Röder Jennifer, Felgner Pascal, Hensel Michael
Abteilung Mikrobiologie, Universität Osnabrück, Osnabrück, Germany.
CellNanOs-Center of Cellular Nanoanalytics, Fachbereich Biologie/Chemie, Universität Osnabrück, Osnabrück, Germany.
Cell Microbiol. 2021 Oct;23(10):e13374. doi: 10.1111/cmi.13374. Epub 2021 Jul 12.
Salmonella enterica serovar Typhimurium (STM) is an invasive, facultative intracellular pathogen and acquisition of nutrients from host cells is essential for survival and proliferation of intracellular STM. The nutritional environment of intracellular STM is only partially understood. We deploy bacteria harbouring reporter plasmids to interrogate the environmental cues acting on intracellular STM, and flow cytometry allows analyses on level of single STM. Phosphorus is a macro-element for cellular life, and in STM inorganic phosphate (P ), homeostasis is mediated by the two-component regulatory system PhoBR, resulting in expression of the high affinity phosphate transporter pstSCAB-phoU. Using fluorescent protein reporters, we investigated P availability for intracellular STM at single-cell level over time. We observed that P concentration in the Salmonella-containing vacuole (SCV) is limiting and activates the promoter of pstSCAB-phoU encoding a high affinity phosphate uptake system. Correlation between reporter activation by STM in defined media and in host cells indicates P concentration less 10 μM within the SCV. STM proliferating within the SCV experience increasing P limitations. Activity of the Salmonella pathogenicity island 2 (SPI2)-encoded type III secretion system (T3SS) is crucial for efficient intracellular proliferation, and SPI2-T3SS-mediated endosomal remodelling also reliefs P limitation. STM that are released from SCV to enter the cytosol of epithelial cells did not indicate P limitations. Addition of P to culture media of infected cells partially relieved P limitations in the SCV, as did inhibition of intracellular proliferation. We conclude that availability of P is critical for intracellular lifestyle of STM, and P acquisition is maintained by multiple mechanisms. Our work demonstrates the use of bacterial pathogens as sensitive single-cell reporters for their environment in host cell or host organisms. TAKE AWAY: Salmonella strains were engineered to report their intracellular niche and the availability of inorganic phosphate (P ) on level of single intracellular bacteria Within the Salmonella-containing vacuole (SCV), P is limited and limitation increases with bacterial proliferation Salmonella located in host cell cytosol are not limited in P availability Remodelling of the host cell endosomal system mediated by T3SS-2 reliefs P limitation in the SCV.
肠炎沙门氏菌鼠伤寒血清型(STM)是一种侵袭性兼性细胞内病原体,从宿主细胞获取营养对于细胞内STM的存活和增殖至关重要。目前对细胞内STM的营养环境仅了解一部分。我们利用携带报告质粒的细菌来探究作用于细胞内STM的环境线索,流式细胞术可在单个STM水平上进行分析。磷是细胞生命的一种宏量元素,在STM中,无机磷酸盐(P)的稳态由双组分调节系统PhoBR介导,导致高亲和力磷酸盐转运体pstSCAB-phoU的表达。我们使用荧光蛋白报告基因,随时间在单细胞水平上研究细胞内STM的磷可用性。我们观察到含沙门氏菌液泡(SCV)中的磷浓度具有限制性,并激活了编码高亲和力磷酸盐摄取系统的pstSCAB-phoU的启动子。STM在限定培养基和宿主细胞中报告基因激活之间的相关性表明SCV内磷浓度低于10μM。在SCV内增殖的STM经历越来越严重的磷限制。沙门氏菌致病岛2(SPI2)编码的III型分泌系统(T3SS)的活性对于有效的细胞内增殖至关重要,并且SPI2-T3SS介导的内体重塑也缓解了磷限制。从SCV释放进入上皮细胞胞质溶胶的STM未显示出磷限制。向感染细胞的培养基中添加磷部分缓解了SCV中的磷限制,抑制细胞内增殖也有同样效果。我们得出结论,磷的可用性对于STM的细胞内生存方式至关重要,并且通过多种机制维持磷的获取。我们的工作证明了使用细菌病原体作为其在宿主细胞或宿主生物体内环境的敏感单细胞报告基因。要点:对沙门氏菌菌株进行工程改造,以在单个细胞内细菌水平上报告其细胞内生态位和无机磷酸盐(P)的可用性。在含沙门氏菌液泡(SCV)内,P是有限的,并且随着细菌增殖限制加剧。位于宿主细胞胞质溶胶中的沙门氏菌在磷可用性方面不受限制。由T3SS-2介导的宿主细胞内体系统重塑缓解了SCV中的磷限制。