COMPARISON OF RESTRICTION ENZYME ANALYSIS VERSUS PULSED-FIELD GRADIENT GEL-ELECTROPHORESIS AS A TYPING SYSTEM FOR TORULOPSIS-GLABRATA AND CANDIDA SPECIES OTHER THAN CANDIDA-ALBICANS

被引:63
作者
VAZQUEZ, JA
BECKLEY, A
DONABEDIAN, S
SOBEL, JD
ZERVOS, MJ
机构
[1] WILLIAM BEAUMONT HOSP, ROYAL OAK, MI 48072 USA
[2] VET ADM MED CTR, ALLEN PK, MI 48101 USA
关键词
D O I
10.1128/JCM.31.8.2021-2030.1993
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Candida species have recently emerged as important nosocomial pathogens. Because of the lack of a reliable system for detecting differences within the same species, little is known about the epidemiology of infection with Candida species. We describe a typing system for Torulopsis glabrata and the non-C. albicans Candida species that uses contour-clamped homogeneous electric field electrophoresis (CHEF), a version of pulsed-field gradient gel electrophoresis, and compared it with restriction enzyme analysis (REA) of genomic DNA. One hundred seventeen clinical isolates from 40 patients were evaluated. CHEF and REA were performed on each of the isolates, and the results of the two procedures were compared. The REA procedure revealed 8 different types of Candida lusitaniae, 20 of Torulopsis glabrata, 5 of Candida tropicalis, 3 of Candida parapsilosis, and 7 of Candida kefyr, whereas the CHEF method revealed 14 different types of C. lusitaniae, 16 of T. glabrata, 10 of C. tropicalis, 10 of C. parapsilosis, and 7 of C. kefyr. The CHEF technique yielded unique patterns of electrophoretic karyotypes that could be used to distinguish intraspecies variations. When compared with REA, CHEF demonstrated greater sensitivity in recognizing subtle strain-to-strain variations in most isolates and will be a useful epidemiologic tool for studying non-C. albicans Candida species and T. glabrata.
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页码:2021 / 2030
页数:10
相关论文
共 66 条
[1]   USE OF LOW-FREQUENCY-CLEAVAGE RESTRICTION ENDONUCLEASES FOR DNA ANALYSIS IN EPIDEMIOLOGICAL INVESTIGATIONS OF NOSOCOMIAL BACTERIAL-INFECTIONS [J].
ALLARDETSERVENT, A ;
BOUZIGES, N ;
CARLESNURIT, MJ ;
BOURG, G ;
GOUBY, A ;
RAMUZ, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 1989, 27 (09) :2057-2061
[2]   CATHETER-ASSOCIATED CANDIDA-UTILIS FUNGEMIA IN A PATIENT WITH ACQUIRED IMMUNODEFICIENCY SYNDROME - SPECIES VERIFICATION WITH A MOLECULAR PROBE [J].
ALSINA, A ;
MASON, M ;
UPHOFF, RA ;
RIGGSBY, WS ;
BECKER, JM ;
MURPHY, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (04) :621-624
[3]   SECULAR TRENDS IN NOSOCOMIAL PRIMARY BLOOD-STREAM INFECTIONS IN THE UNITED-STATES, 1980-1989 [J].
BANERJEE, SN ;
EMORI, TG ;
CULVER, DH ;
GAYNES, RP ;
JARVIS, WR ;
HORAN, T ;
EDWARDS, JR ;
TOLSON, J ;
HENDERSON, T ;
MARTONE, WJ .
AMERICAN JOURNAL OF MEDICINE, 1991, 91 :S86-S89
[4]   EMERGENCE OF A NEW OPPORTUNISTIC PATHOGEN, CANDIDA-LUSITANIAE [J].
BLINKHORN, RJ ;
ADELSTEIN, D ;
SPAGNUOLO, PJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1989, 27 (02) :236-240
[5]  
BODEY GP, 1984, AM J MED, V77, P13
[6]  
BODEY GP, 1982, SEMIN HEMATOL, V19, P193
[7]  
BROSS J, 1989, AM J MED, V87, P614, DOI 10.1016/S0002-9343(89)80392-4
[8]   ELECTROPHORETIC SEPARATIONS OF LARGE DNA-MOLECULES BY PERIODIC INVERSION OF THE ELECTRIC-FIELD [J].
CARLE, GF ;
FRANK, M ;
OLSON, MV .
SCIENCE, 1986, 232 (4746) :65-68
[9]   DEVELOPMENT OF DNA PROBES FOR CANDIDA-ALBICANS [J].
CHEUNG, LL ;
HUDSON, JB .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1988, 10 (03) :171-179
[10]   MODIFICATIONS OF A CANDIDA-ALBICANS BIOTYPING SYSTEM [J].
CHILDRESS, CM ;
HOLDER, IA ;
NEELY, AN .
JOURNAL OF CLINICAL MICROBIOLOGY, 1989, 27 (06) :1392-1394