Genotypic assessment of isoniazid and rifampin resistance in Mycobacterium tuberculosis: A blind study at reference laboratory level

被引:257
作者
Telenti, A
Honore, N
Bernasconi, C
March, J
Ortega, A
Heym, B
Takiff, HE
Cole, ST
机构
[1] INST PASTEUR,UNITE GENET MOL BACTERIENNE,F-75724 PARIS 15,FRANCE
[2] HOP AMBROISE PARE,F-92104 BOULOGNE,FRANCE
[3] INST SALUD CARLOS III,CIC,MADRID 28029,SPAIN
[4] INST VENEZOLANO INVEST CIENT,CARACAS,VENEZUELA
关键词
D O I
10.1128/JCM.35.3.719-723.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Progress in understanding the basis of resistance to isoniazid (INH) and rifampin (RMP) has allowed molecular tests for the detection of drug-resistant tuberculosis to be developed, Consecutive isolates (n = 95) of Mycobacterium tuberculosis, from a Spanish reference laboratory investigating outbreaks of multidrug-resistant tuberculosis, were coded and sent to two external laboratories for genotypic analysis of INH and RMP resistance by PCR-single-strand conformation polymorphism (SSCP) analysis of specific regions of four genes: part of the coding sequence of katG and the promoter regions of inhA and ahpC for INH and the RMP resistance region of rpoB, After correction for the presence of outbreak strains and multiple isolates from single patients, RMP resistance was detected successfully by PCR-SSCP in >96% of the RMP-resistant strains, PCR-SSCP had a sensitivity of 87% for INH resistance detection, and mutations in katG, inhA, katG-inhA, ahpC, and kaG-ahpC were identified in 36.8, 31.6, 2.6, 13.2, and 2.6%, respectively, of the unique strains, Specificity was 100%, Molecular detection of resistance to the two main antituberculous drugs, INH and RMP, can be accomplished accurately by using a strategy which limits analysis to four genetic regions, This may allow the expedient analysis of drug resistance by reference laboratories.
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页码:719 / 723
页数:5
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共 28 条
[11]  
KAPUR V, 1995, ARCH PATHOL LAB MED, V119, P138
[12]   Characterization of the catalase-peroxidase gene (katG) and inhA locus in isoniazid-resistant and -susceptible strains of Mycobacterium tuberculosis by automated DNA sequencing: Restricted array of mutations associated with drug resistance [J].
Musser, JM ;
Kapur, V ;
Williams, DL ;
Kreiswirth, BN ;
vanSoolingen, D ;
vanEmbden, JDA .
JOURNAL OF INFECTIOUS DISEASES, 1996, 173 (01) :196-202
[13]   NEW ISONIAZID/ETHIONAMIDE RESISTANCE GENE MUTATION AND SCREENING FOR MULTIDRUG-RESISTANT MYCOBACTERIUM-TUBERCULOSIS STRAINS [J].
RISTOW, M ;
MOHLIG, M ;
RIFAI, M ;
SCHATZ, H ;
FELDMANN, K ;
PFEIFFER, A .
LANCET, 1995, 346 (8973) :502-503
[14]   CHARACTERIZATION OF THE KATG AND INHA GENES OF ISONIAZID-RESISTANT CLINICAL ISOLATES OF MYCOBACTERIUM-TUBERCULOSIS [J].
ROUSE, DA ;
LI, ZM ;
BAI, GH ;
MORRIS, SL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (11) :2472-2477
[15]   THE NEW DIAGNOSTIC MYCOBACTERIOLOGY LABORATORY [J].
SALFINGER, M ;
PFYFFER, GE .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1994, 13 (11) :961-979
[16]   Mutations in pncA, a gene encoding pyrazinamidase/nicotinamidase, cause resistance to the antituberculous drug pyrazinamide in tubercle bacillus [J].
Scorpio, A ;
Zhang, Y .
NATURE MEDICINE, 1996, 2 (06) :662-667
[17]   DISPARATE RESPONSES TO OXIDATIVE STRESS IN SAPROPHYTIC AND PATHOGENIC MYCOBACTERIA [J].
SHERMAN, DR ;
SABO, PJ ;
HICKEY, MJ ;
ARAIN, TM ;
MAHAIRAS, GG ;
YUAN, Y ;
BARRY, CE ;
STOVER, CK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (14) :6625-6629
[18]  
SOECKLE MY, 1993, J INFECT DIS, V168, P1063
[19]   CLONING AND NUCLEOTIDE-SEQUENCE OF MYCOBACTERIUM-TUBERCULOSIS GYRA AND GYRB GENES AND DETECTION OF QUINOLONE RESISTANCE MUTATIONS [J].
TAKIFF, HE ;
SALAZAR, L ;
GUERRERO, C ;
PHILIPP, W ;
HUANG, WM ;
KREISWIRTH, B ;
COLE, ST ;
JACOBS, WR ;
TELENTI, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (04) :773-780
[20]   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