Abrahamian Melania, Ah-Fong Audrey M V, Davis Carol, Andreeva Kalina, Judelson Howard S
Department of Plant Pathology and Microbiology, University of California, Riverside, California, United States of America.
PLoS Pathog. 2016 Dec 9;12(12):e1006097. doi: 10.1371/journal.ppat.1006097. eCollection 2016 Dec.
To help learn how phytopathogens feed from their hosts, genes for nutrient transporters from the hemibiotrophic potato and tomato pest Phytophthora infestans were annotated. This identified 453 genes from 19 families. Comparisons with a necrotrophic oomycete, Pythium ultimum var. ultimum, and a hemibiotrophic fungus, Magnaporthe oryzae, revealed diversity in the size of some families although a similar fraction of genes encoded transporters. RNA-seq of infected potato tubers, tomato leaves, and several artificial media revealed that 56 and 207 transporters from P. infestans were significantly up- or down-regulated, respectively, during early infection timepoints of leaves or tubers versus media. About 17 were up-regulated >4-fold in both leaves and tubers compared to media and expressed primarily in the biotrophic stage. The transcription pattern of many genes was host-organ specific. For example, the mRNA level of a nitrate transporter (NRT) was about 100-fold higher during mid-infection in leaves, which are nitrate-rich, than in tubers and three types of artificial media, which are nitrate-poor. The NRT gene is physically linked with genes encoding nitrate reductase (NR) and nitrite reductase (NiR), which mobilize nitrate into ammonium and amino acids. All three genes were coregulated. For example, the three genes were expressed primarily at mid-stage infection timepoints in both potato and tomato leaves, but showed little expression in potato tubers. Transformants down-regulated for all three genes were generated by DNA-directed RNAi, with silencing spreading from the NR target to the flanking NRT and NiR genes. The silenced strains were nonpathogenic on leaves but colonized tubers. We propose that the nitrate assimilation genes play roles both in obtaining nitrogen for amino acid biosynthesis and protecting P. infestans from natural or fertilization-induced nitrate and nitrite toxicity.
为了帮助了解植物病原体如何从宿主获取营养,对半活体营养型马铃薯和番茄害虫致病疫霉的营养转运蛋白基因进行了注释。这确定了来自19个家族的453个基因。与坏死营养型卵菌终极腐霉变种和半活体营养型真菌稻瘟病菌的比较表明,尽管编码转运蛋白的基因比例相似,但一些家族的大小存在差异。对感染的马铃薯块茎、番茄叶片和几种人工培养基进行RNA测序,结果显示,在叶片或块茎感染早期与培养基相比,致病疫霉分别有56个和207个转运蛋白显著上调或下调。与培养基相比,约17个转运蛋白在叶片和块茎中均上调了4倍以上,且主要在活体营养阶段表达。许多基因的转录模式具有宿主器官特异性。例如,在感染中期,富含硝酸盐的叶片中硝酸盐转运蛋白(NRT)的mRNA水平比块茎和三种硝酸盐含量低的人工培养基中高约100倍。NRT基因与编码硝酸盐还原酶(NR)和亚硝酸还原酶(NiR)的基因在物理上相连,后者将硝酸盐转化为铵和氨基酸。这三个基因是共同调控的。例如,这三个基因主要在马铃薯和番茄叶片感染中期表达,但在马铃薯块茎中几乎不表达。通过DNA定向RNA干扰产生了这三个基因均下调的转化体,沉默从NR靶点扩散到侧翼的NRT和NiR基因。沉默菌株在叶片上无致病性,但能定殖于块茎。我们认为,硝酸盐同化基因在获取氮用于氨基酸生物合成以及保护致病疫霉免受天然或施肥诱导的硝酸盐和亚硝酸盐毒性方面均发挥作用。