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Molecular Identification of Selected Streptomyces Strains Isolated from Mexican Tropical Soils and their Anti-Candida Activity

The increasing incidence of Candida albicans infections and resistance to current antifungal therapies has led to the search for new and more effective antifungal compounds. Actinobacterial species from the Streptomyces genus are recognized as some of the major producers of antimicrobial compounds....

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Autores principales: Escalante-Réndiz, Diana, de-la-Rosa-García, Susana, Tapia-Tussell, Raúl, Martín, Jesús, Reyes, Fernando, Vicente, Francisca, Gamboa-Angulo, Marcela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6603721/
https://www.ncbi.nlm.nih.gov/pubmed/31151174
http://dx.doi.org/10.3390/ijerph16111913
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author Escalante-Réndiz, Diana
de-la-Rosa-García, Susana
Tapia-Tussell, Raúl
Martín, Jesús
Reyes, Fernando
Vicente, Francisca
Gamboa-Angulo, Marcela
author_facet Escalante-Réndiz, Diana
de-la-Rosa-García, Susana
Tapia-Tussell, Raúl
Martín, Jesús
Reyes, Fernando
Vicente, Francisca
Gamboa-Angulo, Marcela
author_sort Escalante-Réndiz, Diana
collection PubMed
description The increasing incidence of Candida albicans infections and resistance to current antifungal therapies has led to the search for new and more effective antifungal compounds. Actinobacterial species from the Streptomyces genus are recognized as some of the major producers of antimicrobial compounds. Therefore, the aims of this study were: (1) the identification of Streptomyces strains isolated from Mexican tropical acidic soils, (2) the evaluation of their antifungal activity on C. albicans, and (3) the exploration of the presence of polyketide synthase genes in their genome and antifungal secondary metabolites in their extracts. Four actinobacterial strains, isolated from previously unexplored soils with antibacterial antecedents, were selected. These strains were identified as Streptomyces angustmyceticus S6A-03, Streptomyces manipurensis S3A-05 and S3A-09, and Streptomyces parvisporogenes S2A-04, according to their molecular analyses. The ethanol extract of the lyophilized supernatant of S. parvisporogenes displayed the most interesting antifungal activity against C. albicans, with a minimum inhibitory concentration (MIC) of 0.5 mg/mL. Type I polyketide synthase (PKS-I) and non-ribosomal peptide synthase (NRPS) genes were detected in all strains. In addition, type II PKS genes (PKS-II) were also found in S. manipurensis S3A-05 and S. parvisporogenes. LC-UV-HRMS analysis of the active organic extract of S. parvisporogenes indicated the presence of the known antifungal compound carbazomycin G as the major component.
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spelling pubmed-66037212019-07-17 Molecular Identification of Selected Streptomyces Strains Isolated from Mexican Tropical Soils and their Anti-Candida Activity Escalante-Réndiz, Diana de-la-Rosa-García, Susana Tapia-Tussell, Raúl Martín, Jesús Reyes, Fernando Vicente, Francisca Gamboa-Angulo, Marcela Int J Environ Res Public Health Article The increasing incidence of Candida albicans infections and resistance to current antifungal therapies has led to the search for new and more effective antifungal compounds. Actinobacterial species from the Streptomyces genus are recognized as some of the major producers of antimicrobial compounds. Therefore, the aims of this study were: (1) the identification of Streptomyces strains isolated from Mexican tropical acidic soils, (2) the evaluation of their antifungal activity on C. albicans, and (3) the exploration of the presence of polyketide synthase genes in their genome and antifungal secondary metabolites in their extracts. Four actinobacterial strains, isolated from previously unexplored soils with antibacterial antecedents, were selected. These strains were identified as Streptomyces angustmyceticus S6A-03, Streptomyces manipurensis S3A-05 and S3A-09, and Streptomyces parvisporogenes S2A-04, according to their molecular analyses. The ethanol extract of the lyophilized supernatant of S. parvisporogenes displayed the most interesting antifungal activity against C. albicans, with a minimum inhibitory concentration (MIC) of 0.5 mg/mL. Type I polyketide synthase (PKS-I) and non-ribosomal peptide synthase (NRPS) genes were detected in all strains. In addition, type II PKS genes (PKS-II) were also found in S. manipurensis S3A-05 and S. parvisporogenes. LC-UV-HRMS analysis of the active organic extract of S. parvisporogenes indicated the presence of the known antifungal compound carbazomycin G as the major component. MDPI 2019-05-30 2019-06 /pmc/articles/PMC6603721/ /pubmed/31151174 http://dx.doi.org/10.3390/ijerph16111913 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
Escalante-Réndiz, Diana
de-la-Rosa-García, Susana
Tapia-Tussell, Raúl
Martín, Jesús
Reyes, Fernando
Vicente, Francisca
Gamboa-Angulo, Marcela
Molecular Identification of Selected Streptomyces Strains Isolated from Mexican Tropical Soils and their Anti-Candida Activity
title Molecular Identification of Selected Streptomyces Strains Isolated from Mexican Tropical Soils and their Anti-Candida Activity
title_full Molecular Identification of Selected Streptomyces Strains Isolated from Mexican Tropical Soils and their Anti-Candida Activity
title_fullStr Molecular Identification of Selected Streptomyces Strains Isolated from Mexican Tropical Soils and their Anti-Candida Activity
title_full_unstemmed Molecular Identification of Selected Streptomyces Strains Isolated from Mexican Tropical Soils and their Anti-Candida Activity
title_short Molecular Identification of Selected Streptomyces Strains Isolated from Mexican Tropical Soils and their Anti-Candida Activity
title_sort molecular identification of selected streptomyces strains isolated from mexican tropical soils and their anti-candida activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6603721/
https://www.ncbi.nlm.nih.gov/pubmed/31151174
http://dx.doi.org/10.3390/ijerph16111913
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