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24The nucleotide second messenger c-di-AMP negatively regulates potassium and osmolyte 25 uptake in Staphylococcus aureus and many other bacteria. c-di-AMP is also important for 26 growth and an S. aureus strain deleted for the c-di-AMP cyclase gene dacA is unable to 27 survive in rich medium unless it acquires compensatory mutations. Previously, we have 28 shown that an S. aureus dacA mutant can grow after the acquisition of inactivating mutants 29 in opuD, encoding the main glycine-betaine osmolyte transporter, or mutations in alsT, 30 encoding a predicted amino acid transporter. Using the size of bacterial cells as a proxy for 31 their osmotic balance, we show that inactivation of OpuD helps bacteria to re-establish their 32 osmotic balance, while inactivation of AlsT does not and bacteria remain enlarged, a 33 characteristic of S. aureus cells unable to produce c-di-AMP. We show that AlsT is the main 34 glutamine transporter in S. aureus, thus revealing that S. aureus can survive without c-di-
35AMP when glutamine uptake is prevented. Using a bioinformatics approach combined with 36 uptake assays, we identified GltS as the main glutamate transporter in S. aureus. Using WT 37 and mutant strain, we show that glutamine is preferred over glutamate for bacterial growth 38 and that its uptake represses c-di-AMP production. Glutamine and glutamate are important 39 players in osmotic regulation, but their cellular levels also serve as a key indicator of 40 nitrogen availability in bacterial cells. Therefore, we not only provide a further connection 41 between the c-di-AMP signalling network and osmotic regulation in S. aureus but also to 42 central nitrogen metabolism.