Pathogenic Nocardia, Rhodococcus, and related organisms are highly susceptible to imidazole antifungals

被引:11
作者
Dabbs, ER [1 ]
Naidoo, S [1 ]
Lephoto, C [1 ]
Nikitina, N [1 ]
机构
[1] Univ Witwatersrand, Sch Mol & Cell Biol, ZA-2050 Wits, South Africa
关键词
D O I
10.1128/AAC.47.4.1476-1478.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Rhodococcus equi and species of Nocardia and Gordonia may be human opportunistic pathogens. We find that these, as well as several isolates from closely related genera, are highly susceptible to the imidazoles bifonazole, clotrimazole, econazole, and miconazole, whose MICs are less than or equal to1 mug/ml. In liquid cultures 1 mug of the drug/ml was bacteriostatic and 10 mug/ml was bactericidal. On solid media at 10 mug of azole/ml no resistant mutants could be isolated. An MIC of 1 to 15 mug/ml was observed with ketoconazole, whereas none of these organisms was inhibited by the triazoles fluconazole and voriconazole (100 mug/ml). Imidazoles may offer the prospect of treatment of nocardioform mycetomas and may provide the basis for the development of additional antimicrobial agents to combat these pathogens.
引用
收藏
页码:1476 / 1478
页数:3
相关论文
共 26 条
[1]   Rhodococcus equi and Nocardia brasiliensis infection of the brain and liver in a patient with acute nonlymphoblastic leukemia [J].
Akan, H ;
Akova, M ;
Ataoglu, H ;
Aksu, G ;
Arslan, Ö ;
Koç, H .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1998, 17 (10) :737-739
[2]  
BEMERMELCHIOR P, 1998, CLIN INFECT DIS, V29, P1340
[3]   PRIMARY CUTANEOUS NOCARDIA-OTITIDISCAVIARUM INFECTION - CASE-REPORT AND REVIEW [J].
CLARK, NM ;
BRAUN, DK ;
PASTERNAK, A ;
CHENOWETH, CE .
CLINICAL INFECTIOUS DISEASES, 1995, 20 (05) :1266-1270
[4]  
CLOTET B, 1993, J ACQ IMMUN DEF SYND, V6, P429
[5]  
Finkelstein A, 1973, Membranes, V2, P377
[6]   Antifungal agents: Chemotherapeutic targets and immunologic strategies [J].
Georgopapadakou, NH ;
Walsh, TJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (02) :279-291
[7]   Azole-antifungal binding to a novel cytochrome P450 from Mycobacterium tuberculosis:: implications for treatment of tuberculosis [J].
Guardiola-Diaz, HM ;
Foster, LA ;
Mushrush, D ;
Vaz, ADN .
BIOCHEMICAL PHARMACOLOGY, 2001, 61 (12) :1463-1470
[8]   Cutaneous and pulmonary infections caused by Mycobacterium vaccae [J].
Hachem, R ;
Raad, I ;
Rolston, KVI ;
Whimbey, E ;
Katz, R ;
Tarrand, J ;
Libshitz, H .
CLINICAL INFECTIOUS DISEASES, 1996, 23 (01) :173-175
[9]  
HARVEY RL, 1991, REV INFECT DIS, V13, P139
[10]   Pathogenesis and virulence of Rhodococcus equi [J].
Hondalus, MK .
VETERINARY MICROBIOLOGY, 1997, 56 (3-4) :257-268