A MOLECULAR ANALYSIS: DETECTION OF PLASMID-BORNE QNR GENES IN QUINOLONE-RESISTANT SALMONELLA TYPHI ISOLATES FROM PATIENTS AT A TERTIARY CARE HOSPITAL IN BAHAWALPUR, PAKISTAN

Main Article Content

Safdar Ali
Muhammad Rizwan
Maria Rasool
Rafia Anwar
Maimona Sadia
Irfan Ahmad
Areej Safdar
Laiba Qadir

Keywords

Salmonella, Typhoid fever, Gene, qnrS

Abstract

Introduction: Typhoid fever is caused by Salmonella typhi, which is known for being resistant to several antibiotics. It is one of the leading causes of death and infections in developing nations, and also a frequent cause of illnesses in Pakistan. The major cause of this infection is to face a significant challenge in dealing with higher-level quinolone-resistant S. typhi strains. To combat this challenge a study was designed to determine the presence of the qnr genes among S. typhi isolated from stool of patient samples.


Methodology: Stool samples of patients with suspected typhoid fever were collected by standard methods in sterile disposable containers. After analysis of stool, microscopic observations and culture analysis, S. typhi was isolated, antibiotic susceptibility testing was carried out, and the bacterial genome was extracted by boiling method. PCR for detection of qnr genes including qnr AqnrB and qnrS was done by specific primers, then PCR products were run using gel electrophoresis and visualized by gel documentation system.


Results: Out of 150 isolates, 13 (8.7%) were positive for S. typhi.  Antibiotic resistance among the isolates in decreasing order were as follows: imipenems (100.0%), cefuroxime (100.0%), cefotaxime (100.0%), nalidixic acid (92.3%), amoxicillin/clavulanic acid (84.6%), ceftriaxone/sulbactam (84.6%), ciprofloxacin (84.6%), gentamicin (76.9%), levofloxacin (46.2%) and ofloxacin (46.2%).The most common antibiotic resistant phenotype was AUG- CTX-IMP-OFX-CN-NA-CXM-CRO-CIP-LBC at 30.4%. Multiple antibiotic resistance (MAR) was observed in 100% (13/13) of the isolates with the common MAR indices being 1.0 (30.8%), 0.7 (23.5%), 0.8 (23.1%) and 0.9 (15.4%). The only positive PMQR genes were qnrS and aac(6)-Ib-cr with percentage occurrence of 50.0% respectively.


Conclusion: The S. typhi isolates showed lower resistance to ofloxacin, levofloxacin, and gentamicin, and all isolates were MAR, with resistance to 10 antibiotics being the most predominant. In addition, qnrS resistance gene was the most common gene expressed.

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References

1. World Health Organization. Critically important antimicrobials for human medicine, 5th Revision 2016. 2017.http://www.who.int/foodsafety/publications/antimicrobials-fifth/en/.
2. Hooper DC, Jacoby GA. Mechanisms of drug resistance: quinolone resistance. Annals of the New York academy of sciences. 2015 Sep;1354(1):12-31.
3. Yanat B, Rodríguez-Martínez JM, Touati A. Plasmid-mediated quinolone resistance in Enterobacteriaceae: a systematic review with a focus on Mediterranean countries. European Journal of Clinical Microbiology & Infectious Diseases. 2017 Mar;36:421-35.
4. Crump JA, Barrett TJ, Nelson JT, Angulo FJ. Reevaluating fluoroquinolone breakpoints for Salmonella enterica serotype Typhi and for non-Typhi salmonellae. Clinical Infectious Diseases. 2003 Jul 1;37(1):75-81.
5. Van TT, Nguyen HN, Smooker PM, Coloe PJ. The antibiotic resistance characteristics of non-typhoidal Salmonella enterica isolated from food-producing animals, retail meat and humans in South East Asia. International Journal of Food Microbiology. 2012 Mar 15;154(3):98-106.
6. Cavaco LM, Aarestrup FM. Evaluation of quinolones for use in detection of determinants of acquired quinolone resistance, including the new transmissible resistance mechanisms qnrA, qnrB, qnrS, and aac (6′) Ib-cr, in Escherichia coli and Salmonella enterica and determinations of wild-type distributions. Journal of Clinical Microbiology. 2009 Sep;47(9):2751-8.
7. Jacoby GA, Strahilevitz J, Hooper DC. Plasmid‐mediated quinolone resistance. Plasmids: Biology and Impact in Biotechnology and Discovery. 2015 May 30:475-503.
8. Rodríguez-Martínez JM, Machuca J, Cano ME, Calvo J, Martínez-Martínez L, & Pascual A(2016).
9. Plasmid-mediated quinolone resistance: Two decades on. Drug Resistance Updates, 29, 13–29. 10.1016/j.drup.2016.09.001. [PubMed: 27912841]
10. Herrera-Sánchez MP, Castro-Vargas RE, Fandiño-de-Rubio LC, Rodríguez-Hernández R,Rondón-Barragán IS. Molecular identification of fluoroquinolone resistance in Salmonella spp. Isolated from broiler farms and human samples obtained from two regions in Colombia. Veterinary World.2021 Jul;14 (7):1767.
11. Cheesbrough M. District laboratory practice in tropical countries: Cambridge university press; 2006.
12. Ali, S., Jalees, M. M., Ashraf, W., Sadia, M., Anwar, R., Zafar, & Mannan, A. (2024). Emergence Of Extensive Drug Resistance Typhoid In Hospitalized Covid-19 Patients In South Punjab, Pakistan. Journal of Population Therapeutics and Clinical Pharmacology, 31(2), 753-763.
13. Krumperman PH. Multiple antibiotic resistance indexing of Escherichia coli to identify high-risk sources of fecal contamination of foods. Applied and environmental microbiology. 1983 Jul; 46(1):165-70.
14. Abimiku RH, Ngwai YB, Nkene IH, Bassey BE, Tsaku PA, Ibrahim T, Tama SC, Ishaleku D, Pennap GR. Molecular Diversity and extended spectrum beta-lactamase resistance of diarrheagenic Escherichia coli from patients attending selected health care facilities in Nasarawa state, Nigeria. International Journal of Pathogen Research. 2019 Sep 2;3(1):1-8.
15. Jang S, Kelley KW, Johnson RW. Luteolin reduces IL-6 production in microglia by inhibiting JNK phosphorylation and activation of AP-1. Proceedings of the National Academy of Sciences. 2008 May 27;105(21):7534-9.
16. Aljanaby AA, Medhat AR. Research article prevalence of some antimicrobials resistance associated-genes in Salmonella typhi isolated from patients infected with typhoid fever. J. Biol. Sci. 2017;17(4):171-84.
17. Jubair HH, Al-Buhamrah NA, Al-Fatlawi SG. Molecular characterization of quinolones resistant Salmonella typhi isolates from patients infected with Typhoid fever in Al-Najaf province, Iraq. Journal of Population Therapeutics and Clinical Pharmacology. 2023 Mar 13;30(3):11-9.
18. Rahman BA, Wasfy MO, Maksoud MA, Hanna N, Dueger E, House B. Multi-drug resistance and reduced susceptibility to ciprofloxacin among Salmonella enterica serovar Typhi isolates from the Middle East and Central Asia. New microbes new Infect. 2014;2(4):88–92.
19. Aljanaby AAJ, Medhat AR. Research article prevalence of some antimicrobials resistance associated-genes in Salmonella typhi isolated from patients infected with typhoid fever. J Biol Sci.2017;17(4):171–84.
20. AL-Fatlawy HNK, AL-Hadrawi HAN. Molecular Profiling of Class I Integron Gene in MDR Salmonella Typhi Isolates. J Pure Appl Microbiol. 2020;14:1825–33.
21. Njum AA, Hassan RN, Alwan JA. Identification of Antibiotic-Resistant Genes in Salmonella Typhi Isolated From Typhoid Patient in Samawa City. Iraqi J Sci. 2019;60(5):980–4.
22. Fasema R, Bassey BE, Ngwai YB, Nkene IH, Abimiku RH, Parom SK, Yahaya I. Plasmid- mediated Quinolone Resistance Genes in Salmonella typhi from Patients Attending Selected General Hospitals in Abuja Municipal, Nigeria. Asian Journal of Biochemistry, Genetics and Molecular Biology. 2020 Jul 6;4(2):45-59.
23. Dong N, Li Y, Zhao J, Ma H, Wang J, Liang B, et al. The phenotypic and molecular characteristics, of antimicrobial resistance of Salmonella enterica subsp. enterica serovar Typhimurium in Henan Province, China. BMC Infect Dis. 2020;20(1):1–11.
24. Malehmir S, Ranjbar R, Harzandi N. The molecular study of antibiotic resistance to quinolones in Salmonella enterica strains isolated in Tehran, Iran. Open Microbiol J. 2017;11:189.
25. Salman HA, Abdulmohsen AM, Falih MN, Romi ZM. serovar Typhi isolated from Iraqi subjects. 2021;14:1922–8.
26. Tadesse G, Tessema TS, Beyene G, Aseffa A. Molecular epidemiology of fluoroquinolone resistant Salmonella in Africa: A systematic review and meta-analysis. PLoS One. 2018;13 (2):e0192575.
27. Kim H Bin, Park CH, Kim CJ, Kim E-C, Jacoby GA, Hooper DC. Prevalence of plasmid-mediated quinolone resistance determinants over a 9-year period. Antimicrob Agents Chemother. 2009;53 (2):639–45.
28. Geetha VK, Yugendran T, Srinivasan R, Harish BN. Plasmid-mediated quinolone resistance in typhoidal Salmonellae: a preliminary report from South India. Indian J Med Microbiol. 2014;32(1):31–4.