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Two Photon Intravital Microscopy of Lyme Borrelia in Mice
Alexia A Belperron1, Jialing Mao2, Linda K Bockenstedt2
1Department of Internal Medicine/Section of Rheumatology, Yale University School of Medicine, New Haven, CT, 06520, USA. alexia.belperron@yale.edu.
Abstract:
Two-photon intravital microscopy is a powerful tool that allows visualization of cells in intact tissues in a live animal in real time. In recent years, this advanced technology has been applied to understand pathogen-host interactions using fluorescently labeled bacteria. In particular, infectious fluorescent transformants of the Lyme disease spirochete Borrelia burgdorferi, an Ixodes tick-transmitted pathogen, have been imaged by two-photon intravital microscopy to study bacterial motility and interactions of the pathogen with feeding ticks and host tissues. Here, we describe the techniques and equipment used to image mammalian-adapted spirochetes in the skin of living mice in vivo and in joints ex vivo using two-photon intravital microscopy.