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A Murine Skin Infection Model Capable of Differentiating the Dermatopathology of Community-Associated MRSA Strain USA300 from Other MRSA Strains

机译:一种小鼠皮肤感染模型可以区分社区相关的MRSA菌株USA300的皮肤病从其他MRSA菌株

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摘要

USA300 is a predominant and highly virulent community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) strain that is a leading cause of skin and soft tissue infections. We established a murine intradermal infection model capable of demonstrating dermatopathological differences between USA300 and other MRSA strains. In this model, USA300 induced dermonecrosis, uniformly presenting as extensive open lesions with a histologically documented profound inflammatory cell infiltrate extending below the subcutis. In contrast, USA400 and a colonizing control strain M92 caused only localized non-ulcerated skin infections associated with a mild focal inflammatory infiltrate. It was also determined that the dermonecrosis induced by USA300 was associated with significantly increased neutrophil recruitment, inhibition of an antibacterial response, and increased production of cytokines/chemokines associated with disease severity. These results suggest that induction of severe skin lesions by USA300 is related to over-activation of neutrophils, inhibition of host antibacterial responses, and selective alteration of host cytokine/chemokine profiles.
机译:USA300是一种主要和高毒性的群体相关的甲氧西林抗葡萄球菌(CA-MRSA)菌株,是皮肤和软组织感染的主要原因。我们建立了一种小鼠皮内感染模型,其能够在USA300和其他MRSA菌株之间证明皮肤病理论差异。在该模型中,USA300诱导皮塞骨,均匀地呈现为广泛的开裂病变,具有组织学上记录的深刻炎症细胞浸润,延伸下方。相比之下,USA400和殖民控制菌株M92仅引起与轻度局灶性炎症浸润相关的局部的非溃疡性皮肤感染。还确定USA300诱导的DermoNecrosy与显着增加的中性粒细胞募集,抑制抗菌反应的抑制,以及增加与疾病严重程度相关的细胞因子/趋化因子的产生。这些结果表明,USA300诱导严重的皮肤病变与中性粒细胞的过度激活有关,抑制宿主抗菌反应,以及宿主细胞因子/趋化因子谱的选择性改变。

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