A Murine Skin Wound Infection Model to Study the Immune Response against a Bacterial Pathogen

0 weergaven • 4:00 min. • July 8th, 2025

Take an anesthetized mouse engineered to express a fluorescent protein in neutrophils. Shave the dorsum and create a circular cut. Excise the cut skin to reveal the fascia — a connective tissue layer underneath.

Take a syringe containing a suspension of Staphylococcus aureus — a pathogenic bacterium — genetically modified to produce bioluminescence. Inject the suspension between the fascia and the underlying tissue generating a localized wound infection.

The pattern recognition receptors on stromal cells in the fascia recognize the pathogen-associated molecular patterns on the bacteria. This binding induces the release of pro-inflammatory cytokines and chemoattractants — resulting in inflammation.

Chemoattractants recruit circulatory neutrophils at the infection site. Incoming neutrophils engulf the bacteria into a phagosome that fuses with cytoplasmic granules, causing antimicrobial peptide release.

NADPH oxidase — an enzyme complex — assembles on the phagosome membrane and produces reactive oxygen species or ROS. The antimicrobial peptides and ROS cause bacterial degradation.

As a counter-response, the bacteria secrete virulence factors that permeabilize the neutrophil membrane,

Bekijk het volledige transcript en krijg toegang tot duizenden wetenschappelijke video's

Inloggen

Meer video's verkennen

Staphylococcus aureus-infectie