| Literature DB >> 27001539 |
Martine Deplanche1,2, Ludmila Alekseeva1,2,3, Ksenia Semenovskaya1,2, Chih-Lung Fu4, Frederic Dessauge5, Laurence Finot5, Wolfram Petzl6, Holm Zerbe6, Yves Le Loir1,2, Pascal Rainard7,8, David G E Smith9, Pierre Germon7,8, Michael Otto4, Nadia Berkova10,2.
Abstract
The role of the recently described interleukin-32 (IL-32) in Staphylococcus aureus-induced mastitis, an inflammation of the mammary gland, is unclear. We determined expression of IL-32, IL-6, and IL-8 in S. aureus- and Escherichia coli-infected bovine mammary gland epithelial cells. Using live bacteria, we found that in S. aureus-infected cells, induction of IL-6 and IL-8 expression was less pronounced than in E. coli-infected cells. Notably, IL-32 expression was decreased in S. aureus-infected cells, while it was increased in E. coli-infected cells. We identified the staphylococcal phenol-soluble modulin (PSM) peptides as key contributors to these effects, as IL-32, IL-6, and IL-8 expression by epithelial cells exposed to psm mutant strains was significantly increased compared to that in cells exposed to the isogenic S. aureus wild-type strain, indicating that PSMs inhibit the production of these interleukins. The use of genetically complemented strains confirmed this observation. Inasmuch as the decreased expression of IL-32, which is involved in dendritic cell maturation, impairs immune responses, our results support a PSM-dependent mechanism that allows for the development of chronic S. aureus-related mastitis.Entities:
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Year: 2016 PMID: 27001539 PMCID: PMC4907149 DOI: 10.1128/IAI.01330-15
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441