Mycobacterium tuberculosis (Mtb) is responsible for about two million deaths worldwide each year with approximately ten million new cases annually. Like several other intracellular pathogens, the preferred niche for this organism throughout most of the infection, is a modified phagosome-like compartment of the host macrophage. While there are clearly advantages to this pathogenic strategy, growth within a host-derived membrane also poses many challenges. Perhaps the most fundamental is the acquisition of nutrients. How Mtb, or any other vacuolar pathogen, obtains nutrients in this niche is unclear. Furthermore, the environment found inside the phagosome is not static, but rather changes as the disease progresses. Infection with Mtb can be divided into at least two distinct stages: the early preimmune/acute phase and the late postimmune/chronic phase. Previously we used a global genetic interaction mapping strategy to characterize a cholesterol uptake system, called "Mce4." This transporter is only required for survival during the chronic stages of infection, suggesting that the nutrients available to the bacterium change as disease progresses. The carbon source(s) used in the acute phase remains unclear. Using a high-throughput screen for transposon mutants that are defective for growth in acute infection, we have found two putative carbohydrate uptake systems and a hexose kinase that are critical for growth during this phase. The putative sugar importers sugABC, rv2038c-2040c and the hexose kinase ppgK, are important for survival during the early stages of infection suggesting that carbohydrates may serve as important nutrients during this phase. We propose a model in which the adaptive immune response alters the compartment in which Mtb resides, and the bacterium adjusts by shifting from carbohydrate to a cholesterol-based metabolism. To test this hypothesis, we propose to characterize these carbohydrate transporters and hexose kinase, identify the host substrates that serve as nutrients, and identify new therapeutic targets. These studies will provide valuable new drug targets and insight regarding how pathogens adapt in nutrient limited environments inside the host.

Public Health Relevance

Part of Mycobacteria tuberculosis (Mtb) success in virulence, is due to its ability to acquire nutrients during infection. We have developed a high-throughput genetic interaction screen for Mtb, to identify pathways needed for nutrient uptake and survival inside the host. Data from these genetic interaction screens can be used to determine what nutrients are required for infection in the host.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32AI093049-03
Application #
8499233
Study Section
Special Emphasis Panel (ZRG1-F13-C (20))
Program Officer
Jacobs, Gail G
Project Start
2011-07-01
Project End
2014-06-30
Budget Start
2013-07-01
Budget End
2014-06-30
Support Year
3
Fiscal Year
2013
Total Cost
$55,670
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Genetics
Type
Schools of Medicine
DUNS #
603847393
City
Worcester
State
MA
Country
United States
Zip Code
01655
Padilla-Benavides, Teresita; Long, Jarukit E; Raimunda, Daniel et al. (2013) A novel P(1B)-type Mn2+-transporting ATPase is required for secreted protein metallation in mycobacteria. J Biol Chem 288:11334-47