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
相关论文
共 37 条
[31]   RAPID IDENTIFICATION OF MYCOBACTERIA TO THE SPECIES LEVEL BY POLYMERASE CHAIN-REACTION AND RESTRICTION ENZYME ANALYSIS [J].
TELENTI, A ;
MARCHESI, F ;
BALZ, M ;
BALLY, F ;
BOTTGER, EC ;
BODMER, T .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (02) :175-178
[32]   Evaluation of INNO-LiPA MYCOBACTERIA v2: Improved reverse hybridization multiple DNA probe assay for mycobacterial identification [J].
Tortoli, E ;
Mariottini, A ;
Mazzarelli, G .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (09) :4418-4420
[33]   Commercial DNA Probes for Mycobacteria Incorrectly Identify a Number of Less Frequently Encountered Species [J].
Tortoli, Enrico ;
Pecorari, Monica ;
Fabio, Giuliana ;
Messino, Massimino ;
Fabio, Anna .
JOURNAL OF CLINICAL MICROBIOLOGY, 2010, 48 (01) :307-310
[34]   High-Throughput Identification of Bacteria and Yeast by Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry in Conventional Medical Microbiology Laboratories [J].
van Veen, S. Q. ;
Claas, E. C. J. ;
Kuijper, Ed J. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2010, 48 (03) :900-907
[35]   Fatal Mycobacterium abscessus endocarditis misidentified as Corynebacterium spp. [J].
Williamson, John C. ;
Miano, Todd A. ;
Morgan, Michael R. ;
Palavecino, Elizabeth L. .
SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 2010, 42 (03) :222-224
[36]   Then and now: use of 16S rDNA gene sequencing for bacterial identification and discovery of novel bacteria in clinical microbiology laboratories [J].
Woo, P. C. Y. ;
Lau, S. K. P. ;
Teng, J. L. L. ;
Tse, H. ;
Yuen, K. -Y. .
CLINICAL MICROBIOLOGY AND INFECTION, 2008, 14 (10) :908-934
[37]   THE SUPEROXIDE-DISMUTASE GENE, A TARGET FOR DETECTION AND IDENTIFICATION OF MYCOBACTERIA BY PCR [J].
ZOLG, JW ;
PHILIPPISCHULZ, S .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (11) :2801-2812