Minimum inhibitory concentration of carbapenems and tigecycline against Salmonella spp.

Author:

Capoor Malini R.1,Nair Deepthi1,Posti Jitendra1,Singhal Smita2,Deb Monorama1,Aggarwal Pushpa1,Pillai Parukutty3

Affiliation:

1. Department of Microbiology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India

2. New Drug Discovery, Ranbaxy Research Laboratories, Gurgaon, India

3. Department of Microbiology, Majeedia Hospital, Hamdard University, New Delhi, India

Abstract

Antimicrobial resistance in Salmonella spp. is of grave concern, more so in quinolone-resistant and extended-spectrum β-lactamase (ESBL)-producing isolates that cause complicated infections. The MIC of azithromycin, ciprofloxacin, cefixime, cefepime, ceftriaxone, gatifloxacin, imipenem, levofloxacin, meropenem and ofloxacin (E-test strip) and tigecycline and faropenem (agar dilution) against 210 Salmonella spp. was determined. MIC90 (defined as the antimicrobial concentration that inhibited growth of 90 % of the strains) of the carbapenems (imipenem and meropenem) for Salmonella Typhi and Salmonella Paratyphi A was 0.064 μg ml−1. MIC90 of faropenem was 0.25 μg ml−1 for S. Typhi, S. Paratyphi A and Salmonella Typhimurium. The MIC90 of azithromycin for all Salmonella spp. ranged from 8 to 16 μg ml−1. Tigecycline showed an MIC90 of 2 μg ml−1 for S. Typhi, 1 μg ml−1 for S. Paratyphi A and 4 μg ml−1 for S. Typhimurium. We concluded that tigecycline and the carbapenems are likely to have roles in the final stage of treatment of quinolone-resistant and ESBL-producing multidrug-resistant salmonellae.

Publisher

Microbiology Society

Subject

Microbiology (medical),General Medicine,Microbiology

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