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© Giulia Manina, Institut Pasteur
Mycobacterium tuberculosis dual fluorescent reporter of metabolic activity. Green (active bacilli) and red fluorescence (quiescent bacilli) are merged, 100X magnification.
Scientific Fields
Diseases
Organisms
Applications
Technique
Starting Date
07
Sep 2015
Status
Ongoing
Members
3
Structures
4
Instituts
1

About

A deeper understanding of mycobacterial individuality entails looking at this phenomenon in the fluctuating host environment. Micro-fabrication of host-mimicking platforms (either cell- or tissue-based) by standard photolithography or 3D-printing techniques could allow us to visualize and perturb single-infection events in real-time, aiming to gather dynamic and mechanistic insights of the infection process ex vivo.

An ideal long-term goal is to explore bacterial individuality and tuberculosis complexity by “in vivo imaging” of mice infected with bioluminescent reporters. This technique could provide a broader view into the spatiotemporal dynamics of infection and into the role of different bacterial subpopulations within discrete host niches. Nonetheless, the current technological constraints, such as detection limit, cannot be overlooked.