tedizolid. 19 20 21 22 Mycobacterium abscessus has emerged as a significant pathogen responsible for chronic 23 pulmonary infections in cystic fibrosis (CF) patients, which are difficult to treat due to 24 resistance to a broad range of antibiotics. The initial phase of the recommended treatment 25 in CF patients includes imipenem used without any β-lactamase inhibitor in spite of the 26 production of the β-lactamase Bla Mab . Here, we determine whether the addition of 27 tedizolid, a once-daily oxazolidinone, improves the activity of imipenem alone or in 28 combination with a β-lactamase inhibitor, avibactam, and rifabutin. 29 The activity of the drugs was evaluated against M. abscessus CIP104536 by determining in 30 vitro and intracellular antibacterial activities. The impact of Bla Mab inhibition by avibactam 31 on antibiotic activity was assessed by comparing CIP104536 and its β-lactamase-deficient 32 derivative (∆bla Mab ). 33 The minimal inhibitory concentrations (MICs) of tedizolid against M. abscessus CIP104536 34 and ∆bla Mab were 4 µg/mL. Tedizolid combined with imipenem showed a moderate 35 synergistic effect with fractional inhibitory concentration (FIC) indexes of 0.41 and 0.38 for 36 CIP104536 and ∆bla Mab , respectively. For both strains, the addition of tedizolid at 2 µg/mL, 37 corresponding to the peak serum concentration, increased the intracellular efficacy of 38 imipenem at 8 and 32 µg/mL. Addition of avibactam and rifabutin improved the activity of 39 the imipenem-tedizolid combination against CIP104536S. 40 The imipenem-tedizolid combination should be further considered for the treatment of M. 41 abscessus pulmonary infections in CF patients. The efficacy of the treatment might benefit 42 from the use of a β-lactamase inhibitor, such as avibactam, and the addition of rifabutin. 43 44 45 46