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Author Spotlight: Advancements in Understanding and Combatting Shigella Infections
Published on: February 9, 2024
The Emergence of Quinolone Resistant Shigella sonnei, Pondicherry, India
Ankita Das1, Mailan Natarajan1, Jharna Mandal1
1Department of Microbiology, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India.
Abstract:
Ciprofloxacin resistant Shigella sonnei across the globe have been increasing alarmingly. In order to understand the emergence of S.sonnei with respect to ciprofloxacin resistance in our patient population, the following study was carried out. Of the 184 Shigella sp. Isolated from 2012 to 2015, 34 S.sonnei which were confirmed by standard methods and subjected to antimicrobial susceptibility testing were selected. The minimum inhibitory concentrations (MICs) of 16/34 quinolone resistant isolates tested ranged from 4micrograms/ml to 16micrograms/ml for ciprofloxacin, from 16 micrograms/ml to 64 micrograms/ml for ofloxacin and from 16micrograms/ml to 64micrograms/ml for levofloxacin. Sequence determination of the quinolone resistance determining regions of gyrA, gyrB, parC, and parE genes showed mutations in GyrA at Gln69/Trp, Phe71/Ser, Ser72/Pro, Met75/Leu, Ser90/Cys, Met94/Leu, His106/Pro, Asn161/His, Thr163/Ala and in ParC at Ala64/Asp. Among the plasmid-mediated quinolone resistance (PMQRs) targets investigated,qnrB was the most (93.7%) prevalent followed by qnrC (18.7%). None hadqnrA, qnrS and qepA. Two (0.1%) of the isolates harboured theaac(6')-lb gene. Drug accumulation assay detected the presence of efflux pump activity in 9/15 (60%) among ciprofloxacin resistant isolates. All isolates harboured the ipaH gene followed by ial (17.6%), sen (11.7%), set1A&set1B (5.8%) genes. None had stx1 element. PCR for Enterobacterial repetitive intergenic consensus (ERIC) sequences resulted in 4 unique clusters, of which Type III was the most (44%) dominant but there was no correlation between the ERIC types and the antibiotic resistance pattern or the virulence profile. A documented increase in S.sonnei harbouring the qnrgenes and some unusual genes like set1Aand indicate an ongoing process of horizontal gene transfer. The accumulation of novel mutations in GyrA and ParC in the presence of efflux pump and PMQR genes contributed to the raised MIC to quinolones. These findings are crucial in our understanding of quinolone resistance in these isolates.
Insights
Ciprofloxacin resistance in Shigella sonnei is rising globally. This study identified novel mutations and plasmid-mediated quinolone resistance genes contributing to high quinolone minimum inhibitory concentrations (MICs) in patient isolates.
Area of Science:
- Microbiology
- Genetics
- Infectious Diseases
Background:
- Global increase in ciprofloxacin-resistant Shigella sonnei strains.
- Need to understand resistance mechanisms in local patient populations.
Purpose of the Study:
- Investigate the emergence of ciprofloxacin resistance in Shigella sonnei.
- Identify genetic mutations and resistance mechanisms contributing to quinolone resistance.
Main Methods:
- Antimicrobial susceptibility testing of Shigella sonnei isolates.
- Sequence determination of quinolone resistance-determining regions (QRDRs) of gyrA, gyrB, parC, and parE genes.
- Detection of plasmid-mediated quinolone resistance (PMQR) genes and efflux pump activity.
Main Results:
- Elevated MICs for ciprofloxacin, ofloxacin, and levofloxacin in resistant isolates.
- Identified mutations in GyrA and ParC genes.
- Prevalence of qnrB (93.7%) and qnrC (18.7%) PMQR genes; presence of aac(6')-lb in 0.1% of isolates.
- Efflux pump activity detected in 60% of ciprofloxacin-resistant isolates.
- Presence of virulence genes ipaH, ial, sen, set1A, and set1B.
Conclusions:
- Accumulation of novel mutations in GyrA and ParC, along with efflux pumps and PMQR genes, contributes to high quinolone MICs.
- Ongoing horizontal gene transfer indicated by the presence of qnr genes and unusual genes like set1A.
- Findings are crucial for understanding quinolone resistance in Shigella sonnei.
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