Effect of Matricaria aurea Essential Oils on Biofilm Development, Virulence Factors and Quorum Sensing-Dependent Genes of Pseudomonas aeruginosa

Author:

Qaralleh Haitham1,Saghir Sultan Ayesh Mohammed2ORCID,Al-limoun Muhamad O.3ORCID,Dmor Saif M.2ORCID,Khleifat Khaled1ORCID,Al-Ahmad Basma Ezzat Mustafa4ORCID,Al-Omari Laila5,Tabana Yasser67,Mothana Ramzi A.8ORCID,Al-Yousef Hanan M.8ORCID,Alqahtani Abdulaziz M.8

Affiliation:

1. Department of Medical Laboratory Sciences, Mutah University, Mutah 61710, Jordan

2. Department of Medical Analysis, Princess Aisha Bint Al-Hussein College of Nursing and Medical Sciences, Al-Hussein Bin Talal University, Ma’an 71111, Jordan

3. Department of Biological Sciences, Faculty of Science, Mutah University, Mutah 61710, Jordan

4. Department of Fundamental Dental Medical Sciences, Kulliyyah of Dentistry, International Islamic University Malaysia, Kuantan 25200, Pahang, Malaysia

5. Faculty of Allied Medical Sciences, Al-Ahliyya Amman University, Amman 19111, Jordan

6. Faculty of Pharmacy and Pharmaceutical Sciences, University of Alberta, Edmonton, AB T6G 2E1, Canada

7. Department of Biochemistry, University of Alberta, Edmonton, AB T6G 2R3, Canada

8. Department of Pharmacognosy, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia

Abstract

The emergence of drug-resistant microorganisms presents a substantial global public health threat. The increase in pathogens resistant to commonly prescribed antibiotics underscores the urgent requirement to explore alternative treatment strategies. This study adopts a novel approach by harnessing natural resources, specifically essential oils (EO), to combat bacterial pathogenicity. The primary aim of this research was to analyze the chemical composition of the aerial part of the Matricaria aurea (M. aureas) EO and evaluate its potential for inhibiting quorum sensing (QS) and disrupting biofilm formation in Pseudomonas aeruginosa (P. aeruginosa). The gas chromatography-mass spectrometry (GCMS) analysis unveiled that α-bisabolol oxide A constituted the predominant portion, comprising 64.8% of the total, with β-bisabolene at 6.3% and α-farnesene at 4.8% following closely behind. The antibiofilm efficacy was observed at concentrations of 0.3, 0.15, and 0.08 mg/mL, demonstrating negligible effects on cell viability. Furthermore, the EO from M. aurea effectively inhibited the formation of P. aeruginosa biofilms by diminishing aggregation, hydrophobicity, and swarming motility. Significantly, the EO treatment resulted in a conspicuous decrease in the production of pyocyanin, rhamnolipid, and extracellular polymeric substances (EPS), along with a reduction in the enzymatic activity of protease and chitinase. The EO effectively hindered QS by disrupting QS mechanisms, resulting in a marked decline in the secretion of N-Acyl homoserine lactone (AHL) molecules and the expression of phazA1 and aprA genes. This investigation offers compelling evidence supporting the potential of M. aurea EO as a promising therapeutic candidate for addressing infectious diseases induced by biofilm formation.

Funder

King Saud University, Riyadh, Saudi Arabia

Publisher

MDPI AG

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