Genotype distribution of Candida albicans isolates by 25S intron analysis with regard to invasiveness

被引:31
作者
Karahan, ZC
Güriz, H
Agirbasli, H
Balaban, N
Göçmen, JS
Aysev, D
Akar, N
机构
[1] Ankara Univ, Div Pediat Mol Pathol & Genet, Fac Med, TR-06100 Ankara, Turkey
[2] Ankara Univ, Microbiol Lab, Dept Pediat, Fac Med, TR-06100 Ankara, Turkey
[3] Istanbul Univ, Microbiol Lab Fdn Children Leukemia, Fac Med, Istanbul, Turkey
[4] Ankara Numune Educ & Invest Hosp, Microbiol & Clin Microbiol Dept, Ankara, Turkey
[5] Ankara Univ, Microbiol Lab, Dept Chest Dis, Fac Med, TR-06100 Ankara, Turkey
关键词
Candida albicans; genotypes; invasiveness;
D O I
10.1111/j.1439-0507.2004.01022.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The aim of this study was to genotype Candida albicans strains isolated from patients with invasive and non-invasive deep-seated infections. For this purpose, 301 C. albicans isolates (81 invasive and 220 non-invasive) were genotyped by using specific PCR primers designed to span the transposable group I intron of the 25S rDNA gene. Fifty-three of the 81 invasive isolates were genotype A (65.4%), eight were genotype B (9.9%) and 20 were genotype C (24.7%), while 98 of the 220 non-invasive isolates were genotype A (44.6%), 46 were genotype B (20.9%) and 76 were genotype C (34.5%). Genotype A was more prevalent among invasive isolates and genotypes B and C were more prevalent among non-invasive isolates (P = 0.0046). Genotypes D and E which represent C. dubliniensis were not found. These results indicate that there may be a relationship between C. albicans genotypes and invasiveness; genotype A being more invasive than others. The presence or absence of the transposable group I intron in the 25S rDNA gene may be important in determining the invasiveness of C. albicans.
引用
收藏
页码:465 / 469
页数:5
相关论文
共 28 条
[1]  
Baran J, 2001, SCAND J INFECT DIS, V33, P137, DOI 10.1080/003655401750065544
[2]   Risk factors for candidal bloodstream infections in surgical intensive care unit patients: The NEMIS Prospective Multicenter Study [J].
Blumberg, HM ;
Jarvis, WR ;
Soucie, JM ;
Edwards, JE ;
Patterson, JE ;
Pfaller, MA ;
Rangel-Frausto, MS ;
Rinaldi, MG ;
Saiman, L ;
Wiblin, RT ;
Wenzel, RP .
CLINICAL INFECTIOUS DISEASES, 2001, 33 (02) :177-186
[3]   Microsatellite polymorphism in the promoter sequence of the elongation factor 3 gene of Candida albicans as the basis for a typing system [J].
Bretagne, S ;
Costa, JM ;
Besmond, C ;
Carsique, R ;
Calderone, R .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (07) :1777-1780
[4]   Comparative genotyping of Candida albicans bloodstream and nonbloodstream isolates at a polymorphic microsatellite locus [J].
Dalle, F ;
Franco, N ;
Lopez, J ;
Vagner, O ;
Caillot, D ;
Chavanet, P ;
Cuisenier, B ;
Aho, S ;
Lizard, S ;
Bonnin, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (12) :4554-4559
[5]   Investigation of Candida dubliniensis in Candida spp.-positive hemocultures [J].
Dolapci, I ;
Tekeli, A ;
Gocmen, JS ;
Aysev, D ;
Guriz, H .
APMIS, 2002, 110 (05) :391-395
[6]   Phylogenetic analysis and rapid identification of Candida dubliniensis based on analysis of ACT1 intron and exon sequences [J].
Donnelly, SM ;
Sullivan, DJ ;
Shanley, DB ;
Coleman, DC .
MICROBIOLOGY-UK, 1999, 145 :1871-1882
[7]   Epidemiology of nosocomial fungal infections [J].
Fridkin, SK ;
Jarvis, WR .
CLINICAL MICROBIOLOGY REVIEWS, 1996, 9 (04) :499-&
[8]   Secular trends of candidemia over 12 years in adult patients at a tertiary care hospital [J].
Garbino, J ;
Kolarova, L ;
Rohner, P ;
Lew, D ;
Pichna, P ;
Pittet, D .
MEDICINE, 2002, 81 (06) :425-433
[9]   Candidemia in a neonatal intensive care unit: trends during fifteen years and clinical features of 111 cases [J].
Kossoff, EH ;
Buescher, ES ;
Karlowicz, MG .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1998, 17 (06) :504-508
[10]   COLONIZING POPULATIONS OF CANDIDA-ALBICANS ARE CLONAL IN ORIGIN BUT UNDERGO MICROEVOLUTION THROUGH C1 FRAGMENT REORGANIZATION AS DEMONSTRATED BY DNA-FINGERPRINTING AND C1 SEQUENCING [J].
LOCKHART, SR ;
FRITCH, JJ ;
MEIER, AS ;
SCHROPPEL, K ;
SRIKANTHA, T ;
GALASK, R ;
SOLL, DR .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (06) :1501-1509