Affiliations 

  • 1 Department of Biology, College of Sciences, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia. Electronic address: shalmejale@pnu.edu.sa
  • 2 High Institute of Nursing Professions and Health Techniques Casablanca, Casablanca, 20250, Morocco. Electronic address: naceiri.mrabti.hanae@gmail.com
  • 3 Department of Biology, College of Science, Qassim University, Qassim, 51452, Saudi Arabia. Electronic address: 140208@qu.edu.sa
  • 4 Department of Laboratory Medicine, Faculty of Applied Medical Sciences, Umm Al-Qura University, Makkah, 21955, Saudi Arabia. Electronic address: hmsaggaf@uqu.edu.sa
  • 5 Department of Laboratory Medicine, Faculty of Applied Medical Sciences, Umm Al-Qura University, Makkah, 21955, Saudi Arabia. Electronic address: aaqasem@uqu.edu.sa
  • 6 Department of Medical Laboratory, College of Applied Medical Sciences-Shaqra, Shaqra University, Shaqra 11961, Saudi Arabia
  • 7 Laboratory of Human Pathologies Biology, Department of Biology, Faculty of Sciences, Mohammed V University in Rabat, Rabat, 10106, Morocco; Sunway Biofunctional Molecules Discovery Centre, School of Medical and Life Sciences, Sunway University, Sunway City, Malaysia. Electronic address: a.bouyahya@um5r.ac.ma
  • 8 Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah, 51452, Saudi Arabia. Electronic address: Fshbrmy@qu.edu.sa
  • 9 Faculty of Medicine and Pharmacy Guelmim 81000, Ibnou Zohr University, Agadir, Morocco. Electronic address: n.elhachlafi@uiz.ac.ma
Microb Pathog, 2025 Jan 31;200:107357.
PMID: 39894234 DOI: 10.1016/j.micpath.2025.107357

Abstract

Acorus calamus is a medicinal plant known for its multifaceted health benefits, especially against inflammation and infectious ailments. In the current work, we attempt to investigate the volatile constituents of A. calamus essential oil (ACEO) and, for the first time, to elucidate its antibacterial mechanism. Gas chromatography coupled to a mass spectrometer (GC-MS) was used to investigate phytochemical substances. The GC-MS analysis detected β-asarone (71.13 %), an aromatic anisole as main component, followed by α-asarone (12.07 %), β-calacorene (3.01 %), methyl isoeugenol (2.16 %). ACEO exhibited remarkable antibacterial activity, as demonstrated by significant inhibition zones against several bacteria that were tested. Gram-positive strains, Staphylococcus aureus and Bacillus subtilis, showed inhibition zones measuring 20.11 ± 0.28 mm and 18.06 ± 1.36 mm, respectively, while Gram-negative bacteria, Pseudomonas aeruginosa, and Escherichia coli, displayed slightly smaller zones of 15.58 ± 0.68 mm and 16.00 ± 0.04 mm. The results of ACEO were competitive with Tetracycline and Cefoperazone. Furthermore, ACEO demonstrated low MICs (ranging from 0.125 % to 1.0 %) and MBCs (ranging between 0.125 % and 2.0 %), with MBC/MIC ratios consistently below 4.0, confirming its bactericidal nature. Time-kill kinetics represented high lethality of ACEO at MIC levels against Staphylococcus aureus and Pseudomonas aeruginosa, resulting in a significant reduction in colony-forming units within 12-24 h. The antibacterial mechanisms of ACEO were investigated, demonstrating its potential to disrupt the integrity of the cell membrane and enhance membrane permeability. This disruption results in the release of genetic material (RNA and DNA) and proteins from the bacterial cell. Significant anti-biofilm activity further highlights the potential of the tested compounds in combating biofilm-associated infections. Scanning electron microscopy (SEM) images revealed significant inhibition of bacterial adhesion (First step of biofilm formation) on used surface as well as possible morphological changes in bacterial cells treated with ACEO.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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