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Isolation and Characterization of Anti-Adenoviral Secondary Metabolites from Marine Actinobacteria
Adenovirus infections in immunocompromised patients are associated with high mortality rates. Currently, there are no effective anti-adenoviral therapies available. It is well known that actinobacteria can produce secondary metabolites that are attractive in drug discovery due to their structural di...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944516/ https://www.ncbi.nlm.nih.gov/pubmed/24477283 http://dx.doi.org/10.3390/md12020799 |
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author | Strand, Mårten Carlsson, Marcus Uvell, Hanna Islam, Koushikul Edlund, Karin Cullman, Inger Altermark, Björn Mei, Ya-Fang Elofsson, Mikael Willassen, Nils-Peder Wadell, Göran Almqvist, Fredrik |
author_facet | Strand, Mårten Carlsson, Marcus Uvell, Hanna Islam, Koushikul Edlund, Karin Cullman, Inger Altermark, Björn Mei, Ya-Fang Elofsson, Mikael Willassen, Nils-Peder Wadell, Göran Almqvist, Fredrik |
author_sort | Strand, Mårten |
collection | PubMed |
description | Adenovirus infections in immunocompromised patients are associated with high mortality rates. Currently, there are no effective anti-adenoviral therapies available. It is well known that actinobacteria can produce secondary metabolites that are attractive in drug discovery due to their structural diversity and their evolved interaction with biomolecules. Here, we have established an extract library derived from actinobacteria isolated from Vestfjorden, Norway, and performed a screening campaign to discover anti-adenoviral compounds. One extract with anti-adenoviral activity was found to contain a diastereomeric 1:1 mixture of the butenolide secondary alcohols 1a and 1b. By further cultivation and analysis, we could isolate 1a and 1b in different diastereomeric ratio. In addition, three more anti-adenoviral butenolides 2, 3 and 4 with differences in their side-chains were isolated. In this study, the anti-adenoviral activity of these compounds was characterized and substantial differences in the cytotoxic potential between the butenolide analogs were observed. The most potent butenolide analog 3 displayed an EC(50) value of 91 μM and no prominent cytotoxicity at 2 mM. Furthermore, we propose a biosynthetic pathway for these compounds based on their relative time of appearance and structure. |
format | Online Article Text |
id | pubmed-3944516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-39445162014-03-07 Isolation and Characterization of Anti-Adenoviral Secondary Metabolites from Marine Actinobacteria Strand, Mårten Carlsson, Marcus Uvell, Hanna Islam, Koushikul Edlund, Karin Cullman, Inger Altermark, Björn Mei, Ya-Fang Elofsson, Mikael Willassen, Nils-Peder Wadell, Göran Almqvist, Fredrik Mar Drugs Adenovirus infections in immunocompromised patients are associated with high mortality rates. Currently, there are no effective anti-adenoviral therapies available. It is well known that actinobacteria can produce secondary metabolites that are attractive in drug discovery due to their structural diversity and their evolved interaction with biomolecules. Here, we have established an extract library derived from actinobacteria isolated from Vestfjorden, Norway, and performed a screening campaign to discover anti-adenoviral compounds. One extract with anti-adenoviral activity was found to contain a diastereomeric 1:1 mixture of the butenolide secondary alcohols 1a and 1b. By further cultivation and analysis, we could isolate 1a and 1b in different diastereomeric ratio. In addition, three more anti-adenoviral butenolides 2, 3 and 4 with differences in their side-chains were isolated. In this study, the anti-adenoviral activity of these compounds was characterized and substantial differences in the cytotoxic potential between the butenolide analogs were observed. The most potent butenolide analog 3 displayed an EC(50) value of 91 μM and no prominent cytotoxicity at 2 mM. Furthermore, we propose a biosynthetic pathway for these compounds based on their relative time of appearance and structure. MDPI 2014-01-28 /pmc/articles/PMC3944516/ /pubmed/24477283 http://dx.doi.org/10.3390/md12020799 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Strand, Mårten Carlsson, Marcus Uvell, Hanna Islam, Koushikul Edlund, Karin Cullman, Inger Altermark, Björn Mei, Ya-Fang Elofsson, Mikael Willassen, Nils-Peder Wadell, Göran Almqvist, Fredrik Isolation and Characterization of Anti-Adenoviral Secondary Metabolites from Marine Actinobacteria |
title | Isolation and Characterization of Anti-Adenoviral Secondary Metabolites from Marine Actinobacteria |
title_full | Isolation and Characterization of Anti-Adenoviral Secondary Metabolites from Marine Actinobacteria |
title_fullStr | Isolation and Characterization of Anti-Adenoviral Secondary Metabolites from Marine Actinobacteria |
title_full_unstemmed | Isolation and Characterization of Anti-Adenoviral Secondary Metabolites from Marine Actinobacteria |
title_short | Isolation and Characterization of Anti-Adenoviral Secondary Metabolites from Marine Actinobacteria |
title_sort | isolation and characterization of anti-adenoviral secondary metabolites from marine actinobacteria |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944516/ https://www.ncbi.nlm.nih.gov/pubmed/24477283 http://dx.doi.org/10.3390/md12020799 |
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