• 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

左氧氟沙星单独及与DnaK抑制剂联合使用对革兰氏阴性杆菌(包括耐左氧氟沙星菌株)的活性。

Activity of levofloxacin alone and in combination with a DnaK inhibitor against gram-negative rods, including levofloxacin-resistant strains.

作者信息

Credito Kim, Lin Gengrong, Koeth Laura, Sturgess Michael A, Appelbaum Peter C

机构信息

Department of Pathology, Hershey Medical Center, PA 17033, USA.

出版信息

Antimicrob Agents Chemother. 2009 Feb;53(2):814-7. doi: 10.1128/AAC.01132-08. Epub 2008 Nov 17.

DOI:10.1128/AAC.01132-08
PMID:19015359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2630640/
Abstract

Synergy time-kill testing of levofloxacin alone and in combination with CHP-105, a representative DnaK inhibitor, against 50 gram-negative rods demonstrated that 34 of the 50 strains tested showed significant synergy between levofloxacin and CHP-105 after 12 h and 24 h. Fourteen of these 34 organisms were quinolone resistant (levofloxacin MICs of > or =4 microg/ml).

摘要

单独使用左氧氟沙星以及将其与具有代表性的DnaK抑制剂CHP-105联合使用,对50株革兰氏阴性杆菌进行协同时间杀菌试验,结果显示,在12小时和24小时后,所测试的50株菌株中有34株在左氧氟沙星和CHP-105之间表现出显著协同作用。这34种微生物中有14种对喹诺酮耐药(左氧氟沙星最低抑菌浓度≥4微克/毫升)。

相似文献

1
Activity of levofloxacin alone and in combination with a DnaK inhibitor against gram-negative rods, including levofloxacin-resistant strains.左氧氟沙星单独及与DnaK抑制剂联合使用对革兰氏阴性杆菌(包括耐左氧氟沙星菌株)的活性。
Antimicrob Agents Chemother. 2009 Feb;53(2):814-7. doi: 10.1128/AAC.01132-08. Epub 2008 Nov 17.
2
Activity of amikacin, ertapenem, ciprofloxacin and levofloxacin alone and in combination against resistant nosocomial pathogens by time-kill.阿米卡星、厄他培南、环丙沙星和左氧氟沙星单独及联合应用对耐药医院病原体的时间杀菌活性。
West Indian Med J. 2008 Mar;57(2):106-11.
3
Activities of levofloxacin, ofloxacin, and ciprofloxacin, alone and in combination with amikacin, against acinetobacters as determined by checkerboard and time-kill studies.通过棋盘法和时间杀菌研究测定左氧氟沙星、氧氟沙星和环丙沙星单独及与阿米卡星联合使用时对不动杆菌的活性。
Antimicrob Agents Chemother. 1997 May;41(5):1073-6. doi: 10.1128/AAC.41.5.1073.
4
Anti-anaerobic activity of levofloxacin alone and combined with clindamycin and metronidazole.
Diagn Microbiol Infect Dis. 2000 Nov;38(3):181-3. doi: 10.1016/s0732-8893(00)00190-5.
5
Comparative activity of trovafloxacin, alone and in combination with other agents, against gram-negative nonfermentative rods.曲伐沙星单独及与其他药物联合应用对革兰阴性非发酵菌的比较活性
Antimicrob Agents Chemother. 1997 Jul;41(7):1475-81. doi: 10.1128/AAC.41.7.1475.
6
[In vitro activity of prulifloxacin, levofloxacin and ciprofloxacin against urinary pathogens].[普卢利沙星、左氧氟沙星和环丙沙星对尿路病原体的体外活性]
Infez Med. 2006 Mar;14(1):24-8.
7
The North American component (the United States and Canada) of an International Comparative MIC trial monitoring ofloxacin resistance.一项国际比较性最低抑菌浓度(MIC)试验中对氧氟沙星耐药性监测的北美部分(美国和加拿大)。
Diagn Microbiol Infect Dis. 1993 Aug-Sep;17(2):157-61. doi: 10.1016/0732-8893(93)90027-5.
8
Susceptibilities of non-Pseudomonas aeruginosa gram-negative nonfermentative rods to ciprofloxacin, ofloxacin, levofloxacin, D-ofloxacin, sparfloxacin, ceftazidime, piperacillin, piperacillin-tazobactam, trimethoprim-sulfamethoxazole, and imipenem.非铜绿假单胞菌革兰氏阴性非发酵菌对环丙沙星、氧氟沙星、左氧氟沙星、D-氧氟沙星、司帕沙星、头孢他啶、哌拉西林、哌拉西林-他唑巴坦、甲氧苄啶-磺胺甲恶唑和亚胺培南的敏感性。
Antimicrob Agents Chemother. 1996 Mar;40(3):772-5. doi: 10.1128/AAC.40.3.772.
9
In vitro antibacterial potency and spectrum of ABT-492, a new fluoroquinolone.新型氟喹诺酮类药物ABT-492的体外抗菌效力及抗菌谱
Antimicrob Agents Chemother. 2003 Oct;47(10):3260-9. doi: 10.1128/AAC.47.10.3260-3269.2003.
10
Quinolones sensitize gram-negative bacteria to antimicrobial peptides.喹诺酮类药物使革兰氏阴性菌对抗菌肽敏感。
Antimicrob Agents Chemother. 2006 Jul;50(7):2361-7. doi: 10.1128/AAC.01437-05.

引用本文的文献

1
Gram-negative quorum sensing signalling enhances biofilm formation and virulence traits in gram-positive pathogen .革兰氏阴性群体感应信号增强革兰氏阳性病原体中的生物膜形成和毒力特性。
J Oral Microbiol. 2023 May 11;15(1):2208901. doi: 10.1080/20002297.2023.2208901. eCollection 2023.
2
Targeting the Proteostasis Network for Mycobacterial Drug Discovery.针对蛋白质稳态网络进行分枝杆菌药物研发。
ACS Infect Dis. 2018 Apr 13;4(4):478-498. doi: 10.1021/acsinfecdis.7b00231. Epub 2018 Mar 2.
3
The inactivation of RNase G reduces the Stenotrophomonas maltophilia susceptibility to quinolones by triggering the heat shock response.核糖核酸酶G的失活通过触发热休克反应降低了嗜麦芽窄食单胞菌对喹诺酮类药物的敏感性。
Front Microbiol. 2015 Oct 19;6:1068. doi: 10.3389/fmicb.2015.01068. eCollection 2015.
4
Analysis of the bacterial heat shock response to photodynamic therapy-mediated oxidative stress.分析细菌热休克反应对光动力治疗介导的氧化应激的响应。
Photochem Photobiol. 2011 May-Jun;87(3):707-13. doi: 10.1111/j.1751-1097.2011.00902.x. Epub 2011 Feb 22.

本文引用的文献

1
Activity of meropenem with and without ciprofloxacin and colistin against Pseudomonas aeruginosa and Acinetobacter baumannii.美罗培南联合或不联合环丙沙星及黏菌素对铜绿假单胞菌和鲍曼不动杆菌的活性。
Antimicrob Agents Chemother. 2008 Jan;52(1):333-6. doi: 10.1128/AAC.00689-07. Epub 2007 Oct 29.
2
High-throughput screen for small molecules that modulate the ATPase activity of the molecular chaperone DnaK.用于筛选调节分子伴侣DnaK的ATP酶活性的小分子的高通量筛选。
Anal Biochem. 2008 Jan 15;372(2):167-76. doi: 10.1016/j.ab.2007.08.020. Epub 2007 Aug 22.
3
Activity of daptomycin alone and in combination with rifampin and gentamicin against Staphylococcus aureus assessed by time-kill methodology.采用时间杀菌法评估达托霉素单独使用以及与利福平、庆大霉素联合使用对金黄色葡萄球菌的活性。
Antimicrob Agents Chemother. 2007 Apr;51(4):1504-7. doi: 10.1128/AAC.01455-06. Epub 2007 Jan 12.
4
Fatty acyl benzamido antibacterials based on inhibition of DnaK-catalyzed protein folding.基于抑制DnaK催化的蛋白质折叠的脂肪酰苯甲酰胺类抗菌剂。
J Biol Chem. 2007 Feb 16;282(7):4437-4446. doi: 10.1074/jbc.M607667200. Epub 2006 Dec 14.
5
Treatment options for multidrug-resistant bacteria.耐多药细菌的治疗选择。
Expert Rev Anti Infect Ther. 2006 Aug;4(4):601-18. doi: 10.1586/14787210.4.4.601.
6
Designer antibacterial peptides kill fluoroquinolone-resistant clinical isolates.设计抗菌肽可杀死耐氟喹诺酮临床分离株。
J Med Chem. 2005 Aug 11;48(16):5349-59. doi: 10.1021/jm050347i.
7
Epidemiology and control of antibiotic resistance in the intensive care unit.重症监护病房中抗生素耐药性的流行病学及控制
Curr Opin Infect Dis. 2004 Aug;17(4):309-16. doi: 10.1097/01.qco.0000136927.29802.68.
8
Development of novel antibacterial peptides that kill resistant isolates.开发能够杀死耐药菌株的新型抗菌肽。
Peptides. 2002 Dec;23(12):2071-83. doi: 10.1016/s0196-9781(02)00244-9.
9
Identification of crucial residues for the antibacterial activity of the proline-rich peptide, pyrrhocoricin.富含脯氨酸的肽——红蝽菌素抗菌活性关键残基的鉴定
Eur J Biochem. 2002 Sep;269(17):4226-37. doi: 10.1046/j.1432-1033.2002.03119.x.
10
Insect peptides with improved protease-resistance protect mice against bacterial infection.具有增强蛋白酶抗性的昆虫肽可保护小鼠免受细菌感染。
Protein Sci. 2000 Apr;9(4):742-9. doi: 10.1110/ps.9.4.742.