SBIR/STTR Research Award

Development of a Genotype-linked Antibiotic Resistance Platform for Real Time Pathogen Risk Classification and Epidemiology

Award identifier eef6ac67a3484bb16086c0d38f142d9ed49a62841cdd87f2b87f894be666c1faAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$219,655

Program and phase

STTR · Phase I

Award year

2016

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
MAVERIX BIOMICS, INC.
Proposal award date
2016-08-01
Contract end date
2017-07-31
UEI
Not reported
Solicitation number
PA15-270
Topic code
NIAID

Research abstract

Project Summary Antibiotic resistance has become a pressing public health concern due to the rise of pathogenic bacterial strains with mutations that reduce or eliminate the effectiveness of drugs to treat infections Beta lactamases produced by some bacteria provide resistance by degrading beta lactams one of most widely used class of antibiotics Originally restricted to penicillins mutant beta lactamases that confer resistance to antibiotics including monobactams and most cephalosporins known as extended spectrum beta lactamases or ESBLs are widespread Clinical isolates are currently characterized for ESBL resistance using inhibition zone tests against a panel of lactam antibiotics but the results produced by these tests are difficult to standardize and do not translate consistently into clinical practice In addition these tests typically produce no information about the genetic basis for the observed resistance nor the relatedness to other potentially characterized strains Here we propose the development of a sequence based analysis platform and knowledgebase for analyzing molecular signatures of extended spectrum beta lactamase resistance that can initially market to health institutions and companies monitoring the spread of EBSL resistance The platform will consist of an analysis kit that extracts positively selected variants beta lactamase sequences and other genomic information relevant to the ESBL phenotype from whole genome sequences of clinical samples A total of samples will be analyzed of which ESBL resistant samples provided by the Mercy Center at UC Merced will be newly sequenced and the rest will be obtained from a published study from the University of Washington A cloud based searchable database with interactive visualization will be served as the repository of the ESBL resistant features identified in the clinical samples By leveraging the metadata exchange standards being developed for broad sharing of human genomic data the rapidly expanding Global Alliance for Genomics and Health application program interface our work will represent the initial extension of this API for sharing microbial centric data The ultimate goal of this project is to create an accurate predictive resistance classifier using beta lactamase gene sequences and other genomic markers that are linked to known treatment outcomes and strain phenotypes We will develop this new classifier based on published methods found to be effective with HIV genotype phenotype prediction ESBL resistant features obtained from the clinical samples in this study will be used for training and testing of the classifier The powerful combination of sharable database and analytic tools in a single platform will significantly advance knowledge of antibiotic resistant bacteria facilitate epidemiological monitoring of the spread of ESBL resistance and represents a key first step to develop a diagnostic tool to counter ESBL resistance using whole genome sequences !Project Narrative Infectious diseases caused by antibiotic resistant bacteria are difficult to treat and represent a serious threat to human health world wide This project will develop a platform of pathogen search tools with simple interfaces for clinical researchers to rapidly match and analyze molecular signatures of extended spectrum beta lactamase resistance Broad application of this cloud based database and search technology should significantly advance knowledge of antibiotic resistant bacteria enable more effective targeted treatment and limit future outbreaks by establishing real time pathogen signature data sharing

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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