Affiliation:
1. Aberdeen Fungal Group, School of Medical Sciences, Institute of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom
Abstract
ABSTRACT
The echinocandin antifungal drugs inhibit synthesis of the major fungal cell wall polysaccharide β(1,3)-glucan. Echinocandins have good efficacy against
Candida albicans
but reduced activity against other
Candida
species, in particular
Candida parapsilosis
and
Candida guilliermondii
. Treatment of
Candida albicans
with a sub-MIC level of caspofungin has been reported to cause a compensatory increase in chitin content and to select for sporadic echinocandin-resistant
FKS1
point mutants that also have elevated cell wall chitin. Here we show that elevated chitin in response to caspofungin is a common response in various
Candida
species. Activation of chitin synthesis was observed in isolates of
C. albicans
,
Candida tropicalis
,
C. parapsilosis
, and
C. guilliermondii
and in some isolates of
Candida krusei
in response to caspofungin treatment. However,
Candida glabrata
isolates demonstrated no exposure-induced change in chitin content. Furthermore, isolates of
C. albicans
,
C. krusei
,
C. parapsilosis
, and
C. guilliermondii
which were stimulated to have higher chitin levels via activation of the calcineurin and protein kinase C (PKC) signaling pathways had reduced susceptibility to caspofungin. Isolates containing point mutations in the
FKS1
gene generally had higher chitin levels and did not demonstrate a further compensatory increase in chitin content in response to caspofungin treatment. These results highlight the potential of increased chitin synthesis as a potential mechanism of tolerance to caspofungin for the major pathogenic
Candida
species.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
165 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献