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Adaptive evolution of Moniliophthora PR-1 proteins towards its pathogenic lifestyle

BACKGROUND: Plant pathogenesis related-1 (PR-1) proteins belong to the CAP superfamily and have been characterized as markers of induced defense against pathogens. Moniliophthora perniciosa and Moniliophthora roreri are hemibiotrophic fungi that respectively cause the witches’ broom disease and fros...

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Autores principales: Vasconcelos, Adrielle A., José, Juliana, Tokimatu, Paulo M., Camargo, Antonio P., Teixeira, Paulo J. P. L., Thomazella, Daniela P. T., do Prado, Paula F. V., Fiorin, Gabriel L., Costa, Juliana L., Figueira, Antonio, Carazzolle, Marcelo F., Pereira, Gonçalo A. G., Baroni, Renata M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120714/
https://www.ncbi.nlm.nih.gov/pubmed/33990179
http://dx.doi.org/10.1186/s12862-021-01818-5
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author Vasconcelos, Adrielle A.
José, Juliana
Tokimatu, Paulo M.
Camargo, Antonio P.
Teixeira, Paulo J. P. L.
Thomazella, Daniela P. T.
do Prado, Paula F. V.
Fiorin, Gabriel L.
Costa, Juliana L.
Figueira, Antonio
Carazzolle, Marcelo F.
Pereira, Gonçalo A. G.
Baroni, Renata M.
author_facet Vasconcelos, Adrielle A.
José, Juliana
Tokimatu, Paulo M.
Camargo, Antonio P.
Teixeira, Paulo J. P. L.
Thomazella, Daniela P. T.
do Prado, Paula F. V.
Fiorin, Gabriel L.
Costa, Juliana L.
Figueira, Antonio
Carazzolle, Marcelo F.
Pereira, Gonçalo A. G.
Baroni, Renata M.
author_sort Vasconcelos, Adrielle A.
collection PubMed
description BACKGROUND: Plant pathogenesis related-1 (PR-1) proteins belong to the CAP superfamily and have been characterized as markers of induced defense against pathogens. Moniliophthora perniciosa and Moniliophthora roreri are hemibiotrophic fungi that respectively cause the witches’ broom disease and frosty pod rot in Theobroma cacao. Interestingly, a large number of plant PR-1-like genes are present in the genomes of both species and many are up-regulated during the biotrophic interaction. In this study, we investigated the evolution of PR-1 proteins from 22 genomes of Moniliophthora isolates and 16 other Agaricales species, performing genomic investigation, phylogenetic reconstruction, positive selection search and gene expression analysis. RESULTS: Phylogenetic analysis revealed conserved PR-1 genes (PR-1a, b, d, j), shared by many Agaricales saprotrophic species, that have diversified in new PR-1 genes putatively related to pathogenicity in Moniliophthora (PR-1f, g, h, i), as well as in recent specialization cases within M. perniciosa biotypes (PR-1c, k, l) and M. roreri (PR-1n). PR-1 families in Moniliophthora with higher evolutionary rates exhibit induced expression in the biotrophic interaction and positive selection clues, supporting the hypothesis that these proteins accumulated adaptive changes in response to host–pathogen arms race. Furthermore, although previous work showed that MpPR-1 can detoxify plant antifungal compounds in yeast, we found that in the presence of eugenol M. perniciosa differentially expresses only MpPR-1e, k, d, of which two are not linked to pathogenicity, suggesting that detoxification might not be the main function of most MpPR-1. CONCLUSIONS: Based on analyses of genomic and expression data, we provided evidence that the evolution of PR-1 in Moniliophthora was adaptive and potentially related to the emergence of the parasitic lifestyle in this genus. Additionally, we also discuss how fungal PR-1 proteins could have adapted from basal conserved functions to possible roles in fungal pathogenesis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12862-021-01818-5.
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spelling pubmed-81207142021-05-17 Adaptive evolution of Moniliophthora PR-1 proteins towards its pathogenic lifestyle Vasconcelos, Adrielle A. José, Juliana Tokimatu, Paulo M. Camargo, Antonio P. Teixeira, Paulo J. P. L. Thomazella, Daniela P. T. do Prado, Paula F. V. Fiorin, Gabriel L. Costa, Juliana L. Figueira, Antonio Carazzolle, Marcelo F. Pereira, Gonçalo A. G. Baroni, Renata M. BMC Ecol Evol Research BACKGROUND: Plant pathogenesis related-1 (PR-1) proteins belong to the CAP superfamily and have been characterized as markers of induced defense against pathogens. Moniliophthora perniciosa and Moniliophthora roreri are hemibiotrophic fungi that respectively cause the witches’ broom disease and frosty pod rot in Theobroma cacao. Interestingly, a large number of plant PR-1-like genes are present in the genomes of both species and many are up-regulated during the biotrophic interaction. In this study, we investigated the evolution of PR-1 proteins from 22 genomes of Moniliophthora isolates and 16 other Agaricales species, performing genomic investigation, phylogenetic reconstruction, positive selection search and gene expression analysis. RESULTS: Phylogenetic analysis revealed conserved PR-1 genes (PR-1a, b, d, j), shared by many Agaricales saprotrophic species, that have diversified in new PR-1 genes putatively related to pathogenicity in Moniliophthora (PR-1f, g, h, i), as well as in recent specialization cases within M. perniciosa biotypes (PR-1c, k, l) and M. roreri (PR-1n). PR-1 families in Moniliophthora with higher evolutionary rates exhibit induced expression in the biotrophic interaction and positive selection clues, supporting the hypothesis that these proteins accumulated adaptive changes in response to host–pathogen arms race. Furthermore, although previous work showed that MpPR-1 can detoxify plant antifungal compounds in yeast, we found that in the presence of eugenol M. perniciosa differentially expresses only MpPR-1e, k, d, of which two are not linked to pathogenicity, suggesting that detoxification might not be the main function of most MpPR-1. CONCLUSIONS: Based on analyses of genomic and expression data, we provided evidence that the evolution of PR-1 in Moniliophthora was adaptive and potentially related to the emergence of the parasitic lifestyle in this genus. Additionally, we also discuss how fungal PR-1 proteins could have adapted from basal conserved functions to possible roles in fungal pathogenesis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12862-021-01818-5. BioMed Central 2021-05-14 /pmc/articles/PMC8120714/ /pubmed/33990179 http://dx.doi.org/10.1186/s12862-021-01818-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Vasconcelos, Adrielle A.
José, Juliana
Tokimatu, Paulo M.
Camargo, Antonio P.
Teixeira, Paulo J. P. L.
Thomazella, Daniela P. T.
do Prado, Paula F. V.
Fiorin, Gabriel L.
Costa, Juliana L.
Figueira, Antonio
Carazzolle, Marcelo F.
Pereira, Gonçalo A. G.
Baroni, Renata M.
Adaptive evolution of Moniliophthora PR-1 proteins towards its pathogenic lifestyle
title Adaptive evolution of Moniliophthora PR-1 proteins towards its pathogenic lifestyle
title_full Adaptive evolution of Moniliophthora PR-1 proteins towards its pathogenic lifestyle
title_fullStr Adaptive evolution of Moniliophthora PR-1 proteins towards its pathogenic lifestyle
title_full_unstemmed Adaptive evolution of Moniliophthora PR-1 proteins towards its pathogenic lifestyle
title_short Adaptive evolution of Moniliophthora PR-1 proteins towards its pathogenic lifestyle
title_sort adaptive evolution of moniliophthora pr-1 proteins towards its pathogenic lifestyle
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120714/
https://www.ncbi.nlm.nih.gov/pubmed/33990179
http://dx.doi.org/10.1186/s12862-021-01818-5
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