Citrus Research and Education Center, Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Lake Alfred, Florida, United States of America.
PLoS Genet. 2021 Jan 19;17(1):e1009310. doi: 10.1371/journal.pgen.1009310. eCollection 2021 Jan.
Transcription activator-like effectors (TALEs) are virulence factors of Xanthomonas that induce the expression of host susceptibility (S) genes by specifically binding to effector binding elements (EBEs) in their promoter regions. The DNA binding specificity of TALEs is dictated by their tandem repeat regions, which are highly variable between different TALEs. Mutation of the EBEs of S genes is being utilized as a key strategy to generate resistant crops against TALE-dependent pathogens. However, TALE adaptations through rearrangement of their repeat regions is a potential obstacle for successful implementation of this strategy. We investigated the consequences of TALE adaptations in the citrus pathogen Xanthomonas citri subsp. citri (Xcc), in which PthA4 is the TALE required for pathogenicity, whereas CsLOB1 is the corresponding susceptibility gene, on host resistance. Seven TALEs, containing two-to-nine mismatching-repeats to the EBEPthA4 that were unable to induce CsLOB1 expression, were introduced into Xcc pthA4:Tn5 and adaptation was simulated by repeated inoculations into and isolations from sweet orange for a duration of 30 cycles. While initially all strains failed to promote disease, symptoms started to appear between 9-28 passages in four TALEs, which originally harbored two-to-five mismatches. Sequence analysis of adapted TALEs identified deletions and mutations within the TALE repeat regions which enhanced putative affinity to the CsLOB1 promoter. Sequence analyses suggest that TALEs adaptations result from recombinations between repeats of the TALEs. Reintroduction of these adapted TALEs into Xcc pthA4:Tn5 restored the ability to induce the expression of CsLOB1, promote disease symptoms and colonize host plants. TALEs harboring seven-to-nine mismatches were unable to adapt to overcome the incompatible interaction. Our study experimentally documented TALE adaptations to incompatible EBE and provided strategic guidance for generation of disease resistant crops against TALE-dependent pathogens.
转录激活子样效应因子(TALEs)是黄单胞菌的毒力因子,通过特异性结合其启动子区域中的效应子结合元件(EBE),诱导宿主易感性(S)基因的表达。TALEs 的 DNA 结合特异性由其串联重复区决定,不同 TALEs 之间的重复区高度可变。通过突变 S 基因的 EBE 被用作产生抗 TALE 依赖性病原体的抗性作物的关键策略。然而,TALE 通过重复区的重排进行适应是成功实施该策略的潜在障碍。我们研究了柑橘病原菌柑橘溃疡病菌(Xanthomonas citri subsp. citri,Xcc)中 TALE 适应的后果,其中 PthA4 是致病性所必需的 TALE,而 CsLOB1 是相应的易感性基因,对宿主抗性的影响。引入了 7 个 TALEs,它们的重复区与 EBE PthA4 有两到九个错配重复,无法诱导 CsLOB1 的表达,然后通过重复接种和从甜橙中分离进行模拟适应,持续 30 个循环。虽然最初所有菌株都未能促进疾病,但在四个 TALEs 中,最初含有两到五个错配重复的菌株在 9-28 个传代后开始出现症状。适应性 TALEs 的序列分析确定了 TALE 重复区的缺失和突变,这些突变增强了对 CsLOB1 启动子的假定亲和力。序列分析表明,TALEs 的适应是由 TALEs 重复之间的重组引起的。将这些适应性 TALEs 重新引入 Xcc pthA4:Tn5 中,恢复了诱导 CsLOB1 表达、促进疾病症状和定植宿主植物的能力。含有七到九个错配的 TALEs 无法适应克服不兼容的相互作用。我们的研究从实验上证明了 TALE 对不相容 EBE 的适应,并为针对 TALE 依赖性病原体的抗性作物的产生提供了战略指导。