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Production of Ramoplanin and Ramoplanin Analogs by Actinomycetes

Ramoplanin is a glycolipodepsipeptide antibiotic obtained from fermentation of Actinoplanes sp. ATCC 33076 that exhibits activity against clinically important multi-drug-resistant, Gram-positive pathogens including vancomycin-resistant Enterococcus (VRE), methicillin-resistant Staphylococcus aureus...

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Autores principales: de la Cruz, Mercedes, González, Ignacio, Parish, Craig A., Onishi, Russell, Tormo, José R., Martín, Jesús, Peláez, Fernando, Zink, Debbie, El Aouad, Noureddine, Reyes, Fernando, Genilloud, Olga, Vicente, Francisca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337499/
https://www.ncbi.nlm.nih.gov/pubmed/28321210
http://dx.doi.org/10.3389/fmicb.2017.00343
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author de la Cruz, Mercedes
González, Ignacio
Parish, Craig A.
Onishi, Russell
Tormo, José R.
Martín, Jesús
Peláez, Fernando
Zink, Debbie
El Aouad, Noureddine
Reyes, Fernando
Genilloud, Olga
Vicente, Francisca
author_facet de la Cruz, Mercedes
González, Ignacio
Parish, Craig A.
Onishi, Russell
Tormo, José R.
Martín, Jesús
Peláez, Fernando
Zink, Debbie
El Aouad, Noureddine
Reyes, Fernando
Genilloud, Olga
Vicente, Francisca
author_sort de la Cruz, Mercedes
collection PubMed
description Ramoplanin is a glycolipodepsipeptide antibiotic obtained from fermentation of Actinoplanes sp. ATCC 33076 that exhibits activity against clinically important multi-drug-resistant, Gram-positive pathogens including vancomycin-resistant Enterococcus (VRE), methicillin-resistant Staphylococcus aureus (MRSA), and vancomycin-intermediate resistant Clostridium difficile. It disrupts bacterial cell wall through a unique mechanism of action by sequestering the peptidoglycan intermediate Lipid II and therefore does not show cross-resistance with other antibiotics. However, while demonstrating excellent antimicrobial activity in systemic use in animal models of infection, ramoplanin presents low local tolerability when injected intravenously. As a consequence of this limitation, new derivatives are desirable to overcome this issue. During a natural product screening program developed to discover compounds that disrupt bacterial cell wall synthesis by inhibiting peptidoglycan transglycosylation through binding to the intermediate Lipid II, 49 actinomycete strains were identified by HR-LCMS as producers of ramoplanin-related compounds. The producing strains were isolated from environmental samples collected worldwide comprising both tropical and temperate areas. To assess the diversity of this microbial population, the 49 isolates were initially identified to the genus level on the basis of their micromorphology, and 16S sequencing confirmed the initial identification of the strains. These analyses resulted in the identification of members of genus Streptomyces, as well as representatives of the families Micromonosporaceae, Nocardiaceae, Thermomonosporaceae, and Pseudonocardiaceae, suggesting that the production of ramoplanins is relatively widespread among Actinomycetes. In addition, all of these isolates were tested against a panel of Gram-positive and Gram-negative bacteria, filamentous fungi, and yeast in order to further characterize their antimicrobial properties. This work describes the diversity of actinomycete strains that produced ramoplanin-related compounds, and the analysis of the antimicrobial activity exhibited by these isolates. Our results strongly suggest the presence of new ramoplanin-analogs among these actinomycete producers.
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spelling pubmed-53374992017-03-20 Production of Ramoplanin and Ramoplanin Analogs by Actinomycetes de la Cruz, Mercedes González, Ignacio Parish, Craig A. Onishi, Russell Tormo, José R. Martín, Jesús Peláez, Fernando Zink, Debbie El Aouad, Noureddine Reyes, Fernando Genilloud, Olga Vicente, Francisca Front Microbiol Microbiology Ramoplanin is a glycolipodepsipeptide antibiotic obtained from fermentation of Actinoplanes sp. ATCC 33076 that exhibits activity against clinically important multi-drug-resistant, Gram-positive pathogens including vancomycin-resistant Enterococcus (VRE), methicillin-resistant Staphylococcus aureus (MRSA), and vancomycin-intermediate resistant Clostridium difficile. It disrupts bacterial cell wall through a unique mechanism of action by sequestering the peptidoglycan intermediate Lipid II and therefore does not show cross-resistance with other antibiotics. However, while demonstrating excellent antimicrobial activity in systemic use in animal models of infection, ramoplanin presents low local tolerability when injected intravenously. As a consequence of this limitation, new derivatives are desirable to overcome this issue. During a natural product screening program developed to discover compounds that disrupt bacterial cell wall synthesis by inhibiting peptidoglycan transglycosylation through binding to the intermediate Lipid II, 49 actinomycete strains were identified by HR-LCMS as producers of ramoplanin-related compounds. The producing strains were isolated from environmental samples collected worldwide comprising both tropical and temperate areas. To assess the diversity of this microbial population, the 49 isolates were initially identified to the genus level on the basis of their micromorphology, and 16S sequencing confirmed the initial identification of the strains. These analyses resulted in the identification of members of genus Streptomyces, as well as representatives of the families Micromonosporaceae, Nocardiaceae, Thermomonosporaceae, and Pseudonocardiaceae, suggesting that the production of ramoplanins is relatively widespread among Actinomycetes. In addition, all of these isolates were tested against a panel of Gram-positive and Gram-negative bacteria, filamentous fungi, and yeast in order to further characterize their antimicrobial properties. This work describes the diversity of actinomycete strains that produced ramoplanin-related compounds, and the analysis of the antimicrobial activity exhibited by these isolates. Our results strongly suggest the presence of new ramoplanin-analogs among these actinomycete producers. Frontiers Media S.A. 2017-03-06 /pmc/articles/PMC5337499/ /pubmed/28321210 http://dx.doi.org/10.3389/fmicb.2017.00343 Text en Copyright © 2017 de la Cruz, González, Parish, Onishi, Tormo, Martín, Peláez, Zink, El Aouad, Reyes, Genilloud and Vicente. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
de la Cruz, Mercedes
González, Ignacio
Parish, Craig A.
Onishi, Russell
Tormo, José R.
Martín, Jesús
Peláez, Fernando
Zink, Debbie
El Aouad, Noureddine
Reyes, Fernando
Genilloud, Olga
Vicente, Francisca
Production of Ramoplanin and Ramoplanin Analogs by Actinomycetes
title Production of Ramoplanin and Ramoplanin Analogs by Actinomycetes
title_full Production of Ramoplanin and Ramoplanin Analogs by Actinomycetes
title_fullStr Production of Ramoplanin and Ramoplanin Analogs by Actinomycetes
title_full_unstemmed Production of Ramoplanin and Ramoplanin Analogs by Actinomycetes
title_short Production of Ramoplanin and Ramoplanin Analogs by Actinomycetes
title_sort production of ramoplanin and ramoplanin analogs by actinomycetes
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337499/
https://www.ncbi.nlm.nih.gov/pubmed/28321210
http://dx.doi.org/10.3389/fmicb.2017.00343
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