Evaluation of a membrane array for detection of Mycobacterium tuberculosis complex and nontuberculous mycobacteria in positive liquid cultures

被引:12
作者
Lu, Po-Liang [1 ,2 ]
Lin, Yao-Cheng [3 ]
Yang, Yuan-Chieh [1 ,4 ]
Jou, Ruwen [5 ]
Huang, Su Chiao [1 ]
Jenh, Yi-Shan [3 ]
Huang, Hsin-Hui [3 ]
Chang, Tsung Chain [3 ]
机构
[1] Kaohsiung Med Univ Hosp, Dept Lab Med, Kaohsiung, Taiwan
[2] Kaohsiung Med Univ Hosp, Dept Internal Med, Kaohsiung, Taiwan
[3] Natl Cheng Kung Univ, Coll Med, Dept Med Lab Sci & Biotechnol, Tainan 70101, Taiwan
[4] Kaohsiung Med Univ, Dept Med Lab Sci & Biotechnol, Kaohsiung, Taiwan
[5] Ctr Dis Control, Dept Hlth, Reference Lab Mycobacteriol, Taipei, Taiwan
关键词
Mycobacterium tuberculosis complex; Nontuberculous mycobacteria; Molecular diagnosis; Array; CLINICAL-SAMPLES; IDENTIFICATION; ASSAY; GENOTYPE; INFECTIONS; SPECIMENS;
D O I
10.1016/j.diagmicrobio.2013.01.009
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Molecular identification of mycobacteria in positive Mycobacteria Growth Indicator Tube (MGIT) cultures can accelerate mycobacterial diagnosis. A membrane hybridization array (Blue Point) was evaluated for this purpose in 284 positive MGIT cultures. Discrepant results were resolved by testing with the GenoType Mycobacterium kit, TBc ID test, sequencing of the 16S rRNA gene and internal transcribed spacer. Total recovery from culture and the array (if confirmed) was considered 100%. The sensitivity, specificity, positive, and negative predictive values of the array for detection of Mycobacterium tuberculosis complex were 99.4%, 100%, 100%, and 99.2%, respectively, while the corresponding values of culture were 95.1%, 100%, 100%, and 93.8%, respectively, with significant differences in sensitivity and negative predictive value being found between the 2 methods. The recoveries of nontuberculous mycobacteria and mixed cultures of the array were also significantly higher than those of culture. The array can be adopted in routine mycobacteriology laboratory. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:337 / 341
页数:5
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