Trends in antimicrobial susceptibility pattern of Salmonella species isolated from bacteremia patients at a tertiary care center in Northern India
•Salmonella Typhi is a predominant serovar causing sepsis.•Fluoroquinolone resistance is emerging among Salmonella serovars.•Pefloxacin can be used as a marker for fluoroquinolone resistance.•Re-emergence of azithromycin, chloramphenicol and co-trimoxazole sensitivity. The study was done to assess t...
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Veröffentlicht in: | Diagnostic microbiology and infectious disease 2024-08, Vol.109 (4), p.116354, Article 116354 |
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Zusammenfassung: | •Salmonella Typhi is a predominant serovar causing sepsis.•Fluoroquinolone resistance is emerging among Salmonella serovars.•Pefloxacin can be used as a marker for fluoroquinolone resistance.•Re-emergence of azithromycin, chloramphenicol and co-trimoxazole sensitivity.
The study was done to assess the antimicrobial susceptibility pattern among Salmonella enterica serovars causing bacteremia in Northern India. In this observational study, blood samples positive for Salmonella enterica serovars from January 2021 to April 2023 were studied. Species identification was done using MALDI-ToF MS. Serotyping was done using slide agglutination method. Antimicrobial susceptibility was interpreted as per the CLSI guidelines. During the study period, 32 Salmonella enterica serovars were isolated. Salmonella enterica serovar Typhi was the predominant serovar, followed by Salmonella enterica serovar Paratyphi A. All isolates were susceptible to ceftriaxone, chloramphenicol, co-trimoxazole and cefotaxime. Pefloxacin showed 100% resistance. Resistance to nalidixic acid was found in 81.2% isolates. Of the isolates resistant to nalidixic acid, 19(73.08%) isolates were resistant to ciprofloxacin also. This changing susceptibility pattern necessitates continuous surveillance of antibiogram of Salmonella isolates to rationalize the treatment protocols for invasive salmonellosis and prevent emergence of resistant strains. |
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ISSN: | 0732-8893 1879-0070 1879-0070 |
DOI: | 10.1016/j.diagmicrobio.2024.116354 |