Abstract

BackgroundSmall non-coding RNA (sRNA) short sequences regulate various biological processes in all organisms, including bacteria that are animal or plant pathogens. Virulent or pathogenicity-associated sRNAs have been increasingly elucidated in animal pathogens but little is known about similar category of sRNAs in plant-pathogenic bacteria. This is particularly true regarding rice bacterial blight pathogen Xanthomonas oryzae pathovar oryzae (Xoo) as studies on the virulent role of Xoo sRNAs is very limited at present.ResultsThe number and genomic distribution of sRNAs in Xoo were determined by bioinformatics analysis based on high throughput sequencing (sRNA-Seq) of the bacterial cultures from virulence-inducing and standard growth media, respectively. A total of 601 sRNAs were identified in the Xoo genome and ten virulent sRNA candidates were screened out based on significant differences of their expression levels between the culture conditions. In addition, trans3287 and trans3288 were also selected as candidates due to high expression levels in both media. The differential expression of 12 sRNAs evidenced by the sRNA-Seq data was confirmed by a convincing quantitative method. Based on genetic analysis of Xoo ΔsRNA mutants generated by deletion of the 12 single sRNAs, trans217 and trans3287 were characterized as virulent sRNAs. They are essential not only for the formation of bacterial blight in a susceptible rice variety Nipponbare but also for the induction of hypersensitive response (HR) in nonhost plant tobacco. Xoo Δtrans217 and Δtrans3287 mutants fail to induce bacterial blight in Nipponbare and also fail to induce the HR in tobacco, whereas, genetic complementation restores both mutants to the wild type in the virulent performance and HR induction. Similar effects of gene knockout and complementation were found in the expression of hrpG and hrpX genes, which encode regulatory proteins of the type III secretion system. Consistently, secretion of a type III effector, PthXo1, is blocked in Δtrans217 or Δtrans3287 bacterial cultures but retrieved by genetic complementation to both mutants.ConclusionsThe genetic analysis characterizes trans217 and trans3287 as pathogenicity-associated sRNAs essential for the bacterial virulence on the susceptible rice variety and for the HR elicitation in the nonhost plant. The molecular evidence suggests that both virulent sRNAs regulate the bacterial virulence by targeting the type III secretion system.

Highlights

  • Small non-coding RNA short sequences regulate various biological processes in all organisms, including bacteria that are animal or plant pathogens

  • Aggregate information on the genomic profile of Small RNA (sRNAs) The genomic cDNA libraries of Xanthomonas oryzae pathovar oryzae (Xoo) used in sRNA-Seq were prepared from cultures of the international standard strain PXO99A grown on the standard growth medium polypeptone sucrose agar (PSA) or X. oryzae growth medium recipe 2 (XOM2), which induces gene expression related to the bacterial virulence [38]

  • The number of sRNA reads from XOM2 was found to be less than that of PSA, suggesting that virulence induction impairs the expression of potential sRNAs in the bacterial genome

Read more

Summary

Introduction

Small non-coding RNA (sRNA) short sequences regulate various biological processes in all organisms, including bacteria that are animal or plant pathogens. Small non-coding RNAs (sRNAs) are characteristic of unique nucleotide (nt) sequences comprising 50–500 nt under most circumstances and constitute a universal group of post-transcriptional regulators for gene expression [1,2,3] They function by base pairing with target mRNAs via limited and extended complementarity, which are used to distinguish two categories, namely cis-sRNAs and transsRNAs, respectively [2]. RNAIII governs the expression of SA1000 mRNA, which hypothetically encodes a fibrinogen binding protein indispensable for bacterial adhesion to host surfaces and invasion of host tissues [25] These demonstrations suggest that bacterial RNAs use distinct mechanisms while cooperating with different functional partners to regulate pathogenicity and virulence

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call