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Diversity and Antimicrobial Potential of Predatory Bacteria from the Peruvian Coastline
The microbiome of three different sites at the Peruvian Pacific coast was analyzed, revealing a lower bacterial biodiversity at Isla Foca than at Paracas and Manglares, with 89 bacterial genera identified, as compared to 195 and 173 genera, respectively. Only 47 of the bacterial genera identified we...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666416/ https://www.ncbi.nlm.nih.gov/pubmed/29023396 http://dx.doi.org/10.3390/md15100308 |
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author | Linares-Otoya, Luis Linares-Otoya, Virginia Armas-Mantilla, Lizbeth Blanco-Olano, Cyntia Crüsemann, Max Ganoza-Yupanqui, Mayar L. Campos-Florian, Julio König, Gabriele M. Schäberle, Till F. |
author_facet | Linares-Otoya, Luis Linares-Otoya, Virginia Armas-Mantilla, Lizbeth Blanco-Olano, Cyntia Crüsemann, Max Ganoza-Yupanqui, Mayar L. Campos-Florian, Julio König, Gabriele M. Schäberle, Till F. |
author_sort | Linares-Otoya, Luis |
collection | PubMed |
description | The microbiome of three different sites at the Peruvian Pacific coast was analyzed, revealing a lower bacterial biodiversity at Isla Foca than at Paracas and Manglares, with 89 bacterial genera identified, as compared to 195 and 173 genera, respectively. Only 47 of the bacterial genera identified were common to all three sites. In order to obtain promising strains for the putative production of novel antimicrobials, predatory bacteria were isolated from these sampling sites, using two different bait organisms. Even though the proportion of predatory bacteria was only around 0.5% in the here investigated environmental microbiomes, by this approach in total 138 bacterial strains were isolated as axenic culture. 25% of strains showed antibacterial activity, thereby nine revealed activity against clinically relevant methicillin resistant Staphylococcus aureus (MRSA) and three against enterohemorrhagic Escherichia coli (EHEC) strains. Phylogeny and physiological characteristics of the active strains were investigated. First insights into the chemical basis of the antibacterial activity indicated the biosynthetic production of the known compounds ariakemicin, kocurin, naphthyridinomycin, pumilacidins, resistomycin, and surfactin. However, most compounds remained elusive until now. Hence, the obtained results implicate that the microbiome present at the various habitats at the Peruvian coastline is a promising source for heterotrophic bacterial strains showing high potential for the biotechnological production of antibiotics. |
format | Online Article Text |
id | pubmed-5666416 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-56664162017-11-09 Diversity and Antimicrobial Potential of Predatory Bacteria from the Peruvian Coastline Linares-Otoya, Luis Linares-Otoya, Virginia Armas-Mantilla, Lizbeth Blanco-Olano, Cyntia Crüsemann, Max Ganoza-Yupanqui, Mayar L. Campos-Florian, Julio König, Gabriele M. Schäberle, Till F. Mar Drugs Article The microbiome of three different sites at the Peruvian Pacific coast was analyzed, revealing a lower bacterial biodiversity at Isla Foca than at Paracas and Manglares, with 89 bacterial genera identified, as compared to 195 and 173 genera, respectively. Only 47 of the bacterial genera identified were common to all three sites. In order to obtain promising strains for the putative production of novel antimicrobials, predatory bacteria were isolated from these sampling sites, using two different bait organisms. Even though the proportion of predatory bacteria was only around 0.5% in the here investigated environmental microbiomes, by this approach in total 138 bacterial strains were isolated as axenic culture. 25% of strains showed antibacterial activity, thereby nine revealed activity against clinically relevant methicillin resistant Staphylococcus aureus (MRSA) and three against enterohemorrhagic Escherichia coli (EHEC) strains. Phylogeny and physiological characteristics of the active strains were investigated. First insights into the chemical basis of the antibacterial activity indicated the biosynthetic production of the known compounds ariakemicin, kocurin, naphthyridinomycin, pumilacidins, resistomycin, and surfactin. However, most compounds remained elusive until now. Hence, the obtained results implicate that the microbiome present at the various habitats at the Peruvian coastline is a promising source for heterotrophic bacterial strains showing high potential for the biotechnological production of antibiotics. MDPI 2017-10-12 /pmc/articles/PMC5666416/ /pubmed/29023396 http://dx.doi.org/10.3390/md15100308 Text en © 2017 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 Linares-Otoya, Luis Linares-Otoya, Virginia Armas-Mantilla, Lizbeth Blanco-Olano, Cyntia Crüsemann, Max Ganoza-Yupanqui, Mayar L. Campos-Florian, Julio König, Gabriele M. Schäberle, Till F. Diversity and Antimicrobial Potential of Predatory Bacteria from the Peruvian Coastline |
title | Diversity and Antimicrobial Potential of Predatory Bacteria from the Peruvian Coastline |
title_full | Diversity and Antimicrobial Potential of Predatory Bacteria from the Peruvian Coastline |
title_fullStr | Diversity and Antimicrobial Potential of Predatory Bacteria from the Peruvian Coastline |
title_full_unstemmed | Diversity and Antimicrobial Potential of Predatory Bacteria from the Peruvian Coastline |
title_short | Diversity and Antimicrobial Potential of Predatory Bacteria from the Peruvian Coastline |
title_sort | diversity and antimicrobial potential of predatory bacteria from the peruvian coastline |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666416/ https://www.ncbi.nlm.nih.gov/pubmed/29023396 http://dx.doi.org/10.3390/md15100308 |
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