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Transcriptome and metabolome analyses revealed the response mechanism of pepper roots to Phytophthora capsici infection

BACKGROUND: Phytophthora root rot caused by the oomycete Phytophthora capsici is the most devastating disease in pepper production worldwide, and current management strategies have not been effective in preventing this disease. Therefore, the use of resistant varieties was regarded as an important p...

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Autores principales: Lei, Gang, Zhou, Kun-Hua, Chen, Xue-Jun, Huang, Yue-Qin, Yuan, Xin-Jie, Li, Ge-Ge, Xie, Yuan-Yuan, Fang, Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589972/
https://www.ncbi.nlm.nih.gov/pubmed/37864214
http://dx.doi.org/10.1186/s12864-023-09713-7
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author Lei, Gang
Zhou, Kun-Hua
Chen, Xue-Jun
Huang, Yue-Qin
Yuan, Xin-Jie
Li, Ge-Ge
Xie, Yuan-Yuan
Fang, Rong
author_facet Lei, Gang
Zhou, Kun-Hua
Chen, Xue-Jun
Huang, Yue-Qin
Yuan, Xin-Jie
Li, Ge-Ge
Xie, Yuan-Yuan
Fang, Rong
author_sort Lei, Gang
collection PubMed
description BACKGROUND: Phytophthora root rot caused by the oomycete Phytophthora capsici is the most devastating disease in pepper production worldwide, and current management strategies have not been effective in preventing this disease. Therefore, the use of resistant varieties was regarded as an important part of disease management of P. capsici. However, our knowledge of the molecular mechanisms underlying the defense response of pepper roots to P. capsici infection is limited. METHODS: A comprehensive transcriptome and metabolome approaches were used to dissect the molecular response of pepper to P. capsici infection in the resistant genotype A204 and the susceptible genotype A198 at 0, 24 and 48 hours post-inoculation (hpi). RESULTS: More genes and metabolites were induced at 24 hpi in A204 than A198, suggesting the prompt activation of defense responses in the resistant genotype, which can attribute two proteases, subtilisin-like protease and xylem cysteine proteinase 1, involved in pathogen recognition and signal transduction in A204. Further analysis indicated that the resistant genotype responded to P. capsici with fine regulation by the Ca(2+)- and salicylic acid-mediated signaling pathways, and then activation of downstream defense responses, including cell wall reinforcement and defense-related genes expression and metabolites accumulation. Among them, differentially expressed genes and differentially accumulated metabolites involved in the flavonoid biosynthesis pathways were uniquely activated in the resistant genotype A204 at 24 hpi, indicating a significant role of the flavonoid biosynthesis pathways in pepper resistance to P. capsici. CONCLUSION: The candidate transcripts may provide genetic resources that may be useful in the improvement of Phytophthora root rot-resistant characters of pepper. In addition, the model proposed in this study provides new insight into the defense response against P. capsici in pepper, and enhance our current understanding of the interaction of pepper–P. capsici. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09713-7.
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spelling pubmed-105899722023-10-22 Transcriptome and metabolome analyses revealed the response mechanism of pepper roots to Phytophthora capsici infection Lei, Gang Zhou, Kun-Hua Chen, Xue-Jun Huang, Yue-Qin Yuan, Xin-Jie Li, Ge-Ge Xie, Yuan-Yuan Fang, Rong BMC Genomics Research BACKGROUND: Phytophthora root rot caused by the oomycete Phytophthora capsici is the most devastating disease in pepper production worldwide, and current management strategies have not been effective in preventing this disease. Therefore, the use of resistant varieties was regarded as an important part of disease management of P. capsici. However, our knowledge of the molecular mechanisms underlying the defense response of pepper roots to P. capsici infection is limited. METHODS: A comprehensive transcriptome and metabolome approaches were used to dissect the molecular response of pepper to P. capsici infection in the resistant genotype A204 and the susceptible genotype A198 at 0, 24 and 48 hours post-inoculation (hpi). RESULTS: More genes and metabolites were induced at 24 hpi in A204 than A198, suggesting the prompt activation of defense responses in the resistant genotype, which can attribute two proteases, subtilisin-like protease and xylem cysteine proteinase 1, involved in pathogen recognition and signal transduction in A204. Further analysis indicated that the resistant genotype responded to P. capsici with fine regulation by the Ca(2+)- and salicylic acid-mediated signaling pathways, and then activation of downstream defense responses, including cell wall reinforcement and defense-related genes expression and metabolites accumulation. Among them, differentially expressed genes and differentially accumulated metabolites involved in the flavonoid biosynthesis pathways were uniquely activated in the resistant genotype A204 at 24 hpi, indicating a significant role of the flavonoid biosynthesis pathways in pepper resistance to P. capsici. CONCLUSION: The candidate transcripts may provide genetic resources that may be useful in the improvement of Phytophthora root rot-resistant characters of pepper. In addition, the model proposed in this study provides new insight into the defense response against P. capsici in pepper, and enhance our current understanding of the interaction of pepper–P. capsici. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09713-7. BioMed Central 2023-10-20 /pmc/articles/PMC10589972/ /pubmed/37864214 http://dx.doi.org/10.1186/s12864-023-09713-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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
Lei, Gang
Zhou, Kun-Hua
Chen, Xue-Jun
Huang, Yue-Qin
Yuan, Xin-Jie
Li, Ge-Ge
Xie, Yuan-Yuan
Fang, Rong
Transcriptome and metabolome analyses revealed the response mechanism of pepper roots to Phytophthora capsici infection
title Transcriptome and metabolome analyses revealed the response mechanism of pepper roots to Phytophthora capsici infection
title_full Transcriptome and metabolome analyses revealed the response mechanism of pepper roots to Phytophthora capsici infection
title_fullStr Transcriptome and metabolome analyses revealed the response mechanism of pepper roots to Phytophthora capsici infection
title_full_unstemmed Transcriptome and metabolome analyses revealed the response mechanism of pepper roots to Phytophthora capsici infection
title_short Transcriptome and metabolome analyses revealed the response mechanism of pepper roots to Phytophthora capsici infection
title_sort transcriptome and metabolome analyses revealed the response mechanism of pepper roots to phytophthora capsici infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589972/
https://www.ncbi.nlm.nih.gov/pubmed/37864214
http://dx.doi.org/10.1186/s12864-023-09713-7
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