- Title
- Paradoxical effect of 1-(1-naphthylmethyl)-piperazine on resistance to tetracyclines in multidrug-resistant Acinetobacter baumannii
- Creator
- Bean, David; Wareham, David
- Date
- 2009
- Type
- Text; Journal article
- Identifier
- http://researchonline.federation.edu.au/vital/access/HandleResolver/1959.17/74032
- Identifier
- vital:7155
- Identifier
-
https://doi.org/10.1093/jac/dkn493
- Identifier
- ISSN:0305-7453
- Abstract
- Objectives The efflux inhibitor 1-(1-naphthylmethyl)-piperazine (NMP) has been demonstrated to reverse multidrug resistance in Acinetobacter baumannii. We investigated the interaction of NMP with tigecycline and three other tetracyclines on clinical isolates of A. baumannii. Methods One hundred and four clinical isolates of Acinetobacter were tested for susceptibility to tigecycline, minocycline, doxycycline and tetracycline by disc diffusion, and tigecycline MICs were determined by Etest, both in the presence and absence of NMP. Tigecycline MICs and zones of inhibition were interpreted using the BSAC guidelines. An OXA carbapenemase multiplex PCR was also performed on each isolate. Results Mean zones of inhibition for tetracycline, doxycycline and minocycline increased by 11.3%, 22.9% and 11.2%, respectively, in the presence of NMP. In contrast, tigecycline susceptibility was decreased in the presence of NMP, with mean zones of inhibition decreasing by 8.4%. Based on PCR results, all but six isolates belonged to the OXA-23 clone 1. Conclusions Susceptibility to tigecycline of the A. baumannii OXA-23 clone 1 prevalent in the UK is reduced (∼2-fold) by the presence of the efflux inhibitor NMP. NMP does not have the same effect on susceptibility to other tetracyclines.; C1
- Relation
- Journal of Antimicrobial Chemotherapy Vol. 63, no. 2 (2009), p. 349-352
- Rights
- © British Society for Antimicrobial Chemotherapy
- Rights
- No open access
- Rights
- This metadata is freely available under a CCO license
- Subject
- Acinetobacter; Tigecycline; Efflux inhibitor; 1115 Pharmacology and Pharmaceutical Sciences; 0605 Microbiology; 1108 Medical Microbiology
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