BACKGROUND: Citrus Huanglongbing (HLB) is the most catastrophic citrus disease worldwide. SEC-dependent effectors (SDEs) play prominent roles in HLB pathogenesis, and 86 were predicted from the genome of Candidatus Liberibacter asiaticus. Nevertheless, little is known about the comprehensive picture of effector action mechanisms. In this study, RNA-seq was performed to explore the gene expression profiling of transgenic citrus plants expressing a CLas SDE, CLIBASIA_00185 (0185-OE). RESULTS: A total of 6,506 differentially expressed genes (DEGs) were identified between 0185-OEs and the wild-type (WT) control through RNA-seq. Gene ontology (GO) analysis indicated that molecular functions associated with cellular process, cell part, binding, and catalysis activity were affected. Kyoto encyclopedia of genes and genomes (KEGG) pathway analysis revealed that DEGs were enriched in pathways including primary and secondary metabolisms. Further analysis demonstrated that DEGs implicated in sugar metabolism, phenylpropanoid biosynthesis, and endocytosis pathway were markedly induced in 0185-OE group compared to those in WTs. Ten genes were chosen to verify RNA-seq data with qRT-PCR, and their expression patterns were in good agreement with those of RNA-seq. CONCLUSIONS: The transcriptomic analysis demonstrated that CLIBASIA_00185 (CLas0185) governed sugar metabolism, phenylpropanoid biosynthesis and endocytosis for pathogen survival and development. The results determined a prominent role of CLas0185 in HLB pathogenicity that could be a target for disease management. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-025-11922-1.
A Candidatus liberibacter Asiaticus effector, CLIBASIA_00185 controls sugar metabolism, phenylpropanoid biosynthesis, and endocytosis pathway in Citrus sinensis.
CLIBASIA_00185 是一种 Candidatus liberibacter Asiaticus 效应子,控制柑橘中的糖代谢、苯丙素生物合成和内吞途径
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作者:Zhang Shushe, Lu Yaobin, He Jun, Zhou Changyong, Wang Xuefeng
| 期刊: | BMC Genomics | 影响因子: | 3.700 |
| 时间: | 2025 | 起止号: | 2025 Aug 2; 26(1):717 |
| doi: | 10.1186/s12864-025-11922-1 | 研究方向: | 代谢 |
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