SBIR-STTR Award

Enzymatic Therapies For Cystic Fibrosis Biofilms
Award last edited on: 10/7/11

Sponsored Program
SBIR
Awarding Agency
NIH : NIAID
Total Award Amount
$227,829
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Phillip Brumm

Company Information

C56 Technologies Inc (AKA: C5•6 Technologies~C5-6 Technologies Inc)

2905 Parmenter Street
Middleton, WI 53562
   (608) 836-3587
   dmead@c56technologies.com
   www.c56technologies.com
Location: Single
Congr. District: 02
County: Dane

Phase I

Contract Number: 1R43AI094728-01
Start Date: 3/1/11    Completed: 8/31/11
Phase I year
2011
Phase I Amount
$227,829
Improved therapy has transformed cystic fibrosis (CF) from a disease characterized by death in early childhood to a chronic illness with a median survival of approximately 30 years. However, there is still no cure for this devastating genetic disease affecting approximately 30,000 Americans and many questions about molecular pathogenesis, with important implications for therapy, remain to be answered. Approximately 80% of cystic fibrosis patients develop Pseudomonas aeruginosa infections of the lungs, which are a major cause of morbidity and mortality in this genetic disease. These chronic infections are resistant to antibiotic therapies. Recent studies suggest that the antibiotic resistance of P. aeruginosa in the CF lung is due to the formation of biofilms that are impervious to antibiotics. The P. aeruginosa biofilm is composed of bacterial cells surrounded by a three dimensional matrix of diverse substances, including polysaccharides, proteins, nucleic acids, and lipids;the major structural component appears to be polysaccharides produced by the P. aeruginosa cells. The proposed work will systematically test the ability of 80 polysaccharide-degrading enzymes to breakdown or weaken the P. aeruginosa biofilm. A sensitive test to determine the amount of polysaccharide degradation has been developed and those enzymes that actively degrade the biofilm will be combined to make a synergistic enzyme cocktail. The optimal enzyme mixture will then be tested in combination with Tobramycin to test the hypothesis that enzymatic degradation of the P. aeruginosa polysaccharide biofilm components will increase the sensitivity of P. aeruginosa to antibiotic treatment, resulting in improved outcomes for patients.

Public Health Relevance:
There is an unmet need for new therapies to extend the life and health of cystic fibrosis patients, a fatal disease affecting tens of thousands of Americans. Pseudomonas aeruginosa is the pathogen responsible for most CF patients succumbing to this genetic disease. The proposed development of enzymes that attack and degrade the antibiotic resistant biofilm formed by Pseudomonas aeruginosa has the potential to extend the quality and quantity of life, with important implications for numerous other diseases that are impacted by the formation of biofilms.

Thesaurus Terms:
Affect;American;Antibiotic Agents;Antibiotic Drugs;Antibiotic Resistance;Antibiotic Therapy;Antibiotic Treatment;Antibiotics;Area;Biological Models;Cf Patients;Carbohydrates;Catheters;Cells;Cessation Of Life;Chronic;Chronic Disease;Chronic Illness;Cloning;Complex;Culture Media;Cystic Fibrosis;D-Streptamine, O-3-Amino-3-Deoxy-Alpha-D-Glucopyranosyl-(1-6)-O-(2,6-Diamino-2,3,6-Trideoxy-Alpha-D-Ribo-Hexopyranosyl-(1-4))-2-Deoxy-;Death;Development;Development And Research;Disease;Disorder;Dose;Effectiveness;Enzymes;Family;Future;Generalized Growth;Genetic Condition;Genetic Diseases;Glycans;Goals;Growth;Health;Hereditary Disease;Human;Human, General;Hydrolysis;Implant;Infection;Life;Lipids;Lung;Man (Taxonomy);Man, Modern;Measures;Methods;Microbial Biofilms;Miscellaneous Antibiotic;Model System;Models, Biologic;Molecular;Molecular Disease;Morbidity;Morbidity - Disease Rate;Mortality;Mortality Vital Statistics;Mucoviscidosis;Nebramycin Factor 6;Nucleic Acids;Outcome;P. Aeruginosa;P.Aeruginosa;Pathogenesis;Patients;Phase;Polysaccharides;Predisposition;Production;Proteins;Pseudomonas Aeruginosa;Pseudomonas Pyocyanea;Qol;Quality Of Life;R &D;R&D;Regimen;Research;Residual;Residual State;Resistance To Antibiotics;Resistance, Antibiotic;Resistant To Antibiotics;Respiratory System, Lung;Sampling;Susceptibility;System;System, Loinc Axis 4;Technology;Testing;Therapeutic;Tissue Growth;Tobramycin;Tobrex;Work;Antibiotic Resistant;Biofilm;Chronic Disease /Disorder;Chronic Disease/Disorder;Chronic Disorder;Cystic Fibrosis Patients;Disease /Disorder;Disease/Disorder;Early Childhood;Experiment;Experimental Research;Experimental Study;Gene Product;Genetic Disorder;Growth Media;Hereditary Disorder;Improved;In Vitro Model;Meetings;Novel Therapeutic Intervention;Ontogeny;Pathogen;Patients With Cf;Patients With Cystic Fibrosis;Pulmonary;Research And Development;Research Study;Response;Sugar;Treatment Of Bacterial Diseases;Treatment Of Bacterial Infectious Disease

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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