Ecological immunology of a flea vector (Ctenocephalides felis)

  • Funded by National Institutes of Health (NIH)
  • Total publications:0 publications

Grant number: 5R16AI170530-02

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Key facts

  • Disease

    Plague
  • Start & end year

    2023
    2027
  • Known Financial Commitments (USD)

    $177,500
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    ASSISTANT PROFESSOR Lisa Brown
  • Research Location

    United States of America
  • Lead Research Institution

    GEORGIA SOUTHERN UNIVERSITY
  • Research Priority Alignment

    N/A
  • Research Category

    Animal and environmental research and research on diseases vectors

  • Research Subcategory

    Vector biology

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

PROJECT SUMMARY/ABSTRACT Fleas are obligate vectors of bacterial pathogens that cause severe diseases in humans, including murine typhus and bubonic plague. To resist or limit infection, fleas possess an innate immune system that provides defense against microbial invasion and colonization. However, in their natural habitats, flea populations are made up of individuals that differ not only their genetic background, but also in regard to factors such as sex, age, diet, infection history, gut microbiota, and exposure to environmental stressors. These non-genetic factors have been shown to have important consequences on the outcome of infection in other disease vectors; yet, no studies to date have addressed the impact of these ecological parameters on flea immune responses. The proposed research aims to fill these knowledge gaps in flea ecological immunology, with the primary goals being to determine the intrinsic factors that affect the antibacterial response in adults, and to determine the effect of larval ecology on subsequent infections as adults. Specifically, we propose to compare the strength of immune defense mechanisms in adult cat fleas (Ctenocephalides felis) based on sex, age, and infection history (Specific Aim 1), as well as following larval exposure to food quantity, larval density, and insecticides (Specific Aim 2). This project will provide valuable insight into the variability of flea immunity under natural conditions, which can directly affect pathogen transmission dynamics and alter disease prevalence outcomes within a vector population. Data arising from this project could aid in the development of novel strategies to control the spread of flea-borne pathogens to humans.