DNA macrorestriction profiles and antifungal susceptibility of Candida (Torulopsis) glabrata

被引:12
作者
Cormican, MG [1 ]
Hollis, RJ [1 ]
Pfaller, MA [1 ]
机构
[1] UNIV IOWA,COLL MED,DEPT PATHOL,DEPT MED MICROBIOL,IOWA CITY,IA 52242
关键词
D O I
10.1016/S0732-8893(96)00083-1
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Candida (Torulopsis) glabrata is an emerging nosocomial pathogen that may be relatively resistant to fluconazole. A series of 75 isolates (blood, urine, tissue, and other sites) from 16 patients (1 to 12 isolates per patient) at a single university medical center were analyzed by pulsed field gel electrophoresis (PFGE) of restriction endonuclease digests of chromosomal DNA. The MICs of the isolates for amphotericin B, flucytosine, fluconazole, and itraconazole, were determined by a microdilution broth method. A preliminary study of seven restriction enzymes, three producing small fragments (Hinf I, Hind III, Eco XI) and four producing large fragments (fag I, BssH II, Sfi I, Not I) identified Not I as giving interpretable banding patterns. Isolates were considered of different types if they differed by two or move bands. Sixteen distinct DNA types (A to P) were identified. Karyotyping was used an additional technique to compare strains with a common PFGE type. Most patients were colonized or infected with a single type at multiple body sites and over time. One PFGE type was shared by four patients housed in different areas of the institution at different times. For two of these four patients, the karyotype was also indistintuishable. Five patients were each colonized with two distinct types. The MIC of the strains studied were amphotericin B 0.5-1.0 mu g/ml (MIC(90) = 1.0 mu g/ ml), 5-fluorocytosine 0.25 --> 256 mu g/ml (MIC(90) = 2 mu g/ml), fluconazole 0.25 --> 128 mu g/ml (MIC(90) = 32 mu g/ml), and itraconazole 0.06-8.0 mu g/ml (MIC(90) = 2.0 mu g/ml). Molecular typing by PFGE using Not I digestion is It useful technique for epidemiological investigation as epidemiologically related isolates are generally identical and epidemiologically unrelated isolates are different by this method.
引用
收藏
页码:83 / 87
页数:5
相关论文
共 23 条
  • [1] TORULOPSIS-GLABRATA INFECTIONS IN PATIENTS WITH CANCER - INCREASING INCIDENCE AND RELATIONSHIP TO COLONIZATION
    AISNER, J
    SCHIMPFF, SC
    SUTHERLAND, JC
    YOUNG, VM
    WIERNIK, PH
    [J]. AMERICAN JOURNAL OF MEDICINE, 1976, 61 (01) : 23 - 28
  • [2] BECKSAGUE CM, 1993, J INFECT DIS, V167, P1247, DOI 10.1093/infdis/167.5.1247
  • [3] GENOTYPIC VARIATION AND SLIME PRODUCTION AMONG BLOOD AND CATHETER ISOLATES OF CANDIDA-PARAPSILOSIS
    BRANCHINI, ML
    PFALLER, MA
    RHINECHALBERG, J
    FREMPONG, T
    ISENBERG, HD
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (02) : 452 - 456
  • [4] CHUNG KJK, 1992, MED MYCOL, P280
  • [5] COMPARISON OF PULSED-FIELD GEL-ELECTROPHORESIS WITH ISOENZYME PROFILES AS A TYPING SYSTEM FOR CANDIDA-TROPICALIS
    DOEBBELING, BN
    LEHMANN, PF
    HOLLIS, RJ
    WU, LC
    WIDMER, AF
    VOSS, A
    PFALLER, MA
    [J]. CLINICAL INFECTIOUS DISEASES, 1993, 16 (03) : 377 - 383
  • [6] COLLABORATIVE COMPARISON OF BROTH MACRODILUTION AND MICRODILUTION ANTIFUNGAL SUSCEPTIBILITY TESTS
    ESPINELINGROFF, A
    KISH, CW
    KERKERING, TM
    FROMTLING, RA
    BARTIZAL, K
    GALGIANI, JN
    VILLAREAL, K
    PFALLER, MA
    GERARDEN, T
    RINALDI, MG
    FOTHERGILL, A
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (12) : 3138 - 3145
  • [7] *NAT COMM CLIN LA, 1995, M27T NAT COMM CLIN L
  • [8] EPIDEMIOLOGIC TYPING METHODS FOR MYCOSES
    PFALLER, MA
    [J]. CLINICAL INFECTIOUS DISEASES, 1992, 14 : S4 - S10
  • [9] IN-VITRO SUSCEPTIBILITIES OF CLINICAL YEAST ISOLATES TO 3 ANTIFUNGAL AGENTS DETERMINED BY THE MICRODILUTION METHOD
    PFALLER, MA
    BARRY, AL
    [J]. MYCOPATHOLOGIA, 1995, 130 (01) : 3 - 9
  • [10] Application of CHROMagar Candida for rapid screening of clinical specimens for Candida albicans, Candida tropicalis, Candida krusei, and Candida (Torulopsis) glabrata
    Pfaller, MA
    Houston, A
    Coffmann, S
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (01) : 58 - 61