In vitro activity of meropenem-vaborbactam combinations and eravacycline against carbapenem-resistant Acinetobacter...

Treatment of carbapenem-resistant Acinetobacter baumannii (CRAB) presents a growing clinical challenge. This study evaluated the in vitro efficacy of eravacycline and the potential synergistic activity of meropenem-vaborbactam in combination with either gentamicin or ceftazidime against carbapenemase-producing Acinetobacter baumannii isolates. A total of 25 CRAB isolates were collected from different clinical samples. Antimicrobial susceptibility was determined via disc diffusion. Meropenem was tested by both disc diffusion and gradient strips. Polymerase chain reaction (PCR) was used to screen these isolates for the carbapenemase genes bla_OXA-51, bla_OXA-23, bla_IMP, bla_VIM, bla_OXA-48, bla_NDM and bla_KPC. Extensively drug-resistant (XDR) CRAB isolates were selected for evaluating colistin, eravacycline and the in vitro synergy of antimicrobial combinations via gradient strips for meropenem-vaborbactam, gentamicin, and ceftazidime. All CRAB isolates were sensitive to tigecycline and were either multidrug resistant or XDR. The minimum inhibitory concentrations (MIC50s and MIC90s) of meropenem were 32 μg/mL and 256 μg/mL, respectively. Among these genes, bla_OXA-23 was the most prevalent gene. The MIC₅₀ and MIC₉₀ of colistin were 1 and 2 μg/mL, respectively. The MIC₅₀ and MIC₉₀ of eravacycline were 0.125 μg/mL and 0.5 μg/mL, respectively. Meropenem-vaborbactam in combination with ceftazidime or gentamicin showed synergy in 45.5% and 36.4% of the XDR isolates and additivity/indifference in 54.5% and 63.6% of them, respectively, with no antagonism. Our findings suggest that eravacycline, as well as combination therapies involving meropenem-vaborbactam with either gentamicin or ceftazidime, may offer promising therapeutic potential for CRAB infections pending further clinical evaluation. These agents demonstrated notable in vitro activity, including potential synergistic effects, particularly against isolates harboring carbapenemase enzymes.