Use of the genotype MTBDR assay for rapid detection of rifampin and isoniazid resistance in Mycobacterium tuberculosis complex isolates

被引:164
作者
Hillemann, D
Weizenegger, M
Kubica, T
Richter, E
Niemann, S
机构
[1] Forschungszentrum Borstel, Natl Reference Mycobacteria, D-23845 Borstel, Germany
[2] Limbach Lab, Dept Microbiol, D-69126 Heidelberg, Germany
关键词
D O I
10.1128/JCM.43.8.3699-3703.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A commercially available DNA strip assay (Genotype MTBDR; Hain Lifescience, Nehren, Germany) was evaluated for its ability to detect mutations conferring resistance to rifampin (RMP) and isoniazid (INH) in clinical Mycobacterium tuberculosis complex isolates. A total of 103 multidrug-resistant (MDR; i.e., at least resistant to RMP and INH) and 40 fully susceptible strains isolated in Germany in 2001 in which resistance mutations have been previously defined by DNA sequencing and real-time PCR analysis were investigated. The Genotype MTBDR assay identified 102 of the 103 MDR strains with mutations in the rpoB gene (99%) and 91 strains (88.4%) with mutations in codon 315 of katG. All 40 susceptible strains showed a wild-type MTBDR hybridization pattern. The concordance between the MTBDR assay and the DNA sequencing results was 100%. Compared to conventional drug susceptibility testing, the sensitivity and specificity were 99 and 100% for RMP resistance and 88.4 and 100% for INH resistance, respectively. In conclusion, the MTBDR assay is a rapid and easy-to-perform test for the detection of the most common mutations found in MDRM. tuberculosis strains that can readily be included in a routine laboratory work flow.
引用
收藏
页码:3699 / 3703
页数:5
相关论文
共 30 条
[21]   Evaluation of genotype MTBC assay for differentiation of clinical Mycobacterium tuberculosis complex isolates [J].
Richter, E ;
Weizenegger, M ;
Rüsch-Gerdes, S ;
Niemann, S .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (06) :2672-2675
[22]   Evaluation of the INNO-LiPA Rif.TB assay, a reverse hybridization assay for the simultaneous detection of Mycobacterium tuberculosis complex and its resistance to rifampin [J].
Rossau, R ;
Traore, H ;
DeBeenhouwer, H ;
Mijs, W ;
Jannes, G ;
DeRijk, P ;
Portaels, F .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (10) :2093-2098
[23]   Molecular characterization of rifampin- and isoniazid-resistant Mycobacterium tuberculosis strains isolated in Poland [J].
Sajduda, A ;
Brzostek, A ;
Poplawska, M ;
Augustynowicz-Kopec, E ;
Zwolska, Z ;
Niemann, S ;
Dziadek, J ;
Hillemann, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (06) :2425-2431
[24]   The genetics and biochemistry of isoniazid resistance in Mycobacterium tuberculosis [J].
Slayden, RA ;
Barry, CE .
MICROBES AND INFECTION, 2000, 2 (06) :659-669
[25]   Analysis of the oxyR-ahpC region in isoniazid-resistant and -susceptible Mycobacterium tuberculosis complex organisms recovered from diseased humans and animals in diverse localities [J].
Sreevatsan, S ;
Pan, X ;
Zhang, Y ;
Deretic, V ;
Musser, JM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (03) :600-606
[26]   DETECTION OF RIFAMPICIN-RESISTANCE MUTATIONS IN MYCOBACTERIUM-TUBERCULOSIS [J].
TELENTI, A ;
IMBODEN, P ;
MARCHESI, F ;
LOWRIE, D ;
COLE, S ;
COLSTON, MJ ;
MATTER, L ;
SCHOPFER, K ;
BODMER, T .
LANCET, 1993, 341 (8846) :647-650
[27]   Genotypic assessment of isoniazid and rifampin resistance in Mycobacterium tuberculosis: A blind study at reference laboratory level [J].
Telenti, A ;
Honore, N ;
Bernasconi, C ;
March, J ;
Ortega, A ;
Heym, B ;
Takiff, HE ;
Cole, ST .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (03) :719-723
[28]   Detection of a point mutation associated with high-level isoniazid resistance in Mycobacterium tuberculosis by using real-time PCR technology with 3′-minor groove binder-DNA probes [J].
van Doorn, HR ;
Claas, ECJ ;
Templeton, KE ;
van der Zanden, AGM ;
Vije, ATK ;
de Jong, MD ;
Dankert, J ;
Kuijper, EJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (10) :4630-4635
[29]   STRAIN IDENTIFICATION OF MYCOBACTERIUM-TUBERCULOSIS BY DNA FINGERPRINTING - RECOMMENDATIONS FOR A STANDARDIZED METHODOLOGY [J].
VANEMBDEN, JDA ;
CAVE, MD ;
CRAWFORD, JT ;
DALE, JW ;
EISENACH, KD ;
GICQUEL, B ;
HERMANS, P ;
MARTIN, C ;
MCADAM, R ;
SHINNICK, TM ;
SMALL, PM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (02) :406-409
[30]  
Zhang Y, 2000, MOLECULAR GENETICS OF MYCOBACTERIA, P235