Investigating Immune Evasion Genes Expression and Biofilm Formation of Klebsiella pneumoniae Isolates from Patients with Ventilator-associated pneumonia

سال انتشار: 1404
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 12

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شناسه ملی سند علمی:

JR_REMJ-13-3_003

تاریخ نمایه سازی: 30 بهمن 1404

چکیده مقاله:

Background: Klebsiella pneumoniae, a leading opportunistic pathogen, exhibits increasing multidrug resistance (MDR) and biofilm formation, posing significant challenges in hospital environments, especially in developing regions such as Iran. This study aimed to characterize the antibiotic resistance profiles, biofilm-formation capacity, and expression levels of immune evasion genes (fimH-۱, mrkD, traT) in K. pneumoniae isolates from patients with ventilator-associated pneumonia. Methods: Thirty Klebsiella pneumoniae isolates were obtained from sputum samples of patients with ventilator-associated pneumonia. Antibiotic susceptibility was determined using the Kirby-Bauer disk diffusion method. Biofilm formation was quantified by a crystal violet assay. The presence and expression of immune evasion genes were evaluated by polymerase chain reaction (PCR) and quantitative real-time PCR, respectively. Results: High resistance rates were observed, including ۱۰۰% to ampicillin-sulbactam, ۹۶.۶۶% to ciprofloxacin, ۹۳.۳۳% to cefepime, and ۸۳.۳۳% to imipenem. ۵۰% of isolates were strong biofilm formers, ۳۳.۳% moderate, and ۱۶.۷% weak. mrkD and fimH-۱ genes were detected in ۱۰۰% and ۹۶.۶۶% of isolates, respectively, while traT was present in ۳۰%. Gene expression analysis revealed significant upregulation of fimH-۱ (p=۰.۰۰۵) and mrkD (p<۰.۰۰۰۱), while traT expression showed no significant change (p=۰.۲۸۰۳). No significant correlation was found between the prevalence of immune evasion genes and biofilm production (p > ۰.۰۵). Conclusion: This study highlights a high prevalence of Multidrug-Resistant Klebsiella pneumoniae isolates with strong biofilm formation and upregulated immune evasion genes among patients with ventilator-associated pneumonia.The significant upregulation of fimH-۱ and mrkD suggests enhanced adaptation for persistence against host defenses. These findings underscore the urgent need for targeted interventions to control K. pneumoniae infections amid the growing threat of antibiotic resistance.

نویسندگان

Babak Beikzadeh

Department of Cell and Molecular Biology & Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran.

Marjan Gerami

Department of Cell and Molecular Biology & Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran.

Mahshid Azizi

Department of Cell and Molecular Biology & Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran.

Hafez Mozayyan Esfahani

Department of Cell and Molecular Biology & Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran. Email: Hafezmozayyan@gmail.com, ORCID: https://orcid.org/۰۰۰۹-۰۰۰۶-۶۷۸۸-۸۹۲۳

Soodabeh Rostami

Infectious Diseases and Tropical Medicine Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

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