Phenotypic and molecular analysis of Pseudomonas aeruginosa virulence and association with antibiotic resistance in Egypt

Authors

  • Salah AI Ali Clinical Pathology Department, Faculty of Medicine, Zagazig University, Sharqia, Egypt https://orcid.org/0009-0005-1041-6872
  • Aya A Ghamry Medical Microbiology and Immunology Department, Faculty of Medicine (for Girls), Al-Azhar University, Cairo, Egypt
  • Amal M Soliman Medical Microbiology and Immunology Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt
  • Abdullah M Abdo Botany and Microbiology Department, Faculty of Science, Al-Azhar University, Cairo, Egypt
  • Nagwan G El-Menofy Microbiology and Immunology Department, Faculty of Pharmacy (Girls), Al-Azhar University, Cairo, Egypt https://orcid.org/0000-0001-6928-9170
  • Manal M Al-Gerby Clinical Pathology Department, Faculty of Medicine, Zagazig University, Sharqia, Egypt
  • Haytham K Mahrous Clinical Pathology Department, Faculty of Medicine, Zagazig University, Sharqia, Egypt

DOI:

https://doi.org/10.3855/jidc.20957

Keywords:

P. aeruginosa, virulence, genotypic, resistance, nosocomial infections

Abstract

Introduction: Pseudomonas aeruginosa is a common nosocomial pathogen with multidrug resistance (MDR) and virulence factors (VFs). This study assessed the VFs and their associations with MDR and non-MDR isolates.

Methodology: One hundred clinical isolates were analyzed for 12 VFs, encoding genes, and phenotypic traits. Antibiotic resistance patterns and correlations between VFs and MDR were investigated.

Results: Aztreonam showed the highest resistance rate among MDR (94.7%) and ceftazidime showed the highest resistance rate among non-MDR isolates (44.2%). Carbapenems demonstrated the greatest susceptibility. VF positivity rates included 91% for algD, 90% for lasB, 86% for toxA, 82% for exoS, 19% for exoU, 78% for aprA, 75% for plcH, 94% for pigment production, 93% for biofilm formation, 72% for hemolysin, 65% for lipase, and 36% for DNase. Strong biofilm formation correlated with algD and lasB (93%). Pigment production was linked with lasB and toxA (94%). Strong biofilm formation was significantly higher in MDR isolates and resistant strains, than non-MDR isolates. No significant differences in VFs were observed between susceptible and resistant strains for lasB, algD, toxA, plcH, exoU, or general biofilm production; except for strong biofilm formation. Certain VFs correlated with susceptible isolates: exoS with tobramycin, aprA with aztreonam and piperacillin-tazobactam, pigment production with imipenem, DNase with aztreonam and norfloxacin, and lipase with tobramycin and ceftazidime.

Conclusions: P. aeruginosa isolates displayed diverse VFs, biofilm-forming abilities, and MDR profiles; with strong biofilm formation closely linked to MDR. Targeting biofilm-related genes (algD, lasB) could offer effective therapeutic interventions, helping mitigate MDR infections and improve clinical outcomes.

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Published

2025-05-31

How to Cite

1.
Ali SA, Ghamry AA, Soliman AM, Abdo AM, El-Menofy NG, Al-Gerby MM, Mahrous HK (2025) Phenotypic and molecular analysis of Pseudomonas aeruginosa virulence and association with antibiotic resistance in Egypt. J Infect Dev Ctries 19:712–722. doi: 10.3855/jidc.20957

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Section

Original Articles