Dominant, Heritable Resistance to Stewart’s Wilt in Maize Is Associated with an Enhanced Vascular Defense Response to Infection with Pantoea stewartii

Author:

Doblas-Ibáñez Paula1ORCID,Deng Kaiyue1,Vasquez Miguel F.1,Giese Laura2,Cobine Paul A.3,Kolkman Judith M.4,King Helen1,Jamann Tiffany M.5,Balint-Kurti Peter6ORCID,De La Fuente Leonardo7,Nelson Rebecca J.4,Mackey David2ORCID,Smith Laurie G.1

Affiliation:

1. Section of Cell and Developmental Biology, University of California at San Diego, La Jolla, CA 92093, U.S.A.

2. Department of Horticulture and Crop Sciences, The Ohio State University, Columbus, OH 43210, U.S.A.

3. Department of Biological Sciences, Auburn University, Auburn, AL 36849, U.S.A.

4. School of Integrative Plant Science, Cornell University, Ithaca, NY 14853, U.S.A.

5. Department of Crop Sciences, University of Illinois Urbana-Champaign, Urbana, IL 61801, U.S.A.

6. United States Department of Agriculture–Agricultural Research Service, Plant Science Research Unit, Raleigh, NC 27695, U.S.A. and Department of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC 27695, U.S.A.

7. Department of Entomology and Plant Pathology, Auburn University

Abstract

Vascular wilt bacteria such as Pantoea stewartii, the causal agent of Stewart’s bacterial wilt of maize (SW), are destructive pathogens that are difficult 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 pan1 mutations are highly resistant to SW. However, current evidence suggests that other genes introgressed along with pan1 are responsible for resistance. Genomic analyses of pan1 lines were used to identify candidate resistance genes. In-depth comparison of P. stewartii interaction with susceptible and resistant maize lines revealed an enhanced vascular defense response in pan1 lines characterized by accumulation of electron-dense materials in xylem conduits visible by electron microscopy. We propose that this vascular defense response restricts P. stewartii spread through the vasculature, reducing both systemic bacterial colonization of the xylem network and consequent wilting. Though apparently unrelated to the resistance phenotype of pan1 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.

Funder

National Institute of Food and Agriculture

Publisher

Scientific Societies

Subject

Agronomy and Crop Science,General Medicine,Physiology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3