Rapid identification of mycobacteria from positive MGIT broths of primary cultures by MALDI-TOF mass spectrometry

被引:27
作者
Huang, Tsi-Shu [1 ]
Lee, Chia-Chien [1 ]
Tu, Hui-Zin [1 ]
Lee, Susan Shin-Jung [1 ,2 ,3 ]
机构
[1] Kaohsiung Vet Gen Hosp, Dept Pathol & Lab Med, Div Microbiol, Kaohsiung, Taiwan
[2] Kaohsiung Vet Gen Hosp, Dept Internal Med, Div Infect Dis, Kaohsiung, Taiwan
[3] Natl Yang Ming Univ, Fac Med, Sch Med, Taipei, Taiwan
关键词
DESORPTION IONIZATION-TIME; RESTRICTION ENZYME ANALYSIS; 16S RIBOSOMAL-RNA; NONTUBERCULOUS MYCOBACTERIA; ROUTINE IDENTIFICATION; TUBERCULOSIS COMPLEX; LIQUID; GENE; DIAGNOSIS; HSP65;
D O I
10.1371/journal.pone.0192291
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Rapid identification of mycobacteria is important for timely treatment and the implementation of public health measures. The MGIT system ensures rapid detection of mycobacteria, but identification is usually delayed by days to weeks due to further subculture on solid medium. Matrix-assisted laser desorption time-of-flight mass spectrometry (MALDI-TOF MS) was demonstrated to effectively identify mycobacteria isolates subcultured from solid or liquid media. Reports of identification directly from MGIT broths of both sterile and non-sterile clinical specimens, omitting the subculture step, were limited and not satisfactory before. Our identification method dramatically shortened delay from detection to identification of mycobacteria. Methodology We assessed the performance of the Vitek MS IVD version 3.0 for direct identification of NTM and M.tuberculosis from primary MGIT cultures, and assessed two sample preparation methods. Results Direct identification of NTM from positive MGIT broths, using MALDI-TOF VITEK MS with IVD v.3.0, generated high rates of acceptable results reaching 96.4% (80/83), and up to 100% (83/83) for sample preparations including a 0.1% SDS washing step. The sensitivity of VITEK MS to identify M.tuberculosis from MGIT tubes was 58/72 (80.6%), when using immunochromatography (ICA) test as gold standard. A characteristic colony clumping, wool-like appearance was observed in 48, and all 58 (100%) were correctly identified as M.tuberculosis using MALDI-TOF. The detection rate of M.tuberculosis complex was low (10/24, 41.6%) in the 24 MGIT tubes that was polymicrobial. Our method significantly reduced both the reagent cost and turnaround time. Conclusions Based on a simplified protocol, we showed that MALDI-TOF MS can be used for rapid identification of NTM directly from primary MGIT cultures within the routine clinical laboratory workflow. However, we recommend an initial ICA test to screen for M.tuberculosis complex, due to a low identification rate of M.tuberculosis in the presence of polymicrobial cultures using MALDI-TOF.
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页数:15
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