AUTHOR=Sharma Swati , Banerjee Tuhina , Yadav Ghanshyam , Kumar Ashok 

TITLE=Susceptibility profile of blaOXA-23 and metallo-β-lactamases co-harbouring isolates of carbapenem resistant Acinetobacter baumannii (CRAB) against standard drugs and combinations

JOURNAL=Frontiers in Cellular and Infection Microbiology

VOLUME=12

YEAR=2023

URL=https://www.frontiersin.org/journals/cellular-and-infection-microbiology/articles/10.3389/fcimb.2022.1068840

DOI=10.3389/fcimb.2022.1068840

ISSN=2235-2988

ABSTRACT=<sec><title>Background</title><p>The rapid emergence of carbapenem resistant <italic>Acinetobacter baumannii</italic> (CRAB) has resulted in an alarming situation worldwide. Realizing the dearth of literature on susceptibility of CRAB in genetic context in the developing region, this study was performed to determine the susceptibility profile against standard drugs/combinations and the association of <italic>in-vitro</italic> drug synergy with the prevalent molecular determinants.</p></sec><sec><title>Methods and findings</title><p>A total of 356 clinical isolates of <italic>A. baumannii</italic> were studied. Confirmation of the isolates was done by amplifying <italic>recA</italic> and ITS region genes. Susceptibility against standard drugs was tested by Kirby Bauer disc diffusion. Minimum inhibitory concentration (MIC), MIC<sub>50</sub> and MIC<sub>90</sub> values against imipenem, meropenem, doripenem, ampicillin/sulbactam, minocycline, amikacin, polymyxin B, colistin and tigecycline was tested as per guidelines. Genes encoding enzymes classes A (<italic>bla</italic><sub>GES</sub>, <italic>bla</italic><sub>IMI/NMC-A</sub>, <italic>bla</italic><sub>SME</sub>, <italic>bla</italic><sub>KPC</sub>), B (<italic>bla</italic><sub>IMP</sub>, <italic>bla</italic><sub>VIM</sub>, <italic>bla</italic><sub>NDM</sub>) and D (<italic>bla</italic><sub>OXA-51,</sub><italic>bla</italic><sub>OXA-23</sub> and <italic>bla</italic><sub>OXA-58</sub>) were detected by multiplex polymerase chain reaction. Synergy against meropenem-sulbactam and meropenem-colistin combinations was done by checkerboard MIC method. Correlation of drug synergy and carbapenemase encoding genes was statistically analyzed.</p></sec><sec><title>Results</title><p>Of the total, resistance above 90% was noted against gentamicin, ciprofloxacin, levofloxacin, ceftazidime, cefepime, ceftriaxone, cotrimoxazole and piperacillin/tazobactam. By MIC, resistance rates from highest to lowest was seen against imipenem 89.04% (n=317), amikacin 80.33% (n=286), meropenem 79.49% (n=283), doripenem 77.80% (n=277), ampicillin/sulbactam 71.62% (n=255), tigecycline 55.61% (n=198), minocycline 14.04% (n=50), polymyxin B 10.11% (n=36), and colistin 2.52% (n=9). CRAB was 317 (89.04%), 81.46% (n=290) were multidrug resistant and 13.48% (n=48) were extensively drug resistant. All the CRAB isolates harboured <italic>bla</italic><sub>OXA-51</sub> gene (100%) and 94% (n=298) <italic>bla</italic><sub>OXA-23</sub> gene. The <italic>bla</italic><sub>IMP</sub> gene was most prevalent 70.03% (n=222) followed by <italic>bla</italic><sub>NDM,</sub> 59.62% (n=189). Majority (87.69%, 278) were co-producers of classes D and B carbapenemases, <italic>bla</italic><sub>OXA-23</sub> with <italic>bla</italic><sub>IMP</sub> and <italic>bla</italic><sub>NDM</sub> being the commonest. Synergy with meropenem-sulbactam and meropenem-colistin was 47% and 57% respectively. Reduced synergy (<italic>p</italic>= &lt;0.0001) was noted for those harbouring <italic>bla</italic><sub>OXA-51</sub>+bla<sub>OXA-23</sub>with <italic>bla</italic><sub>NDM</sub> gene alone or co-producers.</p></sec><sec><title>Conclusion</title><p>Presence of <italic>bla</italic><sub>NDM</sub> gene was a significant cause of synergy loss in meropenem-sulbactam and meropenem-colistin. In <italic>bla</italic><sub>NDM</sub> endemic regions, tigecycline, minocycline and polymyxins could be viable options against CRAB isolates with more than one carbapenemase encoding genes.</p></sec>