Comparison of the Copan WASPLab incorporating the BioRad expert system against the SlRscan 2000 automatic for routine antimicrobial disc diffusion susceptibility testing

被引:11
作者
Cherkaoui, A. [1 ]
Renzi, G. [1 ]
Fischer, A. [1 ]
Azam, N. [1 ]
Schorderet, D. [1 ]
Vuilleumier, N. [2 ,3 ]
Schrenzel, J. [1 ,4 ,5 ]
机构
[1] Geneva Univ Hosp, Dept Diagnost, Div Lab Med, Bacteriol Lab, 4 Rue Gabrielle Perret Gentil, CH-1205 Geneva, Switzerland
[2] Geneva Univ Hosp, Dept Diagnost, Div Lab Med, Geneva, Switzerland
[3] Fac Med, Dept Med Special, Div Lab Med, Geneva, Switzerland
[4] Geneva Univ Hosp, Dept Med, Div Infect Dis, Genom Res Lab, Geneva, Switzerland
[5] Fac Med, Geneva, Switzerland
关键词
Accuracy; Antimicrobial susceptibility testing; Automation; BioRad expert system; Copan WASPLab; Disc diffusion; Medical value; Quality control; SlRscan; 2000; automatic; Turn-around time; STANDARDIZATION; RESISTANCE; VARIABLES;
D O I
10.1016/j.cmi.2019.11.008
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: This study investigated the agreement at the categorical level between the Copan WASPLab incorporating the BioRad expert system against the SlRscan 2000 automatic for antimicrobial disc diffusion susceptibility testing. Methods: The 338 clinical strains (67 Pseudomonas aeruginosa, 19 methicillin-resistant Staphylococcus aureus, 75 methicillin-sensitive S. aureus and 177 Enterobacterales isolates) analysed in this study were non-duplicate isolates obtained from consecutive clinical samples referred to the clinical bacteriology laboratory at Geneva University Hospitals between June and August 2019. For the WASPLab the inoculum suspension was prepared in strict accordance with the manufacturer's instruction (Copan WASP srl, Brescia, Italy) by adding 2 mL of the 0.5 McFarland primary suspension used for the SlRscan analysis into a sterile tube filled with 4 mL of sterile saline (1:3 dilution). The inoculum (2 x 30 mu L loop/spreader) was spread over the entire surface of Mueller-Hinton agar plates according to the AST streaking pattern defined by Copan. The antibiotic discs were dispensed by the WASP and inoculated media were loaded on conveyors for transfer to the automatic incubators. The plates were incubated for 16 h, and several digital images were acquired. Inhibition zone diameters were automatically read by the WASPLab and were adjusted manually whenever necessary. For the SlRscan 2000 automatic, the antimicrobial disc diffusion susceptibility testing was performed according to the EUCAST guidelines. The gradient strip method was used to resolve discrepancies. Results: The overall categorical agreement between the compared methods reached 99.1% (797/804; 95% CI 98.2%-99.6%), 99.5% (1029/1034; 95% CI 98.9%-99.8%), and 98.8% (2798/2832; 95% CI 98.3%-99.1%) for P. aeruginosa, S. aureus and the Enterobacterales, respectively. Conclusions: WASPLab incorporating the BioRad expert system provides a fully automated solution for antimicrobial disc diffusion susceptibility testing with equal or better accuracy than other available phenotypic methods. (C) 2019 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:619 / 625
页数:7
相关论文
共 14 条
[1]   Clinical Microbiology Is Growing Up: The Total Laboratory Automation Revolution [J].
Bailey, Adam L. ;
Ledeboer, Nathan ;
Burnham, Carey-Ann D. .
CLINICAL CHEMISTRY, 2019, 65 (05) :634-643
[2]   INOCULUM STANDARDIZATION IN ANTI-MICROBIAL SUSCEPTIBILITY TESTING - EVALUATION OF OVERNIGHT AGAR CULTURES AND THE RAPID INOCULUM STANDARDIZATION SYSTEM [J].
BAKER, CN ;
THORNSBERRY, C ;
HAWKINSON, RW .
JOURNAL OF CLINICAL MICROBIOLOGY, 1983, 17 (03) :450-457
[3]  
BAUER AW, 1966, AM J CLIN PATHOL, V45, P493
[4]   Copan WASPLab automation significantly reduces incubation times and allows earlier culture readings [J].
Cherkaoui, A. ;
Renzi, G. ;
Vuilleumier, N. ;
Schrenzel, J. .
CLINICAL MICROBIOLOGY AND INFECTION, 2019, 25 (11) :1430.e5-1430.e12
[5]   Automated Incubation and Digital Image Analysis of Chromogenic Media Using Copan WASPLab Enables Rapid Detection of Vancomycin-Resistant Enterococcus [J].
Cherkaoui, Abdessalam ;
Renzi, Gesuele ;
Charretier, Yannick ;
Blanc, Dominique S. ;
Vuilleumier, Nicolas ;
Schrenzel, Jacques .
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2019, 9
[6]   The role of whole genome sequencing in antimicrobial susceptibility testing of bacteria: report from the EUCAST Subcommittee [J].
Ellington, M. J. ;
Ekelund, O. ;
Aarestrup, F. M. ;
Canton, R. ;
Doumith, M. ;
Giske, C. ;
Grundman, H. ;
Hasman, H. ;
Holden, M. T. G. ;
Hopkins, K. L. ;
Iredell, J. ;
Kahlmeter, G. ;
Koser, C. U. ;
MacGowan, A. ;
Mevius, D. ;
Mulvey, M. ;
Naas, T. ;
Peto, T. ;
Rolain, J. -M. ;
Samuelsen, O. ;
Woodford, N. .
CLINICAL MICROBIOLOGY AND INFECTION, 2017, 23 (01) :2-22
[7]   Prediction of Staphylococcus aureus Antimicrobial Resistance by Whole-Genome Sequencing [J].
Gordon, N. C. ;
Price, J. R. ;
Cole, K. ;
Everitt, R. ;
Morgan, M. ;
Finney, J. ;
Kearns, A. M. ;
Pichon, B. ;
Young, B. ;
Wilson, D. J. ;
Llewelyn, M. J. ;
Paul, J. ;
Peto, T. E. A. ;
Crook, D. W. ;
Walker, A. S. ;
Golubchik, T. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2014, 52 (04) :1182-1191
[8]   Rapid disc diffusion antibiotic susceptibility testing for Pseudomonas aeruginosa, Acinetobacter baumannii and Enterococcus spp. [J].
Hombach, Michael ;
Jetter, Marion ;
Bloechliger, Nicolas ;
Kolesnik-Goldmann, Natalia ;
Keller, Peter M. ;
Boettger, Erik C. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2018, 73 (02) :385-391
[9]   Fully automated disc diffusion for rapid antibiotic susceptibility test results: a proof-of-principle study [J].
Hombach, Michael ;
Jetter, Marion ;
Blochliger, Nicolas ;
Kolesnik-Goldmann, Natalia ;
Bottger, Erik C. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2017, 72 (06) :1659-1668
[10]   Relative contribution of biological variation and technical variables to zone diameter variations of disc diffusion susceptibility testing [J].
Hombach, Michael ;
Ochoa, Carlos ;
Maurer, Florian P. ;
Pfiffner, Tamara ;
Boettger, Erik C. ;
Furrer, Reinhard .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2016, 71 (01) :141-151