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Effect of Candida glabrata FKS1 and FKS2 mutations on echinocandin sensitivity and kinetics of 1,3-beta-D-glucan synthase: implication for the existing susceptibility breakpoint.光滑念珠菌FKS1和FKS2突变对棘白菌素敏感性及1,3-β-D-葡聚糖合酶动力学的影响:对现有药敏折点的意义
Antimicrob Agents Chemother. 2009 Sep;53(9):3690-9. doi: 10.1128/AAC.00443-09. Epub 2009 Jun 22.
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Clinical practice guidelines for the management of candidiasis: 2009 update by the Infectious Diseases Society of America.念珠菌病管理临床实践指南:美国传染病学会2009年更新版
Clin Infect Dis. 2009 Mar 1;48(5):503-35. doi: 10.1086/596757.
3
Breakpoints for susceptibility testing should not divide wild-type distributions of important target species.药敏试验的断点不应划分重要目标菌野生型分布。
Antimicrob Agents Chemother. 2009 Apr;53(4):1628-9. doi: 10.1128/AAC.01624-08. Epub 2009 Feb 2.
4
Correlating echinocandin MIC and kinetic inhibition of fks1 mutant glucan synthases for Candida albicans: implications for interpretive breakpoints.白色念珠菌棘白菌素最低抑菌浓度(MIC)与fks1突变体葡聚糖合酶动力学抑制的相关性:对解释性断点的影响
Antimicrob Agents Chemother. 2009 Jan;53(1):112-22. doi: 10.1128/AAC.01162-08. Epub 2008 Oct 27.
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6
Pyrosequencing to detect mutations in FKS1 that confer reduced echinocandin susceptibility in Candida albicans.焦磷酸测序法检测白色念珠菌中FKS1基因的突变,这些突变会导致对棘白菌素的敏感性降低。
Antimicrob Agents Chemother. 2008 Nov;52(11):4145-8. doi: 10.1128/AAC.00959-08. Epub 2008 Sep 15.
7
Development of caspofungin resistance following prolonged therapy for invasive candidiasis secondary to Candida glabrata infection.光滑念珠菌感染继发侵袭性念珠菌病长期治疗后卡泊芬净耐药性的产生。
Antimicrob Agents Chemother. 2008 Oct;52(10):3783-5. doi: 10.1128/AAC.00473-08. Epub 2008 Aug 1.
8
Mutations in the fks1 gene in Candida albicans, C. tropicalis, and C. krusei correlate with elevated caspofungin MICs uncovered in AM3 medium using the method of the European Committee on Antibiotic Susceptibility Testing.白色念珠菌、热带念珠菌和克鲁斯念珠菌中fks1基因的突变,与采用欧洲抗生素敏感性试验委员会的方法在AM3培养基中发现的卡泊芬净最低抑菌浓度升高相关。
Antimicrob Agents Chemother. 2008 Sep;52(9):3092-8. doi: 10.1128/AAC.00088-08. Epub 2008 Jun 30.
9
Correlation of MIC with outcome for Candida species tested against caspofungin, anidulafungin, and micafungin: analysis and proposal for interpretive MIC breakpoints.针对念珠菌属对卡泊芬净、阿尼芬净和米卡芬净的药敏试验,其最低抑菌浓度(MIC)与结果的相关性:分析及MIC解释性折点建议
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10
EUCAST technical note on fluconazole.欧洲临床微生物与感染病学会(EUCAST)关于氟康唑的技术说明。
Clin Microbiol Infect. 2008 Feb;14(2):193-5. doi: 10.1111/j.1469-0691.2007.01899.x. Epub 2007 Dec 5.

棘白菌素类药物和念珠菌属的野生型 MIC 分布和流行病学折点值

Wild-type MIC distributions and epidemiological cutoff values for the echinocandins and Candida spp.

机构信息

Medical Microbiology Division, C606 GH, Department of Pathology, University of Iowa College of Medicine, Iowa City, IA 52242, USA.

出版信息

J Clin Microbiol. 2010 Jan;48(1):52-6. doi: 10.1128/JCM.01590-09. Epub 2009 Nov 18.

DOI:10.1128/JCM.01590-09
PMID:19923478
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2812271/
Abstract

We tested a global collection of Candida sp. strains against anidulafungin, caspofungin, and micafungin, using CLSI M27-A3 broth microdilution (BMD) methods, in order to define wild-type (WT) populations and epidemiological cutoff values (ECVs). From 2003 to 2007, 8,271 isolates of Candida spp. (4,283 C. albicans, 1,236 C. glabrata, 1,238 C. parapsilosis, 996 C. tropicalis, 270 C. krusei, 99 C. lusitaniae, 88 C. guilliermondii, and 61 C. kefyr isolates) were obtained from over 100 centers worldwide. The modal MICs (in microg/ml) for anidulafungin, caspofungin, and micafungin, respectively, for each species were as follows: C. albicans, 0.03, 0.03, 0.015; C. glabrata, 0.06, 0.03, 0.015; C. tropicalis, 0.03, 0.03, 0.015; C. kefyr, 0.06, 0.015, 0.06; C. krusei, 0.03, 0.06, 0.06; C. lusitaniae, 0.05, 0.25, 0.12; C. parapsilosis, 2, 0.25, 1; and C. guilliermondii, 2, 0.5. 05. The ECVs, expressed in microg/ml (percentage of isolates that had MICs that were less than or equal to the ECV is shown in parentheses) for anidulafungin, caspofungin, and micafungin, respectively, were as follows: 0.12 (99.7%), 0.12 (99.8%), and 0.03 (97.7%) for C. albicans; 0.25 (99.4%), 0.12 (98.5%), and 0.03 (98.2%) for C. glabrata; 0.12 (98.9%), 0.12 (99.4%), and 0.12 (99.1%) for C. tropicalis; 0.25(100%), 0.03 (100%), and 0.12 (100%) for C. kefyr; 0.12 (99.3%), 0.25 (96.3%), and 0.12 (97.8%) for C. krusei; 2 (100%), 0.5 (98.0%), and 0.5 (99.0%) for C. lusitaniae; 4 (100%), 1 (98.6%), and 4 (100%) for C. parapsilosis; 16 (100%), 4 (95.5%), and 4 (98.9%) for C. guilliermondii. These WT MIC distributions and ECVs will be useful in surveillance for emerging reduced echinocandin susceptibility among Candida spp. and for determining the importance of various FKS1 or other mutations.

摘要

我们使用 CLSI M27-A3 肉汤微量稀释(BMD)方法对来自全球 100 多个中心的 8271 株念珠菌属菌株(4283 株白念珠菌、1236 株光滑念珠菌、1238 株近平滑念珠菌、996 株热带念珠菌、270 株克柔念珠菌、99 株葡萄牙念珠菌、88 株季也蒙念珠菌和 61 株假热带念珠菌)进行了安尼拉fungin、卡泊芬净和米卡芬净的测试,以确定野生型(WT)种群和流行病学截止值(ECV)。从 2003 年到 2007 年,8271 株念珠菌属菌株(4283 株白念珠菌、1236 株光滑念珠菌、1238 株近平滑念珠菌、996 株热带念珠菌、270 株克柔念珠菌、99 株葡萄牙念珠菌、88 株季也蒙念珠菌和 61 株假热带念珠菌)来自全球 100 多个中心。各物种分别为安尼拉fungin、卡泊芬净和米卡芬净的模式 MIC(μg/ml)如下:白念珠菌,0.03、0.03、0.015;光滑念珠菌,0.06、0.03、0.015;热带念珠菌,0.03、0.03、0.015;假热带念珠菌,0.06、0.015、0.06;克柔念珠菌,0.03、0.06、0.06;葡萄牙念珠菌,0.05、0.25、0.12;近平滑念珠菌,2、0.25、1;季也蒙念珠菌,2、0.5、0.05。安尼拉fungin、卡泊芬净和米卡芬净的 ECVs(以μg/ml 表示(MICs 等于或小于 ECV 的分离株百分比显示在括号中))分别为:白念珠菌,0.12(99.7%)、0.12(99.8%)和 0.03(97.7%);光滑念珠菌,0.25(99.4%)、0.12(98.5%)和 0.03(98.2%);热带念珠菌,0.12(98.9%)、0.12(99.4%)和 0.12(99.1%);假热带念珠菌,0.25(100%)、0.03(100%)和 0.12(100%);克柔念珠菌,0.12(99.3%)、0.25(96.3%)和 0.12(97.8%);葡萄牙念珠菌,2(100%)、0.5(98.0%)和 0.5(99.0%);近平滑念珠菌,4(100%)、1(98.6%)和 4(100%);季也蒙念珠菌,16(100%)、4(95.5%)和 4(98.9%)。这些 WT MIC 分布和 ECVs 将有助于监测念珠菌属中新兴的棘白菌素敏感性降低,并确定 FKS1 或其他突变的重要性。