TY - JOUR
T1 - Dominant, heritable resistance to stewart's wilt in maize is associated with an enhanced vascular defense response to infection with pantoea stewartii
AU - Doblas-Lbéfiez, Paula
AU - Deng, Kaiyue
AU - Vasquez, Miguel F.
AU - Giese, Laura
AU - Cobine, Paul A.
AU - Kolkman, Judith M.
AU - King, Helen
AU - Jamann, Tiffany M.
AU - Balint-Kurti, Peter
AU - De La Fuente, Leonardo
AU - Nelson, Rebecca J.
AU - MacKey, David
AU - Smith, Laurie G.
N1 - Funding Information:
†Corresponding authors: P. Doblas-Ibáñez; pdoblasibanez@ucsd.edu; and L. G. Smith; lgsmith@ucsd.edu Funding: This work was supported by a grant from the United States Department of Agriculture National Institute of Food and Agriculture (award number 2015-67013-23006). RNA-Seq library preparations and sequencing were conducted at the IGM Genomics Center, University of California (UC) San Diego (UCSD). Tag-Seq library preparations and sequencing were carried out at the DNA Technologies and Expression Analysis Core at the UC Davis Genome Center, supported by National Institute of Health (NIH) Shared Instrumentation Grant 1S10OD010786-01. Transmission electron microscopy and serial block-face scanning electron microscopy were performed at UCSD Electron Microscopy Core Facility, supported by NIH equipment grant 1S10OD023527-01, and UCSD School of Medicine Microscopy Core, supported by Grant P30 NS047101, respectively.
Publisher Copyright:
© 2019 The American Phytopathological Society.
PY - 2019
Y1 - 2019
N2 - Vascular wilt bacteria such as Pantoea stewartii, the causal agent of Stewart's bacterial wilt of maize (SW), are destructive pathogens that are diffith to control. These bacteria colonize the xylem, where they form biofilms that block sap flow leading to characteristic wilting symptoms. Heritable forms of SW resistance exist and are used in maize breeding programs but the underlying genes and mechanisms are mostly unknown. Here, we show that seedlings of maize inbred lines with panl mutations are highly resistant to SW. However, current evidence suggests that other genes introgressed along with panl are responsible for resistance. Genomic analyses of panl lines were used to identify candidate resistance genes. In-depth comparison of R stewartii interaction with susceptible and resistant maize lines revealed an enhanced vascular defense response in panl lines characterized by accumulation of electron-dense materials in xylem conduits visible by electron microscopy. We propose that this vascular defense response restricts R stewartii spread through the vasculature, reducing both systemic bacterial colonization of the xylem network and consequent wilting. Though apparently unrelated to the resistance phenotype ofpanl lines, we also demonstrate that the effector WtsE is essential for P. stewartii xylem dissemination, show evidence for a nutritional immunity response to P. stewartii that alters xylem sap composition, and present the first analysis of maize transcriptional responses to P. stewartii infection.
AB - Vascular wilt bacteria such as Pantoea stewartii, the causal agent of Stewart's bacterial wilt of maize (SW), are destructive pathogens that are diffith to control. These bacteria colonize the xylem, where they form biofilms that block sap flow leading to characteristic wilting symptoms. Heritable forms of SW resistance exist and are used in maize breeding programs but the underlying genes and mechanisms are mostly unknown. Here, we show that seedlings of maize inbred lines with panl mutations are highly resistant to SW. However, current evidence suggests that other genes introgressed along with panl are responsible for resistance. Genomic analyses of panl lines were used to identify candidate resistance genes. In-depth comparison of R stewartii interaction with susceptible and resistant maize lines revealed an enhanced vascular defense response in panl lines characterized by accumulation of electron-dense materials in xylem conduits visible by electron microscopy. We propose that this vascular defense response restricts R stewartii spread through the vasculature, reducing both systemic bacterial colonization of the xylem network and consequent wilting. Though apparently unrelated to the resistance phenotype ofpanl lines, we also demonstrate that the effector WtsE is essential for P. stewartii xylem dissemination, show evidence for a nutritional immunity response to P. stewartii that alters xylem sap composition, and present the first analysis of maize transcriptional responses to P. stewartii infection.
KW - Bacterial pathogenesis
KW - Electron-dense materials
KW - Maize
KW - Pantoea stewartii
KW - Plant responses to pathogens
KW - Secretion and cell wall changes
KW - Stewart's bacterial wilt
KW - Type-3 secretion
KW - Vascular defense response
KW - WtsE
KW - Xylem-dwelling bacteria
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U2 - 10.1094/MPMI-05-19-0129-R
DO - 10.1094/MPMI-05-19-0129-R
M3 - Article
C2 - 31657672
AN - SCOPUS:85075090732
SN - 0894-0282
VL - 32
SP - 1581
EP - 1597
JO - Molecular Plant-Microbe Interactions
JF - Molecular Plant-Microbe Interactions
IS - 12
ER -