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The Staphylococcus aureus Transcriptome during Cystic Fibrosis Lung Infection

机译:囊性纤维化肺部感染中的金黄色葡萄球菌转录组

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Laboratory models have been invaluable for the field of microbiology for over 100?years and have provided key insights into core aspects of bacterial physiology such as regulation and metabolism. However, it is important to identify the extent to which these models recapitulate bacterial physiology within a human infection environment. Here, we performed transcriptomics (RNA-seq), focusing on the physiology of the prominent pathogen Staphylococcus aureus in situ in human cystic fibrosis (CF) infection. Through principal-component and hierarchal clustering analyses, we found remarkable conservation in S. aureus gene expression in the CF lung despite differences in the patient clinic, clinical status, age, and therapeutic regimen. We used a machine learning approach to identify an S. aureus transcriptomic signature of 32 genes that can reliably distinguish between S. aureus transcriptomes in the CF lung and in vitro . The majority of these genes were involved in virulence and metabolism and were used to improve a common CF infection model. Collectively, these results advance our knowledge of S. aureus physiology during human CF lung infection and demonstrate how in vitro models can be improved to better capture bacterial physiology in infection.
机译:实验室模型在微生物学领域已具有100多年的宝贵价值,并为细菌生理学的核心方面(例如调节和代谢)提供了重要见解。但是,重要的是要确定这些模型在人类感染环境中概括细菌生理的程度。在这里,我们进行了转录组学(RNA-seq),重点研究了人类囊性纤维化(CF)感染中原位突出的病原体金黄色葡萄球菌的生理。通过主成分和层次聚类分析,尽管患者临床,临床状况,年龄和治疗方案存在差异,但我们发现CF肺中金黄色葡萄球菌基因表达具有显着的保守性。我们用机器学习方法鉴定了32个基因的金黄色葡萄球菌转录组签名,可以可靠地区分CF肺和体外的金黄色葡萄球菌转录组。这些基因中的大多数与毒力和代谢有关,并用于改善常见的CF感染模型。这些结果共同推动了我们对人CF肺部感染期间金黄色葡萄球菌生理学的了解,并证明了如何改进体外模型以更好地捕获感染中的细菌生理学。

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