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.
引用
收藏
页码:4481 / 4486
页数:6
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