A central role for aspartate in Mycobacterium tuberculosis physiology and virulence

The tuberculosis (TB) bacillus, Mycobacterium tuberculosis, is a facultative intracellular pathogen that multiplies inside macrophages, in which it resides within a specialized compartment, the phagosome, where nutrient sources are likely limited. A number of studies provided compelling evidence that M. tuberculosis has the ability to exploit host-derived carbon sources, such as triglycerides, cholesterol and glucose, and to proliferate inside host cells (Mckinney et al., 2000; Pandey and Sassetti, 2008; Daniel et al., 2011; Marrero et al., 2013). In addition to carbon, nitrogen is an essential constituent of all living organisms. As compared to carbon requirements, little is known about the nature of nitrogencontaining molecules utilized by the TB bacillus during infection. We recently discovered that nitrogen incorporation from exogenous aspartate is required for host colonization by M. tuberculosis (Gouzy et al., 2013). This study highlights, for the first time, the potential of amino acids, and aspartate in particular, as a major nitrogen reservoir supporting M. tuberculosis virulence in vivo. It also opens a series of questions to be addressed in the future. Chief among these questions is the origin and molecular mechanism(s) of transport allowing mycobacterial access to aspartate inside host cells. TB lesions are enriched in aspartate, and this likely relies on global metabolic changes in immune cells during granuloma formation (Somashekar et al., 2011). How nutrients, such as aspartate, access the M. tuberculosis phagosome during infection is an intriguing issue. Using mass spectrometry imaging, we further showed that aspartate can access the mycobacterial phagosome, at least in vitro (Gouzy et al., 2013). In mammalian cells, aspartate uptake relies on transporters of the solute carriers (SLC) superfamily, and in particular on those of the high-affinity glutamate and neutral amino acid (SLC1) and of the cationic amino acid (SLC7) transporter families. Among these transporters, SLC1A2 was reported to mediate aspartate transport inside macrophages (Rimaniol et al., 2001; Ye et al., 2010). Interestingly, we reported the expression of the slc1a2 gene is increased in human macrophages upon M. tuberculosis infection (Tailleux et al., 2008). Increased expression of this transporter could impact considerably the ability of M. tuberculosis to multiply inside macrophages, as it is the case for the neutral amino acid transporter SLC1A5 in the context of Francisella tularensis and Legionella pneumophila infection (Wieland et al., 2005; Barel et al., 2012). These studies suggested the transport of yet to be identified amino acid(s) is important to sustain intracellular multiplication of these two bacterial species. Whether SLC1A2 and/or other members of the SLC superfamily allow M. tuberculosis to access aspartate and multiply inside host cells remains to be evaluated. Another issue raised by our study is: how is nitrogen transferred from aspartate to other nitrogen-containing molecules in M. tuberculosis? Once acquired by the bacillus through its unique aspartate importer AnsP1, we showed this amino acid species mostly serves as a nitrogen provider and barely enters carbon metabolism through the Krebs cycle (Gouzy et al., 2013). Nitrogen assimilation from aspartate must rely on transamination steps allowing the transfer of aspartate-derived nitrogen to glutamate, which in turn, together with glutamine, provides nitrogen to most of biosynthesis pathways. In M. tuberculosis, two aspartate transaminases, called AspB and AspC, are predicted to mediate nitrogen transfer from aspartate to glutamate (Cole et al., 1998). Interestingly, the aspC gene is thought to be essential in M. tuberculosis (Sassetti et al., 2003), which may indicate that AspC is involved mostly in aspartate biosynthesis, rather than in aspartate catabolism and glutamate synthesis. Genetic inactivation of aspC may thus result in aspartate auxotrophy. The aspB gene, on the opposite, is not essential in vitro (Sassetti et al., 2003). Interestingly, aspB is expressed at higher level in bacteria withstanding conditions mimicking the intracellular environment (Fisher et al., 2002). AspB may thus be involved in aspartate-derived nitrogen assimilation during infection, and may be required