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Transcriptome analysis of Citrus limon infected with Citrus yellow vein clearing virus

BACKGROUND: Citrus yellow vein clearing virus (CYVCV) is the causative agent of citrus yellow vein clearing disease, and poses a serious threat to the lemon industry in Asia. The common symptoms of CYVCV-infected lemon plants are leaf crinkling, leaf chlorotic mottling, and yellow vein clearing. How...

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Autores principales: Bin, Yu, Zhang, Qi, Su, Yue, Wang, Chunqing, Jiang, Qiqi, Song, Zhen, Zhou, Changyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9903606/
https://www.ncbi.nlm.nih.gov/pubmed/36750773
http://dx.doi.org/10.1186/s12864-023-09151-5
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author Bin, Yu
Zhang, Qi
Su, Yue
Wang, Chunqing
Jiang, Qiqi
Song, Zhen
Zhou, Changyong
author_facet Bin, Yu
Zhang, Qi
Su, Yue
Wang, Chunqing
Jiang, Qiqi
Song, Zhen
Zhou, Changyong
author_sort Bin, Yu
collection PubMed
description BACKGROUND: Citrus yellow vein clearing virus (CYVCV) is the causative agent of citrus yellow vein clearing disease, and poses a serious threat to the lemon industry in Asia. The common symptoms of CYVCV-infected lemon plants are leaf crinkling, leaf chlorotic mottling, and yellow vein clearing. However, the molecular mechanisms underlying CYVCV-citrus interaction that responsible for symptom occurrence is still unclarified. In this study, RNA-seq was performed to analyze the gene expression patterns of ‘Eureka’ lemon (Citrus limon Burm. f.) plants in response to CYVCV infection. RESULTS: There were 3691 differentially expressed genes (DEGs) identified by comparison between mock and CYVCV-infected lemon plants through RNA-seq. Bioinformatics analyses revealed that these DEGs were components of different pathways involved in phenylpropanoid biosynthesis, brassinosteroid biosynthesis, flavonoid biosynthesis and photosynthesis. Among these, the DEGs related to phytohormone metabolism and photosynthesis pathways were further enriched and analyzed. This study showed that different phytohormone-related genes had different responses toward CYVCV infection, however almost all of the photosynthesis-related DEGs were down-regulated in the CYVCV-infected lemon plants. The obtained RNA-seq data were validated by RT-qPCR using 12 randomly chosen genes, and the results of mRNA expression analysis were consistent with those of RNA-seq. CONCLUSIONS: The phytohormone biosynthesis, signaling and photosynthesis-related genes of lemon plants were probably involved in systemic infection and symptom occurrence of CYVCV. Notably, CYVCV infection had regulatory effects on the biosynthesis and signaling of phytohormone, which likely improve systemic infection of CYVCV. Additionally, CYVCV infection could cause structural changes in chloroplast and inhibition of photosynthesis pathway, which probably contribute to the appearance of leaf chlorotic mottling and yellow vein clearing in CYVCV-infected lemon plants. This study illustrates the dynamic nature of the citrus-CYVCV interaction at the transcriptome level and provides new insights into the molecular mechanism underlying the pathogenesis of CYVCV in lemon plants. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09151-5.
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spelling pubmed-99036062023-02-08 Transcriptome analysis of Citrus limon infected with Citrus yellow vein clearing virus Bin, Yu Zhang, Qi Su, Yue Wang, Chunqing Jiang, Qiqi Song, Zhen Zhou, Changyong BMC Genomics Research BACKGROUND: Citrus yellow vein clearing virus (CYVCV) is the causative agent of citrus yellow vein clearing disease, and poses a serious threat to the lemon industry in Asia. The common symptoms of CYVCV-infected lemon plants are leaf crinkling, leaf chlorotic mottling, and yellow vein clearing. However, the molecular mechanisms underlying CYVCV-citrus interaction that responsible for symptom occurrence is still unclarified. In this study, RNA-seq was performed to analyze the gene expression patterns of ‘Eureka’ lemon (Citrus limon Burm. f.) plants in response to CYVCV infection. RESULTS: There were 3691 differentially expressed genes (DEGs) identified by comparison between mock and CYVCV-infected lemon plants through RNA-seq. Bioinformatics analyses revealed that these DEGs were components of different pathways involved in phenylpropanoid biosynthesis, brassinosteroid biosynthesis, flavonoid biosynthesis and photosynthesis. Among these, the DEGs related to phytohormone metabolism and photosynthesis pathways were further enriched and analyzed. This study showed that different phytohormone-related genes had different responses toward CYVCV infection, however almost all of the photosynthesis-related DEGs were down-regulated in the CYVCV-infected lemon plants. The obtained RNA-seq data were validated by RT-qPCR using 12 randomly chosen genes, and the results of mRNA expression analysis were consistent with those of RNA-seq. CONCLUSIONS: The phytohormone biosynthesis, signaling and photosynthesis-related genes of lemon plants were probably involved in systemic infection and symptom occurrence of CYVCV. Notably, CYVCV infection had regulatory effects on the biosynthesis and signaling of phytohormone, which likely improve systemic infection of CYVCV. Additionally, CYVCV infection could cause structural changes in chloroplast and inhibition of photosynthesis pathway, which probably contribute to the appearance of leaf chlorotic mottling and yellow vein clearing in CYVCV-infected lemon plants. This study illustrates the dynamic nature of the citrus-CYVCV interaction at the transcriptome level and provides new insights into the molecular mechanism underlying the pathogenesis of CYVCV in lemon plants. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09151-5. BioMed Central 2023-02-07 /pmc/articles/PMC9903606/ /pubmed/36750773 http://dx.doi.org/10.1186/s12864-023-09151-5 Text en © The Author(s) 2023 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
Bin, Yu
Zhang, Qi
Su, Yue
Wang, Chunqing
Jiang, Qiqi
Song, Zhen
Zhou, Changyong
Transcriptome analysis of Citrus limon infected with Citrus yellow vein clearing virus
title Transcriptome analysis of Citrus limon infected with Citrus yellow vein clearing virus
title_full Transcriptome analysis of Citrus limon infected with Citrus yellow vein clearing virus
title_fullStr Transcriptome analysis of Citrus limon infected with Citrus yellow vein clearing virus
title_full_unstemmed Transcriptome analysis of Citrus limon infected with Citrus yellow vein clearing virus
title_short Transcriptome analysis of Citrus limon infected with Citrus yellow vein clearing virus
title_sort transcriptome analysis of citrus limon infected with citrus yellow vein clearing virus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9903606/
https://www.ncbi.nlm.nih.gov/pubmed/36750773
http://dx.doi.org/10.1186/s12864-023-09151-5
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