Detection of carbapenemase activity directly from blood culture vials using MALDI-TOF MS: a quick answer for the right decision

被引:52
作者
Carvalhaes, Cecilia G. [1 ]
Cayo, Rodrigo [1 ]
Visconde, Marina F. [1 ]
Barone, Talita [1 ]
Frigatto, Eliete A. M. [2 ]
Okamoto, Debora [3 ]
Assis, Diego M. [3 ,4 ]
Juliano, Luiz [3 ]
Machado, Antonia M. O. [2 ]
Gales, Ana C. [1 ]
机构
[1] Univ Fed Sao Paulo UNIFESP, Dept Med, Disciplina Infectol, Lab Alerta, Sao Paulo, Brazil
[2] Hosp Sao Paulo, Lab Cent, Sao Paulo, Brazil
[3] Univ Fed Sao Paulo UNIFESP, Dept Biofis, Sao Paulo, Brazil
[4] Bruker Daltonics Inc, Atibaia, SP, Brazil
关键词
KPC; OXA-type; oxacillinases; metallo-beta-lactamases; serine-beta-lactamases; DESORPTION IONIZATION-TIME; FLIGHT MASS-SPECTROMETRY; ACINETOBACTER-BAUMANNII; PSEUDOMONAS-AERUGINOSA; CLINICAL MICROBIOLOGY; RAPID IDENTIFICATION; BD PHOENIX; RESISTANCE; BACTERIA; SYSTEM;
D O I
10.1093/jac/dku094
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Recently, matrix-assisted laser desorption ionization-time-of-flight mass spectrometry (MALDI-TOF MS) was successfully applied for the detection of carbapenemase activity directly from Gram-negative colonies. Based on this principle, we evaluated the performance of MALDI-TOF MS for rapid detection of carbapenemase activity directly from positive blood culture vials. A total of 100 blood culture vials were randomly selected. MALDI-TOF MS carbapenemase assay results were confirmed by the detection of carbapenemase-encoding genes. A total of 110 bacterial isolates were recovered. The MALDI-TOF MS carbapenemase assay identified 21 of 29 (72.4%) of the carbapenemase-producing isolates directly from the blood culture vials, especially those encoding KPC-2 (100%) and SPM-1 (100%), after a 4 h incubation period. Although the majority of OXA-23-producing Acinetobacter baumannii isolates were not identified on day 1, all isolates were identified as carbapenemase producers directly from the colony on the next day. The MALDI-TOF MS carbapenemase assay is a feasible and rapid test to identify carbapenemase activity directly from blood culture vials. It may contribute to faster readjustment of empirical antimicrobial therapy and implementation of infection control measures.
引用
收藏
页码:2132 / 2136
页数:5
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