Performance of MALDI Biotyper for Species Identification of Carbapenem-Resistant Enterobacteriaceae by Media Types and Incubation Time.
10.15263/jlmqa.2018.40.3.155
- Author:
Young Eun CHO
1
;
Byoung Hu CHOI
;
Jeonghyun CHANG
;
Heungsup SUNG
;
Mi Na KIM
Author Information
1. Department of Laboratory Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. mnkim@amc.seoul.kr
- Publication Type:Original Article
- Keywords:
Carbapenem-resistant Enterobacteriaceae;
Surveillance;
MALDI-TOF;
Media type;
Incubation time
- MeSH:
Agar;
Enterobacter aerogenes;
Enterobacter cloacae;
Enterobacteriaceae*;
Escherichia coli;
Imipenem;
Klebsiella oxytoca;
Klebsiella pneumoniae;
Mass Spectrometry;
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization*
- From:Journal of Laboratory Medicine and Quality Assurance
2018;40(3):155-160
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: This study was conducted to evaluate the impact of the media type used for direct identification of colonies on the surveillance culture of carbapenem-resistant Enterobacteriaceae (CRE) by matrix assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS). METHODS: CRE surveillance culture isolates were subjected to species identification using the MALDI Biotyper (Bruker Daltonics, Germany) for 2 months starting in March 2017. Four types of media were evaluated: blood agar (BA), Mueller Hinton agar (MH), MacConkey agar (Mac), and MacConkey agar containing imipenem of 1 µg/mL (IMP-Mac). CRE-like colonies on IMP-Mac and their subculture colonies on the other media were tested after overnight incubation and extended incubation for one additional day. The percent identification and score value were analyzed for each media types and incubation time when the identification was correct at the genus level. RESULTS: A total of 117 isolates were identified as 84 Klebsiella pneumoniae, 12 Escherichia coli, 9 Enterobacter cloacae, 5 Klebsiella oxytoca, 4 Enterobacter aerogenes, and 2 Raoultella ornithinolytica. The successful identification rates (SIR) for BA and MH were 98.3% and 97.4% (P=0.9), respectively, while those for Mac and IMP-Mac were 82.1% (P < 0.001) and 70.9% (P < 0.001), respectively. After extended incubation, SIRs were decreased to 96.6%, 96.6% (P=1.0), 61.5% (P < 0.001), and 58.1% (P < 0.001) on BA, MH, Mac, and IMP-Mac, respectively. The average score values were significantly lower for Mac (2.017±0.22) and IMP-Mac (1.978±0.24) than for BA (2.213±0.16) (P < 0.001). CONCLUSIONS: The low performance of the MALDI Biotyper applied directly to the colonies grown on Mac or IMP-Mac indicates that subculture on BA or MH is preferable before identification by MALDI-TOF MS.
