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金黄色葡萄球菌酚溶性调节素损害牛乳腺上皮细胞中白细胞介素的表达。

Staphylococcus aureus Phenol-Soluble Modulins Impair Interleukin Expression in Bovine Mammary Epithelial Cells.

作者信息

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

机构信息

INRA, UMR1253 STLO, Rennes, France.

Agrocampus Ouest, UMR1253 STLO, Rennes, France.

出版信息

Infect Immun. 2016 May 24;84(6):1682-1692. doi: 10.1128/IAI.01330-15. Print 2016 Jun.

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.

摘要

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。

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