Study of plasmid mediated quinolone resistance genes among Escherichia coli and Klebsiella pneumoniae isolated from pediatric patients with sepsis
- PMID: 38783019
- PMCID: PMC11116374
- DOI: 10.1038/s41598-024-61357-z
Study of plasmid mediated quinolone resistance genes among Escherichia coli and Klebsiella pneumoniae isolated from pediatric patients with sepsis
Abstract
The resistance to antibiotics in Gram-negative bacilli causing sepsis is a warning sign of failure of therapy. Klebsiella pneumoniae (K. pneumoniae) and Escherichia coli (E. coli) represent major Gram-negative bacilli associated with sepsis. Quinolone resistance is an emerging resistance among E. coli and K. pneumoniae. Therefore, the present study aimed to study the presence of plasmid-mediated quinolone resistance (PMQR) genes qnrA, qnrB, and qnrS by polymerase chain reaction (PCR) in E. coli and K. pneumoniae isolated from pediatric patients with sepsis. This was a retrospective cross-sectional study that included pediatric patients with healthcare-associated sepsis. The E. coli and K. pneumoniae isolates were identified by microbiological methods. PMQR genes namely qnrA, qnrB, and qnrS were detected in E. coli and K. pneumoniae isolates by PCR. The results were analyzed by SPPS24, and the qualitative data was analyzed as numbers and percentages and comparison was performed by Chi-square test, P was significant if < 0.05. The most prevalent gene detected by PCR was qnrA (75%), followed by qnrB (28.1%), and qnrS (25%). The most frequently detected qnr gene in E coli and K. pneumoniae was qnrA (28.8%, and 16.3% respectively). The present study highlights the high prevalence of ciprofloxacin resistance among E. coli and K. pneumoniae isolated from pediatric patients with healthcare-associated sepsis. There was a high frequency of PMQR genes in E. coli and K. pneumoniae isolated from pediatric patients. Therefore, it is important to monitor the spread of PMQR genes in clinical isolates to ensure efficient antibiotic use in those children. The finding denotes the importance of an antibiotics surveillance program.
Keywords: PMQ,; qnrA; qnrB; qnrS; PCR; Sepsis. Pediatrics.
© 2024. The Author(s).
Conflict of interest statement
The authors declare no competing interests.
Similar articles
-
High Prevalence of Plasmid-Mediated Quinolone Resistance Determinants in Escherichia coli and Klebsiella pneumoniae Isolates from Pediatric Patients in China.Microb Drug Resist. 2017 Jan;23(1):107-114. doi: 10.1089/mdr.2016.0004. Epub 2016 May 11. Microb Drug Resist. 2017. PMID: 27167505
-
High rates of plasmid-mediated quinolone resistance QnrB variants among ciprofloxacin-resistant Escherichia coli and Klebsiella pneumoniae from urinary tract infections in Korea.Microb Drug Resist. 2008 Sep;14(3):221-6. doi: 10.1089/mdr.2008.0834. Microb Drug Resist. 2008. PMID: 18707554
-
[Investigation of plasmid-mediated quinolone resistance genes in quinolone-resistant Escherichia coli and Klebsiella spp. isolates from bloodstream infections].Mikrobiyol Bul. 2016 Apr;50(2):186-95. doi: 10.5578/mb.20935. Mikrobiyol Bul. 2016. PMID: 27175491 Turkish.
-
Determination of gyrA and parC mutations and prevalence of plasmid-mediated quinolone resistance genes in Escherichia coli and Klebsiella pneumoniae isolated from patients with urinary tract infection in Iran.J Glob Antimicrob Resist. 2018 Jun;13:197-200. doi: 10.1016/j.jgar.2018.04.017. Epub 2018 May 7. J Glob Antimicrob Resist. 2018. PMID: 29747008
-
Transferable Mechanisms of Quinolone Resistance from 1998 Onward.Clin Microbiol Rev. 2019 Aug 14;32(4):e00007-19. doi: 10.1128/CMR.00007-19. Print 2019 Sep 18. Clin Microbiol Rev. 2019. PMID: 31413045 Free PMC article. Review.
References
-
- de Souza DC, Gonçalves Martin J, Soares Lanziotti V, de Oliveira CF, Tonial C, de Carvalho WB, et al. The epidemiology of sepsis in paediatric intensive care units in Brazil (the sepsis PREvalence assessment database in Pediatric population, SPREAD PED): An observational study. Lancet Child Adolesc. Heal. 2021;4642:1–9. doi: 10.1016/S2352-4642(21)00286-8. - DOI - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases