Use of the Puccinia sorghi haustorial transcriptome to identify and characterize AvrRp1-D recognized by the maize Rp1-D resistance protein.

IF 5.5 1区 医学 Q1 MICROBIOLOGY
Saet-Byul Kim, Ki-Tae Kim, Solhee In, Namrata Jaiswal, Gir-Won Lee, Seungmee Jung, Abigail Rogers, Libia F Gómez-Trejo, Sujan Gautam, Matthew Helm, Hee-Kyung Ahn, Hye-Young Lee, Quentin D Read, Jongchan Woo, Katerina L Holan, Steven A Whitham, Jonathan D G Jones, Doil Choi, Ralph Dean, Eunsook Park, Peter Balint-Kurti
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Abstract

The common rust disease of maize is caused by the obligate biotrophic fungus Puccinia sorghi. The maize Rp1-D allele imparts resistance against the P. sorghi IN2 isolate by initiating a defense response that includes a rapid localized programmed cell death process, the hypersensitive response (HR). In this study, to identify AvrRp1-D from P. sorghi IN2, we employed the isolation of haustoria, facilitated by a biotin-streptavidin interaction, as a powerful approach. This method proves particularly advantageous in cases where the genome information for the fungal pathogen is unavailable, enhancing our ability to explore and understand the molecular interactions between maize and P. sorghi. The haustorial transcriptome generated through this technique, in combination with bioinformatic analyses such as SignalP and TMHMM, enabled the identification of 251 candidate effectors. We ultimately identified two closely related genes, AvrRp1-D.1 and AvrRp1-D.2, which triggered an Rp1-D-dependent defense response in Nicotiana benthamiana. AvrRp1-D-induced Rp1-D-dependent HR was further confirmed in maize protoplasts. We demonstrated that AvrRp1-D.1 interacts directly and specifically with the leucine-rich repeat (LRR) domain of Rp1-D through yeast two-hybrid assay. We also provide evidence that, in the absence of Rp1-D, AvrRp1-D.1 plays a role in suppressing the plant immune response. Our research provides valuable insights into the molecular interactions driving resistance against common rust in maize.

利用山毛杆线虫病菌丝体转录组鉴定玉米 Rp1-D 抗性蛋白识别的 AvrRp1-D 并确定其特征。
玉米的普通锈病是由强制性生物营养真菌 Puccinia sorghi 引起的。玉米 Rp1-D 等位基因通过启动包括快速局部程序化细胞死亡过程(超敏反应)在内的防御反应,赋予玉米对 P. sorghi IN2 分离物的抗性。在本研究中,为了鉴定 P. sorghi IN2 中的 AvrRp1-D,我们采用了生物素-链霉亲和素相互作用促进的菌丝体分离作为一种有效的方法。在无法获得真菌病原体基因组信息的情况下,这种方法显得尤为有利,从而提高了我们探索和理解玉米与苏铁菌之间分子相互作用的能力。通过这种技术生成的簇状转录组,结合 SignalP 和 TMHMM 等生物信息学分析,我们确定了 251 个候选效应因子。我们最终确定了两个密切相关的基因:AvrRp1-D.1 和 AvrRp1-D.2,它们在烟草中引发了依赖 Rp1-D 的防御反应。在玉米原生质体中进一步证实了 AvrRp1-D 诱导的 Rp1-D 依赖性 HR。我们通过酵母双杂交实验证明,AvrRp1-D.1 与 Rp1-D 的富亮氨酸重复(LRR)结构域有直接和特异性的相互作用。我们还提供证据表明,在 Rp1-D 缺失的情况下,AvrRp1-D.1 在抑制植物免疫反应中发挥作用。我们的研究为揭示驱动玉米抗普通锈病的分子相互作用提供了宝贵的见解。
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来源期刊
PLoS Pathogens
PLoS Pathogens MICROBIOLOGY-PARASITOLOGY
自引率
3.00%
发文量
598
期刊介绍: Bacteria, fungi, parasites, prions and viruses cause a plethora of diseases that have important medical, agricultural, and economic consequences. Moreover, the study of microbes continues to provide novel insights into such fundamental processes as the molecular basis of cellular and organismal function.
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