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Gerard Cangelosi , Ph. D.

Affiliate Member
Seattle Biomedical Research Institute

Affiliate Associate Professor, Departments of Global Health & Epidemiology
University of Washington
Email: jerry.cangelosi@sbri.org

Diseases under study: tuberculosis (TB), MAC disease (M. avium complex)

Mission
The Cangelosi Lab focuses on reducing the transmission and acquisition of infectious diseases, through 1) better case finding made possible by biomarker discovery and improved diagnostic tools; 2) improved detection of pathogens in water, food and other environmental sources; and 3) better understanding of the epidemiology of infectious disease acquisition.

Research
We conduct translational research relevant to global health. Specific interests include:

1)      Improved biomarker discovery tools for infectious disease diagnosis. We are developing novel recombinant antibody-like “probes” to detect pathogen molecules in patient samples. In a new NIAID-funded project entitled “Accelerated Molecular Probe Pipeline”, these methods are being used to identify new biomarkers of infection by Entamoeba histolytica, a significant waterborne gastrointestinal pathogen. The project is an international collaboration with partners in the United States, Australia, and Bangladesh.  

2)      Tuberculosis diagnosis.  With funding from the Foundation for Innovative New Diagnostics (FIND), we are partnering with Response Biomedical, Inc. (Vancouver, Canada) to develop a new point-of-care diagnostic test to detect biomarkers of Mycobacterium tuberculosis in patient samples.

3)      Molecular epidemiology of mycobacterial infections. Pathogens in the genus Mycobacterium cause tuberculosis, leprosy, MAC disease (Mycobacterium avium complex), and other significant diseases. Molecular pathogen detection methods, initially developed for infectious disease diagnosis, are being utilized to better understand the host, pathogen, and environmental factors involved in the acquisition of mycobacterial disease.

4)      Molecular detection of pathogens in environmental and clinical samples. As a method for detecting microorganisms in samples, the polymerase chain reaction (PCR) is fast, sensitive, and specific. However, its widespread use is limited in part by its inability to distinguish viable pathogen cells from dead cells and free nucleic acid fragments. With funding from the US Environmental Protection Agency and other sources, we have shown that PCR tests for ribosomal RNA precursors (pre-rRNA) can overcome this problem. We are developing pre-rRNA tests for pathogen detection in environmental as well as clinical samples. Current targets include Aeromonas hydrophila, MAC, and Mycobacterium tuberculosis.

Collaborations
     *  Seattle-King County Department of Public Health
     *  EPA
     *  PATH
     *  University of Virginia
     *  University of Queensland, Australia
     *  International Centre for Diarrheal Disease Research, Bangladesh (ICDDR,B)
     *  Foundation for Innovative New Diagnostics (FIND)

The National Institutes of Health, US Environmental Protection Agency (EPA), and the Foundation for Innovative New Diagnostics (FIND) currently provide support for Dr. Cangelosi’s research.

 

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