An essential component of the body's defense against infectious disease is the innate immune system. Macrophages and other white blood cells that comprise this system are the first responders to infection and recognize invading pathogens and initiate an immune response. A central feature of this response is the up- regulation and secretion of host inflammatory mediators and Type I Interferons (IFNs). The molecular basis connecting pathogen recognition to Type I IFN production is unclear, but is dependent upon the mitochondrial- and endoplasmic reticulum-localized adapter protein, Stimulator of Interferon Genes (STING). The objective of the study is to characterize the activation of STING-dependent signaling pathway(s) to further the long-term goal of delineating how Type I IFNs are regulated during intracellular infection of macrophages. Certain intracellular pathogens modulate the function of host mitochondria. It is hypothesized that intracellular infection of macrophages causes mitochondrial dysregulation, prompting generation of Reactive Oxygen Species (ROS), activating STING-dependent innate immune pathways, leading to expression of the prototypical type I IFN, IFN-?. The small molecule 5,6-dimethylxanthenone-4-acetic acid (DMXAA) is a potent activator of STING-dependent signaling in macrophages and will be used as a surrogate for intracellular infection. Additionally, STING-dependent activation in macrophages will be examined in response to an intracellular bacterial (Francisella tularensis) or viral (Respiratory Syncytial Virus (RSV)) infection.
The first Aim of the study will be to determine whether mitochondrial ROS generation is sufficient for STING dimerization and activation of downstream signaling components, and establish the necessity of mitochondrial ROS generation for IFN- ? expression during infection or chemical treatment.
The second Aim will establish how mitochondrial function and mitochondrial ROS is modulated by infection or DMXAA treatment. It is predicted that mitochondrial ROS generated during DMXAA treatment, or infection with F. tularensis or RSV, will be necessary for activation of STING-dependent innate immune signaling pathways following ROS-dependent dimerization of STING. Due to the potential commonality of mitochondrial subversion in infectious disease, the mechanism characterized in this project could have wide-ranging applications to other infectious organisms.

Public Health Relevance

The ability of white blood cells such as macrophages to prevent infectious disease hinges on their capacity to rapidly recognize and respond to infection or other danger signals. The proposed work will characterize whether damage to intracellular components alters the signaling pathways required for macrophages to produce type I interferon, a molecule long known to exert potent anti-microbial activity, following chemical stimulation with the anti-tumor compound, 5,6-dimethylxanthenone-4-acetic acid (DMXAA) or infection with two important human pathogens Francisella tularensis and Respiratory Syncytial Virus. These studies are highly relevant to our understanding of the earliest host immune responses to infection.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32AI098167-03
Application #
8594219
Study Section
Special Emphasis Panel (ZRG1-F07-E (20))
Program Officer
Prograis, Lawrence J
Project Start
2012-01-30
Project End
2015-01-29
Budget Start
2014-01-30
Budget End
2015-01-29
Support Year
3
Fiscal Year
2014
Total Cost
$53,942
Indirect Cost
Name
University of Maryland Baltimore
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201