Nutritional virulence of Francisella tularensis

One of the most fundamental aspects of infectious diseases is microbial acquisition of nutrients in vivo, which impacts virulence and antibiotic treatment. Therefore, it is not surprising that part of the innate host defense against microbial infection is to limit access of various invading pathogens to sources of host nutrients (Abu Kwaik and Bumann, 2013; Eisenreich et al., 2013). Despite this host nutritional restriction, there has been a long held presumption that the host cell cytosol is a rich haven of plentiful nutrients sufficient to power proliferation of various intracellular pathogens. However, recent studies on the two intravacuolar pathogens Anaplasma phagocytophilum (Niu et al., 2012), Legionella pneumophila (Price et al., 2011) and the cytosolic pathogen Francisella tularensis (Steele et al., 2013) have clearly shown that the levels of amino acids in the host cell cytosol are not sufficient to meet the tremendous demands for carbon, energy, and nitrogen to power the robust intracellular proliferation of these pathogens (Abu Kwaik and Bumann, 2013). Therefore, these intracellular pathogens have evolved with efficient strategies to boost the levels of host amino acids to meet their demands for high levels of carbon and energy sources (Abu Kwaik and Bumann, 2013). There is an emerging paradigm of specific microbial strategies that directly trigger the host cell to boost the cellular levels of essential microbial nutrients, and this paradigm has been designated as nutritional virulence strategies (Abu Kwaik and Bumann, 2013). This opinion article is focused on nutritional virulence of F. tularensis. Upon entry into mammalian and arthropod-derived cells, the vacuole harboring F. tularensis matures into an acidified late endosome-like phagosome followed by rapid bacterial egress into the cytosol within 30 min of bacterial entry (Akimana and Kwaik, 2011; Asare and Abu Kwaik, 2011). Amino acids are major sources of carbon and energy for F. tularensis but the levels of amino acids in the host cell cytosol are not sufficient to meet the pathogen metabolic needs for the robust intracellular proliferation. Although the mammalian cell cytosol is presumed to have plentiful levels of amino acids, the cells are auxotrophic for His, Lys, Met, Phe, Trp, Leu, Ile,Val, and Thr, while Cys is considered semi-essential and is the most limiting amino acid in mammals (Price et al., 2013). F. tularensis is auxotrophic for six amino acids that include His, placeLys, Met, Cys, Arg, and Tyr. Therefore, mammalian cells have limited capacity to provide 4 of the 6 amino acids essential for F. tularensis, and this synchronization in amino acid auxotrophy could have played a factor in nutritional and metabolic evolution as well as adaptation of F. tularensis to the intracellular environment of mammalian cells (Price et al., 2013). Similar to L. pneumophila, F. tularensis is auxotrophic for Cys and requires high levels of this amino acids, which is metabolized into pyruvate that feeds the TCA cycle as the major metabolic pathway for generation of energy and some amino acids. To boost the cellular levels of Cys in the host cell cytosol, F. tularensis exploits host glutathione (GSH), which is a non-ribosomal tri-peptide (L-γL-glutamyl-L-Cysteinyl-glycine) and is the most abundant source of Cys in the host cytosol (Alkhuder et al., 2009; Meibom and Charbit, 2010). The γ-glutamyl transpeptidase (Ggt) enzyme of F. tularensis cleaves GSH to liberate Cys (Alkhuder et al., 2009; Meibom and Charbit, 2010). The ggt mutant of F. tularensis exhibits a severe intracellular growth defect but is rescued upon supplementation of Cys (Alkhuder et al., 2009). In addition to requirements to boost cellular levels of Cys, F. tularensis signals the host cell to boost levels of all amino acids by triggering the host macroautophagy degradation machinery, which is required for optimal intracellular bacterial growth (Steele et al., 2013). Inhibition of the host macroautophagy diminishes intracellular growth of F. tularensis, but the defect is rescued upon supplementation of excess amino acids or pyruvate (Steele et al., 2013). The macroautophagy degradation pathway triggered by F. tularensis is non-canonical, since it is independent of the ATG5 autophagy pathway. Thus, in addition to degradation of the host GSH, an additional nutritional virulence strategy for F. tularensis is to trigger a major host degradation machinery to boost the cellular levels of amino acids, and both nutritional virulence strategies are required for intracellular proliferation and manifestation of tularemia. Availability of excess amino acids in the host cell cytosol is of no benefit to the pathogen if they are not imported by efficient bacterial transporters. The Francisella genome encodes numerous amino acids transporters and predicted secondary carriers that include the major facilitator superfamily (MFS), such as several putative orthologous of PhtA, which import threonine (Meibom and Charbit, 2010). A novel amino acid transporter, designated AnsP, belongs to the MFS secondary transporters has been recently characterized in F. tularensis (Gesbert et al., 2013). The AnsP MFS transporter imports Asn, which is a non-essential