Antimicrobial peptides to combat MDR ESKAPE pathogens

Information

  • Research Project
  • 9846822
  • ApplicationId
    9846822
  • Core Project Number
    R43AI148004
  • Full Project Number
    1R43AI148004-01
  • Serial Number
    148004
  • FOA Number
    PA-18-574
  • Sub Project Id
  • Project Start Date
    9/5/2019 - 5 years ago
  • Project End Date
    8/31/2020 - 4 years ago
  • Program Officer Name
    XU, ZUOYU
  • Budget Start Date
    9/5/2019 - 5 years ago
  • Budget End Date
    8/31/2020 - 4 years ago
  • Fiscal Year
    2019
  • Support Year
    01
  • Suffix
  • Award Notice Date
    9/3/2019 - 5 years ago
Organizations

Antimicrobial peptides to combat MDR ESKAPE pathogens

Project Summary Bacterial resistance has reached alarming levels in the US and other parts of the world in the past decade. The increase in bacterial infection with drug-resistant (DR) pathogens are resulting in increasing healthcare costs and a decline in positive clinical outcomes. Serious infections leading to sepsis remain a public health concern. In the United States alone, approximately 750,000 patients develop sepsis, which claims 250,000 lives every year with treatment failures often associated with multidrug resistance (MDR) bacterial pathogens as well as the complex pathophysiology of the disease. New therapies for controlling these DR pathogen-induced respiratory infections are urgently needed because: (a) the mortality rate among infected individuals requiring hospitalization remains very high; and (b) overuse of antibiotics has resulted in continuing emergence of additional MDR strains. Our long-term goal is to develop an effective, well tolerated antimicrobial peptide therapeutic to MDR pathogens -specifically the MDR Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa and Enterobacter spp (ESKAPE) pathogens determined to be critical and high priority by the CDC and WHO. There is thus a dire need to develop novel antimicrobial compounds that have a broad spectrum of activity against both Gram-positive and Gram-negative bacteria, yet at the same time, are well tolerated with a low propensity to select for resistant strains of bacteria. This proposal seeks to develop computationally engineered synthetic antimicrobial peptides derived from a normal human protein with very low toxicity but broad-spectrum activity against MDR clinical bacterial isolates. Our lead therapeutic, CM-YPD1, has been validated in vitro and in vivo to have strong efficacy, stability, and safety and acts within minutes. Our multidisciplinary team brings together a unique combination of expertise and technology that will permit the development of a drug that can be used to treat a broad array of MDR bacterial infections.

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    R43
  • Administering IC
    AI
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    298691
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    855
  • Ed Inst. Type
  • Funding ICs
    NIAID:298691\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    CELDARA MEDICAL, LLC
  • Organization Department
  • Organization DUNS
    828763263
  • Organization City
    LEBANON
  • Organization State
    NH
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    037661441
  • Organization District
    UNITED STATES