Kelliher Jessica L, Radin Jana N, Grim Kyle P, Párraga Solórzano Paola K, Degnan Patrick H, Kehl-Fie Thomas E
Department of Microbiology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Departamento de Ciencias de la Vida, Universidad de las Fuerzas Armada ESPE, Sangolquí, Ecuador.
Infect Immun. 2017 Dec 19;86(1). doi: 10.1128/IAI.00631-17. Print 2018 Jan.
During infection, pathogens must obtain all inorganic nutrients, such as phosphate, from the host. Despite the essentiality of phosphate for all forms of life, how obtains this nutrient during infection is unknown. Differing from , the paradigm for bacterial phosphate acquisition, which has two inorganic phosphate (P) importers, genomic analysis suggested that possesses three distinct P transporters: PstSCAB, PitA, and NptA. While and are expressed in phosphate-replete media, expression of all three transporters is induced by phosphate limitation. The loss of a single transporter did not affect However, disruption of any two systems significantly reduced P accumulation and growth in divergent environments. These findings indicate that PstSCAB, PitA, and NptA have overlapping but nonredundant functions, thus expanding the environments in which can successfully obtain P Consistent with this idea, in a systemic mouse model of disease, loss of any one transporter did not decrease staphylococcal virulence. However, loss of NptA in conjunction with either PstSCAB or PitA significantly reduced the ability of to cause infection. These observations suggest that P acquisition via NptA is particularly important for the pathogenesis of While our analysis suggests that NptA homologs are widely distributed among bacteria, closely related less pathogenic staphylococcal species do not possess this importer. Altogether, these observations indicate that P uptake by differs from established models and that acquisition of a third transporter enhances the ability of the bacterium to cause infection.
在感染过程中,病原体必须从宿主获取所有无机营养物质,如磷酸盐。尽管磷酸盐对所有生命形式都至关重要,但在感染期间如何获取这种营养物质尚不清楚。与具有两个无机磷酸盐(P)转运体的细菌磷酸盐获取范例不同,基因组分析表明,[细菌名称]拥有三种不同的P转运体:PstSCAB、PitA和NptA。虽然PstSCAB和PitA在富含磷酸盐的培养基中表达,但所有三种转运体的表达都受磷酸盐限制诱导。单个转运体的缺失并不影响[细菌名称],然而,任何两个系统的破坏都会显著降低在不同环境中的磷积累和生长。这些发现表明,PstSCAB、PitA和NptA具有重叠但非冗余的功能,从而扩展了[细菌名称]能够成功获取磷的环境。与此观点一致,在系统性小鼠疾病模型中,任何一种转运体的缺失都不会降低葡萄球菌的毒力。然而,NptA与PstSCAB或PitA之一同时缺失会显著降低[细菌名称]引起感染的能力。这些观察结果表明,通过NptA获取磷对[细菌名称]的发病机制尤为重要。虽然我们的分析表明NptA同源物在细菌中广泛分布,但致病性较低的密切相关葡萄球菌物种不具有这种转运体。总之,这些观察结果表明,[细菌名称]的磷摄取不同于已建立的模型,并且获得第三种转运体增强了该细菌引起感染的能力。