Abstract

Summary Xanthomonas citri ssp. citri, a polar flagellated bacterium, causes citrus canker disease worldwide. In this study, we found that the X. citri ssp. citri response regulator VemR plays a regulatory role in flagellum‐derived cell motility. Deletion of the vemR gene resulted in a reduction in cell motility, as well as reductions in virulence and exopolysaccharide production. Reverse transcription‐polymerase chain reaction (RT‐PCR) demonstrated that vemR is transcribed in an operon together with rpoN2 and fleQ. In the vemR mutant, the flagellar distal rod gene flgG was significantly down‐regulated. Because flgG is also rpoN2 dependent, we speculated that VemR and RpoN2 physically interact, which was confirmed by yeast two‐hybrid and maltose‐binding protein (MBP) pull‐down assays. This suggested that the transcription of flgG is synergistically controlled by VemR and RpoN2. To confirm this, we constructed a vemR and rpoN2 double mutant. In this mutant, the reductions in cell motility and flgG transcription were unable to be restored by the expression of either vemR or rpoN2 alone. In contrast, the expression of both vemR and rpoN2 together in the double mutant restored the wild‐type phenotype. Together, our data demonstrate that the response regulator VemR functions as an RpoN2 cognate activator to positively regulate the transcription of the rod gene flgG in X. citri ssp. citri.

Highlights

  • Xanthomonas citri ssp. citri (Xcc) is the causal agent of citrus canker disease, and its single polar flagellum plays multiple roles during infection

  • Deletion of vemR leads to reduced virulence on citrus and a hypersensitive response (HR) on non-host tomato

  • To investigate vemR function, a non-polar deletion mutant of Xcc 29-1 was established, and the deletion was confirmed by polymerase chain reaction (PCR) (Fig. S1, see Supporting Information)

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Summary

Introduction

Xanthomonas citri ssp. citri (Xcc) is the causal agent of citrus canker disease, and its single polar flagellum plays multiple roles during infection. Citri (Xcc) is the causal agent of citrus canker disease, and its single polar flagellum plays multiple roles during infection. The bacterial flagellum extends from the cell surface to form a helical propeller. This pronounced structure is composed of three contiguous substructures: the basal body, hook and helical filament (Snyder et al, 2009). The basal body spans the bacterial cell envelope and comprises a ‘drive-shaft’ rod with a series of rings. The assembly of the proximal rod requires cooperative interactions between the FlgB, FlgC and FlgF proteins, whilst FlgG forms the most distal part (Homma et al, 1990). FlgG, flhB and fliC are significantly down-regulated in rpoN2 mutants of Xanthomonas campestris pv. FlgG, flhB and fliC are significantly down-regulated in rpoN2 mutants of Xanthomonas campestris pv. campestris (Hu et al, 2005)

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