TY - JOUR
T1 - Small chromosomes among Danish Candida glabrata isolates originated through different mechanisms
AU - Ahmad, Khadija Mohamed
AU - Ishchuk, Olena P.
AU - Hellborg, Linda
AU - Jørgensen, Gloria Pereira
AU - Skvarc, Miha
AU - Stenderup, Jørgen
AU - Jørck-Ramberg, Dorte
AU - Polakova, Silvia
AU - Piškur, Jure
N1 - © The Author(s) 2013. This article is published with open access at Springerlink.com
PY - 2013
Y1 - 2013
N2 - We analyzed 192 strains of the pathogenic yeast Candida glabrata from patients, mainly suffering from systemic infection, at Danish hospitals during 1985–1999. Our analysis showed that these strains were closely related but exhibited large karyotype polymorphism. Nine strains contained small chromosomes, which were smaller than 0.5 Mb. Regarding the year, patient and hospital, these C. glabrata strains had independent origin and the analyzed small chromosomes were structurally not related to each other (i.e. they contained different sets of genes). We suggest that at least two mechanisms could participate in their origin: (i) through a segmental duplication which covered the centromeric region, or (ii) by a translocation event moving a larger chromosome arm to another chromosome that leaves the centromere part with the shorter arm. The first type of small chromosomes carrying duplicated genes exhibited mitotic instability, while the second type, which contained the corresponding genes in only one copy in the genome, was mitotically stable. Apparently, in patients C. glabrata chromosomes are frequently reshuffled resulting in new genetic configurations, including appearance of small chromosomes, and some of these resulting “mutant” strains can have increased fitness in a certain patient “environment”.
AB - We analyzed 192 strains of the pathogenic yeast Candida glabrata from patients, mainly suffering from systemic infection, at Danish hospitals during 1985–1999. Our analysis showed that these strains were closely related but exhibited large karyotype polymorphism. Nine strains contained small chromosomes, which were smaller than 0.5 Mb. Regarding the year, patient and hospital, these C. glabrata strains had independent origin and the analyzed small chromosomes were structurally not related to each other (i.e. they contained different sets of genes). We suggest that at least two mechanisms could participate in their origin: (i) through a segmental duplication which covered the centromeric region, or (ii) by a translocation event moving a larger chromosome arm to another chromosome that leaves the centromere part with the shorter arm. The first type of small chromosomes carrying duplicated genes exhibited mitotic instability, while the second type, which contained the corresponding genes in only one copy in the genome, was mitotically stable. Apparently, in patients C. glabrata chromosomes are frequently reshuffled resulting in new genetic configurations, including appearance of small chromosomes, and some of these resulting “mutant” strains can have increased fitness in a certain patient “environment”.
U2 - 10.1007/s10482-013-9931-3
DO - 10.1007/s10482-013-9931-3
M3 - Journal article
C2 - 23670790
SN - 0003-6072
VL - 104
SP - 111
EP - 122
JO - Antonie van Leeuwenhoek
JF - Antonie van Leeuwenhoek
IS - 1
ER -