Quercetin
mediated inhibition of Staphylococcus aureus biofilms and the impact
of the isolate phenotype and genotype
E.H. Eldrehmy1,2*,
S.M. Abdel-Hafez1,3, Y.S. Alghamdi1, M.M. Soliman4,5,
S.H. Alotaibi6, A. Alkhedaide3, M.Y. Hassan1,3,
H.H. Amer6,7 and Nada Alqadri1
1Department of
Biology, Turabah University College, Taif University, 21995, Saudi Arabia
2Department of Microbiology,
Faculty of Veterinary Medicine, Zagazig University, Zagazig, 44519, Egypt
3Animal
Reproduction Research Institute, Immunobiology and Immunopharmacology Unit,
Giza,11211, Egypt
4Cinical
Laboratories Sciences, Turabah University College, Taif University, Turabah,
21995, KSA
5Biochemistry
Department, Faculty of Veterinary Medicine, Benha University, Benha 13736,
Egypt
6Chemistry
Department, Turabah University College, Turabah 29541, Taif University, Saudi
Arabia
7Animal Medicine
and Infectious Diseases Department, Faculty of Veterinary Medicine,
University of Sadat City, 32897, Egypt
*Corresponding Author Email : esam2005micro@gmail.com
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Abstract
Aim: This
study was designed to assess the antibiofilm activity of quercetin on characterized
S. aureus isolates.
Methodology: This study evaluated 36 S. aureus isolates,
each of which was identified using Gram staining, culture, biochemical, and
PCR assays. Isolates were cultured and their biofilm production was evaluated
using Congo red agar (CRA) plates, microtiter plate tests and PCR, and the
effects of quercetin were examined.
Results:
The CRA results revealed that eight (22.3%) S. aureus isolates were
strongly positive for biofilm production and an additional 18 isolates (50%)
showed moderate biofilm capacity. The remaining 10 isolates were negative
(27.7%) for biofilm production. S. aureus isolates were divided into
strong positive, intermediate, and negative groups, 27.8%, 44.5%, and 27.7%,
respectively. Scanning electron microscopy showed that the biofilm-producing
isolates appeared as aggregates of cells within a heavy matrix. In addition,
PCR assay identified IcaA and IcaD (66.6% for both) biofilm production genes
in most isolates and IcaC (61.1%), IcaB, FnbB (33.3% for both), and Fib
(22.2%) in several other strains. Quercetin significantly inhibited biofilm
activity in biofilm producing S. aureus isolates in a dose-dependent
manner, with an inhibition rate of 29.6-87.7%.
Interpretation: Biofilm production is dependent on Ica
gene phenotype and strains with an IcaABCD or IcaABD phenotype produce more
biofilm than strains with IcaAD phenotype. Quercetin significantly inhibited S.
aureus biofilm production, irrespective of Ica phenotype.
Key
words:
Biofilm, Congo red agar, Ica operon, PCR, Quercetin, S. aureus
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