub 2011 Sep 27.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验