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Fungal mycelia and bacterial thiamine establish a mutualistic growth mechanism

Exclusivity in physical spaces and nutrients is a prerequisite for survival of organisms, but a few species have been able to develop mutually beneficial strategies that allow them to co-habit. Here, we discovered a mutualistic mechanism between filamentous fungus, Aspergillus nidulans, and bacteriu...

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Autores principales: Abeysinghe, Gayan, Kuchira, Momoka, Kudo, Gamon, Masuo, Shunsuke, Ninomiya, Akihiro, Takahashi, Kohei, Utada, Andrew S, Hagiwara, Daisuke, Nomura, Nobuhiko, Takaya, Naoki, Obana, Nozomu, Takeshita, Norio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7574024/
https://www.ncbi.nlm.nih.gov/pubmed/32962971
http://dx.doi.org/10.26508/lsa.202000878
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author Abeysinghe, Gayan
Kuchira, Momoka
Kudo, Gamon
Masuo, Shunsuke
Ninomiya, Akihiro
Takahashi, Kohei
Utada, Andrew S
Hagiwara, Daisuke
Nomura, Nobuhiko
Takaya, Naoki
Obana, Nozomu
Takeshita, Norio
author_facet Abeysinghe, Gayan
Kuchira, Momoka
Kudo, Gamon
Masuo, Shunsuke
Ninomiya, Akihiro
Takahashi, Kohei
Utada, Andrew S
Hagiwara, Daisuke
Nomura, Nobuhiko
Takaya, Naoki
Obana, Nozomu
Takeshita, Norio
author_sort Abeysinghe, Gayan
collection PubMed
description Exclusivity in physical spaces and nutrients is a prerequisite for survival of organisms, but a few species have been able to develop mutually beneficial strategies that allow them to co-habit. Here, we discovered a mutualistic mechanism between filamentous fungus, Aspergillus nidulans, and bacterium, Bacillus subtilis. The bacterial cells co-cultured with the fungus traveled along mycelia using their flagella and dispersed farther with the expansion of fungal colony, indicating that the fungal mycelia supply space for bacteria to migrate, disperse, and proliferate. Transcriptomic, genetic, molecular mass, and imaging analyses demonstrated that the bacteria reached the mycelial edge and supplied thiamine to the growing hyphae, which led to a promotion of hyphal growth. The thiamine transfer from bacteria to the thiamine non-auxotrophic fungus was directly demonstrated by stable isotope labeling. The simultaneous spatial and metabolic interactions demonstrated in this study reveal a mutualism that facilitates the communicating fungal and bacterial species to obtain an environmental niche and nutrient, respectively.
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spelling pubmed-75740242020-10-27 Fungal mycelia and bacterial thiamine establish a mutualistic growth mechanism Abeysinghe, Gayan Kuchira, Momoka Kudo, Gamon Masuo, Shunsuke Ninomiya, Akihiro Takahashi, Kohei Utada, Andrew S Hagiwara, Daisuke Nomura, Nobuhiko Takaya, Naoki Obana, Nozomu Takeshita, Norio Life Sci Alliance Research Articles Exclusivity in physical spaces and nutrients is a prerequisite for survival of organisms, but a few species have been able to develop mutually beneficial strategies that allow them to co-habit. Here, we discovered a mutualistic mechanism between filamentous fungus, Aspergillus nidulans, and bacterium, Bacillus subtilis. The bacterial cells co-cultured with the fungus traveled along mycelia using their flagella and dispersed farther with the expansion of fungal colony, indicating that the fungal mycelia supply space for bacteria to migrate, disperse, and proliferate. Transcriptomic, genetic, molecular mass, and imaging analyses demonstrated that the bacteria reached the mycelial edge and supplied thiamine to the growing hyphae, which led to a promotion of hyphal growth. The thiamine transfer from bacteria to the thiamine non-auxotrophic fungus was directly demonstrated by stable isotope labeling. The simultaneous spatial and metabolic interactions demonstrated in this study reveal a mutualism that facilitates the communicating fungal and bacterial species to obtain an environmental niche and nutrient, respectively. Life Science Alliance LLC 2020-09-21 /pmc/articles/PMC7574024/ /pubmed/32962971 http://dx.doi.org/10.26508/lsa.202000878 Text en © 2020 Abeysinghe et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Articles
Abeysinghe, Gayan
Kuchira, Momoka
Kudo, Gamon
Masuo, Shunsuke
Ninomiya, Akihiro
Takahashi, Kohei
Utada, Andrew S
Hagiwara, Daisuke
Nomura, Nobuhiko
Takaya, Naoki
Obana, Nozomu
Takeshita, Norio
Fungal mycelia and bacterial thiamine establish a mutualistic growth mechanism
title Fungal mycelia and bacterial thiamine establish a mutualistic growth mechanism
title_full Fungal mycelia and bacterial thiamine establish a mutualistic growth mechanism
title_fullStr Fungal mycelia and bacterial thiamine establish a mutualistic growth mechanism
title_full_unstemmed Fungal mycelia and bacterial thiamine establish a mutualistic growth mechanism
title_short Fungal mycelia and bacterial thiamine establish a mutualistic growth mechanism
title_sort fungal mycelia and bacterial thiamine establish a mutualistic growth mechanism
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7574024/
https://www.ncbi.nlm.nih.gov/pubmed/32962971
http://dx.doi.org/10.26508/lsa.202000878
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