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Method Article

Fluorescence Imaging of Bacterial Colonization in Mouse Kidney Tissue

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March 31st, 2026

In This Article

Abstract

Source: Behera, R. K., et al. A Fluorescence-based Method to Study Bacterial Gene Regulation in Infected Tissues. J. Vis. Exp. (2019)

This video demonstrates a method for preparing infected mouse kidney tissue, staining DNA, and detecting bacterial gene expression using dual fluorescent reporters. Red marks all bacteria, and green highlights infection-responsive cells.

Protocol

All procedures involving animal samples have been reviewed and approved by the appropriate animal ethical review committee.

  1. Harvesting the organs and tissue processing
    1. Euthanize the animals by CO2 inhalation and cervical dislocation as a secondary method, and perform necropsy.
    2. Harvest the kidney (right) and other vital organs (heart, liver, lungs, spleen) and transfer into 15 mL polypropylene tubes containing 10% [v/v] buffered formalin.
    3. Allow the organs to fix in the dark at room temperature with gentle shaking or rotation for at least 24 hours but no more than 48 hours.
    4. Embed organs in a clear tissue freezing medium and store the tissues at -80 °C.
    5. Using a cryostat, section tissue into slices of 10 µm thickness.
    6. Dry the sections on a pre-cleaned, charged glass slide for 20 min in the dark. Apply a hard mounting medium with 4',6-diamidino-2-phenylindole (DAPI) stain and a coverslip. Cure mounted slides at room temperature overnight and transfer to 4 °C for long-term storage.
  2. Laser Scanning Confocal Microscopy and Image Processing
    1. Examine mounted slides to locate lesions using lasers appropriate for the fluorescent reporter being used. In this case, the green (GFP or green fluorescent protein), red (tdTomato), and blue (DAPI) fluorescence signals are used.
    2. Acquire the image using the appropriate objective for visualizing individual cells (e.g., typically 20x or 40x objectives are used).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
C57Bl/6 MiceCharles RiverNA 
Confocal laser scanning microscopeZeissNA 
Cryostat microtomeThermo ScientificNA 
Phosphate buffered saline (PBS)Cellgrow46-013-CM 
Precellys 24 homogenizerBertin LaboratoriesNA 
Sub Xero clear tissue freezing mediumMercedes MedicalMER5000 
Superfrost Plus microscope slidesFisher Scientific12-550-15 
Vectashield Antifade Mounting medium with DAPIVector LaboratoriesH-1500 

Tags

Tissue SectioningNuclear StainingConfocal MicroscopyFluorescent ReportersGene Expression DetectionHost Pathogen InteractionCryostat Sectioning