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Curly top disease, caused by Beet Curly Top Virus (BCTV), is a major threat to sugar beet (), resulting in significant yield losses. This study integrates RNA sequencing, gene network analysis, and experimental validation to uncover key regulatory genes involved in plant responses to viral infection. Network analysis identified nine central hub genes associated with fatty acid metabolism, stress adaptation, and transcriptional regulation. Meanwhile, functional enrichment analysis highlighted chloroplast-associated immune signaling, oxidative stress modulation, and secondary metabolite biosynthesis as critical defense mechanisms. Due to the genomic similarities between BCTV and Beet Curly Top Iran Virus (BCTIV), BCTIV was selected to investigate whether conserved molecular responses exist in sugar beet infected by these phylogenetically related viruses. The upregulation of hub genes - Su1 (EMB3147), Su2 (FRS5), and Su3 (LACS9)- under BCTIV infection was found to mirror patterns observed in BCTV-infected plants, suggesting convergent defense mechanisms against both viruses. A strong correlation (R = 0.995) between qRT-PCR and RNA-Seq data further confirmed that the close genomic proximity of BCTIV to BCTV results in analogous transcriptional reprogramming in the host, supporting the broader relevance of these findings for curly top disease management.
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http://dx.doi.org/10.1016/j.bbrep.2025.102214 | DOI Listing |
Biochem Biophys Rep
September 2025
Department of Plant Protection, Faculty of Agriculture, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Curly top disease, caused by Beet Curly Top Virus (BCTV), is a major threat to sugar beet (), resulting in significant yield losses. This study integrates RNA sequencing, gene network analysis, and experimental validation to uncover key regulatory genes involved in plant responses to viral infection. Network analysis identified nine central hub genes associated with fatty acid metabolism, stress adaptation, and transcriptional regulation.
View Article and Find Full Text PDFACS Synth Biol
August 2025
Instituto de Biología Molecular y Celular de Plantas, CSIC-UPV, Valencia 46022, Spain.
Viral replicons are valuable tools in plant biotechnology, widely utilized to increase recombinant protein production. Their ability to amplify gene dosage in a trigger-dependent manner also opens doors to regulatory applications. This work focuses on optimizing geminivirus-based vectors for Synthetic Biology applications in plants, using autobioluminescence as a sensitive, real-time reporter to characterize gene expression.
View Article and Find Full Text PDFJ Virol
August 2025
Department of Phytopathology, Institute for Sugar Beet Research, Göttingen, Germany.
Intermolecular recombination is a critical process in the evolution of plant viruses, including geminiviruses. In this study, we investigated the impact of geminiviral factors on the homologous recombination frequency (HRF) in a model system involving replicons of the beet curly top virus (BCTVRepl) and the cotton leaf curl Multan betasatellite (CLCuMB), which lacks the β gene. BCTVRepl-cGFP and CLCuMB-nGFP replicated together and exhibited intermolecular recombination, which was monitored by reconstituted GFP fluorescence.
View Article and Find Full Text PDFMethods Mol Biol
June 2025
Cannabis Research Institute, Discovery Partners Institute, University of Illinois System, Chicago, IL, USA.
This chapter presents a protocol for dual interrogation reverse transcriptase quantitative polymerase chain reaction (RT-qPCR) genotyping, a rapid, high-throughput, and economical molecular diagnostic approach for the simultaneous detection of viroid and virus genotypes in plant samples. The method utilizes crude nucleic acid extracts from raw tissue or FTA cards, streamlining sample preparation and enabling field-deployable testing. The incorporation of dual interrogation molecular assays and inhibitor-tolerant polymerases ensures high accuracy and robustness, even with challenging sample types.
View Article and Find Full Text PDFBioresour Technol
October 2025
Guangdong Technology Research Center for Marine Algal Bioengineering, Guangdong Provincial Key Laboratory for Plant Epigenetics, Shenzhen Engineering Laboratory for Marine Algal Biotechnology, Longhua Innovation Institute for Biotechnology, College of Life Sciences and Oceanography, Shenzhen Univers
The advancement of Chlamydomonas reinhardtii chloroplasts as synthetic biology chassis remains constrained by low product yields, a limitation potentially rooted in chloroplast genomic heterogeneity. To address this replicative bottleneck, a geminivirus-inspired expression platform was developed in C. reinhardtii by leveraging replication machinery from the beet curly top virus, building upon its validated efficacy in Nicotiana tabacum.
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