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Assessing the diversity of bacterial communities from marine sponges and their bioactive compounds

Symbiotic bacteria play vital roles in the survival and health of marine sponges. Sponges harbor rich, diverse and species-specific microbial communities. Symbiotic marine bacteria have increasingly been reported as promising source of bioactive compounds. A culturomics-based study was undertaken to...

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Detalles Bibliográficos
Autores principales: Bibi, Fehmida, Naseer, Muhammad Imran, Azhar, Esam Ibraheem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117107/
https://www.ncbi.nlm.nih.gov/pubmed/34025160
http://dx.doi.org/10.1016/j.sjbs.2021.03.042
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author Bibi, Fehmida
Naseer, Muhammad Imran
Azhar, Esam Ibraheem
author_facet Bibi, Fehmida
Naseer, Muhammad Imran
Azhar, Esam Ibraheem
author_sort Bibi, Fehmida
collection PubMed
description Symbiotic bacteria play vital roles in the survival and health of marine sponges. Sponges harbor rich, diverse and species-specific microbial communities. Symbiotic marine bacteria have increasingly been reported as promising source of bioactive compounds. A culturomics-based study was undertaken to study the diversity of bacteria from marine sponges and their antimicrobial potential. We have collected three sponge samples i.e. Acanthaster carteri, Rhytisma fulvum (soft coral) and Haliclona caerulea from north region (Obhur) of Red Sea, Jeddah Saudi Arabia. Total of 144 bacterial strains were isolated from three marine sponges using culture dependent method. Screening of isolated strains showed only 37 (26%) isolates as antagonists against oomycetes pathogens (P. ultimum and P. capsici). Among 37 antagonistic bacteria, only 19 bacterial strains exhibited antibacterial activity against human pathogens (Methicillin-resistant Staphylococcus aureus (MRSA) ATCC 43300, Pseudomonas aeruginosa ATCC 27853, Escherichia coli ATCC 8739, Enterococcus faecalis ATCC 29212). Four major classes of bacteria i.e γ-Proteobacteria, α-Proteobacteria, Firmicutes and Actinobacteria were recorded from three marine sponges where γ-Proteobacteria was dominant class. One potential bacterial strain Halomonas sp. EA423 was selected for identification of bioactive metabolites using GC and LC-MS analyses. Bioactive compounds Sulfamerazine, Metronidazole-OH and Ibuprofen are detected from culture extract of strain Halomonas sp. EA423. Overall, this study gives insight into composition and diversity of antagonistic bacterial community of marine sponges and coral from Red Sea and presence of active metabolites from potential strain. Our results showed that these diverse and potential bacterial communities further need to be studied to exploit their biotechnological significance.
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spelling pubmed-81171072021-05-20 Assessing the diversity of bacterial communities from marine sponges and their bioactive compounds Bibi, Fehmida Naseer, Muhammad Imran Azhar, Esam Ibraheem Saudi J Biol Sci Original Article Symbiotic bacteria play vital roles in the survival and health of marine sponges. Sponges harbor rich, diverse and species-specific microbial communities. Symbiotic marine bacteria have increasingly been reported as promising source of bioactive compounds. A culturomics-based study was undertaken to study the diversity of bacteria from marine sponges and their antimicrobial potential. We have collected three sponge samples i.e. Acanthaster carteri, Rhytisma fulvum (soft coral) and Haliclona caerulea from north region (Obhur) of Red Sea, Jeddah Saudi Arabia. Total of 144 bacterial strains were isolated from three marine sponges using culture dependent method. Screening of isolated strains showed only 37 (26%) isolates as antagonists against oomycetes pathogens (P. ultimum and P. capsici). Among 37 antagonistic bacteria, only 19 bacterial strains exhibited antibacterial activity against human pathogens (Methicillin-resistant Staphylococcus aureus (MRSA) ATCC 43300, Pseudomonas aeruginosa ATCC 27853, Escherichia coli ATCC 8739, Enterococcus faecalis ATCC 29212). Four major classes of bacteria i.e γ-Proteobacteria, α-Proteobacteria, Firmicutes and Actinobacteria were recorded from three marine sponges where γ-Proteobacteria was dominant class. One potential bacterial strain Halomonas sp. EA423 was selected for identification of bioactive metabolites using GC and LC-MS analyses. Bioactive compounds Sulfamerazine, Metronidazole-OH and Ibuprofen are detected from culture extract of strain Halomonas sp. EA423. Overall, this study gives insight into composition and diversity of antagonistic bacterial community of marine sponges and coral from Red Sea and presence of active metabolites from potential strain. Our results showed that these diverse and potential bacterial communities further need to be studied to exploit their biotechnological significance. Elsevier 2021-05 2021-03-23 /pmc/articles/PMC8117107/ /pubmed/34025160 http://dx.doi.org/10.1016/j.sjbs.2021.03.042 Text en © 2021 The Author(s) https://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 Original Article
Bibi, Fehmida
Naseer, Muhammad Imran
Azhar, Esam Ibraheem
Assessing the diversity of bacterial communities from marine sponges and their bioactive compounds
title Assessing the diversity of bacterial communities from marine sponges and their bioactive compounds
title_full Assessing the diversity of bacterial communities from marine sponges and their bioactive compounds
title_fullStr Assessing the diversity of bacterial communities from marine sponges and their bioactive compounds
title_full_unstemmed Assessing the diversity of bacterial communities from marine sponges and their bioactive compounds
title_short Assessing the diversity of bacterial communities from marine sponges and their bioactive compounds
title_sort assessing the diversity of bacterial communities from marine sponges and their bioactive compounds
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117107/
https://www.ncbi.nlm.nih.gov/pubmed/34025160
http://dx.doi.org/10.1016/j.sjbs.2021.03.042
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