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

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 ba...

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Autores principales: Abdelgawad, Mohamed A., Hamed, Ahmed A., Nayl, AbdElAziz A., Badawy, Mona Shaban E. M., Ghoneim, Mohammed M., Sayed, Ahmed M., Hassan, Hossam M., Gamaleldin, Noha M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911721/
https://www.ncbi.nlm.nih.gov/pubmed/35268806
http://dx.doi.org/10.3390/molecules27051704
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author Abdelgawad, Mohamed A.
Hamed, Ahmed A.
Nayl, AbdElAziz A.
Badawy, Mona Shaban E. M.
Ghoneim, Mohammed M.
Sayed, Ahmed M.
Hassan, Hossam M.
Gamaleldin, Noha M.
author_facet Abdelgawad, Mohamed A.
Hamed, Ahmed A.
Nayl, AbdElAziz A.
Badawy, Mona Shaban E. M.
Ghoneim, Mohammed M.
Sayed, Ahmed M.
Hassan, Hossam M.
Gamaleldin, Noha M.
author_sort Abdelgawad, Mohamed A.
collection PubMed
description 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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spelling pubmed-89117212022-03-11 The Chemical Profiling, Docking Study, and Antimicrobial and Antibiofilm Activities of the Endophytic fungi Aspergillus sp. AP5 Abdelgawad, Mohamed A. Hamed, Ahmed A. Nayl, AbdElAziz A. Badawy, Mona Shaban E. M. Ghoneim, Mohammed M. Sayed, Ahmed M. Hassan, Hossam M. Gamaleldin, Noha M. Molecules Article 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. MDPI 2022-03-05 /pmc/articles/PMC8911721/ /pubmed/35268806 http://dx.doi.org/10.3390/molecules27051704 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Abdelgawad, Mohamed A.
Hamed, Ahmed A.
Nayl, AbdElAziz A.
Badawy, Mona Shaban E. M.
Ghoneim, Mohammed M.
Sayed, Ahmed M.
Hassan, Hossam M.
Gamaleldin, Noha M.
The Chemical Profiling, Docking Study, and Antimicrobial and Antibiofilm Activities of the Endophytic fungi Aspergillus sp. AP5
title The Chemical Profiling, Docking Study, and Antimicrobial and Antibiofilm Activities of the Endophytic fungi Aspergillus sp. AP5
title_full The Chemical Profiling, Docking Study, and Antimicrobial and Antibiofilm Activities of the Endophytic fungi Aspergillus sp. AP5
title_fullStr The Chemical Profiling, Docking Study, and Antimicrobial and Antibiofilm Activities of the Endophytic fungi Aspergillus sp. AP5
title_full_unstemmed The Chemical Profiling, Docking Study, and Antimicrobial and Antibiofilm Activities of the Endophytic fungi Aspergillus sp. AP5
title_short The Chemical Profiling, Docking Study, and Antimicrobial and Antibiofilm Activities of the Endophytic fungi Aspergillus sp. AP5
title_sort chemical profiling, docking study, and antimicrobial and antibiofilm activities of the endophytic fungi aspergillus sp. ap5
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911721/
https://www.ncbi.nlm.nih.gov/pubmed/35268806
http://dx.doi.org/10.3390/molecules27051704
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