Effect of sub-inhibitory concentrations of cefepime on biofilm formation by Pseudomonas aeruginosa

Author:

Hagras Soheir A.A.12,Hosny Alaa El-Dien M.S.3,Helmy Omneya M.3,Salem-Bekhit Mounir M.45,Shakeel Faiyaz4,Farrag Hala A.1

Affiliation:

1. Department of Drug Radiation Research, National Center for Radiation Research and Technology (NCRRT), Egyptian Atomic Energy Authority, Cairo, Egypt.

2. Inaya Medical Colleges, Riyadh, Saudi Arabia.

3. Department of Microbiology & Immunology, Faculty of Pharmacy, Cairo University, Cairo, Egypt.

4. Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.

5. Department of Microbiology & Immunology, Faculty of Pharmacy, Al-Azhar University, Cairo, Egypt.

Abstract

This study investigated the effect of cefepime at sub-minimum inhibitory concentrations (sub-MICs) on in vitro biofilm formation (BF) by clinical isolates of Pseudomonas aeruginosa. The effect of cefepime at sub-MIC levels (½–1/256 MIC) on in vitro BF by six clinical isolates of P. aeruginosa was phenotypically assessed following 24 and 48 h of challenge using the tissue culture plate (TCP) assay. Quantitative real-time polymerase chain reaction (qRT-PCR) was employed to observe the change in expression of three biofilm-related genes, namely, a protease-encoding gene (lasA), fimbrial protein-encoding gene (cupA1), and alginate-encoding gene (algC), in a weak biofilm-producing strain of P. aeruginosa following 24 and 48 h of challenge with sub-MICs of cefepime. The BF morphology in response to cefepime was imaged using scanning electron microscopy (SEM). The TCP assay showed strain-, time-, and concentration-dependent changes in in vitro BF in P. aeruginosa following challenge with sub-MICs of cefepime, with a profound increase in strains with inherently no or weak biofilm-producing ability. RT-PCR revealed time-dependent upregulation in the expression of the investigated genes following challenge with ½ and ¼ MIC levels, as confirmed by SEM. Cefepime at sub-MICs could upregulate the expression of BF-related genes and enhance BF by P. aeruginosa clinical isolates.

Publisher

Canadian Science Publishing

Subject

Genetics,Molecular Biology,Applied Microbiology and Biotechnology,General Medicine,Immunology,Microbiology

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