Effect of <i>Achillea fragrantissima</i> Extract on Excision Wound Biofilms of MRSA and <i>Pseudomonas aeruginosa</i> in Diabetic Mice

<i>Achillea fragrantissima</i>, a desert plant commonly known as yarrow, is traditionally used as an antimicrobial agent in folklore medicine in Saudi Arabia. The current study was undertaken to determine its antibiofilm activity against methicillin-resistant <i>Staphylococcus aure...

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Bibliographic Details
Main Authors: Yasir Almuhanna, Mohammed Hussein Alqasmi, Hamood AlSudais, Mohammed Alrouji, Fahd A. Kuriri, Mohammed Alissa, Meshari A. Alsuwat, Mohammed Asad, Babu Joseph
Format: Article
Language:English
Published: MDPI AG 2023-06-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/24/11/9774
Description
Summary:<i>Achillea fragrantissima</i>, a desert plant commonly known as yarrow, is traditionally used as an antimicrobial agent in folklore medicine in Saudi Arabia. The current study was undertaken to determine its antibiofilm activity against methicillin-resistant <i>Staphylococcus aureus</i> (MRSA) and multi-drug-resistant <i>Pseudomonas aeruginosa</i> (MDR-<i>P. aeruginosa</i>) using in vitro and in vivo studies. A biofilm model induced through an excision wound in diabetic mice was used to evaluate its effect in vivo. The skin irritation and cytotoxic effects of the extract were determined using mice and HaCaT cell lines, respectively. The <i>Achillea fragrantissima</i> methanolic extract was analyzed with LC-MS to detect different phytoconstituents, which revealed the presence of 47 different phytoconstituents. The extract inhibited the growth of both tested pathogens in vitro. It also increased the healing of biofilm-formed excision wounds, demonstrating its antibiofilm, antimicrobial, and wound-healing action in vivo. The effect of the extract was concentration-dependent, and its activity was stronger against MRSA than MDR-<i>P. aeruginosa</i>. The extract formulation was devoid of a skin irritation effect in vivo and cytotoxic effect on HaCaT cell lines in vitro.
ISSN:1661-6596
1422-0067