Research Unit of Clinical Microbiology, University of Southern Denmark and Odense University Hospital, J.B. Winsløws Vej 21.2, 5000, Odense, Denmark.
Evaxion Biotech A/S, Copenhagen, Denmark.
Sci Rep. 2021 Mar 16;11(1):6037. doi: 10.1038/s41598-021-84050-x.
Staphylococcus aureus is the cause of serious vascular infections such as sepsis and endocarditis. These infections are notoriously difficult to treat, and it is believed that the ability of S. aureus to invade endothelial cells and persist intracellularly is a key mechanism for persistence despite ongoing antibiotic treatment. Here, we used dual RNA sequencing to study the simultaneous transcriptional response of S. aureus and human endothelial cells during in vitro infections. We revealed discrete and shared differentially expressed genes for both host and pathogen at the different stages of infection. While the endothelial cells upregulated genes involved in interferon signalling and antigen presentation during late infection, S. aureus downregulated toxin expression while upregulating genes related to iron scavenging. In conclusion, the presented data provide an important resource to facilitate functional investigations into host-pathogen interaction during S. aureus invasive infection and a basis for identifying novel drug target sites.
金黄色葡萄球菌是败血症和心内膜炎等严重血管感染的病原体。这些感染的治疗极具挑战性,人们认为金黄色葡萄球菌能够侵入内皮细胞并在细胞内持续存在,这是尽管持续使用抗生素治疗仍能持续存在的关键机制。在这里,我们使用双 RNA 测序来研究金黄色葡萄球菌和人内皮细胞在体外感染过程中的同时转录反应。我们揭示了在感染的不同阶段,宿主和病原体的离散和共享差异表达基因。虽然内皮细胞在晚期感染过程中上调了干扰素信号和抗原呈递相关基因,但金黄色葡萄球菌下调了毒素表达,同时上调了与铁摄取有关的基因。总之,所提供的数据为功能研究提供了重要资源金黄色葡萄球菌侵袭性感染过程中的宿主-病原体相互作用,并为确定新的药物靶位奠定了基础。