Rapid mass production of human influenza vaccine in insects using genome editing

Information

  • Research Project
  • 10326120
  • ApplicationId
    10326120
  • Core Project Number
    R43IP001169
  • Full Project Number
    1R43IP001169-01A1
  • Serial Number
    001169
  • FOA Number
    PA-20-260
  • Sub Project Id
  • Project Start Date
    9/30/2021 - 3 years ago
  • Project End Date
    9/29/2022 - 2 years ago
  • Program Officer Name
  • Budget Start Date
    9/30/2021 - 3 years ago
  • Budget End Date
    9/29/2022 - 2 years ago
  • Fiscal Year
    2021
  • Support Year
    01
  • Suffix
    A1
  • Award Notice Date
    9/21/2021 - 3 years ago
Organizations

Rapid mass production of human influenza vaccine in insects using genome editing

ABSTRACT As the recent COVID-19 pandemic has made clear, the rapid mass production of vaccines for emerging infectious diseases is of paramount importance. The use of the baculovirus/insect cell expression system for in vitro protein expression has been a game changer for vaccine production, but it also introduces challenges: transfection can be difficult, needs to be repeated with every batch, and the final product requires multiple purification steps to remove the residual baculovirus. We propose an alternative approach that could side-step the drawbacks associated with baculovirus/insect cell expression system: in vivo vaccine production in a scalable insect non-mammalian genetic model system. We aim to achieve this by using the CRISPR-Cas9 system to insert viral antigen genes for human and avian influenza into insects that are already mass produced for feed and/or waste management. Both the yellow mealworm (Tenebrio molitor) and the blow fly (Phormia regina) are promising bioreactors for manipulating protein expression in vivo due to their high metabolism and fecundity, ease of rearing, high resilience, and versatility in mass production systems (large-scale production facilities already exist for both insects). Unlike existing transgenic insect hosts such as cabbage looper larvae, both mealworms and blowflies are gregarious and can be cost effectively mass-reared at a scale of several tons per day. By using the CRISPR-Cas9 technique for recombinant protein expression to express influenza antigens in these insects, we will engineer life-stage dependent activation of the antigen production. Using existing technologies to facilitate rapid antigen protein purification, we will confirm the antigen production and characterize it. Finally, we will quantify what impact (if any) the modified genome has on phenotypes relevant to mass production and validate cost considerations for production. This work will set the stage for a steady supply of low-cost and customizable antigens, using insect biomass as an affordable and scalable bioreactor.

IC Name
National Center for Immunization and Respiratory Diseases (NCIRD)
  • Activity
    R43
  • Administering IC
    IP
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    243000
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    103
  • Ed Inst. Type
  • Funding ICs
    ODCDC:243000\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    BETA HATCH INC.
  • Organization Department
  • Organization DUNS
    079938555
  • Organization City
    SEATAC
  • Organization State
    WA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    981482328
  • Organization District
    UNITED STATES