SBIR-STTR Award

Development and validation of a sample-to-answer metagenomics workflow for comprehensive pathogen detection in central nervous system infections
Award last edited on: 2/16/2024

Sponsored Program
SBIR
Awarding Agency
NIH : NIAID
Total Award Amount
$1,928,809
Award Phase
2
Solicitation Topic Code
855
Principal Investigator
Stephane Gourguechon

Company Information

Arc Bio LLC

10 Canal Park Suite 201
Cambridge, MA 02141
   (617) 997-8268
   info@arcbio.com
   www.arcbio.com
Location: Multiple
Congr. District: 07
County: Middlesex

Phase I

Contract Number: 1R44AI167334-01
Start Date: 2/2/2022    Completed: 1/31/2024
Phase I year
2022
Phase I Amount
$997,735
This research will ultimately advance human health by improving the diagnosis and treatment of central nervous system infections including meningitis and encephalitis, where the causative pathogen is not identified in up to 50% of cases. These infections are associated with significant morbidity and mortality; therefore, rapid and accurate diagnosis is crucial for appropriate patient management and to improve outcomes. Unfortunately, due to the variety of organisms that can cause central nervous system infections, current standard of care diagnostic methods suffer from long turnaround times and high false negative rates. Metagenomic next- generation sequencing (mNGS) has emerged as a promising universal detection method for infectious disease, enabling the simultaneous identification and characterization of viral, bacterial, and fungal pathogens directly from the DNA/RNA present in clinical samples. However, despite the increasing adoption of molecular diagnostics in clinical microbiology labs, mNGS has not become widespread due to its cost, turnaround time, and the technical expertise required to produce and analyze the data. The product we are developing addresses all of these obstacles. Galileo ONE - CSF is a sample-to-answer platform that includes all of the reagents, controls, protocols, and software required to detect and report clinically relevant pathogens directly from a cerebrospinal fluid (CSF) sample in ~24 hours. This platform incorporates several proprietary technologies, including a library preparation module that reduces abundant human sequences and a quantitative bioinformatics pipeline that increases sensitivity for sequence variants. This all-in-one bundle allows labs to easily evaluate and adopt mNGS in their own laboratories without the need for extensive genomics or bioinformatics expertise. During our Phase I-equivalent work, we used contrived samples to assess the feasibility of using CSF as a sample type; the results show that we can generate high-quality libraries and detect a representative set of pathogens in CSF using our Galileo ONE workflow, which was initially validated on plasma. Therefore, we are ready to move into the development phase of the product development process. In Phase II, we will perform analytical and preliminary clinical validation of the Galileo ONE - CSF platform, complete development of CSF-specific kit controls, and perform beta testing on contrived and clinical samples with our collaborators. This product will be the first deployed mNGS platform validated for CSF, enabling us to take advantage of the growing market for NGS-based infectious disease diagnostics, which is expected to reach $2.1B by 2027. Galileo ONE - CSF will empower end users, who include researchers, reference laboratories, and pharma/biotech partners, to adopt metagenomics to address the current gap in tools for detecting central nervous system infections.

Public Health Relevance Statement:
NARRATIVE The underlying cause of central nervous system infections remains undiagnosed in up to 50% of cases due to standard of care diagnostics that are slow, insensitive, and focused on subsets of pathogens. The goal of this SBIR is to validate a user-friendly DNA sequencing-based platform that will detect all types of pathogens in a cerebrospinal fluid (CSF) sample with a single test.

Project Terms:
Academic Medical Centers; University Medical Centers; Adoption; Bacteria; Biological Assay; Assay; Bioassay; Biologic Assays; Biotechnology; Biotech; Central Nervous System Infections; CNS infection; Central Nervous System Infectious Disease; Central Nervous System Infectious Disorder; Cerebrospinal Fluid; cerebral spinal fluid; spinal fluid; Communicable Diseases; Infectious Disease Pathway; Infectious Diseases; Infectious Disorder; Diagnosis; Differential Diagnosis; DNA; Deoxyribonucleic Acid; Encephalitis; Brain Inflammation; fungus; Future; Goals; Health; Recording of previous events; History; Human; Modern Man; Infection; Laboratories; Lead; Pb element; heavy metal Pb; heavy metal lead; Libraries; Meningitis; Mission; Morbidity - disease rate; Morbidity; mortality; living system; Organism; Parasites; Patients; Physicians; Blood Plasma; Plasma Serum; Reticuloendothelial System, Serum, Plasma; Plasma; Reagent; Research; Investigators; Researchers; Research Personnel; Non-Polyadenylated RNA; RNA Gene Products; Ribonucleic Acid; RNA; Sales; Sensitivity and Specificity; Software; Computer software; Technology; Testing; Time; Universities; Virus; Work; Technical Expertise; technical skills; Businesses; Diagnostic tests; base; improved; Acute; Clinical; Phase; Variant; Variation; Contracting Opportunities; Contracts; tool; Diagnostic; Adopted; Diagnostic Method; Diagnostic Technique; Diagnostic Procedure; Hour; Protocol; Protocols documentation; American; Performance; rapid diagnosis; microbial; Reporting; Modeling; Sampling; Genomics; Manufacturer Name; Manufacturer; Bio-Informatics; Bioinformatics; Pharmaceutical Agent; Pharmaceuticals; Pharmacological Substance; Pharmacologic Substance; Clinical Microbiology; Address; Symptoms; Data; Detection; Small Business Innovation Research Grant; SBIR; Small Business Innovation Research; Validation; Preparation; Characteristics; Process; Development; developmental; Instruction; cost; Outcome; manufacturing process; pathogen; pathogenic bacteria; bacteria pathogen; bacterial pathogen; Microbe; metagenomic sequencing; metagenome sequencing; Pathogen detection; clinically relevant; clinical relevance; Metagenomics; Functional Metagenomics; user-friendly; commercial application; commercialization; standard of care; effective therapy; effective treatment; product development; next generation sequencing; NGS Method; NGS system; next gen sequencing; nextgen sequencing; targeted treatment; targeted drug therapy; targeted drug treatments; targeted therapeutic; targeted therapeutic agents; targeted therapy; accurate diagnosis; sequencing platform; improved outcome; molecular diagnostics; ineffective therapies; ineffective treatment; DNA sequencing; DNA seq; DNAseq; pathogenic fungus; fungal pathogen; fungi pathogen; pathogenic virus; viral pathogen; virus pathogen; bioinformatics pipeline; bio-informatics pipeline; detection method; detection procedure; detection technique; Prognosis; disease diagnostic

Phase II

Contract Number: 5R44AI167334-02
Start Date: 2/2/2022    Completed: 1/31/2024
Phase II year
2023
Phase II Amount
$931,074
This research will ultimately advance human health by improving the diagnosis and treatment of central nervous system infections including meningitis and encephalitis, where the causative pathogen is not identified in up to 50% of cases. These infections are associated with significant morbidity and mortality; therefore, rapid and accurate diagnosis is crucial for appropriate patient management and to improve outcomes. Unfortunately, due to the variety of organisms that can cause central nervous system infections, current standard of care diagnostic methods suffer from long turnaround times and high false negative rates. Metagenomic next- generation sequencing (mNGS) has emerged as a promising universal detection method for infectious disease, enabling the simultaneous identification and characterization of viral, bacterial, and fungal pathogens directly from the DNA/RNA present in clinical samples. However, despite the increasing adoption of molecular diagnostics in clinical microbiology labs, mNGS has not become widespread due to its cost, turnaround time, and the technical expertise required to produce and analyze the data. The product we are developing addresses all of these obstacles. Galileo ONE - CSF is a sample-to-answer platform that includes all of the reagents, controls, protocols, and software required to detect and report clinically relevant pathogens directly from a cerebrospinal fluid (CSF) sample in ~24 hours. This platform incorporates several proprietary technologies, including a library preparation module that reduces abundant human sequences and a quantitative bioinformatics pipeline that increases sensitivity for sequence variants. This all-in-one bundle allows labs to easily evaluate and adopt mNGS in their own laboratories without the need for extensive genomics or bioinformatics expertise. During our Phase I-equivalent work, we used contrived samples to assess the feasibility of using CSF as a sample type; the results show that we can generate high-quality libraries and detect a representative set of pathogens in CSF using our Galileo ONE workflow, which was initially validated on plasma. Therefore, we are ready to move into the development phase of the product development process. In Phase II, we will perform analytical and preliminary clinical validation of the Galileo ONE - CSF platform, complete development of CSF-specific kit controls, and perform beta testing on contrived and clinical samples with our collaborators. This product will be the first deployed mNGS platform validated for CSF, enabling us to take advantage of the growing market for NGS-based infectious disease diagnostics, which is expected to reach $2.1B by 2027. Galileo ONE - CSF will empower end users, who include researchers, reference laboratories, and pharma/biotech partners, to adopt metagenomics to address the current gap in tools for detecting central nervous system infections.

Public Health Relevance Statement:
NARRATIVE The underlying cause of central nervous system infections remains undiagnosed in up to 50% of cases due to standard of care diagnostics that are slow, insensitive, and focused on subsets of pathogens. The goal of this SBIR is to validate a user-friendly DNA sequencing-based platform that will detect all types of pathogens in a cerebrospinal fluid (CSF) sample with a single test.

Project Terms:
University Medical Centers; Academic Medical Centers; Acceleration; Adoption; Bacteria; Biological Assay; Assay; Bioassay; Biologic Assays; Biotechnology; Biotech; Central Nervous System Infections; CNS infection; Central Nervous System Infectious Disease; Central Nervous System Infectious Disorder; Cerebrospinal Fluid; cerebral spinal fluid; spinal fluid; Communicable Diseases; Infectious Disease Pathway; Infectious Diseases; Infectious Disorder; Diagnosis; Differential Diagnosis; DNA; Deoxyribonucleic Acid; Encephalitis; Brain Inflammation; fungus; Future; Goals; Health; Recording of previous events; History; histories; Human; Modern Man; Infection; Laboratories; Libraries; Marketing; Meningitis; Mission; Morbidity - disease rate; Morbidity; mortality; Organism; living system; Parasites; Patients; Physicians; Plasma; Blood Plasma; Plasma Serum; Reticuloendothelial System, Serum, Plasma; Reagent; Research; Research Personnel; Investigators; Researchers; RNA; Non-Polyadenylated RNA; RNA Gene Products; Ribonucleic Acid; Sales; Sensitivity and Specificity; Computer software; Software; Technology; Testing; Time; Universities; Virus; Work; Technical Expertise; technical skills; Businesses; Diagnostic tests; improved; Acute; Clinical; Phase; Variation; Variant; Contracts; Contracting Opportunities; tool; Diagnostic; Adopted; Diagnostic Procedure; Diagnostic Method; Diagnostic Technique; Hour; Protocols documentation; Protocol; American; Performance; rapid diagnosis; microbial; empowerment; Reporting; Modeling; Sampling; Genomics; Manufacturer; Bio-Informatics; Bioinformatics; Pharmaceutical Agent; Pharmaceuticals; Pharmacological Substance; pharmaceutical; Pharmacologic Substance; Clinical Microbiology; Address; Symptoms; Data; Detection; Small Business Innovation Research Grant; SBIR; Small Business Innovation Research; Validation; validations; Preparation; preparations; Characteristics; Process; Development; developmental; Instruction; cost; Outcome; manufacturing process; pathogen; bacteria pathogen; bacterial pathogen; pathogenic bacteria; Microbe; metagenome sequencing; metagenomic sequencing; Pathogen detection; clinical relevance; clinically relevant; Functional Metagenomics; Metagenomics; user-friendly; commercial application; commercialization; standard of care; effective treatment; effective therapy; product development; NGS Method; NGS system; next gen sequencing; nextgen sequencing; next generation sequencing; targeted drug therapy; targeted drug treatments; targeted therapeutic; targeted therapeutic agents; targeted therapy; targeted treatment; accurate diagnosis; sequencing platform; improved outcome; molecular diagnostics; ineffective treatment; ineffective therapies; DNA seq; DNAseq; DNA sequencing; fungal pathogen; fungi pathogen; pathogenic fungus; viral pathogen; virus pathogen; pathogenic virus; bio-informatics pipeline; bioinformatics pipeline; detection procedure; detection technique; detection method; Prognosis; disease diagnostic; commercial launch; commercial product launch