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Rapid Identification of Mycobacterial Whole Cells in Solid and Liquid Culture Media by Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry
被引:122
作者:
Lotz, Aurelie
[1
,2
]
Ferroni, Agnes
[1
]
Beretti, Jean-Luc
[1
]
Dauphin, Brunhilde
[3
]
Carbonnelle, Etienne
[4
]
Guet-Revillet, Helene
[1
,2
]
Veziris, Nicolas
[5
]
Heym, Beate
[6
]
Jarlier, Vincent
[5
]
Gaillard, Jean-Louis
[6
]
Pierre-Audigier, Catherine
[7
]
Frapy, Eric
[2
]
Berche, Patrick
[1
,2
]
Nassif, Xavier
[1
,2
]
Bille, Emmanuelle
[1
,2
]
机构:
[1] Hop Necker Enfants Malad, AP HP, Microbiol Lab, F-75015 Paris, France
[2] Univ Paris 05, Fac Med, Paris, France
[3] Andromas SAS, Paris, France
[4] Hop Europeen Georges Pompidou, AP HP, Microbiol Lab, Paris, France
[5] Hop La Pitie Salpetriere, AP HP, Natl Reference Ctr Mycobacteria, Paris, France
[6] Hop Ambroise Pare, AP HP, Microbiol Lab, Boulogne, France
[7] Hop Bichat Claude Bernard, AP HP, Microbiol Lab, F-75877 Paris 18, France
关键词:
DESORPTION/IONIZATION-TIME;
MICROBIOLOGY LABORATORIES;
SPECIES IDENTIFICATION;
ROUTINE IDENTIFICATION;
INTACT MYCOBACTERIA;
DNA PROBES;
ASSAY;
BACTERIA;
LEVEL;
GENE;
D O I:
10.1128/JCM.01397-10
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Mycobacterial identification is based on several methods: conventional biochemical tests that require several weeks for accurate identification, and molecular tools that are now routinely used. However, these techniques are expensive and time-consuming. In this study, an alternative method was developed using matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS). This approach allows a characteristic mass spectral fingerprint to be obtained from whole inactivated mycobacterial cells. We engineered a strategy based on specific profiles in order to identify the most clinically relevant species of mycobacteria. To validate the mycobacterial database, a total of 311 strains belonging to 31 distinct species and 4 species complexes grown in Lowenstein-Jensen (LJ) and liquid (mycobacterium growth indicator tube [MGIT]) media were analyzed. No extraction step was required. Correct identifications were obtained for 97% of strains from LJ and 77% from MGIT media. No misidentification was noted. Our results, based on a very simple protocol, suggest that this system may represent a serious alternative for clinical laboratories to identify mycobacterial species.
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页码:4481 / 4486
页数:6
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