Phevamine A, a small molecule that suppresses plant immune responses
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 bacteria–host interactions.
Additional Information
© 2018 the Author(s). Published by PNAS. This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND). Edited by Sheng Yang He, Michigan State University, East Lansing, MI, and approved August 10, 2018 (received for review March 3, 2018) We thank Dr. Albert Bowers for helpful discussions of the manuscript, Dr. Gary Pielak for the naming of the phevamines, Dr. Jillian 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. E.M.O. and T.S.M. contributed equally to this work. Author contributions: E.M.O., T.S.M., J.L.D., and B.L. designed research; E.M.O., T.S.M., J.B.P., O.M.F., and E.-H.C. performed research; J.B.P., O.M.F., J.A.B., E.M., and F.C.S. contributed new reagents/analytic tools; E.M.O., T.S.M., J.L.D., and B.L. analyzed data; and E.M.O., T.S.M., J.L.D., and B.L. wrote the paper. The authors declare no conflict of interest. This article is a PNAS Direct Submission. This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1803779115/-/DCSupplemental.Attached Files
Published - E9514.full.pdf
Supplemental Material - pnas.1803779115.sapp.pdf
Supplemental Material - pnas.1803779115.sd01.xlsx
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Additional details
- PMCID
- PMC6187163
- Eprint ID
- 89811
- Resolver ID
- CaltechAUTHORS:20180920-144411925
- Rita Allen Foundation
- David and Lucile Packard Foundation
- R00 GM099904
- NIH
- 5T32 GM008500
- NIH Predoctoral Fellowship
- R01 GM112739-01
- NIH
- IOS-1257373
- NSF
- Howard Hughes Medical Institute (HHMI)
- Created
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2018-09-20Created from EPrint's datestamp field
- Updated
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2023-03-16Created from EPrint's last_modified field