DETECTION OF MUTATIONS IN GYRA GENE AMONG CIPROFLOXACIN RESISTANT ESCHERICHIA COLI ISOLATED FROM CLINICAL SAMPLES IN BAGHDAD CITY

Authors

  • Mustafa Mahmoud Al-Qaisi Department of medical laboratory techniques, College of Health and Medical Technique-Baghdad, Middle Technical University, Baghdad, Iraq.

DOI:

https://doi.org/10.36320/ajb/v18.i1.24248

Keywords:

Ciprofloxacin Resistance, Escherichia coli, Baghdad City, Iraq.

Abstract

Quinolone resistant Escherichia coli (QREC) isolation rate was elevated due to the prolonged use of this drug in clinical diseases. Various mechanisms play role in developing the quinolone resistance, mutations in DNA gyrase and topoisomerase II are the most common among them. The aim of this study was to identify the mutations in gyrA that correlated with ciprofloxacin resistance among Iraqi E. coli isolates. Out of 600 clinical specimens (Urine, Blood and infected wounds), 70 (11.67%) isolates were identified as E. coli during 2015 -2016. The higher isolation was recorded from infected wound swabs (23.33%), while the prevalence rate of E. coli isolates from urine and blood samples was (12.27% and 4.49%, respectively). The resistance rate of ciprofloxacin for E. coli was recorded (52.86%) with minimum inhibitory concentration (MIC) ≥ 4μg/ml. Non-synonymous mutations, Ser-83 were detected in quinolone resistant determining region (QRDR) of gyrA in all sequenced QREC isolates (Eco U3, Eco U16 and Eco U58) and other mutations (Val-68-Ile, Ser-72-Pro, Arg-73-Cys and Lys-96-Glu) were also detected. Mutation outside this region was also displayed in Eco U16 isolate, at position (Ala-119) near to the active site of gyrA (Tyr-122).

Downloads

Download data is not yet available.

References

1. Farrokh, C., Jordan, K., Auvray, F., Glass, K., Oppegaard, H., Raynaud, S., ... & Cerf, O. (2013). Review of Shiga-toxin-producing Escherichia coli (STEC) and their significance in dairy production. International journal of food microbiology, 162(2), 190-212. doi: 10.1016/j.ijfoodmicro.2012.08.008.

2. Motayo, B. O., Ogiogwa, I. J., Okerentugba, P. O., Innocent-Adiele, H. C., Nwanze, J. C., Onoh, C. C., & Okonko, I. O. (2012). Antimicrobial resistance profile of extra-intestinal Escherichia coli infections in a South-Western Nigerian City. Blood, 27(8). doi: 10.5923/j.microbiology.20120205.05.

3. Rath, S., & Padhy, R. N. (2015). Prevalence of fluoroquinolone resistance in Escherichia coli in an Indian teaching hospital and adjoining communities. Journal of Taibah University Medical Sciences, 10(4), 504-508. doi: 10.1016/j.jtumed.2015.02.009.

4. Dalhoff, A. (2012). Global fluoroquinolone resistance epidemiology and implictions for clinical use. Interdisciplinary perspectives on infectious diseases, 2012(1), 976273. doi: 10.1155/2012/976273.

5. Aldred, K. J., Kerns, R. J., & Osheroff, N. (2014). Mechanism of quinolone action and resistance. Biochemistry, 53(10), 1565-1574. doi: 10.1021/bi5000564.

6. Al-Agamy, M. H. M., Shibl, A. M., & Radwan, H. H. (2012). Detection of mutations in quinolone-resistant determining regions in clinical isolates of Escherichia coli from Saudi Arabia. African Journal of Biotechnology, 11(5), 1054-1058. doi: 10.5897/ajb11.3078.

7. Aldred, K. J., McPherson, S. A., Turnbough Jr, C. L., Kerns, R. J., & Osheroff, N. (2013). Topoisomerase IV-quinolone interactions are mediated through a water-metal ion bridge: mechanistic basis of quinolone resistance. Nucleic acids research, 41(8), 4628-4639. doi: 10.1093/nar/gkt124.

8. Guan, X., Xue, X., Liu, Y., Wang, J., Wang, Y., Wang, J., ... & Pan, L. (2013). Plasmid-mediated quinolone resistance–current knowledge and future perspectives. Journal of International Medical Research, 41(1), 20-30. doi: 10.1177/0300060513475965.

9. Carattoli, A. (2013). Plasmids and the spread of resistance. International journal of medical microbiology, 303(6-7), 298-304. doi: 10.1016/j.ijmm.2013.02.001.

10. Xiong, X., Bromley, E. H., Oelschlaeger, P., Woolfson, D. N., & Spencer, J. (2011). Structural insights into quinolone antibiotic resistance mediated by pentapeptide repeat proteins: conserved surface loops direct the activity of a Qnr protein from a gram-negative bacterium. Nucleic acids research, 39(9), 3917-3927. doi: 10.1093/nar/gkq1296.

11. Guillard, T., Cambau, E., Chau, F., Massias, L., De Champs, C., & Fantin, B. (2013). Ciprofloxacin treatment failure in a murine model of pyelonephritis due to an AAC (6′)-Ib-cr-producing Escherichia coli strain susceptible to ciprofloxacin in vitro. Antimicrobial agents and chemotherapy, 57(12), 5830-5835. doi: 10.1128/aac.01489-13.

12. Liu, Bao-Tao, et al. "Dissemination and characterization of plasmids carrying oqxAB-bla CTX-M genes in Escherichia coli isolates from food-producing animals." PloS one 8.9 (2013): e73947. doi: 10.1371/journal.pone.0073947.

13. McFadden, J. F. (2000). Biochmical testsfor identification of medicalbacteria. Lippincott Williams and wilkins, USA Microbiol. Rev, 2, 15-38.

14. Cockerill, F. R., Wikler, M., Bush, K., Dudley, M., Eliopoulos, G., & Hardy, D. (2012). Clinical and laboratory standards institute. Performance standards for antimicrobial susceptibility testing: twenty-second informational supplement.

15. Zayed, A. A. F., Essam, T. M., Hashem, A. G. M., & El-Tayeb, O. M. (2015). ‘Supermutators’ found amongst highly levofloxacin-resistant E. coli isolates: a rapid protocol for the detection of mutation sites. Emerging microbes & infections, 4(1), 1-8. doi: 10.1038/emi.2015.4.

16. Pdia, U., Okoli, E. N., & Izomoh, I. M. (2006). Antimicrobial susceptibility and plasmid profiles of Escherichia coli isolates obtained from different human clinical specimens in Lagos–Nigeria. J Am Sci, 2, 70-76.

17. Abera, B. (2011). Antimicrobial susceptibility patterns of E. coli from clinical sources in northeast Ethiopia. African health sciences, 11(Suppl 1), S40. doi: 10.4314/ahs.v11i3.70069.

18. Chiller, K., Selkin, B. A., & Murakawa, G. J. (2001, December). Skin microflora and bacterial infections of the skin. In Journal of Investigative dermatology Symposium proceedings (Vol. 6, No. 3, pp. 170-174). Elsevier. doi: 10.1046/j.0022-202x.2001.00043.x.

19. Raza, M. S., Chander, A., & Ranabhat, A. (2013). Antimicrobial susceptibility patterns of the bacterial isolates in post-operative wound infections in a tertiary care hospital, Kathmandu, Nepal. Open journal of medical microbiology, 3(3), 159-163. doi: 10.4236/ojmm.2013.33024.

20. Kader, A. A., Kumar, A., & Dass, S. M. (2004). Antimicrobial resistance patterns of gram-negative bacteria isolated from urine cultures at a general hospital. Saudi Journal of Kidney Diseases and Transplantation, 15(2), 135-139.

21. Hassan, H. G. (2014). ‟Phenotypic and Molecular Characterization of AmpC β-lactamases Among Escherichia coli, Klebsiella spp. & Enterobacter spp. Isolated From Al-Hussein Teaching Hospital in Thi-Qar Governorateˮ. M.Sc. Thesis. College of Heath & Medical Technology/Baghdad, Middle Technical University.

22. Ahmed, A. F. (2016). ‟Molecular study of a number of bacterial adhesion of the bacteria Escherichia coli isolated of urine samples of children under fiveˮ. M.Sc. Thesis. Pure College of Education Sciences / Ibn Al-Haytham. Baghdad University.

23. Fayroz-Ali. (2012) ‟Detection of Quinolone Resistance Genes in Escherichia coli Isolated from Patients with Significant Bacteriuria in Najaf Provinceˮ. PHD. Thesis. College of Medicine. Kufa University.

24. Yaseen, S. S. (2014). Statistical study of urinary tract infection at all in children under the age of five in the city of Kirkuk. Kirkuk Univ J, 9, 22-42.

25. Laupland, K. B., & Church, D. L. (2014). Population-based epidemiology and microbiology of community-onset bloodstream infections. Clinical microbiology reviews, 27(4), 647-664. doi: 10.1128/cmr.00002-14.

26. Duah, P. E. (2013). Detection of mutations in gyra and parc by mama-pcr of quinolone-resistant isolates of escherichia coli from the komfo anokye teaching hospital, kumasi (Doctoral dissertation).

27. Al-Saadi, M. A., Al-Charrakh, A. H., & Al-Greti, S. H. (2011). Prevalence of bacteremia in patients with diabetes mellitus in Karbala, Iraq. Journal of Bacteriology Research, 3(7), 108-116.

28. Alsamarai, A. G. M., Latif, I. A., & Abdulaziz, M. M. (2016). Antibiotic susceptibility of extended spectrum beta lactamase (ESBL) producing Escherichia coli. WJJPPS, 5, 195-215.

29. AL-Alak SKA. ‟Molecular Study of Adherence Factors in Uropathogenic Escherichia coli Related to Fluoroquinolones Resistanceˮ. M.Sc. Thesis. College of Science. Al-Mustansiriyah University. (2012).

30. Kireçci, E., Sleman, D. M., Ahmed, D. Y., Rahman, D. B., & Yazdee, F. S. (2015). Identification of the bacterial types that cause urinary tract infection and antimicrobial susceptibility in Erbil, Iraq. Sky J Microbiol Res, 1, 011-014.

31. Tony Mazzulli, M. (2012). Diagnosis and management of simple and complicated urinary tract infections (UTIs). Can J Urol, 19(1), 42-8.

32. Geetha, V. K., Yugendran, T., Srinivasan, R., & Harish, B. N. (2014). Plasmid-mediated quinolone resistance in typhoidal Salmonellae: a preliminary report from South India. Indian Journal of Medical Microbiology, 32(1), 31-34. doi: 10.4103/0255-0857.124292

33. Hassan, W. M., Hashim, A., & Domany, R. A. A. (2012). Plasmid mediated quinolone resistance determinants qnr, aac (6′)-Ib-cr, and qep in ESBL-producing Escherichia coli clinical isolates from Egypt. Indian journal of medical microbiology, 30(4), 442-447. doi: 10.4103/0255-0857.103766.

34. Sato, T., Yokota, S. I., Uchida, I., Okubo, T., Ishihara, K., Fujii, N., & Tamura, Y. (2011). A fluoroquinolone-resistant Escherichia coli clinical isolate without quinolone resistance-determining region mutations found in Japan. Antimicrobial agents and chemotherapy, 55(8), 3964-3965. doi: 10.1128/aac.00532-11.

35. Hopkins, K. L., Davies, R. H., & Threlfall, E. J. (2005). Mechanisms of quinolone resistance in Escherichia coli and Salmonella: recent developments. International journal of antimicrobial agents, 25(5), 358-373. doi: 10.1016/j.ijantimicag.2005.02.006.

36. Jaktaji, R. P., & Mohiti, E. (2010). Study of mutations in the DNA gyrase gyrA gene of Escherichia coli. Iranian journal of pharmaceutical research: IJPR, 9(1), 43.

37. Barnard, F. M., & Maxwell, A. (2001). Interaction between DNA gyrase and quinolones: effects of alanine mutations at GyrA subunit residues Ser83and Asp87. Antimicrobial agents and chemotherapy, 45(7), 1994-2000. doi: 10.1128/aac.45.7.1994-2000.2001.

38. Bansal, S., & Tandon, V. (2011). Contribution of mutations in DNA gyrase and topoisomerase IV genes to ciprofloxacin resistance in Escherichia coli clinical isolates. International journal of antimicrobial agents, 37(3), 253-255. doi: 10.1016/j.ijantimicag.2010.11.022.

39. Johnning, A., Kristiansson, E., Fick, J., Weijdegård, B., & Larsson, D. J. (2015). Resistance mutations in gyrA and parC are common in Escherichia communities of both fluoroquinolone-polluted and uncontaminated aquatic environments. Frontiers in Microbiology, 6, 1355. doi: 10.3389/fmicb.2015.01355.

Downloads

Published

2026-05-13

How to Cite

Mustafa Mahmoud Al-Qaisi. (2026). DETECTION OF MUTATIONS IN GYRA GENE AMONG CIPROFLOXACIN RESISTANT ESCHERICHIA COLI ISOLATED FROM CLINICAL SAMPLES IN BAGHDAD CITY. Al-Kufa University Journal for Biology, 18(1). https://doi.org/10.36320/ajb/v18.i1.24248

Share