Arthropod exosomes mediate vector-pathogen interactions

Information

  • Research Project
  • 10322352
  • ApplicationId
    10322352
  • Core Project Number
    R01AI141790
  • Full Project Number
    7R01AI141790-03
  • Serial Number
    141790
  • FOA Number
    PA-18-590
  • Sub Project Id
  • Project Start Date
    8/19/2019 - 5 years ago
  • Project End Date
    7/31/2024 - 7 months ago
  • Program Officer Name
    COSTERO-SAINT DENIS, ADRIANA
  • Budget Start Date
    3/1/2021 - 4 years ago
  • Budget End Date
    7/31/2021 - 3 years ago
  • Fiscal Year
    2020
  • Support Year
    03
  • Suffix
  • Award Notice Date
    3/19/2021 - 3 years ago

Arthropod exosomes mediate vector-pathogen interactions

Project Summary/Abstract Ticks transmit several pathogens including flaviviruses that cause diseases in humans. The molecular determinants and mechanisms of arthropod-borne flavivirus transmission to the vertebrate host are poorly understood. In this study, we provide strong preliminary data that show for the first time that a cell line from medically important arthropods, such as ticks, secretes exosomes that mediate transmission of flavivirus RNA and proteins to the human cells. We noted that tick-borne Langat virus (LGTV), a model pathogen closely related to tick-borne encephalitis virus (TBEV), profusely uses tick exosomes for transmission of viral RNA and proteins to the human- skin keratinocytes and blood endothelial cells. Cryo- EM analysis revealed presence of tick exosomes with the size range of 30 to 200 nm in diameter. Detection of both positive and negative LGTV RNA strands and proteins such as Envelope (E) and Non- structural 1 (NS1) inside arthropod exosomes confirmed that tick exosomes contain viral RNA and proteins. Viral RNA and proteins in exosomes derived from tick and mammalian cells were secured, highly infectious and replicative in all tested evaluations. Furthermore, treatment of tick cells with GW4869, a selective inhibitor that blocks exosome production affected LGTV loads and transmission from arthropod to human cells. 1-D gel electrophoresis further revealed presence of several arthropod exosome-enriched tick molecules. These preliminary results form the strong basis for the proposal to characterize role of arthropod exosomes in tick-LGTV interactions. Several approaches that delineate molecular signaling and identification of arthropod exosomal proteins in tick-LGTV interactions are proposed. We hypothesize that tick exosomal-enriched proteins could be considered as ideal candidates for the development of anti- vector vaccines. The proposed aims provide important insights to define molecular basis of the relationship between tick exosomes and pathogens. This is a transformative and a novel study that not only provides information on the role of arthropod exosomes in vector-pathogen interactions but also lead to the development of better strategies to treat or control transmission of pathogens from this and perhaps other vectors of medical importance.

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    R01
  • Administering IC
    AI
  • Application Type
    7
  • Direct Cost Amount
    250000
  • Indirect Cost Amount
    109800
  • Total Cost
    359800
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    855
  • Ed Inst. Type
    SCHOOLS OF VETERINARY MEDICINE
  • Funding ICs
    NIAID:359800\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    VB
  • Study Section Name
    Vector Biology Study Section
  • Organization Name
    UNIVERSITY OF TENNESSEE KNOXVILLE
  • Organization Department
    VETERINARY SCIENCES
  • Organization DUNS
    003387891
  • Organization City
    KNOXVILLE
  • Organization State
    TN
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    37996
  • Organization District
    UNITED STATES