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The genome of the truffle-parasite Tolypocladium ophioglossoides and the evolution of antifungal peptaibiotics
BACKGROUND: Two major mycoparasitic lineages, the family Hypocreaceae and the genus Tolypocladium, exist within the fungal order, Hypocreales. Peptaibiotics are a group of secondary metabolites almost exclusively described from Trichoderma species of Hypocreaceae. Peptaibiotics are produced by nonri...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517408/ https://www.ncbi.nlm.nih.gov/pubmed/26215153 http://dx.doi.org/10.1186/s12864-015-1777-9 |
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author | Quandt, C. Alisha Bushley, Kathryn E. Spatafora, Joseph W. |
author_facet | Quandt, C. Alisha Bushley, Kathryn E. Spatafora, Joseph W. |
author_sort | Quandt, C. Alisha |
collection | PubMed |
description | BACKGROUND: Two major mycoparasitic lineages, the family Hypocreaceae and the genus Tolypocladium, exist within the fungal order, Hypocreales. Peptaibiotics are a group of secondary metabolites almost exclusively described from Trichoderma species of Hypocreaceae. Peptaibiotics are produced by nonribosomal peptide synthetases (NRPSs) and have antibiotic and antifungal activities. Tolypocladium species are mainly truffle parasites, but a few species are insect pathogens. RESULTS: The draft genome sequence of the truffle parasite Tolypocladium ophioglossoides was generated and numerous secondary metabolite clusters were discovered, many of which have no known putative product. However, three large peptaibiotic gene clusters were identified using phylogenetic analyses. Peptaibiotic genes are absent from the predominantly plant and insect pathogenic lineages of Hypocreales, and are therefore exclusive to the largely mycoparasitic lineages. Using NRPS adenylation domain phylogenies and reconciliation of the domain tree with the organismal phylogeny, it is demonstrated that the distribution of these domains is likely not the product of horizontal gene transfer between mycoparasitic lineages, but represents independent losses in insect pathogenic lineages. Peptaibiotic genes are less conserved between species of Tolypocladium and are the product of complex patterns of lineage sorting and module duplication. In contrast, these genes are more conserved within the genus Trichoderma and consistent with diversification through speciation. CONCLUSIONS: Peptaibiotic NRPS genes are restricted to mycoparasitic lineages of Hypocreales, based on current sampling. Phylogenomics and comparative genomics can provide insights into the evolution of secondary metabolite genes, their distribution across a broader range of taxa, and their possible function related to host specificity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1777-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4517408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45174082015-07-29 The genome of the truffle-parasite Tolypocladium ophioglossoides and the evolution of antifungal peptaibiotics Quandt, C. Alisha Bushley, Kathryn E. Spatafora, Joseph W. BMC Genomics Research Article BACKGROUND: Two major mycoparasitic lineages, the family Hypocreaceae and the genus Tolypocladium, exist within the fungal order, Hypocreales. Peptaibiotics are a group of secondary metabolites almost exclusively described from Trichoderma species of Hypocreaceae. Peptaibiotics are produced by nonribosomal peptide synthetases (NRPSs) and have antibiotic and antifungal activities. Tolypocladium species are mainly truffle parasites, but a few species are insect pathogens. RESULTS: The draft genome sequence of the truffle parasite Tolypocladium ophioglossoides was generated and numerous secondary metabolite clusters were discovered, many of which have no known putative product. However, three large peptaibiotic gene clusters were identified using phylogenetic analyses. Peptaibiotic genes are absent from the predominantly plant and insect pathogenic lineages of Hypocreales, and are therefore exclusive to the largely mycoparasitic lineages. Using NRPS adenylation domain phylogenies and reconciliation of the domain tree with the organismal phylogeny, it is demonstrated that the distribution of these domains is likely not the product of horizontal gene transfer between mycoparasitic lineages, but represents independent losses in insect pathogenic lineages. Peptaibiotic genes are less conserved between species of Tolypocladium and are the product of complex patterns of lineage sorting and module duplication. In contrast, these genes are more conserved within the genus Trichoderma and consistent with diversification through speciation. CONCLUSIONS: Peptaibiotic NRPS genes are restricted to mycoparasitic lineages of Hypocreales, based on current sampling. Phylogenomics and comparative genomics can provide insights into the evolution of secondary metabolite genes, their distribution across a broader range of taxa, and their possible function related to host specificity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1777-9) contains supplementary material, which is available to authorized users. BioMed Central 2015-07-28 /pmc/articles/PMC4517408/ /pubmed/26215153 http://dx.doi.org/10.1186/s12864-015-1777-9 Text en © Quandt et al. 2015 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 work is properly credited. 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 Quandt, C. Alisha Bushley, Kathryn E. Spatafora, Joseph W. The genome of the truffle-parasite Tolypocladium ophioglossoides and the evolution of antifungal peptaibiotics |
title | The genome of the truffle-parasite Tolypocladium ophioglossoides and the evolution of antifungal peptaibiotics |
title_full | The genome of the truffle-parasite Tolypocladium ophioglossoides and the evolution of antifungal peptaibiotics |
title_fullStr | The genome of the truffle-parasite Tolypocladium ophioglossoides and the evolution of antifungal peptaibiotics |
title_full_unstemmed | The genome of the truffle-parasite Tolypocladium ophioglossoides and the evolution of antifungal peptaibiotics |
title_short | The genome of the truffle-parasite Tolypocladium ophioglossoides and the evolution of antifungal peptaibiotics |
title_sort | genome of the truffle-parasite tolypocladium ophioglossoides and the evolution of antifungal peptaibiotics |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517408/ https://www.ncbi.nlm.nih.gov/pubmed/26215153 http://dx.doi.org/10.1186/s12864-015-1777-9 |
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