Abstract
Bacterial plant pathogens cause significant crop damage worldwide. They invade plant cells by producing a variety of virulence factors, including small-molecule toxins and phytohormone mimics. Virulence of the model pathogen Pseudomonas syringae pv. tomato DC3000 (Pto) is regulated in part by the sigma factor HrpL. Our study of the HrpL regulon identified an uncharacterized, three-gene operon in Pto that is controlled by HrpL and related to the Erwinia hrp-associated systemic virulence (hsv) operon. Here, we demonstrate that the hsv operon contributes to the virulence of Pto on Arabidopsis thaliana and suppresses bacteria-induced immune responses. We show that the hsv-encoded enzymes in Pto synthesize a small molecule, phevamine A. This molecule consists of L-phenylalanine, L-valine, and a modified spermidine, and is different from known small molecules produced by phytopathogens. We show that phevamine A suppresses a potentiation effect of spermidine and L-arginine on the reactive oxygen species burst generated upon recognition of bacterial flagellin. The hsv operon is found in the genomes of divergent bacterial genera, including ∼37% of P. syringae genomes, suggesting that phevamine A is a widely distributed virulence factor in phytopathogens. Our work identifies a small-molecule virulence factor and reveals a mechanism by which bacterial pathogens overcome plant defense. This work highlights the power of omics approaches in identifying important small molecules in bacteriäChost interactions.
Original language | English |
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Pages (from-to) | E9514-E9522 |
Journal | Proceedings of the National Academy of Sciences of the United States of America |
Volume | 115 |
Issue number | 41 |
DOIs | |
Publication status | Published - 2018 Oct 9 |
Externally published | Yes |
Bibliographical note
Funding Information:Tyrrell for cloning the hsv operon into the pLIC-His vector, Dr. Jake Malone for sharing the pBBR5 plasmid, Dr. Jim Jorgenson and Katherine Simpson for helpful discussion of isolation of phevamines, and Kevin Santa Maria for assistance with MultiGeneBlast. This work is supported by the Rita Allen Foundation and the David and Lucile Packard Foundation (B.L.), National Institutes of Health (R00 GM099904 to B.L., 5T32 GM008500 to J.A.B., and R01 GM112739-01 to F.C.S.), the National Science Foundation (IOS-1257373 to J.L.D.), and the Howard Hughes Medical Institute. J.L.D. is an Investigator of the Howard Hughes Medical Institute, and F.C.S. is a Faculty Scholar of the Howard Hughes Medical Institute.
Publisher Copyright:
© 2018 National Academy of Sciences. All rights reserved.
ASJC Scopus subject areas
- General