Investigation of virulence factor genes and biofilm formation of antibiotic resistant clinical E.coli isolates

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Özet

Purpose: The aim of this study is to investigate the antibiotic sensitivity, presence of virulence genes and biofilm formation capacity of 90 clinical E. coli isolates. Methods: The presence of virulence genes in E. coli isolates were investigated by PCR. Ninety clinical isolates of E. coli were subjected to biofilm quantitative analysis using the semi-quantitative crystal violet staining method. Results: it was observed that the isolates were resistant to quinolone, cephalosporin, aminoglycoside, carbapenem and penicillin group antibiotics. The presence of virulence factor genes were observed in a total of 86/90 E. coli. The highest rate of fim (92.2 %) virulence factor gene was detected in the strains. Afa, pap, cnf, sfa, hly were detected in 30 %, 13 %, 13 %, 3.3 %, 2.2 % respectively. Also, 13 different virulence factor gene patterns were determined in 90 E. coli isolates. Of the 90 E. coli isolates whose biofilm-forming capacities were evaluated, 42 were found to have biofilm-forming capacity. Of these 26 (28.8 %) the weak, 12 (13.3 %) moderate and 4 (4.4 %) strong biofilm-forming. Also, statistical analysis was performed to investigate the relationship between virulence factor genes and biofilm formation, and none of the 7 genes analyzed showed a significant relationship with biofilm formation. Conclusion: since pathogenic E. coli is an important public health problem, investigating antibiotic resistance, virulence factor genes and biofilm formation in bacterial pathogens is important for better treatment options.

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dc.contributor.authorMumin, Yahye Mohamud
dc.contributor.authorYüksel, Gamze
dc.contributor.authorÖzad Düzgün, Azer
dc.date.accessioned2026-10-22T10:22:09.950553646Z
dc.date.available2026-10-22T10:22:09.950553646Z
dc.date.issued2025
dc.description.abstractPurpose: The aim of this study is to investigate the antibiotic sensitivity, presence of virulence genes and biofilm formation capacity of 90 clinical E. coli isolates. Methods: The presence of virulence genes in E. coli isolates were investigated by PCR. Ninety clinical isolates of E. coli were subjected to biofilm quantitative analysis using the semi-quantitative crystal violet staining method. Results: it was observed that the isolates were resistant to quinolone, cephalosporin, aminoglycoside, carbapenem and penicillin group antibiotics. The presence of virulence factor genes were observed in a total of 86/90 E. coli. The highest rate of fim (92.2 %) virulence factor gene was detected in the strains. Afa, pap, cnf, sfa, hly were detected in 30 %, 13 %, 13 %, 3.3 %, 2.2 % respectively. Also, 13 different virulence factor gene patterns were determined in 90 E. coli isolates. Of the 90 E. coli isolates whose biofilm-forming capacities were evaluated, 42 were found to have biofilm-forming capacity. Of these 26 (28.8 %) the weak, 12 (13.3 %) moderate and 4 (4.4 %) strong biofilm-forming. Also, statistical analysis was performed to investigate the relationship between virulence factor genes and biofilm formation, and none of the 7 genes analyzed showed a significant relationship with biofilm formation. Conclusion: since pathogenic E. coli is an important public health problem, investigating antibiotic resistance, virulence factor genes and biofilm formation in bacterial pathogens is important for better treatment options.
dc.identifier.articlenumber107257
dc.identifier.doi10.1016/j.micpath.2024.107257
dc.identifier.eissn1096-1208
dc.identifier.issn0882-4010
dc.identifier.pmid39725043
dc.identifier.scopus2-s2.0-85213058331
dc.identifier.startpage107257
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/14055
dc.identifier.volume199
dc.identifier.wosWOS:001412476200001
dc.language.isoen
dc.publisherAcademic Press
dc.relation.ispartofMicrobial Pathogenesis
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectBiofilm
dc.subjectE.coli
dc.subjectUTI
dc.subjectVirulence factor gene
dc.subject.classificationImmunology
dc.subject.classificationMicrobiology
dc.subject.otherAnti-Bacterial Agents
dc.subject.otherBiofilms
dc.subject.otherDrug Resistance, Bacterial
dc.subject.otherEscherichia coli
dc.subject.otherEscherichia coli Infections
dc.subject.otherEscherichia coli Proteins
dc.subject.otherGenes, Bacterial
dc.subject.otherHumans
dc.subject.otherMicrobial Sensitivity Tests
dc.subject.otherPolymerase Chain Reaction
dc.subject.otherVirulence Factors
dc.subject.otheraminoglycoside
dc.subject.otheramoxicillin
dc.subject.otherampicillin
dc.subject.othercarbapenem
dc.subject.othercefixime
dc.subject.othercefotaxime
dc.subject.otherceftriaxone
dc.subject.othercephalosporin
dc.subject.otherciprofloxacin
dc.subject.otherertapenem
dc.subject.otherfosfomycin
dc.subject.otherimipenem
dc.subject.otherlevofloxacin
dc.subject.othermeropenem
dc.subject.othernitrofurantoin
dc.subject.otherpenicillin derivative
dc.subject.otherpiperacillin plus tazobactam
dc.subject.otherquinolone
dc.subject.othersultamicillin
dc.subject.othertobramycin
dc.subject.othervirulence factor
dc.subject.otherantiinfective agent
dc.subject.otherEscherichia coli protein
dc.subject.otherantibiotic resistance
dc.subject.otherantibiotic sensitivity
dc.subject.otherArticle
dc.subject.otheraspiration
dc.subject.otherbacterium isolation
dc.subject.otherbiofilm
dc.subject.otherDNA isolation
dc.subject.othernonhuman
dc.subject.otherquantitative analysis
dc.subject.otherroom temperature
dc.subject.otherbacterial gene
dc.subject.otherdrug effect
dc.subject.otherEscherichia coli infection
dc.subject.othergenetics
dc.subject.othergrowth, development and aging
dc.subject.otherhuman
dc.subject.otherisolation and purification
dc.subject.othermicrobial sensitivity test
dc.subject.othermicrobiology
dc.titleInvestigation of virulence factor genes and biofilm formation of antibiotic resistant clinical E.coli isolates
dc.typeArticle
dspace.entity.typePublication
rdl.citation.openalex4
rdl.citation.scopus4
rdl.citation.wos4
rdl.departmentDepartment of Biotechnology, Institute of Graduate Education, Gumushane University, Gümüşhane, Turkey
rdl.departmentBursa City Hospital, Bursa, Turkey
rdl.departmentDepartment of Occupational Health and Safety, Faculty of Health Sciences, Gumushane University, Gümüşhane, Turkey
rdl.oa.statusgreen
rdl.oa.statuspreprint
rdl.oa.urlhttps://hdl.handle.net/20.500.12440/6467
rdl.scopus.quartileQ2
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)