CORRELATION BETWEEN ANTIBIOTIC RESISTANCE PHENOTYPES WITH MOBILE GENETIC ELEMENTS (INTEGRON CLASS I) IN UROPATHOGENIC E. coli

Authors

  • Marwa Sh. M.
  • A. H. Ibrahim

DOI:

https://doi.org/10.36103/shxqpf87

Keywords:

Nucleic acids sequencing, PCR, MDR, XDR, PDR.

Abstract

This study was aimed to determine the relationship between Integron class I and multidrug resistance in Uropathogenic E. coli. A total of 302 urine samples were used in this study. 139 Uropathogenic E coli  were collected from hospitalized patients. Then, using biochemical testing and the Vitek II compact system, all of the isolates were diagnosed and confirmed. All E. coli isolates were tested using a disc diffusion procedure to detect their susceptibility to 23 types of antibiotics from different classes, and the result showed that these bacteria were  highly resistant to most used antibiotics especially, Cefotaxime, Ampicillin,  Piperacillin, Trimethoprim- sulfamethoxazole ,Cefepime and Ceftazidime, while the most effective antibiotics were Colistin and Tigecyclin. Also the results show different resistance patterns in which 111 (79.86%) isolate showed multidrug resistance MDR, Extensively drug resistance XDR 18  isolate (12.94%), while Pandrug resistance PDR 3 (2.15%). PCR was used to detect the presence of  integron class I in MDR isolates ,which was found in 87 of isolates with a 483 bp amplification product.  The resolved PCR products were sequenced in both directions (forward and reverse), and the NCBI BLASTn engine revealed 100% sequence similarity between the sequenced  samples and the planned reference1target sequences. These findings revealed that E. coli strains were highly resistant to common antibiotics; however, given the high prevalence of integron class I among these isolates, we can deduce that antibiotic resistance genes were most likely carried on mobile genetic elements (integron) in these isolates.

References

Al-ghanimi, G. M. M., and A. M. Alrubeii. 2024. Effect of elastin hydrolysate on bacteria and some sensory traits of chilled ground beef. Iraqi Journal of Agricultural Sciences, 55(1):422-431. https://doi.org/10.36103/8w3frt36

Ali M.A. and S.S. Mahmood, 2022. Role of rnd-efflux pump in levofloxacin resistance among Acinetobacter baumannii. Iraqi Journal of Agricultural Sciences. 53(3):542- 550. https://doi.org/10.36103/ijas.v53i3.1562

Bennett P. M. 2008. Plasmid-encoded antibiotic resistance: acquisition and transfer of antibiotic resistance genes in bacteria. Br J Pharmacol. 153 (1): 47–57.

Clinical Laboratory Standard Institute 2020. Performance Standard for Antimicrobial Susceptibility testing. M100-S30.

Fasugba O, Gardner A, Mitchell, and B. G, Mnatzaganian, 2015. Ciprofloxacin resistance in community-and hospital-acquired Escherichia coli urinary tract infections: a systematic review and meta-analysis of observational studies. BMC infectious diseases. 15(1): 545.

Fluit A, and F. J. Schmitz, 2004. Resistance integrons and super-integrons. Clinical Microbiology and Infection. 10(4): 272-288.

Japoni, A.; M.; Gudarzi, S.H.; Farshad, E.; Basiri, M.; Ziyaeyan, A.; Alborzi, and N. Rafaatpour, 2008. Assay for integrons and pattern of antibiotic resistance in clinical Escherichia coli strains by PCR-RFLP in southern Iran . Jpn J Infect Dis. 61(1): 85-88.

Leekitcharoenphon, P., M. H. Johansson, K., Munk, P., Malorny, B., M., Skarżyńska, K., Wadepohl, and F. M.Aarestrup, 2021. Genomic evolution of antimicrobial resistance in Escherichia coli. Scientific Reports. 11(1): 1-12.‏

Letunic I, and P. Bork, 2019. Interactive Tree Of Life (iTOL) v4: recent updates and new developments. Nucleic Acids Res. 2;47(W1): W256-W259.

Magiorakos A. P., A. Srinivasan,R. B. Carey, Y. Carmeli,M. E. Falagas, C. G. Giske, S. Harbarth, J. F. Hindler,G. Kahlmeter,B. Olsson-Liljequist, D. L. Paterson,L. B. Rice,J. Stelling, and M. J. Struelens, 2012. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infection. 18(3): 268–281.

Manal M., I. khadhim and A. Kazaal, 2018. Association Between Antibiotic Resistance and Integron Class2 Among Commonsal Escherichia coli Genotypic Groups. AL-Qadisiya Medical Journal.14(25): 18-32.

Mobley H. L. 2016. Measuring Escherichia coli Gene Expression during Human Urinary Tract Infections. Pathogens (Basel, Switzerland). 5(1): 7.

Mohammad Ahangarzadeh Rezaee, Vajihe Sheikhalizade, and Alka Hasani, 2011. Detection of integrons among multi-drug resistant (mdr) escherichia coli strains isolated from clinical specimens in northern west of iran. Brazilian Journal of Microbiology. 42: 1308-1313.

Mohammad Kargar, Zahra Mohammad alipour , Abbas Doosti , Shahrokh Lorzadeh , and Alireza Japoni-Nejad, 2014. High Prevalence of Class 1 to 3 Integrons Among Multidrug- Resistant Diarrheagenic Escherichia coli in Southwest of Iran. Osong Public Health Res Perspect. 5(4): 193-198.

Majda B, A. Barchan, A. Aarab, M. Bakkali, A. Arakrak, and A. Laglaoui 2022. Evaluation of the antibacterial activity of essential oils against E. coli isolated from rabbits. Iraqi Journal of Agricultural Sciences, 53(4):802-809. https://doi.org/10.36103/ijas.v53i4.1592

Odetoyin, B. W., A. S., Labar, A., Lamikanra, A. O., Aboderin, and I. N. Okeke, 2017. Classes 1 and 2 integrons in faecal Escherichia coli strains isolated from mother-child pairs in Nigeria. PloS one. 12(8): e0183383.

Partridge S. R, Tsafnat G, Coiera E,and J. R. Iredell 2009. Gene cassettes and cassette arrays in mobile resistance integrons. FEMS Microbiol Rev. 33(4):757–84.

Phongpaichit S, K, Wuttananupan, and W. Samasanti 2008. Class 1 integrons and multidrug resistance among Escherichia coli isolates from human stools. Southeast Asian J Trop Med Public Health . 39(2):279e87.

Poirel, L., Madec, J. Y., Lupo, A., Schink, A. K., Kieffer, N., Nordmann, P., and S. Schwarz, 2018. Antimicrobial Resistance in Escherichia coli. Microbiology spectrum. 6(4):10.112.

Rezaee M. A, V. Sheikhalizadeh, and A. Hasani, 2012. First report of class 1 and class 2 integrons in multidrug-resistant (MDR) Escherichia coli strains isolated from clinical specimens in northern west of Iran. Jpn J Infect Dis. 65(3): 256e9.

World Health Organization (WHO) 2014. WHO first global report on antibiotic resistance reveals serious, worldwide threat to public health; http://www.who.int/mediacentre/news/releases/2014/amr-report/en/. Cited 17 July 2016.

Ying, L., F., Ji-qian, and T. Lu, 2015. Advanced medical statistics (Vol. 5). World Scientific. Singapore.

Zainab Jaber Hadi; Thanaa A-Turaihi; Hashim Ali Abdualmeer Al-sherees; Alia Essa Bashboosh; Suaad Mohammed H.Rasheed, and Sumaya Najim Abd-ali, 2020. Prevalence of Integrons and Antibiotic Resistance among Escherichia coli isolated from patient suspected with urinary tract infection from Al-Najaf hospitals. Sys Rev Pharm .11(7):258-264.

Omar F. H. and A. H. Ibrahim, 2023. The prevalence of integron class i and ii among multidrug resistance producing Klebsiella pneumonia. Iraqi Journal of Agricultural Sciences.54(3):619- 629. https://doi.org/10.36103/ijas.v54i3.1775

Zhang Z, S. Schwartz, L. Wagner, W. Miller, 2000. A greedy algorithm for aligning DNA sequences. J Comput Biol. 7(1-2):203-14.

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Published

2024-08-26

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How to Cite

Marwa Sh. M., & A. H. Ibrahim. (2024). CORRELATION BETWEEN ANTIBIOTIC RESISTANCE PHENOTYPES WITH MOBILE GENETIC ELEMENTS (INTEGRON CLASS I) IN UROPATHOGENIC E. coli. IRAQI JOURNAL OF AGRICULTURAL SCIENCES, 55(4), 1280-1291. https://doi.org/10.36103/shxqpf87

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