Comparison of 14 Molecular Assays for Detection of Mycobacterium tuberculosis Complex in Bronchoalveolar Lavage Fluid

被引:24
作者
Akkerman, Onno W. [1 ]
van der Werf, Tjip S. [1 ,2 ]
de Boer, Maria [3 ]
de Beer, Jessica L. [4 ]
Rahim, Zeaur [5 ]
Rossen, John W. A. [6 ]
van Soolingen, Dick [4 ,7 ,8 ]
Kerstjens, Huib A. M. [1 ]
van der Zanden, Adri G. M. [3 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Pulmonol & TB, Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Internal Med, Groningen, Netherlands
[3] Lab Med Microbiol & Publ Hlth, Enschede, Netherlands
[4] Natl Inst Publ Hlth & Environm RIVM, CIb LIS, Ctr Infect Dis, TB Reference Lab, Bilthoven, Netherlands
[5] Int Ctr Diarrhoeal Dis Res, Dhaka 1000, Bangladesh
[6] Univ Groningen, Univ Med Ctr Groningen, Dept Med Microbiol, Groningen, Netherlands
[7] Radboud Univ Nijmegen Med Ctr, Dept Med Microbiol, Nijmegen, Netherlands
[8] Radboud Univ Nijmegen Med Ctr, Dept Lung Dis, Nijmegen, Netherlands
关键词
REAL-TIME PCR; INSERTION-SEQUENCE; IS6110; DNA; DIAGNOSIS; AMPLIFICATION; EPIDEMIOLOGY; SPECIMENS; STRAINS; ELEMENT;
D O I
10.1128/JCM.00843-13
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We compared 14 molecular assays for their ability to detect the Mycobacterium tuberculosis complex in bronchoalveolar lavage fluid samples. Three approaches were followed. First, by using DNA from Mycobacterium bovis BCG, we determined the detection limits of the assays using routine molecular methods. Second, in order to determine the analytical sensitivities of the assays, we added one of four M. tuberculosis isolates with various numbers of the insertion sequence IS6110 to N-acetyl-L-cysteine (NALC)-NaOH-treated bronchoalveolar lavage fluid samples in dilutions of 1:10 to 1:10,000,000. Third, intertest variabilities were measured and defined by the standard deviations for the quantitation cycle (Cq) values of three positive test results per dilution per assay. The 14 assays tested had similar analytical sensitivities, except for GeneXpert, which had an analytical sensitivity that was 10- to 100-fold lower than that of the other assays. The MP MTB/NTM test and the in-house TaqMan-10 revealed the best performances for the detection limit and had the highest analytical sensitivities. Most of the tests performed well regarding detection limit and analytical sensitivity for the detection of the M. tuberculosis complex in serial dilutions, and the differences were small. The MP MTB/NTM and the in-house TaqMan-10 assays revealed the best, and GeneXpert the worst, overall performances.
引用
收藏
页码:3505 / 3511
页数:7
相关论文
共 23 条
[1]   Comparison of six methods of extracting Mycobacterium tuberculosis DNA from processed sputum for testing by quantitative real-time PCR [J].
Aldous, WK ;
Pounder, JI ;
Cloud, JL ;
Woods, GL .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (05) :2471-2473
[2]  
ALLEN JL, 1992, MED LAB SCI, V49, P99
[3]   IS6110 - CONSERVATION OF SEQUENCE IN THE MYCOBACTERIUM-TUBERCULOSIS COMPLEX AND ITS UTILIZATION IN DNA FINGERPRINTING [J].
CAVE, MD ;
EISENACH, KD ;
MCDERMOTT, PF ;
BATES, JH ;
CRAWFORD, JT .
MOLECULAR AND CELLULAR PROBES, 1991, 5 (01) :73-80
[4]   Comparison of Diagnostic Performance of Three Real-Time PCR Kits for Detecting Mycobacterium Species [J].
Cho, Sun Young ;
Kim, Min Jin ;
Suh, Jin-Tae ;
Lee, Hee Joo .
YONSEI MEDICAL JOURNAL, 2011, 52 (02) :301-306
[5]   DNA FINGERPRINTING OF MYCOBACTERIUM-BOVIS STRAINS BY RESTRICTION FRAGMENT ANALYSIS AND HYBRIDIZATION WITH INSERTION ELEMENTS IS1081 AND IS6110 [J].
COLLINS, DM ;
ERASMUSON, SK ;
STEPHENS, DM ;
YATES, GF ;
DELISLE, GW .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (05) :1143-1147
[6]   REPETITIVE DNA-SEQUENCES AS PROBES FOR MYCOBACTERIUM-TUBERCULOSIS [J].
EISENACH, KD ;
CRAWFORD, JT ;
BATES, JH .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (11) :2240-2245
[7]   Evaluation of the Quantiplex human immunodeficiency virus type 1 RNA 3.0 Assay in a tertiary-care center [J].
Gale, H .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2000, 7 (01) :122-124
[8]   Comparison of the COBAS AMPLICOR MTB and BDProbeTec ET assays for detection of Mycobacterium tuberculosis in respiratory specimens [J].
Goessens, WHF ;
de Man, P ;
Koeleman, JGM ;
Luijendijk, A ;
te Witt, R ;
Endtz, HP ;
van Belkum, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (06) :2563-2566
[9]   Current evidence on diagnostic accuracy of commercially based nucleic acid amplification tests for the diagnosis of pulmonary tuberculosis [J].
Greco, S. ;
Girardi, E. ;
Navarra, A. ;
Saltini, C. .
THORAX, 2006, 61 (09) :783-790
[10]   Rapid Detection of Mycobacterium tuberculosis and Rifampin Resistance by Use of On-Demand, Near-Patient Technology [J].
Helb, Danica ;
Jones, Martin ;
Story, Elizabeth ;
Boehme, Catharina ;
Wallace, Ellen ;
Ho, Ken ;
Kop, JoAnn ;
Owens, Michelle R. ;
Rodgers, Richard ;
Banada, Padmapriya ;
Safi, Hassan ;
Blakemore, Robert ;
Lan, N. T. Ngoc ;
Jones-Lopez, Edward C. ;
Levi, Michael ;
Burday, Michele ;
Ayakaka, Irene ;
Mugerwa, Roy D. ;
McMillan, Bill ;
Winn-Deen, Emily ;
Christel, Lee ;
Dailey, Peter ;
Perkins, Mark D. ;
Persing, David H. ;
Alland, David .
JOURNAL OF CLINICAL MICROBIOLOGY, 2010, 48 (01) :229-237