Burkholderia pseudomallei multi-centre study to establish EUCAST MIC and zone diameter distributions and epidemiological cut-off values

被引:15
|
作者
Karatuna, O. [1 ]
Dance, D. A. B. [2 ,3 ,4 ]
Matuschek, E. [1 ]
Ahman, J. [1 ]
Turner, P. [3 ,5 ]
Hopkins, J. [3 ,5 ]
Amornchai, P. [6 ]
Wuthiekanun, V [6 ]
Cusack, T-P [2 ,7 ]
Baird, R. [8 ]
Hennessy, J. [8 ]
Norton, R. [9 ]
Armstrong, M. [9 ]
Zange, S. [10 ]
Zoeller, L. [10 ]
Wahab, T. [11 ]
Jacob, D. [12 ]
Grunow, R. [12 ]
Kahlmeter, G. [1 ]
机构
[1] EUCAST Dev Lab, Vaxjo, Sweden
[2] Lao Oxford Mahosot Hosp Wellcome Trust Res Unit, Viangchan, Laos
[3] Univ Oxford, Ctr Trop Med & Global Hlth, Nuffield Dept Med, Oxford, England
[4] London Sch Hyg & Trop Med, Fac Infect & Trop Dis, London, England
[5] Angkor Hosp Children, Cambodia Oxford Med Res Unit, Siem Reap, Cambodia
[6] Mahidol Univ, Fac Trop Med, Mahidol Oxford Trop Med Res Unit, Bangkok, Thailand
[7] Publ Hlth England, Natl Infect Serv, London, England
[8] Royal Darwin Hosp, Darwin, NT, Australia
[9] Townsville Hosp, Townsville, Qld, Australia
[10] Bundeswehr Inst Microbiol, Munich, Germany
[11] Publ Hlth Agcy Sweden, Stockholm, Sweden
[12] Robert Koch Inst, Berlin, Germany
关键词
Melioidosis; Antimicrobial susceptibility testing; Broth microdilution; Minimum inhibitory concentration; MIC determination; Disc diffusion; ECOFF; Clinical breakpoints; Quality control; TRIMETHOPRIM/SULFAMETHOXAZOLE RESISTANCE; ANTIMICROBIAL SUSCEPTIBILITY; TRIMETHOPRIM-SULFAMETHOXAZOLE; ANTIBIOTIC SUSCEPTIBILITY; MELIOIDOSIS; CEFTAZIDIME; DOXYCYCLINE;
D O I
10.1016/j.cmi.2020.07.001
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: Melioidosis, caused by Burkholderia pseudomallei, requires intensive antimicrobial treatment. However, standardized antimicrobial susceptibility testing (AST) methodology based on modern principles for determining breakpoints and ascertaining performance of methods are lacking for B. pseudomallei. This study aimed to establish MIC and zone diameter distributions on which to set epidemiological cut-off (ECOFF) values for B. pseudomallei using standard EUCAST methodology for non-fastidious organisms. Methods: Non-consecutive, non-duplicate clinical B. pseudomallei isolates (9-70 per centre) were tested at eight study centres against eight antimicrobials by broth microdilution (BMD) and the EUCAST disc diffusion method. Isolates without and with suspected resistance mechanisms were deliberately selected. The EUCAST Development Laboratory ensured the quality of study materials, and provided guidance on performance of the tests and interpretation of results. Aggregated results were analysed according to EUCAST recommendations to determine ECOFFs. Results: MIC and zone diameter distributions were generated using BMD and disc diffusion results obtained for 361 B. pseudomallei isolates. MIC and zone diameter ECOFFs (mg/L; mm) were determined for amoxicillin-clavulanic acid (8; 22), ceftazidime (8; 22), imipenem (2; 29), meropenem (2; 26), doxycycline (2; none), tetracycline (8; 23), chloramphenicol (8; 22) and trimethoprim-sulfamethoxazole (4; 28). Conclusions: We have validated the use of standard BMD and disc diffusion methodology for AST of B. pseudomallei. The MIC and zone diameter distributions generated in this study allowed us to establish MIC and zone diameter ECOFFs for the antimicrobials studied. (C) 2020 The Authors. Published by Elsevier Ltd on behalf of European Society of Clinical Microbiology and Infectious Diseases.
引用
收藏
页码:736 / 741
页数:6
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