A DNA polymorphism specific to Candida albicans strains exceptionally successful as human pathogens

被引:13
作者
Giblin, L
Edelmann, A
Zhang, NX
von Maltzahn, NB
Cleland, SB
Sullivan, PA
Schmid, J [1 ]
机构
[1] Massey Univ, Coll Sci, Inst Mol BioSci, Palmerston North, New Zealand
[2] Univ Leipzig, Inst Biochem, D-7010 Leipzig, Germany
关键词
evolution; pathogenicity; repetitive elements;
D O I
10.1016/S0378-1119(01)00548-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A large proportion of infection-causing isolates of the yeast Candida albicans belong to a general-purpose genotype, identifiable by fingerprinting with the moderately repetitive sequence CO. The high prevalence of this group - up to 70% in some patient categories suggests that its members possess genetic determinants. which enhance their success as pathogens compared to other strains. To find such determinants we are comparing the genomes of representatives of the general-purpose genotype cluster with the genomes of other strains. In this paper we describe the identification of a 985 bp HpaII fragment (MU13-4) specific to general-purpose genotype strains. The fragment was present in 90% of these strains, but only in 10% of other strains. The fragment did not hybridize with probe Ca3, used to define the general-purpose cluster. It contains elevated levels of repetitive DNA. Sequences homologous to MU 13-4 are dispersed throughout the chromosomes of general-purpose strains but are rarer or absent in other strains, as judged by Southern hybridization. Using the Stanford C. albicans genome database, we have placed the MU 13-4 fragment next to a CARE-1 element. We also found 79 significant homologies between parts of MU13-4 and 19 other contigs. Attempts to amplify the region surrounding the polymorphic fragment in non-general-purpose genotype strains suggest. as do the hybridization data, that the polymorphism is created by a deletion in non-cluster strains. These results show that it is possible to identify polymorphisms specific to general-purpose genotype strains. Primers against the fragment will allow PCR-based discrimination between general-purpose genotype strains and other strains, facilitating investigations aimed at determining morbidity and mortality caused by general-purpose genotype strains compared to other strains. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:157 / 164
页数:8
相关论文
共 15 条
[1]  
Ausubel FM., 1994, Curr. Protoc. Mol. Biol
[2]   Repetitive sequences (RPSs) in the chromosomes of Candida albicans are sandwiched between two novel stretches, HOK and RB2, common to each chromosome [J].
Chindamporn, A ;
Nakagawa, Y ;
Mizuguchi, I ;
Chibana, H ;
Doi, M ;
Tanaka, K .
MICROBIOLOGY-UK, 1998, 144 :849-857
[3]  
FONZI WA, 1993, GENETICS, V134, P717
[4]   Molecular markers reveal that population structure of the human pathogen Candida albicans exhibits both clonality and recombination [J].
Graser, Y ;
Volovsek, M ;
Arrington, J ;
Schonian, G ;
Presber, W ;
Mitchell, TG ;
Vilgalys, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (22) :12473-12477
[5]   3'-end-forming signals of yeast mRNA [J].
Guo, ZJ ;
Sherman, F .
TRENDS IN BIOCHEMICAL SCIENCES, 1996, 21 (12) :477-481
[6]   CHARACTERIZATION OF CARE-1 - CANDIDA-ALBICANS REPETITIVE ELEMENT-1 [J].
LASKER, BA ;
PAGE, LS ;
LOTT, TJ ;
KOBAYASHI, GS ;
MEDOFF, G .
GENE, 1991, 102 (01) :45-50
[7]  
Magee PT, 1998, ASM NEWS, V64, P505
[8]   PATHOGENICITY DETERMINANTS OF CANDIDA-ALBICANS - POTENTIAL TARGETS FOR IMMUNOTHERAPY [J].
MATTHEWS, RC .
MICROBIOLOGY-SGM, 1994, 140 :1505-1511
[9]  
Odds F.C., 1988, CANDIDA CANDIDOSIS R
[10]  
Sambrook J., 2002, MOL CLONING LAB MANU