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Anti-MRSA Activity of Actinomycin X(2) and Collismycin A Produced by Streptomyces globisporus WA5-2-37 From the Intestinal Tract of American Cockroach (Periplaneta americana)

Methicillin-resistant Staphylococcus aureus (MRSA) is recognized as one of the serious pathogen that causes acquired infections worldwide. Its emerging need to discover novel, safe and potent anti-MRSA drugs. In this study, primary screening by anti-MRSA activity assay found one strain WA5-2-37 isol...

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Autores principales: Chen, Zhiyu, Ou, Peiyu, Liu, Lingyan, Jin, Xiaobao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154055/
https://www.ncbi.nlm.nih.gov/pubmed/32318039
http://dx.doi.org/10.3389/fmicb.2020.00555
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author Chen, Zhiyu
Ou, Peiyu
Liu, Lingyan
Jin, Xiaobao
author_facet Chen, Zhiyu
Ou, Peiyu
Liu, Lingyan
Jin, Xiaobao
author_sort Chen, Zhiyu
collection PubMed
description Methicillin-resistant Staphylococcus aureus (MRSA) is recognized as one of the serious pathogen that causes acquired infections worldwide. Its emerging need to discover novel, safe and potent anti-MRSA drugs. In this study, primary screening by anti-MRSA activity assay found one strain WA5-2-37 isolated from the intestinal tract of Periplaneta americana, exhibited great activity against MRSA ATCC 43300. The strain WA5-2-37 produced actinomycin X(2) and collismycin A which showed strong inhibition of MRSA with minimum inhibitory concentration (MIC) values of 0.25 and 8 μg/mL. The structures of the pure compounds were elucidated by analysis of mass spectrometry (MS), (1)H and (13)C nuclear magnetic resonance (NMR). The strain WA5-2-37 was considered as Streptomyces globisporus on the basis of morphological characteristics, genotypic data, and phylogenetic analysis. This is the first reported naturally occurring strain of S. globisporus isolated from the intestinal tract of P. americana, whereas it has almost been found from plants, marine, and soil previously. Moreover, S. globisporus has not been reported to produce any anti-MRSA substances previously, such as actinomycin X(2) and collismycin A. In conclusion, the insect-derived strain of S. globisporus WA5-2-37 was considered of great potential as a new strain of producing actinomycin X(2), collismycin A or other anti-MRSA compounds.
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spelling pubmed-71540552020-04-21 Anti-MRSA Activity of Actinomycin X(2) and Collismycin A Produced by Streptomyces globisporus WA5-2-37 From the Intestinal Tract of American Cockroach (Periplaneta americana) Chen, Zhiyu Ou, Peiyu Liu, Lingyan Jin, Xiaobao Front Microbiol Microbiology Methicillin-resistant Staphylococcus aureus (MRSA) is recognized as one of the serious pathogen that causes acquired infections worldwide. Its emerging need to discover novel, safe and potent anti-MRSA drugs. In this study, primary screening by anti-MRSA activity assay found one strain WA5-2-37 isolated from the intestinal tract of Periplaneta americana, exhibited great activity against MRSA ATCC 43300. The strain WA5-2-37 produced actinomycin X(2) and collismycin A which showed strong inhibition of MRSA with minimum inhibitory concentration (MIC) values of 0.25 and 8 μg/mL. The structures of the pure compounds were elucidated by analysis of mass spectrometry (MS), (1)H and (13)C nuclear magnetic resonance (NMR). The strain WA5-2-37 was considered as Streptomyces globisporus on the basis of morphological characteristics, genotypic data, and phylogenetic analysis. This is the first reported naturally occurring strain of S. globisporus isolated from the intestinal tract of P. americana, whereas it has almost been found from plants, marine, and soil previously. Moreover, S. globisporus has not been reported to produce any anti-MRSA substances previously, such as actinomycin X(2) and collismycin A. In conclusion, the insect-derived strain of S. globisporus WA5-2-37 was considered of great potential as a new strain of producing actinomycin X(2), collismycin A or other anti-MRSA compounds. Frontiers Media S.A. 2020-04-07 /pmc/articles/PMC7154055/ /pubmed/32318039 http://dx.doi.org/10.3389/fmicb.2020.00555 Text en Copyright © 2020 Chen, Ou, Liu and Jin. 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) and the copyright owner(s) 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
Chen, Zhiyu
Ou, Peiyu
Liu, Lingyan
Jin, Xiaobao
Anti-MRSA Activity of Actinomycin X(2) and Collismycin A Produced by Streptomyces globisporus WA5-2-37 From the Intestinal Tract of American Cockroach (Periplaneta americana)
title Anti-MRSA Activity of Actinomycin X(2) and Collismycin A Produced by Streptomyces globisporus WA5-2-37 From the Intestinal Tract of American Cockroach (Periplaneta americana)
title_full Anti-MRSA Activity of Actinomycin X(2) and Collismycin A Produced by Streptomyces globisporus WA5-2-37 From the Intestinal Tract of American Cockroach (Periplaneta americana)
title_fullStr Anti-MRSA Activity of Actinomycin X(2) and Collismycin A Produced by Streptomyces globisporus WA5-2-37 From the Intestinal Tract of American Cockroach (Periplaneta americana)
title_full_unstemmed Anti-MRSA Activity of Actinomycin X(2) and Collismycin A Produced by Streptomyces globisporus WA5-2-37 From the Intestinal Tract of American Cockroach (Periplaneta americana)
title_short Anti-MRSA Activity of Actinomycin X(2) and Collismycin A Produced by Streptomyces globisporus WA5-2-37 From the Intestinal Tract of American Cockroach (Periplaneta americana)
title_sort anti-mrsa activity of actinomycin x(2) and collismycin a produced by streptomyces globisporus wa5-2-37 from the intestinal tract of american cockroach (periplaneta americana)
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154055/
https://www.ncbi.nlm.nih.gov/pubmed/32318039
http://dx.doi.org/10.3389/fmicb.2020.00555
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