Cryptococcal meningitis kills approximately 625,000 immunocompromised individuals each year, mainly in developing areas of the world. The pathogenic fungus responsible for this disease, Cryptococcus neoformans, enters the host by inhalation; how it specifically targets and invades the brain to cause fatal infection is a central question in the field. Several distinct routes of entry to the central nervous system (CNS) have been proposed and supported by experimental evidence, but gaps remain in mechanistic understanding of these routes. Our goal in this R21 application is to identify host endothelial factors that participate in cryptococcal traversal of the blood-brain barrier (BBB), as a step toward our long-term objective of defining the molecular components and specific roles of the pathways used by C. neoformans to enter the CNS. We have developed a high-throughput screening assay to measure the transit of free C. neoformans across model BBB that have been treated with siRNA.
In Aim 1 we will use it to screen an siRNA library targeting endothelial surface proteins, and will validate hits from the screen for further study.
In Aim 2 we will assess the specificity and roles in BBB transit of selected hits from Aim 1, using a combination of imaging, in vitro assays, and in vivo studies. While these aims are necessarily interdependent, our strong preliminary data and expertise in the required methods support the feasibility of the proposed approach. For all experiments, we will analyze the results using rigorous statistical methods and appropriate controls, and will interpret them in the context of our expertise in the biology of C. neoformans and its host. These innovative studies will be enabled by a close collaboration between a cryptococcal biologist and a neuroimmunologist, a powerful combination that will advance fundamental understanding of a central aspect of fungal pathogenesis. This work will additionally open new areas of investigation of a significant pathogen and develop experimental tools that can be used to explore the biology of other neurotropic pathogens.

Public Health Relevance

Cryptococcus neoformans is a pathogenic fungus that causes serious disease in immunocompromised individuals worldwide. The main target of this organism is the central nervous system (CNS), where it causes infections that kill over 625,000 people annually. This project is designed to elucidate how C. neoformans crosses the physiological barriers that should normally exclude it from the CNS. The results will provide insight into this lethal infection and potential therapeutic strategies, as well as into basic biological processes relevant to diseases caused by this and other neurotropic microbial pathogens.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AI114549-01A1
Application #
8937299
Study Section
Special Emphasis Panel (ZRG1-AARR-K (04))
Program Officer
Duncan, Rory A
Project Start
2015-04-03
Project End
2017-03-31
Budget Start
2015-04-03
Budget End
2016-03-31
Support Year
1
Fiscal Year
2015
Total Cost
$228,750
Indirect Cost
$78,750
Name
Washington University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Santiago-Tirado, Felipe H; Onken, Michael D; Cooper, John A et al. (2017) Trojan Horse Transit Contributes to Blood-Brain Barrier Crossing of a Eukaryotic Pathogen. MBio 8:
Klein, Robyn S; Garber, Charise; Howard, Nicole (2017) Infectious immunity in the central nervous system and brain function. Nat Immunol 18:132-141
Santiago-Tirado, Felipe H; Doering, Tamara L (2017) False friends: Phagocytes as Trojan horses in microbial brain infections. PLoS Pathog 13:e1006680
Gish, Stacey R; Maier, Ezekiel J; Haynes, Brian C et al. (2016) Computational Analysis Reveals a Key Regulator of Cryptococcal Virulence and Determinant of Host Response. MBio 7:e00313-16