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首页> 外文期刊>Frontiers in Microbiology >Effect of Substance P in Staphylococcus aureus and Staphylococcus epidermidis Virulence: Implication for Skin Homeostasis
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Effect of Substance P in Staphylococcus aureus and Staphylococcus epidermidis Virulence: Implication for Skin Homeostasis

机译:P物质对金黄色葡萄球菌表皮葡萄球菌毒力的影响:对皮肤体内稳态的影响

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摘要

Staphylococcus aureus and Staphylococcus epidermidis are two major skin associated bacteria, and Substance P (SP) is a major skin neuropeptide. Since bacteria are known to sense and response to many human hormones, we investigated the effects of SP on Staphylococci virulence in reconstructed human epidermis model and HaCaT keratinocytes. We show that SP is stimulating the virulence of S. aureus and S. epidermidis in a reconstructed human epidermis model. qRT-PCR array analysis of 64 genes expressed by keratinocytes in the response to bacterial infection revealed a potential link between the action of SP on Staphylococci and skin physiopathology. qRT-PCR and direct assay of cathelicidin and human β-defensin 2 secretion also provided that demonstration that the action of SP on bacteria is independent of antimicrobial peptide expression by keratinocytes. Considering an effect of SP on S. aureus and S. epidermidis , we observed that SP increases the adhesion potential of both bacteria on keratinocytes. However, SP modulates the virulence of S. aureus and S. epidermidis through different mechanisms. The response of S. aureus is associated with an increase in Staphylococcal Enterotoxin C2 (SEC2) production and a reduction of exolipase processing whereas in S. epidermidis the effect of SP appears mediated by a rise in biofilm formation activity. The Thermo unstable ribosomal Elongation factor Ef-Tu was identified as the SP-interacting protein in S. aureus and S. epidermidis . SP appears as an inter-kingdom communication factor involved in the regulation of bacterial virulence and essential for skin microflora homeostasis.
机译:金黄色葡萄球菌和表皮葡萄球菌是两种主要的皮肤相关细菌,而P物质(SP)是主要的皮肤神经肽。由于已知细菌能够感应和响应许多人类激素,因此我们在重建的人类表皮模型和HaCaT角质形成细胞中研究了SP对葡萄球菌毒力的影响。我们显示,SP在重建的人类表皮模型中刺激金黄色葡萄球菌和表皮葡萄球菌的毒力。对细菌感染的反应中角质形成细胞表达的64个基因的qRT-PCR阵列分析揭示了SP对葡萄球菌的作用与皮肤生理病理之间的潜在联系。 qRT-PCR和直接测定cathelicidin和人β-defensin2的分泌还表明,SP对细菌的作用独立于角质形成细胞的抗菌肽表达。考虑到SP对金黄色葡萄球菌和表皮葡萄球菌的影响,我们观察到SP增加了两种细菌在角质形成细胞上的粘附潜能。但是,SP通过不同的机制调节金黄色葡萄球菌和表皮葡萄球菌的毒力。金黄色葡萄球菌的反应与葡萄球菌肠毒素C2(SEC2)产生的增加和外脂酶加工的减少有关,而在表皮葡萄球菌中,SP的作用似乎是由生物膜形成活性的增加介导的。热不稳定核糖体延伸因子Ef-Tu被鉴定为金黄色葡萄球菌和表皮葡萄球菌中的SP相互作用蛋白。 SP表现为参与细菌毒力调节的一个王国间交流因子,并且是皮肤微生物群落动态平衡所必需的。

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