Cargando…

A multi-omics analysis of the grapevine pathogen Lasiodiplodia theobromae reveals that temperature affects the expression of virulence- and pathogenicity-related genes

Lasiodiplodia theobromae (Botryosphaeriaceae, Ascomycota) is a plant pathogen and human opportunist whose pathogenicity is modulated by temperature. The molecular effects of temperature on L. theobromae are mostly unknown, so we used a multi-omics approach to understand how temperature affects the m...

Descripción completa

Detalles Bibliográficos
Autores principales: Félix, Carina, Meneses, Rodrigo, Gonçalves, Micael F. M., Tilleman, Laurentijn, Duarte, Ana S., Jorrín-Novo, Jesus V., Van de Peer, Yves, Deforce, Dieter, Van Nieuwerburgh, Filip, Esteves, Ana C., Alves, Artur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739476/
https://www.ncbi.nlm.nih.gov/pubmed/31511626
http://dx.doi.org/10.1038/s41598-019-49551-w
_version_ 1783450952559230976
author Félix, Carina
Meneses, Rodrigo
Gonçalves, Micael F. M.
Tilleman, Laurentijn
Duarte, Ana S.
Jorrín-Novo, Jesus V.
Van de Peer, Yves
Deforce, Dieter
Van Nieuwerburgh, Filip
Esteves, Ana C.
Alves, Artur
author_facet Félix, Carina
Meneses, Rodrigo
Gonçalves, Micael F. M.
Tilleman, Laurentijn
Duarte, Ana S.
Jorrín-Novo, Jesus V.
Van de Peer, Yves
Deforce, Dieter
Van Nieuwerburgh, Filip
Esteves, Ana C.
Alves, Artur
author_sort Félix, Carina
collection PubMed
description Lasiodiplodia theobromae (Botryosphaeriaceae, Ascomycota) is a plant pathogen and human opportunist whose pathogenicity is modulated by temperature. The molecular effects of temperature on L. theobromae are mostly unknown, so we used a multi-omics approach to understand how temperature affects the molecular mechanisms of pathogenicity. The genome of L. theobromae LA-SOL3 was sequenced (Illumina MiSeq) and annotated. Furthermore, the transcriptome (Illumina TruSeq) and proteome (Orbitrap LC-MS/MS) of LA-SOL3 grown at 25 °C and 37 °C were analysed. Proteins related to pathogenicity (plant cell wall degradation, toxin synthesis, mitogen-activated kinases pathway and proteins involved in the velvet complex) were more abundant when the fungus grew at 25 °C. At 37 °C, proteins related to pathogenicity were less abundant than at 25 °C, while proteins related to cell wall organisation were more abundant. On the other hand, virulence factors involved in human pathogenesis, such as the SSD1 virulence protein, were expressed only at 37 °C. Taken together, our results showed that this species presents a typical phytopathogenic molecular profile that is compatible with a hemibiotrophic lifestyle. We showed that L. theobromae is equipped with the pathogenesis toolbox that enables it to infect not only plants but also animals.
format Online
Article
Text
id pubmed-6739476
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-67394762019-09-22 A multi-omics analysis of the grapevine pathogen Lasiodiplodia theobromae reveals that temperature affects the expression of virulence- and pathogenicity-related genes Félix, Carina Meneses, Rodrigo Gonçalves, Micael F. M. Tilleman, Laurentijn Duarte, Ana S. Jorrín-Novo, Jesus V. Van de Peer, Yves Deforce, Dieter Van Nieuwerburgh, Filip Esteves, Ana C. Alves, Artur Sci Rep Article Lasiodiplodia theobromae (Botryosphaeriaceae, Ascomycota) is a plant pathogen and human opportunist whose pathogenicity is modulated by temperature. The molecular effects of temperature on L. theobromae are mostly unknown, so we used a multi-omics approach to understand how temperature affects the molecular mechanisms of pathogenicity. The genome of L. theobromae LA-SOL3 was sequenced (Illumina MiSeq) and annotated. Furthermore, the transcriptome (Illumina TruSeq) and proteome (Orbitrap LC-MS/MS) of LA-SOL3 grown at 25 °C and 37 °C were analysed. Proteins related to pathogenicity (plant cell wall degradation, toxin synthesis, mitogen-activated kinases pathway and proteins involved in the velvet complex) were more abundant when the fungus grew at 25 °C. At 37 °C, proteins related to pathogenicity were less abundant than at 25 °C, while proteins related to cell wall organisation were more abundant. On the other hand, virulence factors involved in human pathogenesis, such as the SSD1 virulence protein, were expressed only at 37 °C. Taken together, our results showed that this species presents a typical phytopathogenic molecular profile that is compatible with a hemibiotrophic lifestyle. We showed that L. theobromae is equipped with the pathogenesis toolbox that enables it to infect not only plants but also animals. Nature Publishing Group UK 2019-09-11 /pmc/articles/PMC6739476/ /pubmed/31511626 http://dx.doi.org/10.1038/s41598-019-49551-w Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Félix, Carina
Meneses, Rodrigo
Gonçalves, Micael F. M.
Tilleman, Laurentijn
Duarte, Ana S.
Jorrín-Novo, Jesus V.
Van de Peer, Yves
Deforce, Dieter
Van Nieuwerburgh, Filip
Esteves, Ana C.
Alves, Artur
A multi-omics analysis of the grapevine pathogen Lasiodiplodia theobromae reveals that temperature affects the expression of virulence- and pathogenicity-related genes
title A multi-omics analysis of the grapevine pathogen Lasiodiplodia theobromae reveals that temperature affects the expression of virulence- and pathogenicity-related genes
title_full A multi-omics analysis of the grapevine pathogen Lasiodiplodia theobromae reveals that temperature affects the expression of virulence- and pathogenicity-related genes
title_fullStr A multi-omics analysis of the grapevine pathogen Lasiodiplodia theobromae reveals that temperature affects the expression of virulence- and pathogenicity-related genes
title_full_unstemmed A multi-omics analysis of the grapevine pathogen Lasiodiplodia theobromae reveals that temperature affects the expression of virulence- and pathogenicity-related genes
title_short A multi-omics analysis of the grapevine pathogen Lasiodiplodia theobromae reveals that temperature affects the expression of virulence- and pathogenicity-related genes
title_sort multi-omics analysis of the grapevine pathogen lasiodiplodia theobromae reveals that temperature affects the expression of virulence- and pathogenicity-related genes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739476/
https://www.ncbi.nlm.nih.gov/pubmed/31511626
http://dx.doi.org/10.1038/s41598-019-49551-w
work_keys_str_mv AT felixcarina amultiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT menesesrodrigo amultiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT goncalvesmicaelfm amultiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT tillemanlaurentijn amultiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT duarteanas amultiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT jorrinnovojesusv amultiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT vandepeeryves amultiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT deforcedieter amultiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT vannieuwerburghfilip amultiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT estevesanac amultiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT alvesartur amultiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT felixcarina multiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT menesesrodrigo multiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT goncalvesmicaelfm multiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT tillemanlaurentijn multiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT duarteanas multiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT jorrinnovojesusv multiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT vandepeeryves multiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT deforcedieter multiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT vannieuwerburghfilip multiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT estevesanac multiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes
AT alvesartur multiomicsanalysisofthegrapevinepathogenlasiodiplodiatheobromaerevealsthattemperatureaffectstheexpressionofvirulenceandpathogenicityrelatedgenes