Abstract

RipX of Ralstonia solanacearum is translocated into host cells by a type III secretion system and acts as a harpin-like protein to induce a hypersensitive response in tobacco plants. The molecular events in association with RipX-induced signaling transduction have not been fully elucidated. This work reports that transient expression of RipX induced a yellowing phenotype in Nicotiana benthamiana, coupled with activation of the defense reaction. Using yeast two-hybrid and split-luciferase complementation assays, mitochondrial ATP synthase F1 subunit α (ATPA) was identified as an interaction partner of RipX from N. benthamiana. Although a certain proportion was found in mitochondria, the YFP-ATPA fusion was able to localize to the cell membrane, cytoplasm, and nucleus. RFP-RipX fusion was found from the cell membrane and cytoplasm. Moreover, ATPA interacted with RipX at both the cell membrane and cytoplasm in vivo. Silencing of the atpA gene had no effect on the appearance of yellowing phenotype induced by RipX. However, the silenced plants improved the resistance to R. solanacearum. Moreover, qRT-PCR and promoter GUS fusion experiments revealed that the transcript levels of atpA were evidently reduced in response to expression of RipX. These data demonstrated that RipX exerts a suppressive effect on the transcription of atpA gene, to induce defense reaction in N. benthamiana.

Highlights

  • The soil-borne pathogen Ralstonia solanacearum is a species complex that causes bacterial wilt disease in a wide range of host plants [1]

  • R. solanacearum isolates possess a meta-repertoire of type-III-dependent effectors, which comprise over 110 candidates that vary in different isolates [2,3]

  • Agrobacterium-mediated transient expression was conducted to assess the response to RipX1 and RipX3 in N. benthamiana

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Summary

Introduction

The soil-borne pathogen Ralstonia solanacearum is a species complex that causes bacterial wilt disease in a wide range of host plants [1]. Transient expression of a few effectors induced hypersensitive response (HR)-like reactions in different plant species. The harpin-like protein RipX (previously named PopA) is purified from the culture supernatant of R. solanacearum GMI1000 and induces an HR in tobacco [13,14]. Tobacco plants transformed with the ripX gene exhibited a promotion of resistance that depends on the salicylic acid (SA) signaling cascade. Plant mitochondrial ATP synthase is a complex motor comprising a membrane-spanning F0 and a soluble F1 component [18]. The RipX showed a suppression effect on atpA gene transcription.

Results
Expression of RipX1 Suppresses the Transcription of atpA Gene
Plant Material and Cultivation
Bacterial Strains and Plasmids
DNA Manipulation
Agrobacterium-Mediated Transient Expression
Histochemical Staining
Confocal Microscopy
Examination of the HR Reaction Induced by RipX
4.10. Split-Luciferase Complementation Assay
4.13. Promoter Activity Assays
4.14. Western Blot Analysis
4.15. Sequence and Data Analysis
Full Text
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