year 20, Issue 1 (January - February 2026)                   Iran J Med Microbiol 2026, 20(1): 12-21 | Back to browse issues page

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Abdi E, Ahmadi A, Azizaian K, Talebi Aghdam R, Taherpour A. Comparison of bax, ibpAB and cspH Genes in Escherichia coli Isolates From Urine and Fecal Samples. Iran J Med Microbiol 2026; 20 (1) :12-21
URL: http://ijmm.ir/article-1-2957-en.html
1- Student Research Committee, Kurdistan University of Medical Sciences, Sanandaj, Iran
2- Health Metrics and Evaluation Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran & Zoonoses Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran
3- Zoonoses Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran
4- Zoonoses Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran , rezaeeit93@gmail.com
Abstract:   (234 Views)

Background and Aim: Antimicrobial resistance (AMR) in Escherichia (E.) coli presents challenges in its clinical management. This study aimed to quantify the prevalence and relative expression levels of bax, ibpA, ibpB, and cspH genes in E. coli isolates obtained from urine and fecal samples of patients diagnosed with urinary tract infections (UTIs).
Materials and Methods: In this cross-sectional investigation, 50 E. coli isolates (25 urinary and 25 fecal) were collected from patients diagnosed with UTI in Sanandaj, Iran. Antimicrobial susceptibility was determined using Kirby-Bauer disk diffusion method. Biofilm-forming capacity was quantified using microtiter plate assay. Quantitative Real-Time PCR (qPCR) was performed to determine gene expression levels of target genes.
Results: Antimicrobial susceptibility testing of urinary isolates revealed maximal sensitivity to nitrofurantoin, ofloxacin, and norfloxacin, while the highest resistance rates were observed for amoxicillin, nalidixic acid, and trimethoprim-sulfamethoxazole. In fecal isolates, the greatest sensitivity was recorded for nitrofurantoin, ofloxacin, and norfloxacin. The genomic prevalence of the bax, ibpA, ibpB, and cspH genes in urinary isolates was 100%. In fecal isolates, ibpA was ubiquitous (100%), while bax, ibpB, and cspH were detected in 96% of the strains. Analysis of relative expression levels showed that the expression of all 4 genes was significantly higher in urinary isolates compared to fecal isolates. No significant difference was observed in biofilm formation capacity between two groups (P>0.05).
Conclusion: This investigation identifies a significant differential expression of bax, ibpA, ibpB, and cspH genes between fecal and urinary E. coli isolates, whereas biofilm-forming capacity remained consistent across sources.

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Type of Study: Original Research Article | Subject: Medical Bacteriology
Received: 2025/11/8 | Accepted: 2026/02/12 | ePublished: 2026/02/28

References
1. Biswas S, Rana R, Bal M, Pati S, Suar M, Ranjit M. Escherichia coli associated urinary tract infection: Epidemiology and possible strategies for control. One Health Bull. 2025;5(2):51-7. [DOI:10.4103/ohbl.ohbl_56_24]
2. Nasrollahian S, Moradi F, Hadi N, Ranjbar S, Ranjbar R. An update on alternative therapy for Escherichia coli causing urinary tract infections; a narrative review. Photodiagnosis Photodyn Ther. 2024;46:104075. [DOI:10.1016/j.pdpdt.2024.104075] [PMID]
3. Nikzad M, Mirnejad R, Babapour E. Evaluation of Antibiotic Resistance and Biofilm Formation Ability Uropathogenic E. coli (UPEC) Isolated From Pregnant Women in Karaj. Iran J Med Microbiol. 2021;15(2):195-211. [DOI:10.30699/ijmm.15.2.195]
4. Ismail MA, Faisal AN, Hadi QN, Mohsein OA. Exploring the genetic variability of Escherichia coli pathotypes in urinary tract infections: implications for diagnostics and treatment. Cent Asian J Med Nat Sci. 2025;6(1):179-91.
5. Gümüş D, Yüksek FK, Uz G, Sefer Ö, Yörük E, Küçüker M. Urine influences growth and virulence gene expressions in Uropathogenic E. coli: a comparison with nutrient limited medium. Clin Exp Health Sci. 2021;11(2):209-14. [DOI:10.33808/clinexphealthsci.686302]
6. Vautrin N, Dahyot S, Leoz M, Caron F, Grand M, Feldmann A, et al. Are Escherichia coli causing recurrent cystitis just ordinary uropathogenic E. coli (UPEC) strains?. Virulence. 2025;16(1):2444689. [DOI:10.1080/21505594.2024.2444689] [PMID] [PMCID]
7. Miwa T, Chadani Y, Taguchi H. Escherichia coli small heat shock protein IbpA is an aggregation‐sensor that self‐regulates its own expression at posttranscriptional levels. Mol Microbiol. 2021;115(1):142-56. [DOI:10.1111/mmi.14606] [PMID]
8. Kim B, Kim JH, Lee Y. Virulence factors associated with Escherichia coli bacteremia and urinary tract infection. Ann Lab Med. 2022;42(2):203-12. [DOI:10.3343/alm.2022.42.2.203] [PMID] [PMCID]
9. Zhang X, Yu Z, Yin L, Li Q, He S, Li H, et al. BAX-mediated ammonia-driven cell death: a novel prognostic and therapeutic target in clear cell renal cell carcinoma. Hum Genom. 2025;19(1):57. [DOI:10.1186/s40246-025-00764-3] [PMID] [PMCID]
10. Zehentner B, Ardern Z, Kreitmeier M, Scherer S, Neuhaus K. A novel pH-regulated, unusual 603 bp overlapping protein coding gene pop is encoded antisense to ompA in Escherichia coli O157: H7 (EHEC). Front Microbiol. 2020;11:377. [DOI:10.3389/fmicb.2020.00377] [PMID] [PMCID]
11. Obuchowski I, Piróg A, Stolarska M, Tomiczek B, Liberek K. Duplicate divergence of two bacterial small heat shock proteins reduces the demand for Hsp70 in refolding of substrates. PLoS Genet. 2019;15(10):e1008479. [DOI:10.1371/journal.pgen.1008479] [PMID] [PMCID]
12. Azaharuddin M, Pal A, Mitra S, Dasgupta R, Basu T. A review on oligomeric polydispersity and oligomers-dependent holding chaperone activity of the small heat-shock protein IbpB of Escherichia coli. Cell Stress Chaperones. 2023;28(6):689-96. [DOI:10.1007/s12192-023-01392-3] [PMID] [PMCID]
13. Yu T, Keto-Timonen R, Jiang X, Virtanen JP, Korkeala H. Insights into the phylogeny and evolution of cold shock proteins: from enteropathogenic yersinia and Escherichia coli to eubacteria. Int J Mol Sci. 2019;20(16):4059. [DOI:10.3390/ijms20164059] [PMID] [PMCID]
14. Janowska MK, Baughman HE, Woods CN, Klevit RE. Mechanisms of small heat shock proteins. Cold Spring Harb Perspect Biol. 2019;11(10):a034025. [DOI:10.1101/cshperspect.a034025] [PMID] [PMCID]
15. Yair Y, Michaux C, Biran D, Bernhard J, Vogel J, Barquist L, et al. Cellular RNA targets of cold shock proteins CspC and CspE and their importance for serum resistance in septicemic Escherichia coli. MSystems. 2022;7(4):e00086-22. [DOI:10.1128/msystems.00086-22] [PMID] [PMCID]
16. Zhou Z, Tang H, Wang W, Zhang L, Su F, Wu Y, et al. A cold shock protein promotes high-temperature microbial growth through binding to diverse RNA species. Cell Discov. 2021;7(1):15. [DOI:10.1038/s41421-021-00246-5] [PMID] [PMCID]
17. Zhang H, Gao Z, Li C, Xu J. Two Cold‐Shock Proteins Characterised as RNA Chaperone of Hyperthermophilic Archaeon Pyrococcus yayanosii. Environ Microbiol. 2025;27(5):e70105. [DOI:10.1111/1462-2920.70105] [PMID]
18. Cardoza E, Singh H. Involvement of CspC in response to diverse environmental stressors in Escherichia coli. J Appl Microbiol. 2022;132(2):785-801. [DOI:10.1111/jam.15219] [PMID]
19. Oudih M, Harhara T. Escherichia coli bacteremia due to urinary tract infection complicated by acute myocarditis: a rare complication. SAGE Open Med Case Rep. 2021;9:2050313X211023674. [DOI:10.1177/2050313X211023674] [PMID] [PMCID]
20. Ghosh M, Shin M, Son YO. Cold shock proteins: Orchestrating cellular defense in response to low temperatures. Jeju J Isl Sci. 2024;1(1):12-9.
21. Dong W, Du P, Huang R, Lv S, Chen H, Guan S. Indole may help the horizontal transmission of antibiotic resistance genes in E. coli under subinhibitory concentrations of cefotaxime stress. Cell Microbiol. 2024;2024(1):9018205. [DOI:10.1155/2024/9018205]
22. Mahale RP, K A, Princy A, Maheshwarappa YD, Sumana MN. Comparative evaluation of biofilm-forming capacity in uropathogenic and commensal Escherichia coli. Front Cell Infect Microbiol. 2025;15:1570422. [DOI:10.3389/fcimb.2025.1570422] [PMID] [PMCID]
23. Sun F, Yuan Q, Wang Y, Cheng L, Li X, Feng W, et al. Sub-minimum inhibitory concentration ceftazidime inhibits Escherichia coli biofilm formation by influencing the levels of the ibpA gene and extracellular indole. J Chemother. 2020;32(1):7-14. [DOI:10.1080/1120009X.2019.1678913] [PMID]
24. Figaj D. The role of heat shock protein (Hsp) chaperones in environmental stress adaptation and virulence of plant pathogenic bacteria. Int J Mol Sci. 2025;26(2):528. [DOI:10.3390/ijms26020528] [PMID] [PMCID]
25. Mahon CR, Lehman DC. Textbook of diagnostic microbiology-E-Book: Textbook of diagnostic microbiology-E-Book. 7th ed. Elsevier Health Sciences; 2022.
26. Blosser S. CLSI M100. 2024.
27. Marin J, Walewski V, Braun T, Dziri S, Magnan M, Denamur E, et al. Genomic evidence of Escherichia coli gut population diversity translocation in leukemia patients. Msphere. 2024;9(10):e00530-24. [DOI:10.1128/msphere.00530-24] [PMID] [PMCID]
28. DeVeaux AL, Hall-Moore C, Shaikh N, Wallace M, Burnham CA, Schnadower D, et al. Metagenomic signatures of extraintestinal bacterial infection in the febrile term infant gut microbiome. Microbiome. 2025;13(1):82. [DOI:10.1186/s40168-025-02079-w] [PMID] [PMCID]
29. Naziri Z, Kilegolan JA, Moezzi MS, Derakhshandeh A. Biofilm formation by uropathogenic Escherichia coli: a complicating factor for treatment and recurrence of urinary tract infections. J Hosp Infect. 2021;117:9-16. [DOI:10.1016/j.jhin.2021.08.017] [PMID]
30. Yan CH, Chen FH, Yang YL, Zhan YF, Herman RA, Gong LC, et al. The transcription factor CsgD contributes to engineered Escherichia coli resistance by regulating biofilm formation and stress responses. Int J Mol Sci. 2023;24(18):13681. [DOI:10.3390/ijms241813681] [PMID] [PMCID]
31. Wang Z, Niu X, Zhong N, Kong L, Nawaz S, Zhang H, et al. FimC binds to the promoter region of agn43 to modulate autoaggregation. Front Cell Infect Microbiol. 2025;15:1591206. [DOI:10.3389/fcimb.2025.1591206] [PMID] [PMCID]
32. Zhang H, Zhang Z, Li J, Qin G. New strategies for biocontrol of bacterial toxins and virulence: Focusing on quorum-sensing interference and biofilm inhibition. Toxins. 2023;15(9):570. [DOI:10.3390/toxins15090570] [PMID] [PMCID]
33. Qasemi A, Rahimi F, Katouli M. Genetic diversity and virulence characteristics of biofilm-producing uropathogenic Escherichia coli. Int Microbiol. 2022;25(2):297-307. [DOI:10.1007/s10123-021-00221-w] [PMID]
34. Tantoso E, Eisenhaber B, Sinha S, Jensen LJ, Eisenhaber F. About the dark corners in the gene function space of Escherichia coli remaining without illumination by scientific literature. Biol Direct. 2023;18(1):7. [DOI:10.1186/s13062-023-00362-0] [PMID] [PMCID]
35. Mirzarazi M, Bashiri S, Hashemi A, Vahidi M, Kazemi B, Bandehpour M. The OmpA of commensal Escherichia coli of CRC patients affects apoptosis of the HCT116 colon cancer cell line. BMC Microbiol. 2022;22(1):139. [DOI:10.1186/s12866-022-02540-y] [PMID] [PMCID]
36. Raffatellu M. Learning from bacterial competition in the host to develop antimicrobials. Nat Med. 2018;24(8):1097-103. [DOI:10.1038/s41591-018-0145-0] [PMID]
37. Contreras-Alvarado LM, Zavala-Vega S, Cruz-Córdova A, Reyes-Grajeda JP, Escalona-Venegas G, Flores V, et al. Molecular epidemiology of multidrug-resistant uropathogenic Escherichia coli O25b strains associated with complicated urinary tract infection in children. Microorganisms. 2021;9(11):2299. [DOI:10.3390/microorganisms9112299] [PMID] [PMCID]
38. Roth A, Yang Y, Puchalla J, Rye HS. Single particle dynamics of protein aggregation and disaggregation in the presence of the sHsp proteins IbpAB. Biochemistry. 2025;64(19):4181-95. [DOI:10.1021/acs.biochem.5c00312] [PMID] [PMCID]
39. Sato Y, Okano K, Honda K. Effects of small heat shock proteins from thermotolerant bacteria on the stress resistance of Escherichia coli to temperature, pH, and hyperosmolarity. Extremophiles. 2024;28(1):12. [DOI:10.1007/s00792-023-01326-y] [PMID] [PMCID]
40. Piróg A, Cantini F, Nierzwicki Ł, Obuchowski I, Tomiczek B, Czub J, et al. Two bacterial small heat shock proteins, IbpA and IbpB, form a functional heterodimer. J Mol Biol. 2021;433(15):167054. [DOI:10.1016/j.jmb.2021.167054] [PMID] [PMCID]
41. Haque MF, Tarusawa T, Ushida C, Ito S, Himeno H. cAMP-CRP-activated E. coli causes growth arrest under stress conditions. Front Microbiol. 2025;16:1597530. [DOI:10.3389/fmicb.2025.1597530] [PMID] [PMCID]

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