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Acinetobacter baumannii: a universal threat to public health? (2008) International Journal of Antimicrobial Agents, 32 (2), pp. 106-119. Cited 144 times. doi: 10.1016/j.ijantimicag.2008.02.013 View at Publisher 35 Ramirez, M.S., Tolmasky, M.E. Aminoglycoside modifying enzymes (2010) Drug Resistance Updates, 13 (6), pp. 151-171. Cited 486 times. http://www.elsevier.com/locate/drup doi: 10.1016/j.drup.2010.08.003 View at Publisher 36 Lee, K., Yong, D., Jeong, S.H., Chong, Y. Multidrug-resistant Acinetobacter spp.: Increasingly problematic nosocomial pathogens (Open Access) (2011) Yonsei Medical Journal, 52 (6), pp. 879-891. Cited 86 times. http://www.eymj.org/Synapse/Data/PDFData/0069YMJ/ymj-52-879.pdf doi: 10.3349/ymj.2011.52.6.879 View at Publisher 37 von Dolinger de Brito, D., Oliveira, E.J., Steffen Abdallah, V.O., da Costa Darini, A.L., Gontijo Filho, P.P. An outbreak of Acinetobacter baumannii septicemia in a Neonatal Intensive Care Unit of a University Hospital in Brazil (2005) Brazilian Journal of Infectious Diseases, 9 (4), pp. 301-309. Cited 43 times. http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702005000400006&lng=en&nrm=iso&tlng=en18742858https://doi.org/10.2174/1874285802014010098https://t.ly/bYOxSCOPUSBackground: Acinetobacter baumannii is one of the most challenging multidrug-resistant (MDR) nosocomial pathogens worldwide. Aminoglycosides are used for the treatment of A. baumannii infections, however, resistance to aminoglycosides is currently emerging, limiting therapeutic choices. Objective: In this study, the prevalence of aminoglycoside resistance and plasmid-mediated mechanisms of aminoglycoside resistance were investigated in A. baumannii clinical isolates collected from ICU patients at a tertiary care hospital in Egypt. Methods: The automated Vitek 2 system was used to identify A. baumannii species and determination of the antimicrobial susceptibility pattern. The identification of A. baumannii was confirmed by the detection of the blaOXA-51-like gene intrinsic to this species. Minimum Inhibitory Concentration (MIC) of gentamicin was determined using E-test following the CLSI breakpoints. Isolates were screened for the prevalence and diversity of the plasmid-carried aminoglycoside-modifying enzymes encoding genes aacC1, aadA1, aadB and aphA6. For genetic diversity analysis, the ERIC-PCR method was performed. Results: All A. baumannii isolates were MDR with high resistance rates to tested antimicrobials. The resistance rate to gentamicin was 92.9% with elevated MICs (≥ 32 μg/mL). The gentamicin-resistant isolates harboured one or more of the studied genes with the prevalence of aphA6 (81%). ERIC-based genotyping revealed that there was no evidence of A. baumannii clonal dissemination among isolates. Conclusion: The study concluded that MDR A. baumannii isolates were highly resistant to gentamicin. The plasmid-carried aminoglycoside-modifying enzymes encoding genes were disseminated among isolates with the AphA6 gene, which was the most prevalent one. The acquisition of more than one aminoglycoside resistance gene was associated with an elevated MIC of gentamicin. Thus, regular surveillance studies of the emerging resistance to antimicrobials and strict measures to control the dissemination of resistance determinants genes are warranteden-USAcinetobacter baumanniiAminoglycoside-modifying enzymesMultidrug resistancePCRPlasmid-mediatedLC-MS/MSGentamicinDissemination of plasmid-mediated aminoglycoside-modifying enzymes among mdr acinetobacter baumannii isolates from a tertiary care Egyptian hospitalArticlehttps://doi.org/10.2174/1874285802014010098