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An Immunogenic and Slow-Growing Cryptococcal Strain Induces a Chronic Granulomatous Infection in Murine Lungs
Telzrow C. L. ; Righi S. E. ; Castro-Lopez N. ; Campuzano A. ; Brooks J. T. ; Carney J. M. ; Wormley F. L. ; Jr ; Andrew Alspaugh J.
Telzrow C. L.
Righi S. E.
Castro-Lopez N.
Campuzano A.
Brooks J. T.
Carney J. M.
Wormley F. L.
Jr
Andrew Alspaugh J.
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American Society for Microbiology
Date
2022
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Abstract
Many successful pathogens cause latent infections, remaining dormant within the host for years but retaining the ability to reactivate to cause symptomatic disease. The human opportunistic fungal pathogen Cryptococcus neoformans establishes latent pulmonary infections in immunocompetent individuals upon inhalation from the environment. These latent infections are frequently characterized by granulomas, or foci of chronic inflammation, that contain dormant and persistent cryptococcal cells. Immunosuppression can cause these granulomas to break down and release fungal cells that proliferate, disseminate, and eventually cause lethal cryptococcosis. This course of fungal latency and reactivation is understudied due to limited models, as chronic pulmonary granulomas do not typically form in mouse cryptococcal infections. A loss-of-function mutation in the Cryptococcus-specific MAR1 gene was previously described to alter cell surface remodeling in response to host signals. Here, we demonstrate that the mar1D mutant strain persists long term in a murine inhalation model of cryptococcosis, inducing a chronic pulmonary granulomatous response. We find that murine infections with the mar1D mutant strain are characterized by reduced fungal burden, likely due to the low growth rate of the mar1D mutant strain at physiological temperature, and an altered host immune response, likely due to inability of the mar1D mutant strain to properly employ virulence factors. We propose that this combination of features in the mar1D mutant strain collectively promotes the induction of a more chronic inflammatory response and enables long-term fungal persistence within these granulomatous regions. ¿ 2022 Telzrow et al.
Contents
Subject
cell cycle defects
cell wall
GM-CSF
granuloma
hypoxia
KEYWORDS Cryptococcus neoformans
Titan cell
cell wall
GM-CSF
granuloma
hypoxia
KEYWORDS Cryptococcus neoformans
Titan cell
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Biology