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Staphylococcus aureus infection dynamics

机译:金黄色葡萄球菌感染动态

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摘要

Staphylococcus aureus is a human commensal that can also cause systemic infections. This transition requires evasion of the immune response and the ability to exploit different niches within the host. However, the disease mechanisms and the dominant immune mediators against infection are poorly understood. Previously it has been shown that the infecting S. aureus population goes through a population bottleneck, from which very few bacteria escape to establish the abscesses that are characteristic of many infections. Here we examine the host factors underlying the population bottleneck and subsequent clonal expansion in S. aureus infection models, to identify underpinning principles of infection. The bottleneck is a common feature between models and is independent of S. aureus strain. Interestingly, the high doses of S. aureus required for the widely used “survival” model results in a reduced population bottleneck, suggesting that host defences have been simply overloaded. This brings into question the applicability of the survival model. Depletion of immune mediators revealed key breakpoints and the dynamics of systemic infection. Loss of macrophages, including the liver Kupffer cells, led to increased sensitivity to infection as expected but also loss of the population bottleneck and the spread to other organs still occurred. Conversely, neutrophil depletion led to greater susceptibility to disease but with a concomitant maintenance of the bottleneck and lack of systemic spread. We also used a novel microscopy approach to examine abscess architecture and distribution within organs. From these observations we developed a conceptual model for S. aureus disease from initial infection to mature abscess. This work highlights the need to understand the complexities of the infectious process to be able to assign functions for host and bacterial components, and why S. aureus disease requires a seemingly high infectious dose and how interventions such as a vaccine may be more rationally developed.
机译:金黄色葡萄球菌是一种人类共鸣,也可能引起全身感染。这种转变需要规避免疫反应,并具有利用宿主内不同生态位的能力。但是,人们对这种疾病的发病机理和主要的免疫介导因子的感染知之甚少。以前已经表明,感染的金黄色葡萄球菌种群经历了种群瓶颈,极少细菌从中逃逸以建立许多感染所特有的脓肿。在这里,我们研究了金黄色葡萄球菌感染模型中人口瓶颈和随后克隆扩展的潜在宿主因素,以确定感染的基本原理。瓶颈是模型之间的共同特征,并且与金黄色葡萄球菌菌株无关。有趣的是,广泛使用的“生存”模型需要高剂量的金黄色葡萄球菌导致种群瓶颈减少,这表明宿主防御能力简直是超负荷的。这对生存模型的适用性提出了质疑。免疫介质的耗竭揭示了关键的断点和全身感染的动态。巨噬细胞(包括肝Kupffer细胞)的丢失导致对感染的敏感性如预期的那样增加,但种群瓶颈也消失了,并且仍然传播到其他器官。相反,嗜中性白细胞耗竭导致更易患疾病,但同时伴随着瓶颈的维持和缺乏系统性扩散。我们还使用了新颖的显微镜方法来检查脓肿的结构及其在器官内的分布。从这些观察结果,我们开发了从最初感染到成熟脓肿的金黄色葡萄球菌疾病的概念模型。这项工作强调需要了解感染过程的复杂性,以便能够为宿主和细菌成分分配功能,以及为什么金黄色葡萄球菌疾病需要看似高的感染剂量,以及如何更合理地开发疫苗等干预措施。

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