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Peltaster fructicola genome reveals evolution from an invasive phytopathogen to an ectophytic parasite

Sooty blotch and flyspeck (SBFS) fungi are unconventional plant pathogens that cause economic losses by blemishing the surface appearance of infected fruit. Here, we introduce the 18.14-Mb genome of Peltaster fructicola, one of the most prevalent SBFS species on apple. This undersized assembly conta...

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Autores principales: Xu, Chao, Chen, Huan, Gleason, Mark L., Xu, Jin-Rong, Liu, Huiquan, Zhang, Rong, Sun, Guangyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786788/
https://www.ncbi.nlm.nih.gov/pubmed/26964666
http://dx.doi.org/10.1038/srep22926
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author Xu, Chao
Chen, Huan
Gleason, Mark L.
Xu, Jin-Rong
Liu, Huiquan
Zhang, Rong
Sun, Guangyu
author_facet Xu, Chao
Chen, Huan
Gleason, Mark L.
Xu, Jin-Rong
Liu, Huiquan
Zhang, Rong
Sun, Guangyu
author_sort Xu, Chao
collection PubMed
description Sooty blotch and flyspeck (SBFS) fungi are unconventional plant pathogens that cause economic losses by blemishing the surface appearance of infected fruit. Here, we introduce the 18.14-Mb genome of Peltaster fructicola, one of the most prevalent SBFS species on apple. This undersized assembly contains only 8,334 predicted protein-coding genes and a very small repertoire of repetitive elements. Phylogenomics and comparative genomics revealed that P. fructicola had undergone a reductive evolution, during which the numbers of orphan genes and genes involved in plant cell wall degradation, secondary metabolism, and secreted peptidases and effectors were drastically reduced. In contrast, the genes controlling 1,8-dihydroxynaphthalene (DHN)-melanin biosynthesis and appressorium-mediated penetration were retained substantially. Additionally, microscopic examination of the surfaces of infected apple indicated for the first time that P. fructicola can not only dissolve epicuticular waxes but also partially penetrate the cuticle proper. Our findings indicate that genome contraction, characterized mainly by the massive loss of pathogenicity-related genes, has played an important role in the evolution of P. fructicola (and by implication other SBFS species) from a plant-penetrating ancestor to a non-invasive ectophyte, displaying a novel form of trophic interaction between plants and fungi.
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spelling pubmed-47867882016-03-11 Peltaster fructicola genome reveals evolution from an invasive phytopathogen to an ectophytic parasite Xu, Chao Chen, Huan Gleason, Mark L. Xu, Jin-Rong Liu, Huiquan Zhang, Rong Sun, Guangyu Sci Rep Article Sooty blotch and flyspeck (SBFS) fungi are unconventional plant pathogens that cause economic losses by blemishing the surface appearance of infected fruit. Here, we introduce the 18.14-Mb genome of Peltaster fructicola, one of the most prevalent SBFS species on apple. This undersized assembly contains only 8,334 predicted protein-coding genes and a very small repertoire of repetitive elements. Phylogenomics and comparative genomics revealed that P. fructicola had undergone a reductive evolution, during which the numbers of orphan genes and genes involved in plant cell wall degradation, secondary metabolism, and secreted peptidases and effectors were drastically reduced. In contrast, the genes controlling 1,8-dihydroxynaphthalene (DHN)-melanin biosynthesis and appressorium-mediated penetration were retained substantially. Additionally, microscopic examination of the surfaces of infected apple indicated for the first time that P. fructicola can not only dissolve epicuticular waxes but also partially penetrate the cuticle proper. Our findings indicate that genome contraction, characterized mainly by the massive loss of pathogenicity-related genes, has played an important role in the evolution of P. fructicola (and by implication other SBFS species) from a plant-penetrating ancestor to a non-invasive ectophyte, displaying a novel form of trophic interaction between plants and fungi. Nature Publishing Group 2016-03-11 /pmc/articles/PMC4786788/ /pubmed/26964666 http://dx.doi.org/10.1038/srep22926 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Xu, Chao
Chen, Huan
Gleason, Mark L.
Xu, Jin-Rong
Liu, Huiquan
Zhang, Rong
Sun, Guangyu
Peltaster fructicola genome reveals evolution from an invasive phytopathogen to an ectophytic parasite
title Peltaster fructicola genome reveals evolution from an invasive phytopathogen to an ectophytic parasite
title_full Peltaster fructicola genome reveals evolution from an invasive phytopathogen to an ectophytic parasite
title_fullStr Peltaster fructicola genome reveals evolution from an invasive phytopathogen to an ectophytic parasite
title_full_unstemmed Peltaster fructicola genome reveals evolution from an invasive phytopathogen to an ectophytic parasite
title_short Peltaster fructicola genome reveals evolution from an invasive phytopathogen to an ectophytic parasite
title_sort peltaster fructicola genome reveals evolution from an invasive phytopathogen to an ectophytic parasite
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786788/
https://www.ncbi.nlm.nih.gov/pubmed/26964666
http://dx.doi.org/10.1038/srep22926
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