4.6 Article

The Chemical Profiling, Docking Study, and Antimicrobial and Antibiofilm Activities of the Endophytic fungi Aspergillus sp. AP5

Journal

MOLECULES
Volume 27, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/molecules27051704

Keywords

Endophytic fungi; chemical profile; antimicrobial; antibiofilm; molecular docking

Funding

  1. Deanship of Scientific Research at Jouf University [DSR-2021-01-0306]

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Growing evidence suggests that Aspergillus niger is a rich source of natural compounds with diverse biological activities. This study found that an endophytic fungus derived from Phragmites australis has antimicrobial and antibiofilm capabilities, and identified the active compounds through chemical analysis and neural-networking pharmacophore-based screening. These findings are important in the development of new antimicrobial and antibiofilm agents.
Growing data suggest that Aspergillus niger, an endophytic fungus, is a rich source of natural compounds with a wide range of biological properties. This study aimed to examine the antimicrobial and antibiofilm capabilities of the Phragmites australis-derived endophyte against a set of pathogenic bacteria and fungi. The endophytic fungus Aspergillus sp. AP5 was isolated from the leaves of P. australis. The chemical profile of the fungal crude extract was identified by spectroscopic analysis using LC-HRESIMS. The fungal-derived extract was evaluated for its antimicrobial activity towards a set of pathogenic bacterial and fungal strains including Staphylococcus aureus, Pseudomonas aeruginosa, Proteus vulgaris, Klebsiella sp., Candida albicans, and Aspergillus niger. Moreover, antibiofilm activity toward four resistant biofilm-forming bacteria was also evaluated. Additionally, a neural-networking pharmacophore-based visual screening predicted the most probable bioactive compounds in the obtained extract. The AP5-EtOAc extract was found to have potent antibacterial activities against S. aureus, E. coli, and Klebsiella sp., while it exhibited low antibacterial activity toward P. Vulgaris and P. aeruginosa and displayed anticandidal activity. The AP5-EtOAc extract had significant antibiofilm activity in S. aureus, followed by P. aeruginosa. The active metabolites' antifungal and/or antibacterial activities may be due to targeting the fungal CYP 51 and/or the bacterial Gyr-B.

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