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Upregulation of a marine fungal biosynthetic gene cluster by an endobacterial symbiont

Fungal-bacterial associations are present in nature, playing important roles in ecological, evolutionary and medicinal processes. Here we report a fungus-bacterial symbiont from marine sediment. The bacterium lives inside the fungal mycelium yet is robust enough to survive independent of its host; t...

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Autores principales: Shao, Mingwei, Sun, Changli, Liu, Xiaoxiao, Wang, Xiaoxue, Li, Wenli, Wei, Xiaoyi, Li, Qinglian, Ju, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7511336/
https://www.ncbi.nlm.nih.gov/pubmed/32968175
http://dx.doi.org/10.1038/s42003-020-01239-y
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author Shao, Mingwei
Sun, Changli
Liu, Xiaoxiao
Wang, Xiaoxue
Li, Wenli
Wei, Xiaoyi
Li, Qinglian
Ju, Jianhua
author_facet Shao, Mingwei
Sun, Changli
Liu, Xiaoxiao
Wang, Xiaoxue
Li, Wenli
Wei, Xiaoyi
Li, Qinglian
Ju, Jianhua
author_sort Shao, Mingwei
collection PubMed
description Fungal-bacterial associations are present in nature, playing important roles in ecological, evolutionary and medicinal processes. Here we report a fungus-bacterial symbiont from marine sediment. The bacterium lives inside the fungal mycelium yet is robust enough to survive independent of its host; the independently grown bacterium can infect the fungal host in vitro and continue to grow progenitively. The bacterial symbiont modulates the fungal host to biosynthesize a polyketide antimicrobial, spiromarmycin. Spiromarmycin appears to endow upon the symbiont pair a protective/defensive means of warding off competitor organisms, be they prokaryotic or eukaryotic microorganisms. Genomic analyses revealed the spiromarmycin biosynthetic machinery to be encoded, not by the bacterium, but rather the fungal host. This unique fungal-bacterial symbiotic relationship and the molecule/s resulting from it dramatically expand our knowledge of marine microbial diversity and shed important insights into endosymbionts and fungal-bacterial relationships.
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spelling pubmed-75113362020-10-08 Upregulation of a marine fungal biosynthetic gene cluster by an endobacterial symbiont Shao, Mingwei Sun, Changli Liu, Xiaoxiao Wang, Xiaoxue Li, Wenli Wei, Xiaoyi Li, Qinglian Ju, Jianhua Commun Biol Article Fungal-bacterial associations are present in nature, playing important roles in ecological, evolutionary and medicinal processes. Here we report a fungus-bacterial symbiont from marine sediment. The bacterium lives inside the fungal mycelium yet is robust enough to survive independent of its host; the independently grown bacterium can infect the fungal host in vitro and continue to grow progenitively. The bacterial symbiont modulates the fungal host to biosynthesize a polyketide antimicrobial, spiromarmycin. Spiromarmycin appears to endow upon the symbiont pair a protective/defensive means of warding off competitor organisms, be they prokaryotic or eukaryotic microorganisms. Genomic analyses revealed the spiromarmycin biosynthetic machinery to be encoded, not by the bacterium, but rather the fungal host. This unique fungal-bacterial symbiotic relationship and the molecule/s resulting from it dramatically expand our knowledge of marine microbial diversity and shed important insights into endosymbionts and fungal-bacterial relationships. Nature Publishing Group UK 2020-09-23 /pmc/articles/PMC7511336/ /pubmed/32968175 http://dx.doi.org/10.1038/s42003-020-01239-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shao, Mingwei
Sun, Changli
Liu, Xiaoxiao
Wang, Xiaoxue
Li, Wenli
Wei, Xiaoyi
Li, Qinglian
Ju, Jianhua
Upregulation of a marine fungal biosynthetic gene cluster by an endobacterial symbiont
title Upregulation of a marine fungal biosynthetic gene cluster by an endobacterial symbiont
title_full Upregulation of a marine fungal biosynthetic gene cluster by an endobacterial symbiont
title_fullStr Upregulation of a marine fungal biosynthetic gene cluster by an endobacterial symbiont
title_full_unstemmed Upregulation of a marine fungal biosynthetic gene cluster by an endobacterial symbiont
title_short Upregulation of a marine fungal biosynthetic gene cluster by an endobacterial symbiont
title_sort upregulation of a marine fungal biosynthetic gene cluster by an endobacterial symbiont
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7511336/
https://www.ncbi.nlm.nih.gov/pubmed/32968175
http://dx.doi.org/10.1038/s42003-020-01239-y
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