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Published on: January 3, 2020
Salicylic acid diminishes Staphylococcus aureus capsular polysaccharide type 5 expression
Lucía P Alvarez1, María S Barbagelata, Mariana Gordiola
1Departamento de Microbiología, Parasitología e Inmunología, Universidad de Buenos Aires, Paraguay C1121ABG Buenos Aires, Argentina.
Salicylic acid (SAL) treatment reduces Staphylococcus aureus capsular polysaccharide (CP) production, increasing bacterial invasion of host cells. This suggests SAL may impact S. aureus persistence and virulence.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Immunology
Background:
- Capsular polysaccharides (CP) of Staphylococcus aureus serotypes 5 and 8 are key virulence factors.
- Salicylic acid (SAL), an aspirin metabolite, is known to influence bacterial virulence factor expression.
Purpose of the Study:
- To investigate the effect of SAL on Staphylococcus aureus capsular polysaccharide production and epithelial cell invasion.
- To elucidate the molecular mechanisms underlying SAL's impact on S. aureus virulence.
Main Methods:
- Exposure of S. aureus strains (Reynolds and Newman) to SAL.
- Assessment of bacterial internalization into MAC-T epithelial cells.
- Analysis of cap5 promoter activity, mgrA and saeRS transcript levels via real-time PCR.
- Quantification of CP5 production.
Main Results:
- SAL pre-exposure significantly increased the internalization of encapsulated S. aureus strains into MAC-T cells.
- SAL treatment decreased cap5 promoter activity and CP5 production in S. aureus Newman.
- SAL exposure led to diminished mgrA transcription and upregulated saeRS transcription.
- Non-encapsulated S. aureus strains showed no significant change in internalization after SAL exposure.
Conclusions:
- Low concentrations of SAL reduce CP production in encapsulated S. aureus, unmasking adhesins and enhancing epithelial cell invasion.
- SAL-induced increased internalization of encapsulated S. aureus may contribute to bacterial persistence in hosts.
- SAL affects global regulators of CP expression (mgrA and saeRS), leading to reduced capsule production.
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