Format

Send to

Choose Destination
See comment in PubMed Commons below
Anal Chem. 2002 Nov 1;74(21):5487-91.

Identification of Staphylococcus aureus and determination of its methicillin resistance by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

Author information

1
Institute of Microbiology and Epidemiology, Fengtai District, Beijing, PR China.

Abstract

To evaluate the performance of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) in identifying Staphylococcus aureus and in determining its methicillin resistance, we analyzed 76 S. aureus clinical isolates using a linear MALDI-TOF MS. Spectral profile data obtained were compared with the database provided with the instrument, and 74% of the isolates were identified as S. aureus, as confirmed by a nuc-based PCR test. The determination of the methicillin resistance in S. aureus is based on the fact that the spectral profiles of methicillin-susceptible S. aureus (MSSA) and methicillin-resistant S. aureus (MRSA) differ greatly from each other. Replicate spectral profiles obtained from each isolate were combined to be a representative spectrum of it, and representative spectral profiles from all the isolates constitute a user's self-established database. All the spectral profiles in the database were classified into two groups based on clustering analysis, and one is for MSSA and another MRSA. There was a little discrepancy between the results from MALDI-TOF MS and from PCR. Seven isolates that are negative for the mecA gene by PCR were identified as MRSA by MALDI-TOF MS. The discrepancy may be partially explained by the heterogeneous nature of methicillin resistance in S. aureus. Our results suggested that comparison of MALDI-TOF MS spectral profiles of microorganism could serve as a simple and rapid method for bacterial identification and antibiotic susceptibility analysis.

PMID:
12433077
[Indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Loading ...
    Support Center