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Marine Bacteria from Rocas Atoll as a Rich Source of Pharmacologically Active Compounds

Rocas Atoll is a unique environment in the equatorial Atlantic Ocean, hosting a large number of endemic species, however, studies on the chemical diversity emerging from this biota are rather scarce. Therefore, the present work aims to assess the metabolomic diversity and pharmacological potential o...

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Autores principales: Velasco-Alzate, Karen Y., Bauermeister, Anelize, Tangerina, Marcelo M. P., Lotufo, Tito M. C., Ferreira, Marcelo J. P., Jimenez, Paula C., Padilla, Gabriel, Lopes, Norberto P., Costa-Lotufo, Letícia V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949966/
https://www.ncbi.nlm.nih.gov/pubmed/31795148
http://dx.doi.org/10.3390/md17120671
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author Velasco-Alzate, Karen Y.
Bauermeister, Anelize
Tangerina, Marcelo M. P.
Lotufo, Tito M. C.
Ferreira, Marcelo J. P.
Jimenez, Paula C.
Padilla, Gabriel
Lopes, Norberto P.
Costa-Lotufo, Letícia V.
author_facet Velasco-Alzate, Karen Y.
Bauermeister, Anelize
Tangerina, Marcelo M. P.
Lotufo, Tito M. C.
Ferreira, Marcelo J. P.
Jimenez, Paula C.
Padilla, Gabriel
Lopes, Norberto P.
Costa-Lotufo, Letícia V.
author_sort Velasco-Alzate, Karen Y.
collection PubMed
description Rocas Atoll is a unique environment in the equatorial Atlantic Ocean, hosting a large number of endemic species, however, studies on the chemical diversity emerging from this biota are rather scarce. Therefore, the present work aims to assess the metabolomic diversity and pharmacological potential of the microbiota from Rocas Atoll. A total of 76 bacteria were isolated and cultured in liquid culture media to obtain crude extracts. About one third (34%) of these extracts were recognized as cytotoxic against human colon adenocarcinoma HCT-116 cell line. 16S rRNA gene sequencing analyses revealed that the bacteria producing cytotoxic extracts were mainly from the Actinobacteria phylum, including Streptomyces, Salinispora, Nocardiopsis, and Brevibacterium genera, and in a smaller proportion from Firmicutes phylum (Bacillus). The search in the spectral library in GNPS (Global Natural Products Social Molecular Networking) unveiled a high chemodiversity being produced by these bacteria, including rifamycins, antimycins, desferrioxamines, ferrioxamines, surfactins, surugamides, staurosporines, and saliniketals, along with several unidentified compounds. Using an original approach, molecular networking successfully highlighted groups of compounds responsible for the cytotoxicity of crude extracts. Application of DEREPLICATOR+ (GNPS) allowed the annotation of macrolide novonestimycin derivatives as the cytotoxic compounds existing in the extracts produced by Streptomyces BRB-298 and BRB-302. Overall, these results highlighted the pharmacological potential of bacteria from this singular atoll.
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spelling pubmed-69499662020-01-16 Marine Bacteria from Rocas Atoll as a Rich Source of Pharmacologically Active Compounds Velasco-Alzate, Karen Y. Bauermeister, Anelize Tangerina, Marcelo M. P. Lotufo, Tito M. C. Ferreira, Marcelo J. P. Jimenez, Paula C. Padilla, Gabriel Lopes, Norberto P. Costa-Lotufo, Letícia V. Mar Drugs Article Rocas Atoll is a unique environment in the equatorial Atlantic Ocean, hosting a large number of endemic species, however, studies on the chemical diversity emerging from this biota are rather scarce. Therefore, the present work aims to assess the metabolomic diversity and pharmacological potential of the microbiota from Rocas Atoll. A total of 76 bacteria were isolated and cultured in liquid culture media to obtain crude extracts. About one third (34%) of these extracts were recognized as cytotoxic against human colon adenocarcinoma HCT-116 cell line. 16S rRNA gene sequencing analyses revealed that the bacteria producing cytotoxic extracts were mainly from the Actinobacteria phylum, including Streptomyces, Salinispora, Nocardiopsis, and Brevibacterium genera, and in a smaller proportion from Firmicutes phylum (Bacillus). The search in the spectral library in GNPS (Global Natural Products Social Molecular Networking) unveiled a high chemodiversity being produced by these bacteria, including rifamycins, antimycins, desferrioxamines, ferrioxamines, surfactins, surugamides, staurosporines, and saliniketals, along with several unidentified compounds. Using an original approach, molecular networking successfully highlighted groups of compounds responsible for the cytotoxicity of crude extracts. Application of DEREPLICATOR+ (GNPS) allowed the annotation of macrolide novonestimycin derivatives as the cytotoxic compounds existing in the extracts produced by Streptomyces BRB-298 and BRB-302. Overall, these results highlighted the pharmacological potential of bacteria from this singular atoll. MDPI 2019-11-28 /pmc/articles/PMC6949966/ /pubmed/31795148 http://dx.doi.org/10.3390/md17120671 Text en © 2019 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Velasco-Alzate, Karen Y.
Bauermeister, Anelize
Tangerina, Marcelo M. P.
Lotufo, Tito M. C.
Ferreira, Marcelo J. P.
Jimenez, Paula C.
Padilla, Gabriel
Lopes, Norberto P.
Costa-Lotufo, Letícia V.
Marine Bacteria from Rocas Atoll as a Rich Source of Pharmacologically Active Compounds
title Marine Bacteria from Rocas Atoll as a Rich Source of Pharmacologically Active Compounds
title_full Marine Bacteria from Rocas Atoll as a Rich Source of Pharmacologically Active Compounds
title_fullStr Marine Bacteria from Rocas Atoll as a Rich Source of Pharmacologically Active Compounds
title_full_unstemmed Marine Bacteria from Rocas Atoll as a Rich Source of Pharmacologically Active Compounds
title_short Marine Bacteria from Rocas Atoll as a Rich Source of Pharmacologically Active Compounds
title_sort marine bacteria from rocas atoll as a rich source of pharmacologically active compounds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949966/
https://www.ncbi.nlm.nih.gov/pubmed/31795148
http://dx.doi.org/10.3390/md17120671
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