【金黄色葡萄球菌毒力调控机制的研究】。

Chikara Kaito
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引用次数: 1

摘要

金黄色葡萄球菌可引起多种人体疾病,包括皮肤感染、肺炎、食物中毒和脑膜炎。耐甲氧西林金黄色葡萄球菌(MRSA)对多种抗生素具有耐药性,导致严重的临床问题。在这篇综述中,我总结了我们的研究评估金黄色葡萄球菌的毒力和鉴定新的毒力调节剂。首先,利用家蚕作为金黄色葡萄球菌的感染模型,鉴定出新的金黄色葡萄球菌毒力因子。一些毒力因子与细菌细胞中的RNA相互作用,调控毒力因子的表达。其次,我们发现金黄色葡萄球菌细胞在软琼脂板上扩散并形成一个巨大的菌落。我们称这种现象为蜂群扩散。高毒力社区获得性MRSA比医院相关性MRSA表现出更高的菌落传播活性。菌落扩散的差异归因于医院相关MRSA携带的可移动遗传元件SCCmec中的特定基因。该基因转录产物抑制了金黄色葡萄球菌毒力基因的主调控因子的翻译,导致菌落扩散、外毒素产生和动物杀伤能力的衰减。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Studies on the regulatory mechanism of Staphylococcus aureus virulence].
Staphylococcus aureus causes various diseases against humans, including skin infection, pneumonia, food poisoning, and meningitis. Methicillin-resistant S. aureus (MRSA) is resistant to a broad range of antibiotics, causing serious clinical problems. In this review, I summarize our studies to evaluate S. aureus virulence and identify novel virulence regulators. First, we utilized silkworms as an infection model of S. aureus and identified novel virulence factors of S. aureus. Some of the virulence factors interact with RNA in bacterial cells and regulate the expression of virulence factors. Second, we found that S. aureus cells spread on soft agar plates and form a giant colony. We call this phenomenon colony-spreading. High virulence community-acquired MRSA exhibits higher colony-spreading activity than hospital-associated MRSA. The difference in colony spreading is attributed to a specific gene in the mobile genetic element SCCmec carried by hospital-associated MRSA. The gene transcription product inhibits translation of a master regulator against S. aureus virulence genes, resulting in the attenuation of colony-spreading, exotoxin production, and animal killing ability.
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