Parasitic nematode (PN) infections remain a major threat to human health worldwide, with more than 1 billion people infected. Children, pregnant women, and the elderly are particularly susceptible to morbidity from nematode infection. Control strategies are restricted to periodic de-worming of infected individuals, which is limited by rapid re-infection rates and the development of drug resistant worm populations. There are no vaccines available for PN infections in humans. Development of new drugs and vaccines will require a better understanding of host factors that participate in the immune response against PN infection. The requirement of a suitable host and the lack of good animal models have limited investigations into mechanisms that animal hosts employ to oppose PN attacks. Here we propose to use a system consisting of three model organisms: an insect, Drosophila melanogaster; the insect and human PN Heterorhabditis gerrardi; and its mutualistic bacteria Photorhabdus asymbiotica. This system is unique because it promises to reveal not only how pathogens evolve virulence but also how two pathogens (worm and bacteria) can synergize to exploit a common host (insect). Despite the identification and characterization of the main NF-?B immune signaling pathways in Drosophila, other evolutionary conserved pathways might regulate host immune mechanisms. It was recently shown that Transforming Growth Factor-beta (TGF-?) superfamily signals modulate the Drosophila immune response to wounding and bacterial infection and we have preliminary evidence suggesting that certain TGF-? pathway signaling molecules are potentially involved in the fly immune response against the nematodes and their associated bacteria. We will use this information to elucidate the exact role of TGF-? signaling components in Drosophila antinematode and antibacterial defense mechanisms.
In Aim 1, we will analyze the Drosophila tissuespecific transcriptional regulation of TGF-? signaling members upon infection with Heterorhabditis and Photorhabdus, and the potential interference of TGF-? signaling with other innate immune pathways.
In Aim 2, we propose to examine whether TGF-? molecules modulate cellular immune functions and whether the latter interact with humoral reactions in response to the pathogens.
In Aim 3, we will explore the involvement of TGF-? signaling in the phenoloxidase/melanization response of Drosophila flies infected with Heterorhabditis axenic or symbiotic nematodes or Photorhabdus bacteria alone. We expect that the results from this project will generate novel insights into the potential role of TGF-? signalng molecules in the host anti-nematode/antibacterial immune response and thus may expose a currently unknown layer of the innate immune system. Such knowledge will contribute significantly to the development of improved practices to control PN in humans.

Public Health Relevance

Parasitic nematodes pose an important health threat, infecting over 1 billion people. This project will investigate the function of TGF-? signaling in he immune response of the genetic insect model Drosophila melanogaster against the nematode parasite Heterorhabditis gerrardi and its mutualistic bacteria Photorhabdus asymbiotica. Results from this project will potentially uncover novel host antiparasitic/antibacterial defense mechanisms that will lead to improved control strategies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI110675-04
Application #
9455583
Study Section
Innate Immunity and Inflammation Study Section (III)
Program Officer
Singleton, Kentner L
Project Start
2015-04-01
Project End
2019-03-31
Budget Start
2018-04-01
Budget End
2019-03-31
Support Year
4
Fiscal Year
2018
Total Cost
Indirect Cost
Name
George Washington University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
043990498
City
Washington
State
DC
Country
United States
Zip Code
20052
Yadav, Shruti; Daugherty, Sean; Shetty, Amol Carl et al. (2017) RNAseq Analysis of the Drosophila Response to the Entomopathogenic Nematode Steinernema. G3 (Bethesda) 7:1955-1967
Cooper, Dustin; Eleftherianos, Ioannis (2017) Memory and Specificity in the Insect Immune System: Current Perspectives and Future Challenges. Front Immunol 8:539
Casanova-Torres, Ángel M; Shokal, Upasana; Morag, Neta et al. (2017) The Global Transcription Factor Lrp Is both Essential for and Inhibitory to Xenorhabdus nematophila Insecticidal Activity. Appl Environ Microbiol 83:
Shokal, Upasana; Kopydlowski, Hannah; Eleftherianos, Ioannis (2017) The distinct function of Tep2 and Tep6 in the immune defense of Drosophila melanogaster against the pathogen Photorhabdus. Virulence 8:1668-1682
Shokal, Upasana; Eleftherianos, Ioannis (2017) The Drosophila Thioester containing Protein-4 participates in the induction of the cellular immune response to the pathogen Photorhabdus. Dev Comp Immunol 76:200-208
Eleftherianos, Ioannis; Yadav, Shruti; Kenney, Eric et al. (2017) Role of Endosymbionts in Insect-Parasitic Nematode Interactions. Trends Parasitol :
Shokal, Upasana; Eleftherianos, Ioannis (2017) Evolution and Function of Thioester-Containing Proteins and the Complement System in the Innate Immune Response. Front Immunol 8:759
Eleftherianos, I; Shokal, U; Yadav, S et al. (2017) Insect Immunity to Entomopathogenic Nematodes and Their Mutualistic Bacteria. Curr Top Microbiol Immunol 402:123-156
Eleftherianos, Ioannis; Castillo, Julio Cesar; Patrnogic, Jelena (2016) TGF-? signaling regulates resistance to parasitic nematode infection in Drosophila melanogaster. Immunobiology 221:1362-1368
Kenney, Eric; Eleftherianos, Ioannis (2016) Entomopathogenic and plant pathogenic nematodes as opposing forces in agriculture. Int J Parasitol 46:13-9

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