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Original Research Article | OPEN ACCESS

Random Amplified Polymorphic DNA (RAPD)-PCR analysis of genotypic and phenotypic characteristics of Methicillin-Resistant Staphylococcus epidermidis (MRSE) strains involved in biofilm formation

Parisa Behshood, Elahe Tajbakhsh

Department of Microbiology, Faculty of Basic Sciences, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran;

For correspondence:-  Elahe Tajbakhsh   Email: e.tajbakhsh@iaushk.ac.ir

Accepted: 01 January 2024        Published: 30 January 2024

Citation: Behshood P, Tajbakhsh E. Random Amplified Polymorphic DNA (RAPD)-PCR analysis of genotypic and phenotypic characteristics of Methicillin-Resistant Staphylococcus epidermidis (MRSE) strains involved in biofilm formation. Trop J Pharm Res 2024; 23(1):993-107 doi: 10.4314/tjpr.v23i1.13

© 2024 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: The current study aims to investigate genotypic and phenotypic aspects of methicillin-resistant Staphylococcus epidermidis (MRSE) strains involved in the biofilm formation and the attendance of the icaADB gene and genotypic characterization of this gene by random amplified polymorphic DNA (RAPD) PCR.
Methods: 60 Staphylococcus epidermidis strains were isolated from clinical specimens, suspected of having the bacteria, from the laboratories of Isfahan. Biofilm formation was measured by the microtiter plate method. The attendance of biofilm formation genes was studied using PCR and all isolates producing biofilm (strong and moderate) were genetically classified by RAPD-PCR.
Results: 37 isolates (61.7%) were MRSE and all positive biofilm strains. The prevalence of biofilm-related genes in the isolates was SesC (100%), SesI (45.9%), icaA (29.7%), icaB (37.8%), icaC (81.08%), icaD (70.2%), arcA (81.08%), and opp3AB (70%). PCR analysis showed that among 30 isolates of strong and medium biofilm production, 70% (21/30) positive for the icaADB gene. The Dendrograms obtained from RAPD-PCR results showed that all nine main clusters were at an 80% similarity level, and there were four isolates of a single type.  
Conclusion: These findings confirmed the high genotypic diversity of biofilm-producing MRSE strains and the relative diffusion of specific clones among clinical samples.

Keywords: Biofilm formation, icaADBC gene, MRSE, RAPD-PCR

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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