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Exploring the genomic traits of fungus-feeding bacterial genus Collimonas

BACKGROUND: Collimonas is a genus belonging to the class of Betaproteobacteria and consists mostly of soil bacteria with the ability to exploit living fungi as food source (mycophagy). Collimonas strains differ in a range of activities, including swimming motility, quorum sensing, extracellular prot...

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Autores principales: Song, Chunxu, Schmidt, Ruth, de Jager, Victor, Krzyzanowska, Dorota, Jongedijk, Esmer, Cankar, Katarina, Beekwilder, Jules, van Veen, Anouk, de Boer, Wietse, van Veen, Johannes A., Garbeva, Paolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4690342/
https://www.ncbi.nlm.nih.gov/pubmed/26704531
http://dx.doi.org/10.1186/s12864-015-2289-3
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author Song, Chunxu
Schmidt, Ruth
de Jager, Victor
Krzyzanowska, Dorota
Jongedijk, Esmer
Cankar, Katarina
Beekwilder, Jules
van Veen, Anouk
de Boer, Wietse
van Veen, Johannes A.
Garbeva, Paolina
author_facet Song, Chunxu
Schmidt, Ruth
de Jager, Victor
Krzyzanowska, Dorota
Jongedijk, Esmer
Cankar, Katarina
Beekwilder, Jules
van Veen, Anouk
de Boer, Wietse
van Veen, Johannes A.
Garbeva, Paolina
author_sort Song, Chunxu
collection PubMed
description BACKGROUND: Collimonas is a genus belonging to the class of Betaproteobacteria and consists mostly of soil bacteria with the ability to exploit living fungi as food source (mycophagy). Collimonas strains differ in a range of activities, including swimming motility, quorum sensing, extracellular protease activity, siderophore production, and antimicrobial activities. RESULTS: In order to reveal ecological traits possibly related to Collimonas lifestyle and secondary metabolites production, we performed a comparative genomics analysis based on whole-genome sequencing of six strains representing 3 recognized species. The analysis revealed that the core genome represents 43.1 to 52.7 % of the genomes of the six individual strains. These include genes coding for extracellular enzymes (chitinase, peptidase, phospholipase), iron acquisition and type II secretion systems. In the variable genome, differences were found in genes coding for secondary metabolites (e.g. tripropeptin A and volatile terpenes), several unknown orphan polyketide synthase-nonribosomal peptide synthetase (PKS-NRPS), nonribosomal peptide synthetase (NRPS) gene clusters, a new lipopeptide and type III and type VI secretion systems. Potential roles of the latter genes in the interaction with other organisms were investigated. Mutation of a gene involved in tripropeptin A biosynthesis strongly reduced the antibacterial activity against Staphylococcus aureus, while disruption of a gene involved in the biosynthesis of the new lipopeptide had a large effect on the antifungal/oomycetal activities. CONCLUSIONS: Overall our results indicated that Collimonas genomes harbour many genes encoding for novel enzymes and secondary metabolites (including terpenes) important for interactions with other organisms and revealed genomic plasticity, which reflect the behaviour, antimicrobial activity and lifestylesof Collimonas spp. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2289-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-46903422015-12-25 Exploring the genomic traits of fungus-feeding bacterial genus Collimonas Song, Chunxu Schmidt, Ruth de Jager, Victor Krzyzanowska, Dorota Jongedijk, Esmer Cankar, Katarina Beekwilder, Jules van Veen, Anouk de Boer, Wietse van Veen, Johannes A. Garbeva, Paolina BMC Genomics Research Article BACKGROUND: Collimonas is a genus belonging to the class of Betaproteobacteria and consists mostly of soil bacteria with the ability to exploit living fungi as food source (mycophagy). Collimonas strains differ in a range of activities, including swimming motility, quorum sensing, extracellular protease activity, siderophore production, and antimicrobial activities. RESULTS: In order to reveal ecological traits possibly related to Collimonas lifestyle and secondary metabolites production, we performed a comparative genomics analysis based on whole-genome sequencing of six strains representing 3 recognized species. The analysis revealed that the core genome represents 43.1 to 52.7 % of the genomes of the six individual strains. These include genes coding for extracellular enzymes (chitinase, peptidase, phospholipase), iron acquisition and type II secretion systems. In the variable genome, differences were found in genes coding for secondary metabolites (e.g. tripropeptin A and volatile terpenes), several unknown orphan polyketide synthase-nonribosomal peptide synthetase (PKS-NRPS), nonribosomal peptide synthetase (NRPS) gene clusters, a new lipopeptide and type III and type VI secretion systems. Potential roles of the latter genes in the interaction with other organisms were investigated. Mutation of a gene involved in tripropeptin A biosynthesis strongly reduced the antibacterial activity against Staphylococcus aureus, while disruption of a gene involved in the biosynthesis of the new lipopeptide had a large effect on the antifungal/oomycetal activities. CONCLUSIONS: Overall our results indicated that Collimonas genomes harbour many genes encoding for novel enzymes and secondary metabolites (including terpenes) important for interactions with other organisms and revealed genomic plasticity, which reflect the behaviour, antimicrobial activity and lifestylesof Collimonas spp. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2289-3) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-24 /pmc/articles/PMC4690342/ /pubmed/26704531 http://dx.doi.org/10.1186/s12864-015-2289-3 Text en © Song et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Song, Chunxu
Schmidt, Ruth
de Jager, Victor
Krzyzanowska, Dorota
Jongedijk, Esmer
Cankar, Katarina
Beekwilder, Jules
van Veen, Anouk
de Boer, Wietse
van Veen, Johannes A.
Garbeva, Paolina
Exploring the genomic traits of fungus-feeding bacterial genus Collimonas
title Exploring the genomic traits of fungus-feeding bacterial genus Collimonas
title_full Exploring the genomic traits of fungus-feeding bacterial genus Collimonas
title_fullStr Exploring the genomic traits of fungus-feeding bacterial genus Collimonas
title_full_unstemmed Exploring the genomic traits of fungus-feeding bacterial genus Collimonas
title_short Exploring the genomic traits of fungus-feeding bacterial genus Collimonas
title_sort exploring the genomic traits of fungus-feeding bacterial genus collimonas
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4690342/
https://www.ncbi.nlm.nih.gov/pubmed/26704531
http://dx.doi.org/10.1186/s12864-015-2289-3
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