首页> 外文期刊>Frontiers in Plant Science >Utilizing “Omic” Technologies to Identify and Prioritize Novel Sources of Resistance to the Oomycete Pathogen Phytophthora infestans in Potato Germplasm Collections
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Utilizing “Omic” Technologies to Identify and Prioritize Novel Sources of Resistance to the Oomycete Pathogen Phytophthora infestans in Potato Germplasm Collections

机译:利用“ Omic”技术鉴定和区分马铃薯种质资源中对卵菌病原体 Phytophthora infestans 的新耐药源

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The greatest threat to potato production world-wide is late blight, caused by the oomycete pathogen Phytophthora infestans . A screen of 126 wild diploid Solanum accessions from the Commonwealth Potato Collection (CPC) with P. infestans isolates belonging to the genotype 13-A2 identified resistances in the species S. bulbocastanum, S. capsicibaccatum, S. microdontum, S. mochiquense, S. okadae, S. pinnatisectum, S. polyadenium, S. tarijense , and S. verrucosum. Effector-omics, allele mining, and diagnostic RenSeq (dRenSeq) were utilized to investigate the nature of resistances in S. okadae accessions. dRenSeq in resistant S. okadae accessions 7129, 7625, 3762, and a bulk of 20 resistant progeny confirmed the presence of full-length Rpi-vnt1.1 under stringent mapping conditions and corroborated allele mining results in the accessions 7129 and 7625 as well as Avr-vnt1 recognition in transient expression assays. In contrast, susceptible S. okadae accession 3761 and a bulk of 20 susceptible progeny lacked sequence homology in the 5′ end compared to the functional Rpi-vnt1.1 gene. Further evaluation of S. okadae accessions with P. infestans isolates that have a broad spectrum of virulence demonstrated that, although S. okadae accessions 7129, 7625, and 7629 contain functional Rpi-vnt1.1 , they also carry a novel resistance gene. We provide evidence that existing germplasm collections are important sources of novel resistances and that “omic” technologies such as dRenSeq-based genomics and effector-omics are efficacious tools to rapidly explore the diversity within these collections.
机译:对全世界马铃薯生产的最大威胁是晚疫病,这是由卵菌病原体疫霉疫霉引起的。对来自英联邦马铃薯病原体分离株(属于基因型13-A2)的126个野生二倍体茄属植物进行筛选,确定了S. bulbocastanum,S。capsicibaccatum,S。microdontum,S。mochiquense,S冈田,S。pinnatisectum,S。polyadenium,S。tarijense和S. verrucosum。效应基因组学,等位基因挖掘和诊断性RenSeq(dRenSeq)用于研究冈田链球菌种的抗性性质。抗性冈田链球菌7129、7625、3762和20个抗性子代中的dRenSeq证实了在严格的定位条件下全长Rpi-vnt1.1的存在,并证实了7129和7625号以及等位基因的挖掘结果瞬时表达测定中的Avr-vnt1识别。相反,与功能性Rpi-vnt1.1基因相比,易感的冈田链球菌登录号3761和大量20个易感后代在5'端缺乏序列同源性。用具有广泛毒力的致病疫霉分离株对冈田链霉菌的进一步评估表明,尽管冈田链霉菌的7129、7625和7629菌株均含有功能性Rpi-vnt1.1,但它们还携带了新的抗性基因。我们提供的证据表明,现有种质资源库是新型抗药性的重要来源,而诸如基于dRenSeq的基因组学和效应基因组学等“组学”技术是快速探索这些资源库中多样性的有效工具。

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