EFFECT OF INHA AND KATG ON ISONIAZID RESISTANCE AND VIRULENCE OF MYCOBACTERIUM-BOVIS

被引:135
作者
WILSON, TM
DELISLE, GW
COLLINS, DM
机构
[1] Agresearch, Wallaceville Animal Research Centre, Upper Hutt
关键词
D O I
10.1111/j.1365-2958.1995.tb02276.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Isoniazid (INH) resistance of the Mycobacterium tuberculosis Complex (MtbC) is associated with both loss of catalase activity and mutation of the inhA gene. However, the relative contributions of these changes to resistance and to the loss of virulence for guineapigs is unknown. In this study, a virulent strain of Mycobacterium bovis, a member of the MtbC, was exposed to increasing concentrations of INH. Two INH-resistant strains were produced which had lost catalase activity. Strain WAg405, which had a higher resistance to INH, also had a mutation in the inhA gene. This demonstrated that loss of catalase activity and mutation of inhA had a cumulative effect on INH resistance. When a functional katG gene was integrated into the genome of WAg405 the INH resistance was greatly reduced. This indicated that most of the resistance had been caused by loss of catalase activity. While the parent INH-sensitive strain was virulent for guinea-pigs, the INH-resistant strains were significantly less virulent. Integration of a functional katG gene into the most resistant strain restored full virulence. This clearly established that katG is a virulence factor for M. bovis and that mutation of the inhA gene has no effect on virulence.
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收藏
页码:1009 / 1015
页数:7
相关论文
共 27 条
  • [1] MUTATIONS IN THE CATALASE-PEROXIDASE GENE FROM ISONIAZID-RESISTANT MYCOBACTERIUM-TUBERCULOSIS ISOLATES
    ALTAMIRANO, M
    MAROSTENMAKI, J
    WONG, A
    FITZGERALD, M
    BLACK, WA
    SMITH, JA
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1994, 169 (05) : 1162 - 1165
  • [2] INHA, A GENE ENCODING A TARGET FOR ISONIAZID AND ETHIONAMIDE IN MYCOBACTERIUM-TUBERCULOSIS
    BANERJEE, A
    DUBNAU, E
    QUEMARD, A
    BALASUBRAMANIAN, V
    UM, KS
    WILSON, T
    COLLINS, D
    DELISLE, G
    JACOBS, WR
    [J]. SCIENCE, 1994, 263 (5144) : 227 - 230
  • [3] ISOLATION AND EXPRESSION OF A GENE-CLUSTER RESPONSIBLE FOR BIOSYNTHESIS OF THE GLYCOPEPTIDOLIPID ANTIGENS OF MYCOBACTERIUM-AVIUM
    BELISLE, JT
    PASCOPELLA, L
    INAMINE, JM
    BRENNAN, PJ
    JACOBS, WR
    [J]. JOURNAL OF BACTERIOLOGY, 1991, 173 (21) : 6991 - 6997
  • [4] BERGLER H, 1994, J BIOL CHEM, V269, P5493
  • [5] FALKOW S, 1988, REV INFECT DIS, V10, pS274
  • [6] THE EMERGENCE OF DRUG-RESISTANT TUBERCULOSIS IN NEW-YORK-CITY
    FRIEDEN, TR
    STERLING, T
    PABLOSMENDEZ, A
    KILBURN, JO
    CAUTHEN, GM
    DOOLEY, SW
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (08) : 521 - 526
  • [7] INVIVO REPACKAGING OF RECOMBINANT COSMID MOLECULES FOR ANALYSES OF SALMONELLA-TYPHIMURIUM, STREPTOCOCCUS-MUTANS, AND MYCOBACTERIAL GENOMIC LIBRARIES
    JACOBS, WR
    BARRETT, JF
    CLARKCURTISS, JE
    CURTISS, R
    [J]. INFECTION AND IMMUNITY, 1986, 52 (01) : 101 - 109
  • [8] JACOBS WR, 1991, METHOD ENZYMOL, V204, P537
  • [9] SOME OBSERVATIONS ON THE PATHOGENICITY OF ISONIAZID-RESISTANT VARIANTS OF TUBERCLE BACILLI
    MIDDLEBROOK, G
    COHN, ML
    [J]. SCIENCE, 1953, 118 (3063) : 297 - 299
  • [10] MIDDLEBROOK G, 1954, AM REV TUBERC PULM, V69, P471