Toxoplasma gondii is an obligate intracellular pathogen with a remarkably broad host range;it is able to infect virtually any nucleated cell of almost any warm-blooded animal. While well-known for the damage Toxoplasma can cause to a developing fetus, it has become a serious opportunistic pathogen in HIV/AIDS and lymphoma patients, as well as in organ transplant patients who are undergoing immunosuppressive therapy. Different strains of Toxoplasma can lead to different disease outcomes, both in humans and in mice. I have identified the secreted Toxoplasma pseudokinase ROP5 as a dominant virulence factor. This K22 award will provide the resources, time, and training to allow me to build an independent research program to determine molecular mechanism of ROP5's profound effect on disease outcome. This work will provide a much-needed interrogation of the interactions between a pathogen and the mammalian immune system, enabling the development of new therapies for toxoplasmosis. I have found that parasites deficient in ROP5 are completely attenuated in their virulence to mice and elicit a stronger pro-inflammatory response during early infection than do wild-type parasites. Furthermore, I have solved the crystal structure of ROP5's pseudokinase domain and found that polymorphisms correlated with strain-specific differences in virulence form a surface near the substrate binding domain. This has led me to hypothesize that ROP5 subverts the host immune system by binding host signaling molecules in its pseudokinase domain, which leads to dysregulation of immune signaling networks. I will test this hypothesis in the following complementary aims: 1) Identify the specific immune cell types and signaling networks modulated by ROP5;2) Determine the physical interactions ROP5 makes in infected host cells and the biochemical mechanism of ROP5's profound effect on virulence.

Public Health Relevance

While well-known for the disease it causes in the developing fetus, for patients of acute HIV/AIDS, or those suffering from lymphoma, and with the advent of immunosuppressive therapies for cancer patients and recipients of organ transplants, Toxoplasma has become a cause of serious disease in adult patients as well. Understanding the molecular mechanisms of pathogenesis and determinants of virulence will provide insight into the design of new therapies for toxoplasmosis, which will be particularly useful in treating the disease in the context of other syndromes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Career Transition Award (K22)
Project #
1K22AI097345-01
Application #
8224279
Study Section
Microbiology and Infectious Diseases B Subcommittee (MID)
Program Officer
Wali, Tonu M
Project Start
2014-06-01
Project End
2016-05-31
Budget Start
2014-06-01
Budget End
2015-05-31
Support Year
1
Fiscal Year
2014
Total Cost
$162,000
Indirect Cost
$12,000
Name
University of Texas Sw Medical Center Dallas
Department
Pharmacology
Type
Schools of Medicine
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390