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2
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In vitro activities of beta-lactam-beta-lactamase inhibitor combinations against Stenotrophomonas maltophilia: correlation between methods for testing inhibitory activity, time-kill curves, and bactericidal activity.β-内酰胺-β-内酰胺酶抑制剂组合对嗜麦芽窄食单胞菌的体外活性:抑制活性检测方法、时间-杀菌曲线与杀菌活性之间的相关性
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本文引用的文献

1
Effect of divalent cations in bacteriological media on the susceptibility of Xanthomonas maltophilia to imipenem, with special reference to zinc ions.细菌培养基中的二价阳离子对嗜麦芽窄食单胞菌对亚胺培南敏感性的影响,特别提及锌离子。
J Antimicrob Chemother. 1993 Jan;31(1):47-55. doi: 10.1093/jac/31.1.47.
2
A changing pattern of susceptibility of Xanthomonas maltophilia to antimicrobial agents: implications for therapy.嗜麦芽窄食单胞菌对抗菌药物敏感性的变化模式:对治疗的启示
Antimicrob Agents Chemother. 1994 Mar;38(3):624-7. doi: 10.1128/AAC.38.3.624.
3
Susceptibilities of 123 Xanthomonas maltophilia strains to clinafloxacin, PD 131628, PD 138312, PD 140248, ciprofloxacin, and ofloxacin.123株嗜麦芽窄食单胞菌对克林沙星、PD 131628、PD 138312、PD 140248、环丙沙星和氧氟沙星的敏感性。
Antimicrob Agents Chemother. 1994 Feb;38(2):369-70. doi: 10.1128/AAC.38.2.369.
4
Rapid identification of metallo- and serine beta-lactamases.金属β-内酰胺酶和丝氨酸β-内酰胺酶的快速鉴定
Antimicrob Agents Chemother. 1994 May;38(5):991-6. doi: 10.1128/AAC.38.5.991.
5
Mucocutaneous and soft tissue infections caused by Xanthomonas maltophilia. A new spectrum.嗜麦芽窄食单胞菌引起的皮肤黏膜及软组织感染。一种新的感染谱。
Ann Intern Med. 1994 Dec 15;121(12):969-73. doi: 10.7326/0003-4819-121-12-199412150-00011.
6
Biochemical properties of inducible beta-lactamases produced from Xanthomonas maltophilia.嗜麦芽窄食单胞菌产生的诱导型β-内酰胺酶的生化特性
Antimicrob Agents Chemother. 1994 Sep;38(9):2143-9. doi: 10.1128/AAC.38.9.2143.
7
Synergistic interaction in vitro with use of three antibiotics simultaneously against Pseudomonas maltophilia.体外同时使用三种抗生素对嗜麦芽窄食单胞菌的协同相互作用。
J Infect Dis. 1980 Oct;142(4):602-7. doi: 10.1093/infdis/142.4.602.
8
Synergism, killing kinetics, and antimicrobial susceptibility of group A and B streptococci.A组和B组链球菌的协同作用、杀菌动力学及抗菌药敏性
Antimicrob Agents Chemother. 1981 May;19(5):716-25. doi: 10.1128/AAC.19.5.716.
9
Purification and properties of inducible penicillin beta-lactamase isolated from Pseudomonas maltophilia.从嗜麦芽窄食单胞菌中分离出的诱导型青霉素β-内酰胺酶的纯化及特性
Antimicrob Agents Chemother. 1982 Oct;22(4):564-70. doi: 10.1128/AAC.22.4.564.
10
Purification and properties of an inducible cephalosporinase from Pseudomonas maltophilia GN12873.嗜麦芽窄食单胞菌GN12873中一种诱导型头孢菌素酶的纯化及特性
Antimicrob Agents Chemother. 1984 Mar;25(3):362-5. doi: 10.1128/AAC.25.3.362.

抗菌药物组合对嗜麦芽窄食单胞菌(嗜麦芽黄单胞菌)的体外活性。

In vitro activities of antimicrobial combinations against Stenotrophomonas (Xanthomonas) maltophilia.

作者信息

Poulos C D, Matsumura S O, Willey B M, Low D E, McGeer A

机构信息

Department of Microbiology, Princess Margaret Hospital, Toronto, Ontario, Canada.

出版信息

Antimicrob Agents Chemother. 1995 Oct;39(10):2220-3. doi: 10.1128/AAC.39.10.2220.

DOI:10.1128/AAC.39.10.2220
PMID:8619571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC162918/
Abstract

Stenotrophomonas (Xanthomonas) maltophilia is inherently resistant to multiple antimicrobial agents. In order to investigate the in vitro potential of combinations of antimicrobial agents, we obtained 230 epidemiologically unrelated clinical isolates from seven hospitals across Canada and from Northwestern Memorial Hospital in Chicago. Ticarcillin-clavulanate combined with ciprofloxacin or trimethoprim-sulfamethoxazole were assayed for synergy against 31 ticarcillin-resistant strains of S. maltophilia by using microtiter checkerboard panels and against 20 strains by using time-kill methodology. The combination of ciprofloxacin with ceftazidime was also evaluated by time-kill studies. Ticarcillin-clavulanate plus trimethoprim-sulfamethoxazole demonstrated synergy by checkerboard panels, with fractional inhibitory concentration indices ranging from 0.033 to 0.49, and by time-kill studies for all 20 strains tested. Synergy between ticarcillin-clavulanate plus ciprofloxacin was found by the checkerboard method for 24 of 31 strains (77%), with fractional inhibitory concentration indices ranging from 0.188 to 0.75. A correlation between synergy by the checkerboard method and the reference time-kill study method was not observed for ticarcillin-clavulanate plus ciprofloxacin, with results for 3 of 10 strains being nonconcordant. Synergy with both ticarcillin-clavulanate plus ciprofloxacin and ceftazidime plus ciprofloxacin by the time-kill method was found to correlate with ciprofloxacin MICs of <32 micrograms/ml and zone diameters of >15 mm on Mueller-Hinton agar. Evaluation of these combinations in vivo may be warranted.

摘要

嗜麦芽窄食单胞菌(嗜麦芽黄单胞菌)对多种抗菌药物具有内在抗性。为了研究抗菌药物联合使用的体外潜力,我们从加拿大的七家医院以及芝加哥的西北纪念医院获取了230株无流行病学关联的临床分离株。通过微量滴定棋盘法检测替卡西林 - 克拉维酸联合环丙沙星或甲氧苄啶 - 磺胺甲恶唑对31株耐替卡西林嗜麦芽窄食单胞菌的协同作用,并通过时间 - 杀菌方法检测对20株菌的协同作用。还通过时间 - 杀菌研究评估了环丙沙星与头孢他啶的联合作用。替卡西林 - 克拉维酸加甲氧苄啶 - 磺胺甲恶唑通过棋盘法显示出协同作用,部分抑菌浓度指数范围为0.033至0.49,并且通过时间 - 杀菌研究对所有20株受试菌株均显示协同作用。替卡西林 - 克拉维酸加环丙沙星通过棋盘法在31株菌中的24株(77%)中发现有协同作用,部分抑菌浓度指数范围为0.188至0.75。对于替卡西林 - 克拉维酸加环丙沙星,未观察到棋盘法与参考时间 - 杀菌研究方法之间的协同作用相关性,10株菌中有3株结果不一致。通过时间 - 杀菌法发现,替卡西林 - 克拉维酸加环丙沙星以及头孢他啶加环丙沙星的协同作用与环丙沙星在穆勒 - 欣顿琼脂上的最低抑菌浓度<32微克/毫升和抑菌圈直径>15毫米相关。可能有必要对这些联合用药进行体内评估。