Cryptococcus neoformans is a fungal pathogen that causes serious disease in immunocompromised patients and results in an annual death toll of over 600,000. Cryptococcosis is contracted by inhalation of the infectious particle, which leads to a primary pulmonary infection. C. neoformans is a facultative intracellular pathogen. After initial engulfment by phagocytic cells in the lungs it may lyse or exit these cells and disseminate throughout the mammalian host, either in the bloodstream or by entering additional phagocytes. The consequence of dissemination to the brain is lethal meningitis. Several C. neoformans virulence factors have been implicated in the pathogenesis of this disease, including formation of the protective pigment melanin, the presence on fungal cells of an extensive polysaccharide capsule, and secretion of certain proteins. Host factors also play a role in infection, and host phagocytes have been implicated in pathogen latency and dissemination. Despite the demonstration of host phagocytic cell involvement in this disease, there has been no effort to systematically identify and study genes that are significant for the infection process. In preliminary studies, I developed and optimized a high-throughput imaging assay to efficiently evaluate the interactions between C. neoformans and RNAi-treated human macrophage-like cell lines. I then screened a subset of host genes to identify factors important in these interactions, by using commercially available siRNA libraries to down-regulate expression of genes encoding 901 human kinases and phosphatases in the host cells and then performing interaction assays. This screen identified 8 genes as having specific roles in host:fungal interactions;in this application I propose to study two of them in detail. The broad, long-term objectives of this project are to identify host genes that play a significant role in fungal pathogenesis and to discover their mechanisms of involvement.
Aim 1 is designed to test the roles of two candidate host genes in models relevant to pathogenesis, including mouse primary cells in vitro and models of infection.
Aim 2 is designed to elucidate the cellular mechanisms by which the products of the two host genes of interest influence host:fungal interactions. These studies will elucidate key aspects of pathogenesis of this important disease by defining how specific host factors affect the interaction of phagocytic cells with C. neoformans. This work will increase understanding of cryptococcosis and potentially aid in the development of therapeutic or preventive strategies to fight this disease.

Public Health Relevance

Cryptococcus neoformans is an opportunistic fungal pathogen that causes life-threatening disease in immunocompromised individuals, resulting in an annual death toll of over 600,000 globally. Host factors play an important role in pathogen latency and dissemination, so identifying these factors and defining the mechanisms underlying host:pathogen interactions will increase understanding of this disease. Most of the burden of cryptococcosis falls on HIV-positive individuals in regions with limited access to health care;thi research could aid in designing effective host-targeted therapeutics and interventions that could decrease prevalence of this often fatal infection.

National Institute of Health (NIH)
National Institute of Allergy and Infectious Diseases (NIAID)
Postdoctoral Individual National Research Service Award (F32)
Project #
Application #
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Duncan, Rory A
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
Washington University
Schools of Medicine
Saint Louis
United States
Zip Code
Srikanta, Deepa; Hole, Camaron R; Williams, Matthew et al. (2017) RNA Interference Screening Reveals Host CaMK4 as a Regulator of Cryptococcal Uptake and Pathogenesis. Infect Immun 85:
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