Affiliation:
1. School of Medical Sciences, Institute of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom
Abstract
ABSTRACT
Candida albicans
cells with increased cell wall chitin have reduced echinocandin susceptibility
in vitro
. The aim of this study was to investigate whether
C. albicans
cells with elevated chitin levels have reduced echinocandin susceptibility
in vivo
. BALB/c mice were infected with
C. albicans
cells with normal chitin levels and compared to mice infected with high-chitin cells. Caspofungin therapy was initiated at 24 h postinfection. Mice infected with chitin-normal cells were successfully treated with caspofungin, as indicated by reduced kidney fungal burdens, reduced weight loss, and decreased
C. albicans
density in kidney lesions. In contrast, mice infected with high-chitin
C. albicans
cells were less susceptible to caspofungin, as they had higher kidney fungal burdens and greater weight loss during early infection. Cells recovered from mouse kidneys at 24 h postinfection with high-chitin cells had 1.6-fold higher chitin levels than cells from mice infected with chitin-normal cells and maintained a significantly reduced susceptibility to caspofungin when tested
in vitro
. At 48 h postinfection, caspofungin treatment induced a further increase in chitin content of
C. albicans
cells harvested from kidneys compared to saline treatment. Some of the recovered clones had acquired, at a low frequency, a point mutation in
FKS1
resulting in a S645Y amino acid substitution, a mutation known to confer echinocandin resistance. This occurred even in cells that had not been exposed to caspofungin. Our results suggest that the efficacy of caspofungin against
C. albicans
was reduced
in vivo
due to either elevation of chitin levels in the cell wall or acquisition of
FKS1
point mutations.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
177 articles.
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