• 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

LY146032:体外活性及耐药性发展

LY146032: activity and resistance development in vitro.

作者信息

Mouton R P, Mulders S L

机构信息

Department of Medical Microbiology, University Hospital Leiden, The Netherlands.

出版信息

J Antimicrob Chemother. 1987 Oct;20(4):513-7. doi: 10.1093/jac/20.4.513.

DOI:10.1093/jac/20.4.513
PMID:2824427
Abstract

LY146032, a new lipopeptide antibiotic, was compared with vancomycin, teicoplanin, cefamandole and ciprofloxacin, against 107 clinical isolates comprising methicillin-susceptible and methicillin-resistant Staphylococcus spp., Streptococcus faecalis and Corynebacterium spp. All staphylococci were susceptible to all agents, except that some of the methicillin-resistant strains were resistant to cefamandole. Only LY146032 and ciprofloxacin were bactericidal to Str. faecalis. Development of resistance was studied by serial transfers of ten selected strains. A stable greater than or equal to eight-fold increase of the MIC over the breakpoint was found to develop to a variable extent against all agents tested. Simultaneous development of resistance to any of the other antibiotics was registered in 11/200 tests.

摘要

将新型脂肽抗生素LY146032与万古霉素、替考拉宁、头孢孟多和环丙沙星进行比较,以检测其对107株临床分离菌的抗菌活性,这些分离菌包括对甲氧西林敏感和耐药的葡萄球菌属、粪肠球菌和棒状杆菌属。所有葡萄球菌对所有药物均敏感,但部分耐甲氧西林菌株对头孢孟多耐药。只有LY146032和环丙沙星对粪肠球菌有杀菌作用。通过对10株选定菌株进行连续传代研究耐药性的产生。发现对所有受试药物,MIC在断点之上稳定地出现了至少8倍的增加,且程度各异。在200次试验中,有11次出现了对其他任何一种抗生素同时产生耐药性的情况。

相似文献

1
LY146032: activity and resistance development in vitro.LY146032:体外活性及耐药性发展
J Antimicrob Chemother. 1987 Oct;20(4):513-7. doi: 10.1093/jac/20.4.513.
2
In vitro activity of LY146032 (daptomycin) against selected aerobic bacteria.LY146032(达托霉素)对特定需氧菌的体外活性。
Eur J Clin Microbiol. 1987 Feb;6(1):91-6. doi: 10.1007/BF02097209.
3
Activity of LY146032 compared with that of methicillin, cefazolin, cefamandole, cefuroxime, ciprofloxacin, and vancomycin against staphylococci as determined by kill-kinetic studies.通过杀菌动力学研究确定LY146032与甲氧西林、头孢唑林、头孢孟多、头孢呋辛、环丙沙星和万古霉素对葡萄球菌的活性比较。
Antimicrob Agents Chemother. 1987 Aug;31(8):1210-5. doi: 10.1128/AAC.31.8.1210.
4
Comparative in vitro activity of LY146032 (daptomycin) against gram-positive cocci.LY146032(达托霉素)对革兰氏阳性球菌的体外活性比较
Eur J Clin Microbiol. 1987 Feb;6(1):96-9. doi: 10.1007/BF02097210.
5
In vitro postantibiotic effect of daptomycin (LY146032) against Enterococcus faecalis and methicillin-susceptible and methicillin-resistant Staphylococcus aureus strains.达托霉素(LY146032)对粪肠球菌以及甲氧西林敏感和耐药金黄色葡萄球菌菌株的体外抗生素后效应
Antimicrob Agents Chemother. 1989 Aug;33(8):1198-200. doi: 10.1128/AAC.33.8.1198.
6
In vitro activity of LY146032 (daptomycin), a new peptolide.新型缩酚肽LY146032(达托霉素)的体外活性
Eur J Clin Microbiol. 1987 Feb;6(1):84-90. doi: 10.1007/BF02097208.
7
Activity of daptomycin against enterococci and coagulase-negative staphylococci (CNS): relationship between CNS susceptibility and slime production.
J Chemother. 1993 Jun;5(3):151-4. doi: 10.1080/1120009x.1993.11739224.
8
In vitro selection of bacteria resistant to LY146032, a new cyclic lipopeptide.对新型环脂肽LY146032具有抗性的细菌的体外筛选
Antimicrob Agents Chemother. 1988 Jan;32(1):24-6. doi: 10.1128/AAC.32.1.24.
9
Comparative in vitro activity of LY146032 (daptomycin), a new lipopeptide antimicrobial.新型脂肽类抗菌药物LY146032(达托霉素)的体外活性比较
Eur J Clin Microbiol. 1987 Feb;6(1):100-3. doi: 10.1007/BF02097211.
10
Comparative in-vitro activity of LY146032 a new peptolide, with vancomycin and eight other agents against gram-positive organisms.新型缩肽类抗生素LY146032与万古霉素及其他八种药物对革兰氏阳性菌的体外活性比较
J Antimicrob Chemother. 1987 Aug;20(2):191-6. doi: 10.1093/jac/20.2.191.

引用本文的文献

1
In vivo pharmacodynamic activity of daptomycin.达托霉素的体内药效学活性。
Antimicrob Agents Chemother. 2004 Jan;48(1):63-8. doi: 10.1128/AAC.48.1.63-68.2004.
2
Resistance studies with daptomycin.达托霉素的耐药性研究。
Antimicrob Agents Chemother. 2001 Jun;45(6):1799-802. doi: 10.1128/AAC.45.6.1799-1802.2001.
3
Teicoplanin and daptomycin bactericidal activities in the presence of albumin or serum under controlled conditions of pH and ionized calcium.在pH值和离子钙受控条件下,替考拉宁和达托霉素在白蛋白或血清存在时的杀菌活性。
Antimicrob Agents Chemother. 1993 Mar;37(3):605-9. doi: 10.1128/AAC.37.3.605.
4
In vitro development and stability of tolerance to cloxacillin and vancomycin in Staphylococcus aureus.金黄色葡萄球菌对氯唑西林和万古霉素耐受性的体外发育及稳定性
Eur J Clin Microbiol Infect Dis. 1994 Sep;13(9):741-6. doi: 10.1007/BF02276057.
5
Teicoplanin. A reappraisal of its antimicrobial activity, pharmacokinetic properties and therapeutic efficacy.替考拉宁:对其抗菌活性、药代动力学特性及治疗效果的重新评估
Drugs. 1994 May;47(5):823-54. doi: 10.2165/00003495-199447050-00008.
6
Influence of Ly146032 on chemotaxis, chemiluminescence of PMN and lymphocyte transformation in vitro.
Infection. 1989 Nov-Dec;17(6):374-7. doi: 10.1007/BF01645548.
7
In vitro activities of vancomycin and teicoplanin against coagulase-negative staphylococci isolated from neutropenic patients.万古霉素和替考拉宁对从中性粒细胞减少患者中分离出的凝固酶阴性葡萄球菌的体外活性。
Antimicrob Agents Chemother. 1990 May;34(5):901-3. doi: 10.1128/AAC.34.5.901.
8
Failure of teicoplanin therapy in two neutropenic patients with staphylococcal septicemia who recovered after administration of vancomycin.两名中性粒细胞减少且患有葡萄球菌败血症的患者接受替考拉宁治疗失败,给予万古霉素后康复。
Eur J Clin Microbiol Infect Dis. 1990 Feb;9(2):145-7. doi: 10.1007/BF01963643.
9
In vitro pharmacodynamic effects of concentration, pH, and growth phase on serum bactericidal activities of daptomycin and vancomycin.浓度、pH值和生长阶段对达托霉素和万古霉素血清杀菌活性的体外药效学作用
Antimicrob Agents Chemother. 1992 Dec;36(12):2709-14. doi: 10.1128/AAC.36.12.2709.