Source: UNIVERSITY OF NEBRASKA submitted to NRP
IMPROVED WHITE MOLD RESISTANCE IN DRY AND SNAP BEANS THROUGH MULTI-SITE SCREENING AND PATHOGEN CHARACTERIZATION THROUGHOUT MAJOR PRODUCTION AREAS
Sponsoring Institution
Agricultural Research Service/USDA
Project Status
ACTIVE
Funding Source
Reporting Frequency
Annual
Accession No.
0428409
Grant No.
(N/A)
Cumulative Award Amt.
(N/A)
Proposal No.
(N/A)
Multistate No.
(N/A)
Project Start Date
Jul 1, 2016
Project End Date
Dec 31, 2020
Grant Year
(N/A)
Program Code
[(N/A)]- (N/A)
Recipient Organization
UNIVERSITY OF NEBRASKA
(N/A)
LINCOLN,NE 68583
Performing Department
PLANT PATHOLOGY DIVISION
Non Technical Summary
(N/A)
Animal Health Component
35%
Research Effort Categories
Basic
35%
Applied
35%
Developmental
30%
Classification

Knowledge Area (KA)Subject of Investigation (SOI)Field of Science (FOS)Percent
21214101020100%
Knowledge Area
212 - Pathogens and Nematodes Affecting Plants;

Subject Of Investigation
1410 - Beans (dry);

Field Of Science
1020 - Physiology;
Goals / Objectives
1) Identify and/or verify resistance to white mold in wide cross and adapted dry and snap bean lines; 2) Assess the phenotypic and genotypic variation, including fungicide sensitivity in bean isolates of Sclerotinia sclerotiorum collected from major production areas.
Project Methods
Multiple field locations and greenhouse straw tests will be used to screen for white mold reaction of putative sources of resistance. These lines will be provided by bean breeders and plant pathologists from recombinant inbred line populations, interspecific hybridizations, and advanced breeding lines. Field plots will be located in areas of Oregon, Michigan, Wisconsin, France, North Dakota, Nebraska, and Washington with a history of white mold. Five field locations plus Colorado will conduct greenhouse straw tests. The population genetics and fungicide sensitivity of 366 S. sclerotiorum greenhouse and field isolates collected over years at screening trial sites and in bean grower fields will be determined by haplotypes identified by the use of new microsatellite-specific primers. The aggressiveness of the new collection of S. sclerotiorum isolates will be determined by the straw test. Fungicide sensitivity using mycelium and ascospores will be determined for all isolates to guide the use of this disease management tool. Pathogen population knowledge will guide use of relevant specific screening isolates for breeders and plant pathologists.