Cargando…
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...
Autores principales: | , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783597556526219264 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7574024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Life Science Alliance LLC |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT abeysinghegayan fungalmyceliaandbacterialthiamineestablishamutualisticgrowthmechanism AT kuchiramomoka fungalmyceliaandbacterialthiamineestablishamutualisticgrowthmechanism AT kudogamon fungalmyceliaandbacterialthiamineestablishamutualisticgrowthmechanism AT masuoshunsuke fungalmyceliaandbacterialthiamineestablishamutualisticgrowthmechanism AT ninomiyaakihiro fungalmyceliaandbacterialthiamineestablishamutualisticgrowthmechanism AT takahashikohei fungalmyceliaandbacterialthiamineestablishamutualisticgrowthmechanism AT utadaandrews fungalmyceliaandbacterialthiamineestablishamutualisticgrowthmechanism AT hagiwaradaisuke fungalmyceliaandbacterialthiamineestablishamutualisticgrowthmechanism AT nomuranobuhiko fungalmyceliaandbacterialthiamineestablishamutualisticgrowthmechanism AT takayanaoki fungalmyceliaandbacterialthiamineestablishamutualisticgrowthmechanism AT obananozomu fungalmyceliaandbacterialthiamineestablishamutualisticgrowthmechanism AT takeshitanorio fungalmyceliaandbacterialthiamineestablishamutualisticgrowthmechanism |