Affiliation:
1. Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania
2. VA Pittsburgh Health System, Pittsburgh, Pennsylvania
3. Department of Pathology, University of Colorado, Denver, Colorado
Abstract
ABSTRACT
We previously showed that
Candida albicans
orf19.4590, which we have renamed
RFX2
, expresses a protein that is reactive with antibodies in persons with candidiasis. In this study, we demonstrate that
C. albicans RFX2
shares some functional redundancy with
Saccharomyces cerevisiae RFX1
. Complementation of an
S. cerevisiae rfx1
mutant with
C. albicans RFX2
partially restored UV susceptibility and the repression of DNA damage response genes. DNA damage- and UV-induced genes
RAD6
and
DDR48
were derepressed in a
C. albicans rfx2
null mutant strain under basal conditions, and the mutant was significantly more resistant to UV irradiation, heat shock, and ethanol than wild-type strain SC5314. The
rfx2
mutant was hyperfilamentous on solid media and constitutively expressed hypha-specific genes
HWP1
,
ALS3
,
HYR1
,
ECE1
, and
CEK1
. The mutant also demonstrated increased invasion of solid agar and significantly increased adherence to human buccal epithelial cells. During hematogenously disseminated candidiasis, mice infected with the mutant had a significantly delayed time to death compared to the wild type. During oropharyngeal candidiasis, mice infected with the mutant had significantly lower tissue burdens in the oral cavity and esophagus at 7 days and they were less likely to develop disseminated infections because of mucosal translocation. The data demonstrate that
C. albicans
Rfx2p regulates DNA damage responses, morphogenesis, and virulence.
Publisher
American Society for Microbiology
Subject
Molecular Biology,General Medicine,Microbiology
Cited by
43 articles.
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