Related Experiment Video
Updated: Jun 11, 2025

Quantifying the Cytotoxicity of Staphylococcus aureus Against Human Polymorphonuclear Leukocytes
Published on: January 3, 2020
The Relative Importance of Cytotoxins Produced by Methicillin-Resistant Staphylococcus aureus Strain USA300 for
Tyler K Nygaard1, Timothy R Borgogna1, Kyler B Pallister1
1Department of Microbiology Cell Biology, Montana State University, Bozeman, MT 59718, USA.
Abstract:
Staphylococcus aureus (S. aureus) is a prominent Gram-positive bacterial pathogen that expresses numerous cytotoxins known to target human polymorphonuclear leukocytes (PMNs or neutrophils). These include leukocidin G/H (LukGH, also known as LukAB), the Panton-Valentine leukocidin (PVL), γ-hemolysin A/B (HlgAB), γ-hemolysin B/C (HlgBC), leukocidin E/D (LukED), α-hemolysin (Hla), and the phenol-soluble modulin-α peptides (PSMα). However, the relative contribution of each of these cytotoxins in causing human PMN lysis is not clear. In this study, we used a library of cytotoxin deletion mutants in the clinically relevant methicillin-resistant S. aureus (MRSA) isolate LAC (strain ST8:USA300) to determine the relative importance of each for causing human PMN lysis upon exposure to extracellular components as well as following phagocytosis. Using flow cytometry to examine plasma membrane permeability and assays quantifying lactose dehydrogenase release, we found that PVL was the dominant extracellular factor causing human PMN lysis produced by USA300. In contrast, LukGH was the most important cytotoxin causing human PMN lysis immediately following phagocytosis with contributions from the other bicomponent leukocidins only observed at later time points. These results not only clarify the relative importance of different USA300 cytotoxins for causing human PMN destruction but also demonstrate how two apparently redundant virulence factors play distinctive roles in promoting S. aureus pathogenesis.
Insights
Staphylococcus aureus cytotoxins have distinct roles in human neutrophil destruction. Panton-Valentine leukocidin (PVL) is key extracellularly, while leukocidin G/H (LukGH) is critical post-phagocytosis.
Area of Science:
- Microbiology
- Immunology
- Pathogenesis
Background:
- Staphylococcus aureus produces multiple cytotoxins targeting human neutrophils (PMNs).
- The specific roles of these cytotoxins in PMN lysis are not fully understood.
- Methicillin-resistant S. aureus (MRSA) USA300 is a significant human pathogen.
Purpose of the Study:
- To determine the relative contribution of S. aureus cytotoxins in human PMN lysis.
- To differentiate cytotoxin roles in extracellular versus intracellular contexts.
- To elucidate the distinct functions of virulence factors in S. aureus pathogenesis.
Main Methods:
- Utilized a library of S. aureus cytotoxin deletion mutants (MRSA strain USA300).
- Assessed human PMN lysis using flow cytometry for plasma membrane permeability.
- Quantified lactate dehydrogenase (LDH) release to measure cell damage.
Main Results:
- Panton-Valentine leukocidin (PVL) was the primary extracellular factor causing PMN lysis.
- Leukocidin G/H (LukGH) was the most important cytotoxin immediately after phagocytosis.
- Other bicomponent leukocidins contributed to PMN lysis at later time points.
Conclusions:
- PVL and LukGH have distinct, non-redundant roles in S. aureus-mediated PMN destruction.
- Understanding these specific roles clarifies S. aureus pathogenesis mechanisms.
- This study highlights the differential impact of cytotoxins during host-pathogen interaction.
Related Concept Videos
Defense Against Bacterial Pathogens
Phagocytes
Phagocytes are the frontline soldiers of the immune system. They include neutrophils and macrophages. Neutrophils are the most abundant type of white blood cell and are quickly mobilized to the site of infection. Macrophages are larger cells that patrol...
Antimicrobial Proteins
Interferons
Interferons (IFNs) are proteins produced by lymphocytes, macrophages, and fibroblasts infected with viruses. While IFNs cannot prevent viruses from entering and...

