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Background  Carbapenemase-producing  Enterobacteriaceae  (CPE), particularly carbapenemase-producing  Klebsiella pneumoniae  isolates, are important causative agents of nosocomial infections associated with significant mortality rates mostly in critical wards. The rapid detection and typing of these strains is critical either for surveillance purposes and to prevent outbreaks and optimize antibiotic therapy. In this study, the MALDI-TOF MS method was used to detect rapidly these isolates from blood cultures (BCs) and to obtain proteomic profiles enable to discriminate between carbapenemase-producing and non-carbapenemase-producing strains.    Results  Fifty-five  K. pneumoniae  strains were tested. Identification and carbapenemase-production detection assay using Ertapenem were performed both from bacterial pellets extracted directly from BCs flasks and from subcultures of these strains. For all isolates, a complete antimicrobial susceptibility testing and a genotypic characterization were performed.  We found 100% agreement between the carbapenemase-producing profile generated by MALDI TOF MS and that obtained using conventional methods. The assay detected and discriminated different carbapenemase-producing  K. pneumoniae  isolates within 30 min to 3 h after incubation with Ertapenem.    Conclusions  MALDI-TOF MS is a promising, rapid and economical method for the detection of carbapenemase-producing  K. pneumoniae  strains that could be successfully introduced into the routine diagnostic workflow of clinical microbiology laboratories.

bmc microbiology

Rapid detection of carbapenemase-producing Klebsiella pneumoniae strains derived from blood cultures by Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry (MALDI-TOF MS)