Transcriptomic profiling reveals the complex interaction between a bipartite begomovirus and a cucurbitaceous host plant.


Journal

BMC genomics
ISSN: 1471-2164
Titre abrégé: BMC Genomics
Pays: England
ID NLM: 100965258

Informations de publication

Date de publication:
18 Sep 2024
Historique:
received: 08 07 2024
accepted: 09 09 2024
medline: 19 9 2024
pubmed: 19 9 2024
entrez: 18 9 2024
Statut: epublish

Résumé

Begomoviruses are major constraint in the production of many crops. Upon infection, begomoviruses may substantially modulate plant biological processes. While how monopartite begomoviruses interact with their plant hosts has been investigated extensively, bipartite begomoviruses-plant interactions are understudied. Moreover, as one of the major groups of hosts, cucurbitaceous plants have been seldom examined in the interaction with begomoviruses. We profiled the zucchini transcriptomic changes induced by a bipartite begomovirus squash leaf curl China virus (SLCCNV). We identified 2275 differentially-expressed genes (DEGs), of which 1310 were upregulated and 965 were downregulated. KEGG enrichment analysis of the DEGs revealed that many pathways related to primary and secondary metabolisms were enriched. qRT-PCR verified the transcriptional changes of twelve selected DEGs induced by SLCCNV infection. Close examination revealed that the expression levels of all the DEGs of the pathway Photosynthesis were downregulated upon SLCCNV infection. Most DEGs in the pathway Plant-pathogen interaction were upregulated, including some positive regulators of plant defenses. Moreover, the majority of DEGs in the MAPK signaling pathway-plant were upregulated. Our findings indicates that SLCCNV actively interact with its cucurbitaceous plant host by suppressing the conversion of light energy to chemical energy and inducing immune responses. Our study not only provides new insights into the interactions between begomoviruses and host plants, but also adds to our knowledge on virus-plant interactions in general.

Sections du résumé

BACKGROUND BACKGROUND
Begomoviruses are major constraint in the production of many crops. Upon infection, begomoviruses may substantially modulate plant biological processes. While how monopartite begomoviruses interact with their plant hosts has been investigated extensively, bipartite begomoviruses-plant interactions are understudied. Moreover, as one of the major groups of hosts, cucurbitaceous plants have been seldom examined in the interaction with begomoviruses.
RESULTS RESULTS
We profiled the zucchini transcriptomic changes induced by a bipartite begomovirus squash leaf curl China virus (SLCCNV). We identified 2275 differentially-expressed genes (DEGs), of which 1310 were upregulated and 965 were downregulated. KEGG enrichment analysis of the DEGs revealed that many pathways related to primary and secondary metabolisms were enriched. qRT-PCR verified the transcriptional changes of twelve selected DEGs induced by SLCCNV infection. Close examination revealed that the expression levels of all the DEGs of the pathway Photosynthesis were downregulated upon SLCCNV infection. Most DEGs in the pathway Plant-pathogen interaction were upregulated, including some positive regulators of plant defenses. Moreover, the majority of DEGs in the MAPK signaling pathway-plant were upregulated.
CONCLUSION CONCLUSIONS
Our findings indicates that SLCCNV actively interact with its cucurbitaceous plant host by suppressing the conversion of light energy to chemical energy and inducing immune responses. Our study not only provides new insights into the interactions between begomoviruses and host plants, but also adds to our knowledge on virus-plant interactions in general.

Identifiants

pubmed: 39294575
doi: 10.1186/s12864-024-10781-6
pii: 10.1186/s12864-024-10781-6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

876

Subventions

Organisme : Scientific Research and Development Fund Project of Zhejiang Agriculture and Forestry University
ID : 2023LFR070
Organisme : Zhejiang Provincial Natural Science Foundation
ID : No. LQ22C140003

Informations de copyright

© 2024. The Author(s).

Références

Tatineni S, Hein GL. Plant viruses of agricultural importance: current and future perspectives of virus disease management strategies. Phytopathol. 2023;113:117–41.
doi: 10.1094/PHYTO-05-22-0167-RVW
Osterbaan LJ, Fuchs M. Dynamic interactions between plant viruses and their hosts for symptom development. J Plant Pathol. 2019;101:885–95.
doi: 10.1007/s42161-019-00323-5
Ye J, Zhang LL, Zhang X, Wu XJ, Fang RX. Plant defense networks against insect-borne pathogens. Trends Plant Sci. 2021;26(3):272–87.
doi: 10.1016/j.tplants.2020.10.009 pubmed: 33277186
Rubio L, Galipienso L, Ferriol I. Detection of plant viruses and disease management: relevance of genetic diversity and evolution. Front Plant Sci. 2020;11:1092.
doi: 10.3389/fpls.2020.01092 pubmed: 32765569 pmcid: 7380168
Fiallo-Olivé E, Navas-Castillo J, Begomoviruses. What is the secret(s) of their success? Trends Plant Sci. 2023;28:715–27.
doi: 10.1016/j.tplants.2023.01.012 pubmed: 36805143
Wang XW, Blanc S. Insect transmission of plant single-stranded DNA viruses. Annu Rev Entomol. 2021;66:389–05.
doi: 10.1146/annurev-ento-060920-094531 pubmed: 32931313
Wang HL, Lei T, Wang XW, Cameron S, Navas-Castillo J, et al. A comprehensive framework for the delimitation of species within the Bemisia tabaci cryptic complex, a global pest-species group. Insect Sci. 2024;0:1–22.
Fiallo-Olivé E, Lett JM, Martin DP, Roumagnac P, Varsani A, Zerbini FM, Navas-Castillo J, ICTV Report Consortium. ICTV virus taxonomy profile: Geminiviridae 2021. J Gen Virol. 2021;102:001696.
doi: 10.1099/jgv.0.001696 pubmed: 34919512 pmcid: 8744271
Rojas MR, Hagen C, Lucas WJ, Gilbertson RL. Exploiting chinks in the plant’s armor: evolution and emergence of geminiviruses. Annu Rev Phytopathol. 2005;43:361–94.
doi: 10.1146/annurev.phyto.43.040204.135939 pubmed: 16078889
Hanley-Bowdoin L, Bejarano ER, Robertson D, Mansoor S. Geminiviruses: masters at redirecting and reprogramming plant processes. Nat Rev Microbiol. 2013;11(11):777–88.
doi: 10.1038/nrmicro3117 pubmed: 24100361
Kamal H, Zafar MM, Razzaq A, Parvaiz A, Ercisli S, et al. Functional role of geminivirus encoded proteins in the host: past and present. Biotechnol J. 2024;19(6):e2300736.
doi: 10.1002/biot.202300736 pubmed: 38900041
Góngora-Castillo E, Ibarra-Laclette E, Trejo-Saavedra DL, Rivera-Bustamante RF. Transcriptome analysis of symptomatic and recovered leaves of geminivirus-infected pepper (Capsicum annuum). Virol J. 2012;9:295.
doi: 10.1186/1743-422X-9-295 pubmed: 23185982 pmcid: 3546870
Pierce EJ, Rey MEC. Assessing global transcriptome changes in response to South African cassava mosaic virus [ZA-99] infection in susceptible Arabidopsis thaliana. PLoS ONE. 2013;8(6):e67534.
doi: 10.1371/journal.pone.0067534 pubmed: 23826319 pmcid: 3694866
Allie F, Pierce EJ, Okoniewski MJ, Rey C. Transcriptional analysis of South African cassava mosaic virus-infected susceptible and tolerant landraces of cassava highlights differences in resistance, basal defense and cell wall associated genes during infection. BMC Genomics. 2014;15:1006.
doi: 10.1186/1471-2164-15-1006 pubmed: 25412561 pmcid: 4253015
Miozzi L, Napoli C, Sardo L, Accotto GP. Transcriptomics of the interaction between the monopartite phloem-limited geminivirus tomato yellow leaf curl Sardinia virus and Solanum lycopersicum highlights a role for plant hormones, autophagy and plant immune system fine tuning during infection. PLoS ONE. 2014;9(2):e89951.
doi: 10.1371/journal.pone.0089951 pubmed: 24587146 pmcid: 3938563
Kushwaha N, Sahu PP, Prasad M, Chakraborty S. Chilli leaf curl virus infection highlights the differential expression of genes involved in protein homeostasis and defense in resistant Chilli plants. Appl Microbiol Biotechnol. 2015;99:4757–70.
doi: 10.1007/s00253-015-6415-6 pubmed: 25693670
Kushwaha NK. Chilli leaf curl virus infection downregulates the expression of the genes encoding chloroplast proteins and stress-related proteins. Physiol Mol Biol Plants. 2019;25(5):1185–96.
doi: 10.1007/s12298-019-00693-1 pubmed: 31564781 pmcid: 6745583
Wu MS, Ding X, Fu X, Lozano-Duran R. Transcriptional reprogramming caused by the geminivirus tomato yellow leaf curl virus in local or systemic infections in Nicotiana Benthamiana. BMC Genomics. 2019;20:542.
doi: 10.1186/s12864-019-5842-7 pubmed: 31272383 pmcid: 6611054
Song L, Wang Y, Zhao L, Zhao T. Transcriptome profiling unravels the involvement of phytohormones in tomato resistance to the tomato yellow leaf curl virus (TYLCV). Horticulturae. 2022;8:143.
doi: 10.3390/horticulturae8020143
Namgial T, Singh AK, Singh NP, Francis A, Chattopadhyay D, et al. Differential expression of genes during recovery of Nicotiana tabacum from tomato leaf curl Gujarat virus infection. Planta. 2023;258:37.
doi: 10.1007/s00425-023-04182-4 pubmed: 37405593 pmcid: 10322791
Romero-Rodríguez B, Petek M, Jiao C, Križnik M, Zagorščak M, et al. Transcriptional and epigenetic changes during tomato yellow leaf curl virus infection in tomato. BMC Plant Biol. 2023;23:651.
doi: 10.1186/s12870-023-04534-y pubmed: 38110861 pmcid: 10726652
Jammes M, Golyaev V, Fuentes A, Laboureau N, Urbino C, et al. Transcriptome and small RNAome profiling uncovers how a recombinant begomovirus evades RDRγ-mediated silencing of viral genes and outcompetes its parental virus in mixed infection. PLoS Pathog. 2024;20(1):e1011941.
doi: 10.1371/journal.ppat.1011941 pubmed: 38215155 pmcid: 10810479
Nagendran KM, Mohankumar S, Aravintharaj R, Balaji CG, Manoranjitham SK, et al. The occurrence and distribution of major viruses infecting cucurbits in Tamil Nadu state, India. Crop Prot. 2017;99:10–6.
doi: 10.1016/j.cropro.2017.05.006
Wu HJ, Li M, Hong N, Peng B, Gu QS. Molecular and biological characterization of melon-infecting squash leaf curl China virus in China. J Integr Agr. 2020;19(2):570–77.
doi: 10.1016/S2095-3119(19)62642-0
Qiu YH, Zhang HJ, Tian W, Fan LG, Du MX, et al. First Report of Squash Leaf Curl China Virus Infecting Tomato in China. Plant Dis. 2022;106(9):2539.
doi: 10.1094/PDIS-10-21-2192-PDN
Pan LL, Chi Y, Liu C, Fan YY, Liu SS. Mutations in the coat protein of a begomovirus result in altered transmission by different species of whitefly vectors. Virus Evol. 2020;6(1):veaa014.
doi: 10.1093/ve/veaa014 pubmed: 32153997 pmcid: 7055206
Kon T, Dolores LM, Bajet NB, Hase S, Takahashi H et al. Molecular characterization of a strain of squash leaf curl China virus from the Philippines. J Phytopathol. 2003;151(10).
Tahir M, Haider M, Briddon R. First report of Squash leaf curl China virus in Pakistan. Australas Plant Dis. 2010;5:21–4.
doi: 10.1071/DN10009
Chen YJ, Lai HC, Lin CC, Neoh ZY, Tsai WS. Genetic diversity, pathogenicity and pseudorecombination of cucurbit-infecting begomoviruses in Malaysia. Plants. 2021;10:2396.
doi: 10.3390/plants10112396 pubmed: 34834759 pmcid: 8624487
Kamal H, Minhas FA, Farooq M, Tripathi D, Hamza M, et al. Silico prediction and validations of domains involved in Gossypium hirsutum SnRK1 protein interaction with cotton leaf curl Multan betasatellite encoded βC1. Front Plant Sci. 2019;10:656.
doi: 10.3389/fpls.2019.00656 pubmed: 31191577 pmcid: 6546731
Breves SS, Silva FA, Euclydes NC, Saia TFF, Jean-Baptiste J et al. Begomovirus–host interactions: viral proteins orchestrating intra and intercellular transport of viral DNA while suppressing host defense mechanisms. Viruses. 2023;15;1593.
Stirbet A, Lazár D, Guo Y, Govindjee G. Photosynthesis: basics, history and modelling. Ann Bot-London. 2020;126:511–37.
doi: 10.1093/aob/mcz171
Liu J, Yang J, Bi HP, Zhang P. Why mosaic? Gene expression profiling of African cassava mosaic virus-infected cassava reveals theeffect of chlorophyll degradation on symptom development. J Integr Plant Biol. 2014;56(2):122–32.
doi: 10.1111/jipb.12133 pubmed: 24237761
Bwalya J, Alazem M, Kim KH. Photosynthesis-related genes induce resistance against soybean mosaic virus: evidence for involvement of the RNA silencing pathway. Mol Plant Pathol. 2022;23(4):543–60.
doi: 10.1111/mpp.13177 pubmed: 34962034
Zhou JM, Zhang YL. Plant immunity: danger perception and signaling. Cell. 2020;181:978–89.
doi: 10.1016/j.cell.2020.04.028 pubmed: 32442407
Zhang MM, Zhang SQ. Mitogen-activated protein kinase cascades in plant signaling. J Integr Plant Biol. 2022;64(2):301–41.
doi: 10.1111/jipb.13215 pubmed: 34984829

Auteurs

Wen-Ze He (WZ)

Zhejiang Key Laboratory of Biology and Ecological Regulation of Crop Pathogens and Insects, Zhejiang A&F University, Hangzhou, 311300, China.

Li Zhao (L)

Hangzhou Agricultural Technology Extension Center, Hangzhou, 310058, China.

Kai Sun (K)

Zhejiang Provincial Key Laboratory of Biometrology and Inspection & Quarantine, College of Life Sciences, China Jiliang University, Hangzhou, 310018, China.

Zhen Feng (Z)

Zhejiang Key Laboratory of Biology and Ecological Regulation of Crop Pathogens and Insects, Zhejiang A&F University, Hangzhou, 311300, China.

Gen Zhou (G)

Zhejiang Key Laboratory of Biology and Ecological Regulation of Crop Pathogens and Insects, Zhejiang A&F University, Hangzhou, 311300, China.

Qiong Rao (Q)

Zhejiang Key Laboratory of Biology and Ecological Regulation of Crop Pathogens and Insects, Zhejiang A&F University, Hangzhou, 311300, China. qiong.rao@zafu.edu.cn.

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