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Rapid Inactivation of Pathogens On Microscope Slides: A Platform for Improving Mass Spectrometry for Imaging of Samples from Infected Tissue

Rapid Inactivation of Pathogens On Microscope Slides: A Platform for Improving Mass Spectrometry for Imaging of Samples from Infected Tissue
Rapid Inactivation of Pathogens On Microscope Slides: A Platform for Improving Mass Spectrometry for Imaging of Samples from Infected Tissue

Category: Research Poster

Author(s): Yvette Cruz

Presenter(s): Yvette Cruz

Molecular imaging using mass spectrometry (MSI) enables identification of the changes in diseased versus neighboring cells within a tissue sample, including demonstrating delays in drug delivery to sites of need for effective treatment. Despite this, MSI for infectious disease research is hampered by the need to inactivate pathogens within tissue samples before analysis. Current inactivation techniques utilize a stepwise process of freezing excised tissues, inactivation via UV, X-ray, or gamma irradiation, then processing samples for MSI. This is a laborious and time-consuming process and is not efficient for studying dynamic cellular interactions during time of tissue harvest. We hypothesize that alternate inactivation strategies can be conducted “on-slide” reducing the delay from tissue sample collection to MSI and improving the capture of dynamic interactions. In this study, we used Mycobacterium bovis Bacillus Calmette-Guerin (BCG), an attenuated Mycobacterium that can be manipulated in standard laboratory conditions to test our hypothesis. We tested chemical and UV on-slide inactivated methods and found promising preliminary results using UV exposure on-slide. Our aim is to develop a protocol using BCG as our model organism, expand our protocols for use with virulent M. tuberculosis-infected tissue samples and eventually other high containment pathogens.