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Published on: July 21, 2023
Minimum inhibitory concentration of carbapenems and tigecycline against Salmonella spp
Malini R Capoor1, Deepthi Nair1, Jitendra Posti1
1Department of Microbiology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.
Abstract:
Antimicrobial resistance in Salmonella spp. is of grave concern, more so in quinolone-resistant and extended-spectrum beta-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. MIC(90) (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 microg ml(-1). MIC(90) of faropenem was 0.25 microg ml(-1) for S. Typhi, S. Paratyphi A and Salmonella Typhimurium. The MIC(90) of azithromycin for all Salmonella spp. ranged from 8 to 16 microg ml(-1). Tigecycline showed an MIC(90) of 2 microg ml(-1) for S. Typhi, 1 microg ml(-1) for S. Paratyphi A and 4 microg 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.
Insights
Antimicrobial resistance in Salmonella is a major concern. Tigecycline and carbapenems show promise for treating multidrug-resistant Salmonella infections, including quinolone-resistant and ESBL-producing strains.
Area of Science:
- Microbiology
- Infectious Diseases
- Antimicrobial Resistance
Background:
- Antimicrobial resistance in Salmonella spp. poses a significant threat, particularly in quinolone-resistant and extended-spectrum beta-lactamase (ESBL)-producing strains.
- These resistant strains can lead to complicated infections, necessitating the evaluation of alternative treatment options.
Purpose of the Study:
- To determine the in vitro susceptibility of Salmonella spp. to various antimicrobial agents.
- To evaluate the efficacy of tigecycline, carbapenems, and faropenem against multidrug-resistant Salmonella isolates.
Main Methods:
- Minimum Inhibitory Concentrations (MICs) were determined for 210 Salmonella spp. isolates using E-test strips and agar dilution methods.
- Antimicrobials tested included azithromycin, ciprofloxacin, cefixime, cefepime, ceftriaxone, gatifloxacin, imipenem, levofloxacin, meropenem, ofloxacin, tigecycline, and faropenem.
Main Results:
- Carbapenems (imipenem, meropenem) exhibited a low MIC(90) of 0.064 µg/mL against Salmonella Typhi and Salmonella Paratyphi A.
- Faropenem showed an MIC(90) of 0.25 µg/mL for S. Typhi, S. Paratyphi A, and Salmonella Typhimurium.
- Tigecycline demonstrated MIC(90) values of 2 µg/mL for S. Typhi, 1 µg/mL for S. Paratyphi A, and 4 µg/mL for S. Typhimurium.
Conclusions:
- Tigecycline and carbapenems are effective against quinolone-resistant and ESBL-producing multidrug-resistant Salmonella.
- These agents are considered valuable options for the final stages of treatment for complicated Salmonella infections.
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