Cytotoxicity Assay of <em>Staphylococcus aureus</em> Strains on Neutrophils following Phagocytosis
A subscription to JoVE is required to view this content.  Sign in or start your free trial.
Cytotoxicity Assay of Staphylococcus aureus Strains on Neutrophils following Phagocytosis

Cytotoxicity Assay of Staphylococcus aureus Strains on Neutrophils following Phagocytosis

Please note that all translations are automatically generated. Click here for the English version.

Transcript

Take virulent and less virulent Staphylococcus aureus strains.

Add serum to opsonize the bacteria.

Transfer increasing bacterial concentrations to chilled multi-well plate wells containing neutrophils. Low temperatures prevent neutrophil activation.

Centrifuge to facilitate synchronized phagocytosis.

Neutrophil receptors bind the opsonins, triggering bacterial internalization into phagosomes.

In virulent bacteria, the phagosomal environment triggers the expression of cytolytic toxins.

These toxins form pores, disrupting the phagosomes and compromising the neutrophil membrane integrity.

However, the less virulent bacteria exhibit reduced cytolytic toxin expression.

Post-incubation, detach the neutrophils and transfer them to flow cytometer tubes containing fluorescent propidium iodide (PI) dye.

The dye enters the neutrophils with compromised membranes and stains the DNA.

Using a flow cytometer, analyze the neutrophils for PI staining.

A concentration-dependent increase in the proportion of PI-positive neutrophils following phagocytosis of the virulent strain, as compared to the less virulent strain, indicates the cytotoxicity of the virulent strain against neutrophils.

Key Terms and Concepts

Scientific Background

Questions This Video Helps You Answer

Applications and Relevance

Related Videos

Read Article