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Updated: Oct 9, 2026

A Mouse Model to Assess Innate Immune Response to Staphylococcus aureus Infection
Published on: February 28, 2019
Association of coagulase and/or pigmentation with the virulence of a capsule-lacking Staphylococcus aureus in
1Botany and Microbiology Department, College of Science, King Saud University, Riyadh, Saudi Arabia.
Abstract:
The effect of pigmentation and coagulase on the virulence of a capsule-lacking Staphylococcus aureus were studied using iron-compromised mice. The presence of either coagulase or pigmentation maintained the viability of this bacterium in the peritoneal cavity. Both coagulase and pigmentation, however, lead not only to maintained viability, but also to its proliferation in the peritoneal macrophages. The iron was found to enhance the virulence of this bacterium, but iron enhancement was contingent on the presence of either pigmentation or coagulase or preferably both.
Insights
Pigmentation and coagulase enhance Staphylococcus aureus virulence, particularly in iron-rich environments. These factors are crucial for bacterial survival and proliferation within host macrophages, impacting infection severity.
Area of Science:
- Microbiology
- Immunology
- Bacterial Pathogenesis
Background:
- Staphylococcus aureus is a significant human pathogen.
- Virulence factors like coagulase and pigmentation influence bacterial survival and infection.
- Capsule-lacking strains present unique challenges in understanding pathogenesis.
Purpose of the Study:
- To investigate the role of coagulase and pigmentation in the virulence of capsule-lacking Staphylococcus aureus.
- To determine the impact of iron availability on bacterial virulence in the presence of these factors.
- To assess bacterial survival and proliferation within the peritoneal cavity and macrophages.
Main Methods:
- Utilized iron-compromised mouse models for infection studies.
- Monitored bacterial viability and proliferation in the peritoneal cavity.
- Examined bacterial interactions with peritoneal macrophages.
- Assessed the influence of coagulase and pigmentation under varying iron conditions.
Main Results:
- Coagulase and pigmentation independently maintained Staphylococcus aureus viability in the peritoneal cavity.
- Both factors promoted bacterial proliferation within peritoneal macrophages.
- Iron significantly enhanced bacterial virulence, but this effect was dependent on the presence of coagulase and/or pigmentation.
- The combined presence of coagulase and pigmentation offered the greatest enhancement of virulence and proliferation.
Conclusions:
- Coagulase and pigmentation are critical virulence determinants for capsule-lacking Staphylococcus aureus.
- These factors are essential for bacterial survival, proliferation, and iron-mediated virulence.
- Understanding these mechanisms is vital for developing targeted therapeutic strategies against Staphylococcus aureus infections.
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