<i>Francisella tularensis</i> Harvests Nutrients Derived via ATG5-Independent Autophagy to Support Intracellular Growth

<div><p><i>Francisella tularensis</i> is a highly virulent intracellular pathogen that invades and replicates within numerous host cell types including macrophages, hepatocytes and pneumocytes. By 24 hours post invasion, <i>F. tularensis</i> replicates up to 1000-fold in the cytoplasm of infected cells. To achieve such rapid intracellular proliferation, <i>F. tularensis</i> must scavenge large quantities of essential carbon and energy sources from the host cell while evading anti-microbial immune responses. We found that macroautophagy, a eukaryotic cell process that primarily degrades host cell proteins and organelles as well as intracellular pathogens, was induced in <i>F. tularensis</i> infected cells. <i>F. tularensis</i> not only survived macroautophagy, but optimal intracellular bacterial growth was found to require macroautophagy. Intracellular growth upon macroautophagy inhibition was rescued by supplying excess nonessential amino acids or pyruvate, demonstrating that autophagy derived nutrients provide carbon and energy sources that support <i>F. tularensis</i> proliferation. Furthermore, <i>F. tularensis</i> did not require canonical, ATG5-dependent autophagy pathway induction but instead induced an ATG5-independent autophagy pathway. ATG5-independent autophagy induction caused the degradation of cellular constituents resulting in the release of nutrients that the bacteria harvested to support bacterial replication. Canonical macroautophagy limits the growth of several different bacterial species. However, our data demonstrate that ATG5-independent macroautophagy may be beneficial to some cytoplasmic bacteria by supplying nutrients to support bacterial growth.</p>