Affiliation:
1. Department of Biological Sciences, Northern Illinois University, Dekalb, Illinois, USA
Abstract
ABSTRACT
Aspergillus fumigatus
is the leading causative agent of invasive aspergillosis (IA). The number of cases is on the rise, with mortality rates as high as 90% among immunocompromised patients. Molecular genetic studies in
A. fumigatus
could provide novel targets to potentially set the basis for antifungal therapies. In the current study, we investigated the role of the transcription factor gene
mtfA
in
A. fumigatus
. Our results revealed that
mtfA
plays a role in the growth and development of the fungus. Deletion or overexpression of
mtfA
leads to a slight reduction in colony growth, as well as a reduction in conidiation levels, in the overexpression strain compared to the wild-type strain. Furthermore, production of the secondary metabolite gliotoxin increased when
mtfA
was overexpressed, coinciding with an increase in the transcription levels of the gliotoxin genes
gliZ
and
gliP
with respect to the wild type. In addition, our study showed that
mtfA
is also necessary for normal protease activity in
A. fumigatus
; deletion of
mtfA
resulted in a reduction of protease activity compared to wild-type levels. Importantly, the absence of
mtfA
caused a decrease in virulence in the
Galleria mellonella
infection model, indicating that
mtfA
is necessary for
A. fumigatus
wild-type pathogenesis.
Publisher
American Society for Microbiology
Subject
Molecular Biology,General Medicine,Microbiology
Cited by
22 articles.
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