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. 2012 May;56(5):2753-5.
doi: 10.1128/AAC.05985-11. Epub 2012 Feb 21.

No decrease in susceptibility to NVC-422 in multiple-passage studies with methicillin-resistant Staphylococcus aureus, S. aureus, Pseudomonas aeruginosa, and Escherichia coli

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No decrease in susceptibility to NVC-422 in multiple-passage studies with methicillin-resistant Staphylococcus aureus, S. aureus, Pseudomonas aeruginosa, and Escherichia coli

Louisa D'Lima et al. Antimicrob Agents Chemother. 2012 May.

Abstract

Twenty-five serial passages of Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus and 50 passages of methicillin-resistant Staphylococcus aureus resulted in no significant increase in NVC-422 MICs, while ciprofloxacin MICs increased 256-fold for E. coli and 32-fold for P. aeruginosa and S. aureus. Mupirocin, fusidic acid, and retapamulin MICs for MRSA increased 64-, 256-, and 16-fold, respectively. No cross-resistance to NVC-422 was observed with mupirocin-, fusidic acid-, and retapamulin-resistant strains.

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Figures

Fig 1
Fig 1
Changes in MICs of NVC-422, mupirocin, and fusidic acid for MRSA ATCC 33591 during 25 passages at 0.5 MIC (determined by the previous passage). Each line shows the result for one representative culture out of seven independent cultures passaged with each antibacterial compound.

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