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Antimicrobial activity and acetylcholinesterase inhibition by extracts from chromatin modulated fungi
Major health challenges as the increasing number of cases of infections by antibiotic multiresistant microorganisms and cases of Alzheimer's disease have led to searching new control drugs. The present study aims to verify a new way of obtaining bioactive extracts from filamentous fungi with po...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790575/ https://www.ncbi.nlm.nih.gov/pubmed/28818332 http://dx.doi.org/10.1016/j.bjm.2017.06.004 |
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author | Lima, Matheus Thomaz Nogueira Silva Santos, Larissa Batista dos Bastos, Rafael Wesley Nicoli, Jacques Robert Takahashi, Jacqueline Aparecida |
author_facet | Lima, Matheus Thomaz Nogueira Silva Santos, Larissa Batista dos Bastos, Rafael Wesley Nicoli, Jacques Robert Takahashi, Jacqueline Aparecida |
author_sort | Lima, Matheus Thomaz Nogueira Silva |
collection | PubMed |
description | Major health challenges as the increasing number of cases of infections by antibiotic multiresistant microorganisms and cases of Alzheimer's disease have led to searching new control drugs. The present study aims to verify a new way of obtaining bioactive extracts from filamentous fungi with potential antimicrobial and acetylcholinesterase inhibitory activities, using epigenetic modulation to promote the expression of genes commonly silenced. For such finality, five filamentous fungal species (Talaromyces funiculosus, Talaromyces islandicus, Talaromyces minioluteus, Talaromyces pinophilus, Penicillium janthinellum) were grown or not with DNA methyltransferases inhibitors (procainamide or hydralazine) and/or a histone deacetylase inhibitor (suberohydroxamic acid). Extracts from T. islandicus cultured or not with hydralazine inhibited Listeria monocytogenes growth in 57.66 ± 5.98% and 15.38 ± 1.99%, respectively. Increment in inhibition of acetylcholinesterase activity was observed for the extract from P. janthinellum grown with procainamide (100%), when compared to the control extract (39.62 ± 3.76%). Similarly, inhibition of acetylcholinesterase activity increased from 20.91 ± 3.90% (control) to 92.20 ± 3.72% when the tested extract was obtained from T. pinophilus under a combination of suberohydroxamic acid and procainamide. Concluding, increases in antimicrobial activity and acetylcholinesterase inhibition were observed when fungal extracts in the presence of DNA methyltransferases and/or histone deacetylase modulators were tested. |
format | Online Article Text |
id | pubmed-5790575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-57905752018-01-31 Antimicrobial activity and acetylcholinesterase inhibition by extracts from chromatin modulated fungi Lima, Matheus Thomaz Nogueira Silva Santos, Larissa Batista dos Bastos, Rafael Wesley Nicoli, Jacques Robert Takahashi, Jacqueline Aparecida Braz J Microbiol Research Paper Major health challenges as the increasing number of cases of infections by antibiotic multiresistant microorganisms and cases of Alzheimer's disease have led to searching new control drugs. The present study aims to verify a new way of obtaining bioactive extracts from filamentous fungi with potential antimicrobial and acetylcholinesterase inhibitory activities, using epigenetic modulation to promote the expression of genes commonly silenced. For such finality, five filamentous fungal species (Talaromyces funiculosus, Talaromyces islandicus, Talaromyces minioluteus, Talaromyces pinophilus, Penicillium janthinellum) were grown or not with DNA methyltransferases inhibitors (procainamide or hydralazine) and/or a histone deacetylase inhibitor (suberohydroxamic acid). Extracts from T. islandicus cultured or not with hydralazine inhibited Listeria monocytogenes growth in 57.66 ± 5.98% and 15.38 ± 1.99%, respectively. Increment in inhibition of acetylcholinesterase activity was observed for the extract from P. janthinellum grown with procainamide (100%), when compared to the control extract (39.62 ± 3.76%). Similarly, inhibition of acetylcholinesterase activity increased from 20.91 ± 3.90% (control) to 92.20 ± 3.72% when the tested extract was obtained from T. pinophilus under a combination of suberohydroxamic acid and procainamide. Concluding, increases in antimicrobial activity and acetylcholinesterase inhibition were observed when fungal extracts in the presence of DNA methyltransferases and/or histone deacetylase modulators were tested. Elsevier 2017-08-01 /pmc/articles/PMC5790575/ /pubmed/28818332 http://dx.doi.org/10.1016/j.bjm.2017.06.004 Text en © 2017 Sociedade Brasileira de Microbiologia. Published by Elsevier Editora Ltda. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Lima, Matheus Thomaz Nogueira Silva Santos, Larissa Batista dos Bastos, Rafael Wesley Nicoli, Jacques Robert Takahashi, Jacqueline Aparecida Antimicrobial activity and acetylcholinesterase inhibition by extracts from chromatin modulated fungi |
title | Antimicrobial activity and acetylcholinesterase inhibition by extracts from chromatin modulated fungi |
title_full | Antimicrobial activity and acetylcholinesterase inhibition by extracts from chromatin modulated fungi |
title_fullStr | Antimicrobial activity and acetylcholinesterase inhibition by extracts from chromatin modulated fungi |
title_full_unstemmed | Antimicrobial activity and acetylcholinesterase inhibition by extracts from chromatin modulated fungi |
title_short | Antimicrobial activity and acetylcholinesterase inhibition by extracts from chromatin modulated fungi |
title_sort | antimicrobial activity and acetylcholinesterase inhibition by extracts from chromatin modulated fungi |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790575/ https://www.ncbi.nlm.nih.gov/pubmed/28818332 http://dx.doi.org/10.1016/j.bjm.2017.06.004 |
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