Centro APTA Citros Sylvio Moreira, CP4, 13490-970, Cordeirópolis-SP, Brazil.
BMC Genomics. 2011 Jan 17;12:39. doi: 10.1186/1471-2164-12-39.
Gummosis and root rot caused by Phytophthora are among the most economically important diseases in citrus. Four F1 resistant hybrids (Pool R), and four F1 susceptible hybrids (Pool S) to P. parasitica, were selected from a cross between susceptible Citrus sunki and resistant Poncirus trifoliata cv. Rubidoux. We investigated gene expression in pools of four resistant and four susceptible hybrids in comparison with their parents 48 hours after P. parasitica inoculation. We proposed that genes differentially expressed between resistant and susceptible parents and between their resistant and susceptible hybrids provide promising candidates for identifying transcripts involved in disease resistance. A microarray containing 62,876 UniGene transcripts selected from the CitEST database and prepared by NimbleGen Systems was used for analyzing global gene expression 48 hours after infection with P. parasitica.
Three pairs of data comparisons (P. trifoliata/C. sunki, Pool R/C. sunki and Pool R/Pool S) were performed. With a filter of false-discovery rate less than 0.05 and fold change greater than 3.0, 21 UniGene transcripts common to the three pairwise comparative were found to be up-regulated, and 3 UniGene transcripts were down-regulated. Among them, our results indicated that the selected transcripts were probably involved in the whole process of plant defense responses to pathogen attack, including transcriptional regulation, signaling, activation of defense genes participating in HR, single dominant genes (R gene) such as TIR-NBS-LRR and RPS4 and switch of defense-related metabolism pathway. Differentially expressed genes were validated by RT-qPCR in susceptible and resistant plants and between inoculated and uninoculated control plants
Twenty four UniGene transcripts were identified as candidate genes for Citrus response to P. parasitica. UniGene transcripts were likely to be involved in disease resistance, such as genes potentially involved in secondary metabolite synthesis, intracellular osmotic adjustment, signal transduction pathways of cell death, oxidative burst and defense gene expression. Furthermore, our microarray data suggest another type of resistance in Citrus-Phytophthora interaction conferred by single dominant genes (R gene) since we encountered two previously reported R genes (TIR-NBS-LRR and RPS4) upregulated in the resistant genotypes relative to susceptible. We identified 7 transcripts with homology in other plants but yet unclear functional characterization which are an interesting pool for further analyses and 3 transcripts where no significant similarity was found. This is the first microarray study addressing an evaluation of transcriptional changes in response to P. parasitica in Citrus.
由疫霉引起的流胶病和根腐病是柑橘中最重要的经济疾病之一。从易感的枳橙和抗性的蓬溪红橘杂交后代中选择了 4 个对疫霉具有抗性的 F1 杂种(Pool R)和 4 个对疫霉敏感的 F1 杂种(Pool S)。我们在接种疫霉后 48 小时,比较了四个抗性和四个敏感杂种与它们的亲本之间的基因表达。我们提出,在抗性和敏感亲本之间以及它们的抗性和敏感杂种之间差异表达的基因提供了鉴定与抗病性相关的转录本的有希望的候选基因。使用 NimbleGen Systems 制备的来自 CitEST 数据库的包含 62876 个 UniGene 转录本的微阵列用于分析接种疫霉后 48 小时的全局基因表达。
进行了三对数据比较(蓬溪红橘/枳橙、Pool R/枳橙和 Pool R/Pool S)。用错误发现率小于 0.05 和倍数变化大于 3.0 的过滤器,发现 21 个 UniGene 转录本在三对比较中共上调,3 个 UniGene 转录本下调。其中,我们的结果表明,所选转录本可能参与植物对病原体攻击的防御反应的全过程,包括转录调控、信号转导、参与 HR 的防御基因的激活、单显性基因(R 基因)如 TIR-NBS-LRR 和 RPS4 以及防御相关代谢途径的转换。在易感和抗性植物以及接种和未接种对照植物之间,通过 RT-qPCR 验证了差异表达的基因。
鉴定了 24 个 UniGene 转录本作为柑橘对疫霉反应的候选基因。UniGene 转录本可能参与抗病性,例如可能参与次生代谢物合成、细胞内渗透调节、细胞死亡信号转导途径、氧化爆发和防御基因表达的基因。此外,我们的微阵列数据表明,柑橘-疫霉互作中存在由单显性基因(R 基因)赋予的另一种类型的抗性,因为我们在抗性基因型中遇到了两个先前报道的 R 基因(TIR-NBS-LRR 和 RPS4)相对于易感型上调。我们鉴定了 7 个在其他植物中具有同源性但功能特征尚不清楚的转录本,这是进一步分析的有趣来源,还有 3 个转录本没有发现显著相似性。这是首次进行微阵列研究,评估柑橘对疫霉的转录变化。