The fungus Cryptococcus neoformans is a respiratory pathogen that is a relatively frequent cause of life-threatening disease in individuals with impaired immunity. Macrophages are critical cells in the control and dissemination of infection in the lung. C. neoformans is a facultative intracellular pathogen that can replicate in macrophage after damaging the phagolysosomal membrane. Fungal damage to the phagolysosomal membrane determines the outcome of the fungal-macrophage interaction. For C. neoformans, as well as other soil pathogenic fungi, the capacity for virulence has been proposed to emerge from interactions with phagocytic predators in the environment that select for traits that can then promote virulence in mammals. In fact, one of the remarkable aspects of C. neoformans pathogenesis is that it is virulent in many different animal hosts and can replicate in phagocytic cells from mammals, fish, insects and protozoa. This poses the fascinating question of how a soil organism with no need for an animal host is able to subvert immune effector cells from so many species. We hypothesize that this capacity for non-specific virulence comes from its ability to undermine host cells with an ?intracellular pathogenesis kit? that includes the intracellular secretion of numerous effector molecules. We have preliminary data that C. neoformans releases many proteins inside murine macrophages that include several well-known virulence factors. In this application we propose to identify proteins made inside human macrophages and amoeba that undermine host cells. A subset of these proteins will then be studied in detail to dissect mechanisms of intracellular pathogenesis.
Three specific aims are proposed:
Aim 1. To identify CN proteins produced intracellularly in human macrophages;
Aim 2. To identify key CN compounds produced during its interaction with amoeba;
Aim 3. To ascertain the mechanism of action of certain CN proteins in the intracellular pathogenic strategy in phagocytic human and protozoan cells. This work will illuminate the mechanisms of C. neoformans intracellular pathogenesis and this information can be relevant to designing improved therapies, antifungal therapies and vaccines.

Public Health Relevance

Cryptococcus neoformans is a major human pathogenic fungus that is acquired by in inhalation into lungs. In the lung the primary host defense system are macrophages that engulf the fungal particles. This application seeks to understand in detail the C. neoformans-macrophage interaction with the ultimate goal of using that information to prevent disease and improve the treatment of cryptococcal disease.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL059842-21
Application #
10093113
Study Section
Pathogenic Eukaryotes Study Section (PTHE)
Program Officer
Mongodin, Emmanuel Franck
Project Start
1997-09-30
Project End
2023-12-31
Budget Start
2021-02-01
Budget End
2022-01-31
Support Year
21
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Microbiology/Immun/Virology
Type
Schools of Public Health
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Vij, Raghav; Cordero, Radames J B; Casadevall, Arturo (2018) The Buoyancy of Cryptococcus neoformans Is Affected by Capsule Size. mSphere 3:
Rizzo, Juliana; Colombo, Ana C; Zamith-Miranda, Daniel et al. (2018) The putative flippase Apt1 is required for intracellular membrane architecture and biosynthesis of polysaccharide and lipids in Cryptococcus neoformans. Biochim Biophys Acta Mol Cell Res 1865:532-541
Casadevall, Arturo (2018) Antibody-based vaccine strategies against intracellular pathogens. Curr Opin Immunol 53:74-80
Jung, Eric H; Meyers, David J; Bosch, Jürgen et al. (2018) Novel Antifungal Compounds Discovered in Medicines for Malaria Venture's Malaria Box. mSphere 3:
Fu, Man Shun; Coelho, Carolina; De Leon-Rodriguez, Carlos M et al. (2018) Cryptococcus neoformans urease affects the outcome of intracellular pathogenesis by modulating phagolysosomal pH. PLoS Pathog 14:e1007144
Goldman, David L; Nieves, Edward; Nakouzi, Antonio et al. (2018) Serum-Mediated Cleavage of Bacillus anthracis Protective Antigen Is a Two-Step Process That Involves a Serum Carboxypeptidase. mSphere 3:
Casadevall, Arturo; Pirofski, Liise-Anne (2018) What Is a Host? Attributes of Individual Susceptibility. Infect Immun 86:
Fu, Man Shun; Casadevall, Arturo (2018) Divalent Metal Cations Potentiate the Predatory Capacity of Amoeba for Cryptococcus neoformans. Appl Environ Microbiol 84:
De Leon-Rodriguez, Carlos M; Rossi, Diego C P; Fu, Man Shun et al. (2018) The Outcome of the Cryptococcus neoformans-Macrophage Interaction Depends on Phagolysosomal Membrane Integrity. J Immunol 201:583-603
Walker, Louise; Sood, Prashant; Lenardon, Megan D et al. (2018) The Viscoelastic Properties of the Fungal Cell Wall Allow Traffic of AmBisome as Intact Liposome Vesicles. MBio 9:

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