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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技术确定马铃薯种质资源中对卵菌病原性致病疫霉的新抗性来源并确定其优先级

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摘要

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,这是由卵菌病原菌疫霉疫霉引起的。从英联邦马铃薯病原体分离株(属于基因型13-A2)中筛选了126个野生二倍体茄属种,鉴定出S. bulbocastanum,S。capsicibaccatum,S。microdontum,S。mochiquense,S冈田,松果链球菌,聚腺链球菌,塔里木链球菌和疣状链球菌。效应组学,等位基因挖掘和诊断性RenSeq(dRenSeq)用于研究冈田链球菌种质的抗性性质。耐药的冈比亚链霉菌种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以及种质的等位基因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球菌的进一步评价表明,尽管冈田链球菌的7129、7625和7629含有功能性Rpi-vnt1.1,但它们也带有新的抗性基因。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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