Deplanche Martine, Alekseeva Ludmila, Semenovskaya Ksenia, Fu Chih-Lung, Dessauge Frederic, Finot Laurence, Petzl Wolfram, Zerbe Holm, Le Loir Yves, Rainard Pascal, Smith David G E, Germon Pierre, Otto Michael, Berkova Nadia
INRA, UMR1253 STLO, Rennes, France.
Agrocampus Ouest, UMR1253 STLO, Rennes, France.
Infect Immun. 2016 May 24;84(6):1682-1692. doi: 10.1128/IAI.01330-15. Print 2016 Jun.
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.
最近发现的白细胞介素-32(IL-32)在金黄色葡萄球菌引起的乳腺炎(一种乳腺炎症)中的作用尚不清楚。我们测定了IL-32、IL-6和IL-8在感染金黄色葡萄球菌和大肠杆菌的牛乳腺上皮细胞中的表达。使用活细菌,我们发现,在感染金黄色葡萄球菌的细胞中,IL-6和IL-8表达的诱导不如在感染大肠杆菌的细胞中明显。值得注意的是,感染金黄色葡萄球菌的细胞中IL-32表达降低,而感染大肠杆菌的细胞中IL-32表达增加。我们确定葡萄球菌酚溶性调节素(PSM)肽是这些效应的关键促成因素,因为与暴露于同基因金黄色葡萄球菌野生型菌株的细胞相比,暴露于psm突变菌株的上皮细胞中IL-32、IL-6和IL-8的表达显著增加,这表明PSM抑制这些白细胞介素的产生。使用基因互补菌株证实了这一观察结果。鉴于参与树突状细胞成熟的IL-32表达降低会损害免疫反应,我们的结果支持一种PSM依赖性机制,该机制导致与金黄色葡萄球菌相关的慢性乳腺炎的发展。