Department of Biological Sciences, Ohio Universitygrid.20627.31, Athens, Ohio, USA.
Department of Cell Biology, Microbiology, and Molecular Biology, University of South Floridagrid.170693.a, Tampa, Florida, USA.
mSphere. 2021 Oct 27;6(5):e0067621. doi: 10.1128/mSphere.00676-21. Epub 2021 Oct 6.
Staphylococcus aureus is a pathogenic bacterium but also a commensal of skin and anterior nares in humans. As S. aureus transits from skins/nares to inside the human body, it experiences changes in temperature. The production and content of S. aureus extracellular vesicles (EVs) have been increasingly studied over the past few years, and EVs are increasingly being recognized as important to the infectious process. Nonetheless, the impact of temperature variation on S. aureus EVs has not been studied in detail, as most reports that investigate EV cargoes and host cell interactions are performed using vesicles produced at 37°C. Here, we report that EVs in S. aureus differ in size and protein/RNA cargo depending on the growth temperature used. We demonstrate that the temperature-dependent regulation of vesicle production in S. aureus is mediated by the alpha phenol-soluble modulin peptides (αPSMs). Through proteomic analysis, we observed increased packaging of virulence factors at 40°C, whereas the EV proteome has greater diversity at 34°C. Similar to the protein content, we perform transcriptomic analysis and demonstrate that the RNA cargo also is impacted by temperature. Finally, we demonstrate greater αPSM- and alpha-toxin-mediated erythrocyte lysis with 40°C EVs, but 34°C EVs are more cytotoxic toward THP-1 cells. Together, our study demonstrates that small temperature variations have great impact on EV biogenesis and shape the interaction with host cells. Extracellular vesicles (EVs) are lipid bilayer spheres that contain proteins, nucleic acids, and lipids secreted by bacteria. They are involved in Staphylococcus aureus infections, as they package virulence factors and deliver their contents inside host cells. The impact of temperature variations experienced by S. aureus during the infectious process on EVs is unknown. Here, we demonstrate the importance of temperature in vesicle production and packaging. High temperatures promote packaging of virulence factors and increase the protein and lipid concentration but reduce the overall RNA abundance and protein diversity in EVs. The importance of temperature changes is highlighted by the fact that EVs produced at low temperature are more toxic toward macrophages, whereas EVs produced at high temperature display more hemolysis toward erythrocytes. Our research brings new insights into temperature-dependent vesiculation and interaction with the host during S. aureus transition from colonization to virulence.
金黄色葡萄球菌是一种病原菌,但也是人类皮肤和鼻腔前部的共生菌。当金黄色葡萄球菌从皮肤/鼻腔进入人体内部时,它会经历温度变化。近年来,人们越来越多地研究金黄色葡萄球菌细胞外囊泡(EVs)的产生和含量,并且越来越认识到 EVs 对感染过程很重要。尽管如此,温度变化对金黄色葡萄球菌 EVs 的影响尚未得到详细研究,因为大多数研究 EV 货物和宿主细胞相互作用的报告都是在 37°C 下使用产生的囊泡进行的。在这里,我们报告说,根据使用的生长温度,金黄色葡萄球菌中的 EV 在大小和蛋白质/RNA 货物方面存在差异。我们证明,金黄色葡萄球菌中囊泡产生的温度依赖性调节是由α酚可溶性调节蛋白肽(αPSM)介导的。通过蛋白质组学分析,我们观察到在 40°C 时毒力因子的包装增加,而在 34°C 时 EV 蛋白质组具有更大的多样性。与蛋白质含量相似,我们进行转录组分析并证明 RNA 货物也受到温度的影响。最后,我们证明用 40°C EV 进行αPSM 和α-毒素介导的红细胞裂解更多,但 34°C EV 对 THP-1 细胞的细胞毒性更大。总之,我们的研究表明,微小的温度变化对 EV 的生物发生有很大的影响,并塑造了与宿主细胞的相互作用。细胞外囊泡(EVs)是由细菌分泌的含有蛋白质、核酸和脂质的双层脂质球体。它们参与金黄色葡萄球菌感染,因为它们包装毒力因子并将其内容物递送到宿主细胞内。金黄色葡萄球菌在感染过程中经历的温度变化对 EVs 的影响尚不清楚。在这里,我们证明了温度在囊泡产生和包装中的重要性。高温促进毒力因子的包装,并增加 EV 中的蛋白质和脂质浓度,但降低 EV 中的总 RNA 丰度和蛋白质多样性。温度变化的重要性体现在这样一个事实上,即低温产生的 EV 对巨噬细胞的毒性更大,而高温产生的 EV 对红细胞的溶血作用更大。我们的研究为金黄色葡萄球菌从定植到毒力的转变过程中,温度依赖性囊泡形成和与宿主的相互作用带来了新的见解。