SBIR-STTR Award

Antigen Detection Assay for the Diagnosis of Melioidosis
Award last edited on: 4/22/19

Sponsored Program
STTR
Awarding Agency
NIH : NIAID
Total Award Amount
$2,594,137
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Raymond L Houghton

Company Information

InBios International Inc

562 First Avenue South Suite 600
Seattle, WA 98104
   (206) 344-5821
   info@inbios.com
   www.inbios.com

Research Institution

University of Nevada - Reno

Phase I

Contract Number: 1R41AI102482-01
Start Date: 6/15/12    Completed: 5/31/14
Phase I year
2012
Phase I Amount
$299,699
Burkholderia pseudomallei is a Gram-negative bacterium that is the causative agent of melioidosis. The bacterium causes significant morbidity and mortality in tropical regions and endemic areas are expanding. Melioidosis is difficult to trea and diagnose due to the fact that B. pseudomallei is resistant to common antibiotics and symptoms are non-specific. Mortality rates reach 45% and 20% in Thailand and Australia respectively, even with antibiotic treatment. Currently, there is no validated diagnostic product for the diagnosis of melioidosis. Culturing of patient samples is the"gold standard"for diagnosis, however this can take 3-5 days. Our goal is to develop a rapid point-of-care lateral flow immunoassay for the detection of the B. pseudomallei capsular antigen (CPS) directly from patient samples. Our previous studies have determined that the CPS is a shed antigen and a prototype LFI has yielded encouraging results. The goals of the project are to (i) produce a library of high affinity CPS specific mAbs (ii) optimize LFI construction, (iii) determine compatibe sample types and sample preparation and (iv) quantify CPS in patient samples. By completing these goals we hope to produce an optimized LFI that possesses sensitivity equal to or greater than culturing of patient samples. To achieve these goals we have established an experienced team. Dr. AuCoin's laboratory is already collaborating with InBios on development of a prototype LFI. In addition, both groups will work closely with experts in endemic areas (Thailand and Australia) who will be conducting evaluation of the LFI with different sample types.

Public Health Relevance:
Melioidosis is a rapidly progressing and frequently fatal disease if left untreated. Burkholderia pseudomallei is the causative agent of melioidosis, this soil dwelling bacterium has been listed as a Category B Select Agent. In the endemic areas (Thailand, Southeast Asia and northern parts of Australia), melioidosis is a public health concern. Rapid diagnosis of melioidosis is needed in order to properly administer effective treatment with antibiotics. At present, the diagnostic"gold standard"is culturing of patient samples, which takes 3-5 days and significantly delays administration of proper treatment. In this application, we offer to develop a point-of-care, cost-effective, and rapid diagnostic for melioidosis that can deliver results within minutes. Such rapid diagnostic test can assist in detecting and monitoring acute and chronic B. pseudomallei infections in the field both in endemic areas as well as following a bioterrorist attack.

Phase II

Contract Number: 5R41AI102482-02
Start Date: 6/15/12    Completed: 5/31/14
Phase II year
2013
(last award dollars: 2016)
Phase II Amount
$2,294,438

Burkholderia pseudomallei is a Gram-negative bacterium that is the causative agent of melioidosis. The bacterium causes significant morbidity and mortality in tropical regions and endemic areas are expanding. Melioidosis is difficult to trea and diagnose due to the fact that B. pseudomallei is resistant to common antibiotics and symptoms are non-specific. Mortality rates reach 45% and 20% in Thailand and Australia respectively, even with antibiotic treatment. Currently, there is no validated diagnostic product for the diagnosis of melioidosis. Culturing of patient samples is the "gold standard" for diagnosis, however this can take 3-5 days. Our goal is to develop a rapid point-of-care lateral flow immunoassay for the detection of the B. pseudomallei capsular antigen (CPS) directly from patient samples. Our previous studies have determined that the CPS is a shed antigen and a prototype LFI has yielded encouraging results. The goals of the project are to (i) produce a library of high affinity CPS specific mAbs (ii) optimize LFI construction, (iii) determine compatibe sample types and sample preparation and (iv) quantify CPS in patient samples. By completing these goals we hope to produce an optimized LFI that possesses sensitivity equal to or greater than culturing of patient samples. To achieve these goals we have established an experienced team. Dr. AuCoin's laboratory is already collaborating with InBios on development of a prototype LFI. In addition, both groups will work closely with experts in endemic areas (Thailand and Australia) who will be conducting evaluation of the LFI with different sample types.

Public Health Relevance Statement:
Melioidosis is a rapidly progressing and frequently fatal disease if left untreated. Burkholderia pseudomallei is the causative agent of melioidosis, this soil dwelling bacterium has been listed as a Category B Select Agent. In the endemic areas (Thailand, Southeast Asia and northern parts of Australia), melioidosis is a public health concern. Rapid diagnosis of melioidosis is needed in order to properly administer effective treatment with antibiotics. At present, the diagnostic "gold standard" is culturing of patient samples, which takes 3-5 days and significantly delays administration of proper treatment. In this application, we offer to develop a point-of-care, cost-effective, and rapid diagnostic for melioidosis that can deliver results within minutes. Such rapid diagnostic test can assist in detecting and monitoring acute and chronic B. pseudomallei infections in the field both in endemic areas as well as following a bioterrorist attack.

NIH Spending Category:
Biodefense; Emerging Infectious Diseases; Infectious Diseases

Project Terms:
Acute; Address; Affinity; Antibiotic Therapy; Antibiotics; Antibody Affinity; Antigens; Area; Attention; Australia; Bacteria; Bedside Testings; Biological Assay; Blood; Burkholderia pseudomallei; Categories; Centers for Disease Control and Prevention (U.S.); China; Chronic; Classification; cost; cost effective; Data; Detection; Development; Diagnosis; diagnosis standard; Diagnostic; Diagnostic Reagent; Diagnostic tests; Disease; effective therapy; Epitopes; Evaluation; experience; Future; Goals; Gold; Gram-Negative Bacteria; Health; Hemagglutination; Hong Kong; Human Resources; Immunoassay; improved; in vivo; Infection; Laboratories; Lateral; Left; Libraries; Melioidosis; microorganism antigen; Monitor; Monoclonal Antibodies; Morbidity - disease rate; Mortality Vital Statistics; novel; Patients; phase 1 study; phase 2 study; point of care; point-of-care diagnostics; Polysaccharides; preclinical study; Preparation; Production; prototype; public health medicine (field); Pus; rapid detection; rapid diagnosis; Research; Resistance; respiratory; Sampling; Schools; Serum; Soil; Southeastern Asia; success; Symptoms; Taiwan; Thailand; Uncertainty; Universities; Urine; Validation; Work