Flow Cytometry Analysis of Intracellular and Emergent Extracellular Listeria monocytogenes In Vitro

Published: September 29, 2023

Abstract

Source: Gayle, P. et al., Using a Bacterial Pathogen to Probe for Cellular and Organismic-level Host Responses. J. Vis. Exp. (2019)

In this video, we quantify intracellular and extracellular Listeria monocytogenes, an intracellular pathogenic bacteria, following their infection of cultured macrophages in vitro using flow cytometry.

Protocol

1. Sampling Processing and Analysis of Intracellular and Emergent Lm by Flow Cytometry (FCM)

  1. Prepare mouse macrophage-like cell line RAW 264.7 in DMEM tissue culture media supplemented with 10% fetal calf serum (henceforth referred to as DMEM/FCS) using a 125 mL flask and a tissue culture incubator maintained at 37 °C/5% CO2. Adjust cells to 1 x 106 cells/mL and add 1 mL (1 x 106 cells) to wells of a 6-well tissue culture dish.
  2. Prepare Listeria monocytogenes, Lm, bacterium inoculum and infect cells with the volume of inoculum corresponding to an MOI of 50 (5 x 107 CFU).
  3. At 1.5 hours post-infection (hpi), collect media from the first set of wells and place in a 1.5 mL microcentrifuge tube with 500 µL of 4% paraformaldehyde (PFA) and place on ice until all wells have been processed.
  4. To collect intracellular Lm, add 1 mL of ds H2O to the well and after 60 s, transfer the resulting water lysate to a 1.5 mL microcentrifuge tube with 500 µL of 4% PFA. Vortex vigorously for 10 seconds and place on ice until all wells have been processed.
  5. For remaining wells, remove media and replace with 1 mL of DMEM/FCS with 5 µg/mL gentamicin to kill extracellular Lm and promptly return cells to the incubator.
  6. After 30 min (2 hpi) remove media and replace with DMEM/FCS without gentamicin.
  7. After 2 and 4 h (4 and 6 hpi) take second and third time points by collecting media and lysates.
  8. Centrifuge tubes at 10,000 x g for 7 min. Remove supernatant without disturbing the pellet.
  9. Suspend each pellet in a staining cocktail of 50 µL of 4% PFA and 15 µL of phalloidin. Incubate tubes in the dark at 4 °C for 20 min.
  10. After incubation add 1 mL of FACS buffer to each tube and pipette up and down to mix.
  11. Spin tubes at 10,000 x g for 7 min. Remove supernatant without disturbing the pellet.
  12. Suspend each pellet in 400 µL of FACS buffer for immediate use, or 200 µL of FACS buffer and 200 µL of 4% PFA if storing for later analysis.
  13. Run samples on flow cytometry and analyze the collected data.

Disclosures

The authors have nothing to disclose.

Materials

BHI (Brain Heart Infusion) broth EMD Milipore 110493
Cell Strainer, 70 µm VWR 10199-656
Collagenase D Roche 11088858001
DMEM media Gibco 11965-092
FACS tubes BD Falcon 352054
FBS – Heat-Inactivated Sigma-Aldrich F4135-500ML
Hanks' Balanced Salt solution Sigma-Aldrich H6648-6X500ML
LB agar Grow Cells MS MBPE-4040
LIVE/DEAD Fixable Yellow Dead Cell Stain kit Life Technologies L349S9
Rhodamine Phalloidin Thermo Fischer R415
SP6800 Spectral Analyzer Sony
TPP Tissue Culture 48-Well Plates MIDSCI TP92048
TPP Tissue Culture 6-Well Plates MIDSCI TP92406

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Cite This Article
Flow Cytometry Analysis of Intracellular and Emergent Extracellular Listeria monocytogenes In Vitro. J. Vis. Exp. (Pending Publication), e21648, doi: (2023).

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