Abstract

BackgroundXanthomonas oryzae pv. oryzae (Xoo) is the causal agent of rice bacterial blight disease. Xoo produces a range of virulence factors, including EPS, extracellular enzyme, iron-chelating siderophores, and type III-secretion dependent effectors, which are collectively essential for virulence. Genetic and genomics evidence suggest that Xoo might use the diffusible signal factor (DSF) type quorum sensing (QS) system to regulate the virulence factor production. However, little is known about the chemical structure of the DSF-like signal(s) produced by Xoo and the factors influencing the signal production.ResultsXoo genome harbours an rpf cluster comprising rpfB, rpfF, rpfC and rpfG. The proteins encoded by these genes are highly homologous to their counterparts in X. campestris pv. campestris (Xcc), suggesting that Xcc and Xoo might use similar mechanisms for DSF biosynthesis and autoregulation. Consistent with in silico analysis, the rpfF mutant was DSF-deficient and the rpfC mutant produced about 25 times higher DSF-like activity than the wild type Xoo strain KACC10331. From the supernatants of rpfC mutant, we purified three compounds showing strong DSF-like activity. Mass spectrometry and NMR analysis revealed that two of them were the previously characterized DSF and BDSF; the third one was a novel unsaturated fatty acid with 2 double bonds and was designated as CDSF in this study. Further analysis showed that all the three DSF-family signals were synthesized via the enzyme RpfF encoded by Xoo2868. DSF and BDSF at a final concentration of 3 μM to the rpfF mutant could fully restore its extracellular xylanase activity and EPS production to the wild type level, but CDSF was less active than DSF and BDSF in induction of EPS and xylanase. DSF and CDSF shared a similar cell density-dependent production time course with the maximum production being detected at 42 h after inoculation, whereas the maximum production of BDSF was observed at 36 h after inoculation. When grown in a rich medium such as YEB, LB, PSA, and NYG, Xoo produced all the three signals with the majority being DSF. Whereas in nutritionally poor XOLN medium Xoo only produced BDSF and DSF but the majority was BDSF.ConclusionsThis study demonstrates that Xoo and Xcc share the conserved mechanisms for DSF biosynthesis and autoregulation. Xoo produces DSF, BDSF and CDSF signals in rich media and CDSF is a novel signal in DSF-family with two double bonds. All the three DSF-family signals promote EPS production and xylanase activity in Xoo, but CDSF is less active than its analogues DSF and BDSF. The composition and ratio of the three DSF-family signals produced by Xoo are influenced by the composition of culture media.

Highlights

  • Xanthomonas oryzae pv. oryzae (Xoo) is the causal agent of rice bacterial blight disease

  • Xoo uses the similar mechanism of X. campestris pv. campestris (Xcc) in autoregulation of diffusible signal factor (DSF) biosynthesis In Xcc, the rpf cluster is involved in DSF biosynthesis, signal sensing and response

  • The genomes of three sequenced Xoo strains (KACC10331, MAFF311018 and PX099A) contain the rpf cluster comprising rpfB, rpfF, rpfG and rpfC, but not rpfH [26,27,28]. These rpf homologous from Xcc and Xoo share more than 86% identify at the amino acids level (Fig. 1A), suggesting the conserved mechanism in DSF biosynthesis and in DSF signalling

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Summary

Introduction

Xanthomonas oryzae pv. oryzae (Xoo) is the causal agent of rice bacterial blight disease. The RpfC/RpfG twocomponent system is involved in sensing and transduction of DSF signal through a conserved phosphorelay mechanism [10,11,12]; RpfG functions in turnover of the second messenger c-di-GMP and Clp is a novel c-diGMP receptor [12,13], which regulates the expression of DSF-dependent genes directly or indirectly via two downstream transcription factors Zur and FhrR [14]. Functional analysis of rpfF or rpfC mutants in different bacterial species suggests that the general role of the DSF-signaling system in the modulation of virulence seems to be conserved, but the regulatory mechanisms and DSF-dependent traits may differ among taxa [8,15,16,17]

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