Objectives
Principal Investigators
 . Gerard Cangelosi
 . Patrick Duffy
 . Jean Feagin
 . Michal Fried
 . Malcolm Gardner
 . Nancy Haigwood
 . Helen Horton
 . Stefan Kappe
 . Peter Myler
 . Marilyn Parsons
 . David Sherman
 . Arnold Smith
 . Joseph Smith
 . Don Sodora
 . Leonidas Stamatatos
 . Ken Stuart
 . Ruobing Wang
 . Theodore White
Senior Scientists
Staff Scientists
Collaborations
Core Technologies

   
 

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Gerard Cangelosi , Ph. D.

Associate Member, Seattle Biomedical Research Institute
Research Assistant Professor, Department of Pathobiology, University of Washington
Email: jerry.cangelosi@sbri.org

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

Mission
Dr. Cangelosi’s work focuses on targeted research, molecular epidemiology, and diagnostic technology brought to bear against tuberculosis and related diseases.

Research
Pathogens in the genus Mycobacterium cause tuberculosis (TB), leprosy, MAC disease (Mycobacterium avium complex), and other significant diseases. TB is among the most devastating public health problems worldwide. It exerts its harshest effects on children, the poor, and people who are underserved by modern medicine.

Serious infections by other mycobacteria, especially MAC, are acquired from environmental sources and are becoming more common in the U.S. and other countries. TB and its cousins are local as well as global problems, and immediate as well as long-term concerns. Accordingly, our program is a mixture of basic and applied research, with the goal of understanding and combating mycobacterial diseases.

Themes
     *  Genetics and genomics of multi-drug resistant MAC
     *  Molecular epidemiology of mycobacterial diseases
     *  Development of novel molecular diagnostic and epidemiological methods

Accomplishments
* Established tuberculosis and MAC DNA fingerprinting services to support disease control efforts in the Pacific Northwest. SBRI's service has been instrumental in the investigation and containmetn of TB outbreaks in Washington State.
* Identified a novel “switch” used by MAC to adapt to diverse environments. The switch affects virulence, drug resistance, and survival in the environment. Understanding the switch will help scientists understand how these important traits work. By connecting individual genes to clinically and epidemiologically important traits, SBRI researchers will identify ways to improve risk assessment and treatment of MAC infections.
* Developed a "pre-RNA"-based method for assessing the viability of bacterial pathogens detected in environmental samples by molecular methods. This method is being applied to contaminants of drinking water, including MAC and Aeromonas hydrophila.
* Collaborated with biotech companies to develop improved technologies for TB diagnosis and molecular epidemiology. These technologies are designed to be sensitive, specific, and low in cost, so that they can be used in resource-poor settings where TB is especially problematic.

Collaborations
     *  Seattle-King County Department of Public Health
     *  EPA
     *  PATH
     *  Montana State University
     *  Foundation for Innovative New Diagnostics (FIND)

The 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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