Aerosol Biology/Small Animal Models Core
Run by Dr. Mark Buller at St. Louis University, the Aerosol Biology/Small Animals
Core supports studies on respiratory routes of infection and/or therapy. The
respiratory tract is susceptible to infection by many organisms that could be
developed as bioweapons. Despite this vulnerability, there is little known about
the molecular pathogenesis of select agents following infection of the respiratory
tract. In particular, the innate and mucosal responses to such infections remain
to be defined. Current studies utilizing the Core focus on smallpox and pneumonic
plague, as these agents are the most widely studied Category A agents in Region
VII. However, the Core is prepared to develop other models to meet new regional
needs. The Core is not limited to studies on pathogens, but can aerosolize and
deliver therapeutics to the respiratory tract and has ongoing studies to test
instruments that can inactivate bioparticles in the air.
MU Innate Immunity Core Facility
Research Projects in the MRCE have a common theme to understand mechanisms of immune
responses to priority pathogens, and participating researchers from five institutions
collaborate to further this frontier. The MU RBL provides state of the art containment
design and engineering as well as centralized resources and education for infectious
disease research. Through the Innate Immunity Core (IIC) we create experimental
opportunities requiring access to live cell sorting and other immunological techniques
on infected samples. The IIC and the RBL are structured to permit flexibility and adaptation
to the changing frontier of infectious disease research. Thus, the IIC provides a unique
capability in region VII that creates opportunities for novel scientific achievements that
further the research mission of the MRCE.
Live Cell Microscopy Core
Directed by Haibing Teng at Washington University School of Medicine, the
MRCE Live Cell Microscopy Core provides investigators a variety of advanced
fluorescence microscopy technologies to study live BSL3 organisms. The
Nikon SFC (Swept Field Confocal) microscope features high
sensitivity/resolution EMCCD and laser technology for 6-D
(x,y,z-slice, time-lapse, multi-color and multi-point fluorescence)
data acquisition. The TILL wide-field microscope features high-speed
calcium and pH imaging. Both systems allow rapid and long term viewing
of processes in live cells. Applications include studies of pathogen-cell
interactions (localization, trafficking, ion concentration and dynamic
turnover). We offer consultation on experimental approaches for image
acquisition, processing and analysis. Equipped with basic apparatus
for cell culture, this facility combines the duo advantage of
state-of-the-art live-cell microscopy and BSL3 containment. For detailed information and to reserve a time,
click here.
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