Affiliation:
1. Department of Medicine and Division of Infectious Diseases, Duke University Medical Center, Durham, North Carolina 27710
Abstract
ABSTRACT
We identified a homologue of the alternative oxidase gene in a screen to identify genes that are preferentially transcribed in response to a shift to 37°C in the human-pathogenic yeast
Cryptococcus neoformans
. Alternative oxidases are nucleus-encoded mitochondrial proteins that have two putative roles: they can function in parallel with the classic cytochrome oxidative pathway to produce ATP, and they may counter oxidative stress within the mitochondria. The
C. neoformans
alternative oxidase gene (
AOX1
) was found to exist as a single copy in the genome, and it encodes a putative protein of 401 amino acids. An
aox1
mutant strain was created using targeted gene disruption, and the mutant strain was reconstituted to wild type using a full-length
AOX1
. Compared to both the wild-type and reconstituted strains, the
aox1
mutant strain was not temperature sensitive but did have significant impairment of both respiration and growth when treated with inhibitors of the classic cytochrome oxidative pathway. The
aox1
mutant strain was also found to be more sensitive to the oxidative stressor tert-butyl hydroperoxide. The
aox1
mutant strain was significantly less virulent than both the wild type and the reconstituted strain in the murine inhalational model, and it also had significantly impaired growth within a macrophage-like cell line. These data demonstrate that the alternative oxidase of
C. neoformans
can make a significant contribution to metabolism, has a role in the yeast's defense against exogenous oxidative stress, and contributes to the virulence composite of this organism, possibly by improving survival within phagocytic cells.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
100 articles.
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