Abstract

Downy mildew of spinach is caused by the obligate oomycete pathogen, Peronospora effusa. The disease causes significant economic losses, especially in the organic sector of the industry where the use of synthetic fungicides is not permitted for disease control. New pathotypes of this pathogen are increasingly reported which are capable of breaking resistance. In this study, we took advantage of new spinach genome resources to conduct RNA-seq analyses of transcriptomic changes in leaf tissue of resistant and susceptible spinach cultivars Solomon and Viroflay, respectively, at an early stage of pathogen establishment (48 hours post inoculation, hpi) to a late stage of symptom expression and pathogen sporulation (168 hpi). Fold change differences in gene expression were recorded between the two cultivars to identify candidate genes for resistance. In Solomon, the hypersensitive inducible genes such as pathogenesis-related gene PR-1, glutathione-S-transferase, phospholipid hydroperoxide glutathione peroxidase and peroxidase were significantly up-regulated uniquely at 48 hpi and genes involved in zinc finger CCCH protein, glycosyltransferase, 1-aminocyclopropane-1-carboxylate oxidase homologs, receptor-like protein kinases were expressed at 48 hpi through 168 hpi. The types of genes significantly up-regulated in Solomon in response to the pathogen suggests that salicylic acid and ethylene signaling pathways mediate resistance. Furthermore, many genes involved in the flavonoid and phenylpropanoid pathways were highly expressed in Viroflay compared to Solomon at 168 hpi. As anticipated, an abundance of significantly down-regulated genes was apparent at 168 hpi, reflecting symptom development and sporulation in cultivar Viroflay, but not at 48 hpi. In the pathogen, genes encoding RxLR-type effectors were expressed during early colonization of cultivar Viroflay while crinkler-type effector genes were expressed at the late stage of the colonization. Our results provide insights on gene expression in resistant and susceptible spinach-P. effusa interactions, which can guide future studies to assess candidate genes necessary for downy mildew resistance in spinach.

Highlights

  • Downy mildew of spinach is caused by the obligate oomycete pathogen, Peronospora effusa

  • Differential gene expression associated with resistant and susceptible crop genotypes has been examined in various pathosystems to understand the molecular basis of plant defense responses[19,44,45,46,47,48]

  • We examined genes expressed in both host and pathogen (P. effusa) sides during host-microbe interactions, at 48 and 168 hpi

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Summary

Introduction

Downy mildew of spinach is caused by the obligate oomycete pathogen, Peronospora effusa. The disease causes significant economic losses, especially in the organic sector of the industry where the use of synthetic fungicides is not permitted for disease control New pathotypes of this pathogen are increasingly reported which are capable of breaking resistance. Increasing numbers of races, or new virulent pathotypes of P. effusa, have been detected using a set of differential spinach cultivars and reported in recent years in the US and other countries[12,13]. The emergence of virulent isolates capable of overcoming resistance genes is more common in pathogens such as downy mildews since they produce many asexual spores and retain high recombination rates[14,15], but their emergence is exacerbated by sexual reproduction, as noted by the presence of oospores in the population[10]. R genes at the RPF1 locus mediated resistance have been reported but functional roles of these genes conferring resistance to different races of P. effusa have not been thoroughly evaluated and validated[28]

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