Host nutrient milieu drives an essential role for aspartate biosynthesis during invasive <i>Staphylococcus aureus</i> infection.

Abstract

The bacterial pathogen <i>Staphylococcus aureus</i> is capable of infecting a broad spectrum of host tissues, in part due to flexibility of metabolic programs. <i>S. aureus</i>, like all organisms, requires essential biosynthetic intermediates to synthesize macromolecules. We therefore sought to determine the metabolic pathways contributing to synthesis of essential precursors during invasive <i>S. aureus</i> infection. We focused specifically on staphylococcal infection of bone, one of the most common sites of invasive <i>S. aureus</i> infection and a unique environment characterized by dynamic substrate accessibility, infection-induced hypoxia, and a metabolic profile skewed toward aerobic glycolysis. Using a murine model of osteomyelitis, we examined survival of <i>S. aureus</i> mutants deficient in central metabolic pathways, including glycolysis, gluconeogenesis, the tricarboxylic acid (TCA) cycle, and amino acid synthesis/catabolism. Despite the high glycolytic demand of skeletal cells, we discovered that <i>S. aureus</i> requires glycolysis for survival in bone. Furthermore, the TCA cycle is dispensable for survival during osteomyelitis, and <i>S. aureus</i> instead has a critical need for anaplerosis. Bacterial synthesis of aspartate in particular is absolutely essential for staphylococcal survival in bone, despite the presence of an aspartate transporter, which we identified as GltT and confirmed biochemically. This dependence on endogenous aspartate synthesis derives from the presence of excess glutamate in infected tissue, which inhibits aspartate acquisition by <i>S. aureus</i> Together, these data elucidate the metabolic pathways required for staphylococcal infection within bone and demonstrate that the host nutrient milieu can determine essentiality of bacterial nutrient biosynthesis pathways despite the presence of dedicated transporters.