Disequilibrium in distribution of resistance mutations among Mycobacterium tuberculosis Beijing and non-beijing strains isolated from patients in Germany

被引:57
作者
Hillemann, D [1 ]
Kubica, T [1 ]
Rüsch-Gerdes, S [1 ]
Niemann, S [1 ]
机构
[1] Forschungszentrum Borstel, Natl Ref Ctr Mycobacteria, D-23845 Borstel, Germany
关键词
D O I
10.1128/AAC.49.3.1229-1231.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Genotypic analysis of 103 multidrug-resistant Mycobacterium tuberculosis strains isolated in Germany in 2001 revealed that mutations in codon 531 (75.7%) of the rpoB gene and codon 315 (88.4%) of the katG gene are most frequent. Beijing genotype strains (60.2% of all isolates) displayed a different distribution of resistance mutations than non-Beijing strains.
引用
收藏
页码:1229 / 1231
页数:3
相关论文
共 23 条
[1]   Silent nucleotide polymorphisms and a phyogeny for Mycobacterium tuberculosis [J].
Baker, L ;
Brown, T ;
Maiden, MC ;
Drobniewski, F .
EMERGING INFECTIOUS DISEASES, 2004, 10 (09) :1568-1577
[2]   Molecular characterization of isoniazid-resistant Mycobacterium tuberculosis clinical isolates in Lithuania [J].
Bakonyte, D ;
Baranauskaite, A ;
Cicenaite, J ;
Sosnovskaja, A ;
Stakenas, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (06) :2009-2011
[3]  
Dobner P, 1997, INT J TUBERC LUNG D, V1, P365
[4]  
Glynn JR, 2002, EMERG INFECT DIS, V8, P843
[5]   Frequency of rpoB mutations inside and outside the cluster I region in rifampin-resistant clinical Mycobacterium tuberculosis isolates [J].
Heep, M ;
Brandstätter, B ;
Rieger, U ;
Lehn, N ;
Richter, E ;
Rüsch-Gerdes, S ;
Niemann, S .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (01) :107-110
[6]   Simultaneous detection and strain differentiation of Mycobacterium tuberculosis for diagnosis and epidemiology [J].
Kamerbeek, J ;
Schouls, L ;
Kolk, A ;
vanAgterveld, M ;
vanSoolingen, D ;
Kuijper, S ;
Bunschoten, A ;
Molhuizen, H ;
Shaw, R ;
Goyal, M ;
vanEmbden, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (04) :907-914
[7]  
Kubica T, 2004, INT J TUBERC LUNG D, V8, P1107
[8]   Novel mutations in ndh in isoniazid-resistant Mycobacterium tuberculosis isolates [J].
Lee, ASG ;
Teo, ASM ;
Wong, SY .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (07) :2157-2159
[9]   Biochemical and genetic data suggest that InhA is not the primary target for activated isoniazid in Mycobacterium tuberculosis [J].
Mdluli, K ;
Sherman, DR ;
Hickey, MJ ;
Kreiswirth, BN ;
Morris, S ;
Stover, CK ;
Barry, CE .
JOURNAL OF INFECTIOUS DISEASES, 1996, 174 (05) :1085-1090
[10]   Inhibition of a Mycobacterium tuberculosis β-ketoacyl ACP synthase by isoniazid [J].
Mdluli, K ;
Slayden, RA ;
Zhu, YQ ;
Ramaswamy, S ;
Pan, X ;
Mead, D ;
Crane, DD ;
Musser, JM ;
Barry, CE .
SCIENCE, 1998, 280 (5369) :1607-1610