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Mechanism of interaction of an endofungal bacterium Serratia marcescens D1 with its host and non-host fungi

Association of bacteria with fungi is a major area of research in infection biology, however, very few strains of bacteria have been reported that can invade and reside within fungal hyphae. Here, we report the characterization of an endofungal bacterium Serratia marcescens D1 from Mucor irregularis...

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Autores principales: Hazarika, Dibya Jyoti, Gautom, Trishnamoni, Parveen, Assma, Goswami, Gunajit, Barooah, Madhumita, Modi, Mahendra Kumar, Boro, Robin Chandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176118/
https://www.ncbi.nlm.nih.gov/pubmed/32320394
http://dx.doi.org/10.1371/journal.pone.0224051
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author Hazarika, Dibya Jyoti
Gautom, Trishnamoni
Parveen, Assma
Goswami, Gunajit
Barooah, Madhumita
Modi, Mahendra Kumar
Boro, Robin Chandra
author_facet Hazarika, Dibya Jyoti
Gautom, Trishnamoni
Parveen, Assma
Goswami, Gunajit
Barooah, Madhumita
Modi, Mahendra Kumar
Boro, Robin Chandra
author_sort Hazarika, Dibya Jyoti
collection PubMed
description Association of bacteria with fungi is a major area of research in infection biology, however, very few strains of bacteria have been reported that can invade and reside within fungal hyphae. Here, we report the characterization of an endofungal bacterium Serratia marcescens D1 from Mucor irregularis SS7 hyphae. Upon re-inoculation, colonization of the endobacterium S. marcescens D1 in the hyphae of Mucor irregularis SS7 was demonstrated using stereo microscopy. However, S. marcescens D1 failed to invade into the hyphae of the tested Ascomycetes (except Fusarium oxysporum) and Basidiomycetes. Remarkably, Serratia marcescens D1 could invade and spread over the culture of F. oxysporum that resulted in mycelial death. Prodigiosin, the red pigment produced by the Serratia marcescens D1, helps the bacterium to invade fungal hyphae as revealed by the increasing permeability in fungal cell membrane. On the other hand, genes encoding the type VI secretion system (T6SS) assembly protein TssJ and an outer membrane associated murein lipoprotein also showed significant up-regulation during the interaction process, suggesting the involvement of T6SS in the invasion process.
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spelling pubmed-71761182020-05-12 Mechanism of interaction of an endofungal bacterium Serratia marcescens D1 with its host and non-host fungi Hazarika, Dibya Jyoti Gautom, Trishnamoni Parveen, Assma Goswami, Gunajit Barooah, Madhumita Modi, Mahendra Kumar Boro, Robin Chandra PLoS One Research Article Association of bacteria with fungi is a major area of research in infection biology, however, very few strains of bacteria have been reported that can invade and reside within fungal hyphae. Here, we report the characterization of an endofungal bacterium Serratia marcescens D1 from Mucor irregularis SS7 hyphae. Upon re-inoculation, colonization of the endobacterium S. marcescens D1 in the hyphae of Mucor irregularis SS7 was demonstrated using stereo microscopy. However, S. marcescens D1 failed to invade into the hyphae of the tested Ascomycetes (except Fusarium oxysporum) and Basidiomycetes. Remarkably, Serratia marcescens D1 could invade and spread over the culture of F. oxysporum that resulted in mycelial death. Prodigiosin, the red pigment produced by the Serratia marcescens D1, helps the bacterium to invade fungal hyphae as revealed by the increasing permeability in fungal cell membrane. On the other hand, genes encoding the type VI secretion system (T6SS) assembly protein TssJ and an outer membrane associated murein lipoprotein also showed significant up-regulation during the interaction process, suggesting the involvement of T6SS in the invasion process. Public Library of Science 2020-04-22 /pmc/articles/PMC7176118/ /pubmed/32320394 http://dx.doi.org/10.1371/journal.pone.0224051 Text en © 2020 Hazarika et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hazarika, Dibya Jyoti
Gautom, Trishnamoni
Parveen, Assma
Goswami, Gunajit
Barooah, Madhumita
Modi, Mahendra Kumar
Boro, Robin Chandra
Mechanism of interaction of an endofungal bacterium Serratia marcescens D1 with its host and non-host fungi
title Mechanism of interaction of an endofungal bacterium Serratia marcescens D1 with its host and non-host fungi
title_full Mechanism of interaction of an endofungal bacterium Serratia marcescens D1 with its host and non-host fungi
title_fullStr Mechanism of interaction of an endofungal bacterium Serratia marcescens D1 with its host and non-host fungi
title_full_unstemmed Mechanism of interaction of an endofungal bacterium Serratia marcescens D1 with its host and non-host fungi
title_short Mechanism of interaction of an endofungal bacterium Serratia marcescens D1 with its host and non-host fungi
title_sort mechanism of interaction of an endofungal bacterium serratia marcescens d1 with its host and non-host fungi
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176118/
https://www.ncbi.nlm.nih.gov/pubmed/32320394
http://dx.doi.org/10.1371/journal.pone.0224051
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