Derivative of plant phenolic compound inhibits the type III secretion system of Dickeya dadantii via HrpX/HrpY two-component signal transduction and Rsm systems

Yan Li, William Hutchins, Xiaogang Wu, Cuirong Liang, Chengfang Zhang, Xiaochen Yuan, Devanshi Khokhani, Xin Chen, Yizhou Che, Qi Wang, Ching Hong Yang

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

Abstract

The type III secretion system (T3SS) is a major virulence factor in many Gram-negative bacterial pathogens and represents a particularly appealing target for antimicrobial agents. Previous studies have shown that the plant phenolic compound p-coumaric acid (PCA) plays a role in the inhibition of T3SS expression of the phytopathogen Dickeya dadantii 3937. This study screened a series of derivatives of plant phenolic compounds and identified that trans-4-hydroxycinnamohydroxamic acid (TS103) has an eight-fold higher inhibitory potency than PCA on the T3SS of D.dadantii. The effect of TS103 on regulatory components of the T3SS was further elucidated. Our results suggest that TS103 inhibits HrpY phosphorylation and leads to reduced levels of hrpS and hrpL transcripts. In addition, through a reduction in the RNA levels of the regulatory small RNA RsmB, TS103 also inhibits hrpL at the post-transcriptional level via the rsmB-RsmA regulatory pathway. Finally, TS103 inhibits hrpL transcription and mRNA stability, which leads to reduced expression of HrpL regulon genes, such as hrpA and hrpN. To our knowledge, this is the first inhibitor to affect the T3SS through both the transcriptional and post-transcriptional pathways in the soft-rot phytopathogen D.dadantii 3937.

Original languageEnglish (US)
Pages (from-to)150-163
Number of pages14
JournalMolecular Plant Pathology
Volume16
Issue number2
DOIs
StatePublished - Feb 1 2015
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2014 BSPP AND JOHN WILEY & SONS LTD.

Keywords

  • Plant phenolic compound
  • Rsm system
  • T3SS inhibitor
  • Two-component signal transduction system
  • Type III secretion system

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