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Introgression of White Mold Resistance From the Secondary Gene Pool

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Title: Introgression of White Mold Resistance From the Secondary Gene Pool


1
Introgression of White Mold Resistance From the
Secondary Gene Pool of Common Bean


Henry Terán-Santofimio
2
Outline
  • ? Importance of Dry Bean
  • ? Dry Bean White Mold
  • ? Objectives
  • ? Breeding Strategy
  • ? Greenhouse and Field Screening
  • ? Results
  • ? Future studies

APS Diseases of Legumes
3
Importance of dry bean
  • According to 2002 census, there were 1,691,775
    acres of dry bean planted in the U.S.
  • Idaho ranked 6th after ND, MI, NE, MN, and CO.
  • Among all counties in the U.S., Twin Falls ranked
    3rd.
  • 60 of beans grown in Idaho belong to the market
    class Pinto


http//www.nass.usda.gov/id
4
Main goals of breeding programs
  • Seed yield
  • Quality of seed
  • End use and cooking
    traits
  • Wide adaptation
  • Resistance to diseases
  • Fungal (Rust, Anthracnose, White mold, etc.)
  • Bacterial (CBB, HBB, etc.)
  • Viral (BCMV, BGMV, Curly Top)




5
Dry Bean White Mold

? Devastating disease across the USA in cool
humid regions ? Caused by Sclerotinia
sclerotiorum ? Wide host range of 400 species ?
Fungus is endemic ? Seed transmitted ? Yield
loss 40, 90

6
Courtesy H. Schwartz, CSU
7
Dry Bean White Mold
  • ? Inadequate resistance to white mold
  • ? Low levels in dry bean, high levels in
    secondary gene pool
  • ? Two mechanisms of resistance
  • ? Avoidance Upright architecture and
    open canopy
  • ? Physiological Quantitatively inherited
  • ? 12 Qtls
  • ? Small effects



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9
White Mold Resistance in Pinto Cultivars Released
from 1944 to 1999.



YR Year of Release
Rating scale, 1No WM symptoms and 9severely
diseased
10
Why Slow Improvement of Resistance?

1. Low Heritability h2 0.01-0.67 2. Large
Environmental Influence 3. Inadequate Screening
Methods 4. Inadequate Breeding Methods 5. Low
Level of Resistance in Dry Beans

11
Research Objectives
  • Introgress white mold resistance genes from the
    secondary gene pool using crosses between ICA
    Pijao with P. coccineus, P. costaricensis, and P.
    polyanthus.
  • Compare the level of resistance obtained with
    known resistant sources of white mold.


12
Gene Pools (GP) of Phaseolus cultivated species
P. coccineus P. costarricensis
P. lunatus
GP4
GP1
GP2
GP3
Phaseolus vulgaris Wild and cultivated
P. Polyanthus
P. acutifolius
13
Phaseolus Species in the Secondary Gene Pool
P. coccineus
P. polyanthus
P. costaricensis
14
Breeding Strategy

1. Introgression of Genes from the Secondary Gene
Pool ? P. coccineus G35171, G35172 ?
P.costaricensis S33720 ? P. polyanthus
G35877 2. Reliable Screening Methodology 3.
Greenhouse and Field Evaluation

15
G35171
16
G35172
17
Source CIAT-URG
G35877
18
S33720
19


Ica Pijao
20
Development of Interspecific Breeding Lines


21
Making Crosses
22
Problems of interspecific crosses
  • Rapid return to Phaseolus. vulgaris
  • Distorted segregation
  • Sterility
  • Instability of expression of white mold
    resistance
  • Presence of highly deleterious genes
  • Delayed maturity


23
P. vulgaris x P. coccineus
F3
F2
F2
F4
24
Greenhouse screening
Temperature 80F-85F/60F-65F Photoperiod
11 hd/13hn Relative humidity 95-100
25
Greenhouse screening Inoculum

Use fresh (
26
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Resistant (1-3)


Susceptible (7-9)
Intermediate (4-6)
28
Greenhouse screening 423 IBL
  • Fort Collins, Colorado from 2002-2006 straw
    test, using 6 pots, 2 plants/pot.
  • Kimberly, Idaho from 2004-2006 Petiole and cut
    branch test, 3 pots, 2 plants/pot.
  • Selection of plants with intermediate and
    resistant reaction.
  • Complete randomized block design in Colorado (12
    plants) and Idaho (6 plants), 2006. (2 replicates)


29
Field screening in Idaho
30
Field screening, Idaho
  • Fields (Kimberly-Parma) were heavily fertilized
    with nitrogen.
  • Sclerotias were broadcast in the fields in late
    fall or early spring.
  • The nursery was inoculated at the beginning-,
    mid- and late flowering stage with ascospores
    (2003), ascosporesmycelial (2004) and mycelial
    (2005-06).
  • Plots were irrigated weekly by gravity
    irrigation.



31
Sprinkler irrigation system
R. Henson 2005
32
Field screening, Idaho
  • 2002-2003 single rows, 3.5 m long, spaced 0.56m
  • 2004-2005 4 rows of 3.5 m, 2 replications.
  • 2006 4 rows of 3.5 m, 3 replications.
  • Randomized complete block design.
  • Reaction to white mold was recorded using a 1
  • to 9 scale, where
  • 9 severely diseased or dead plants.
  • 1 no visible symptoms on stems and pods.


33
Results

Sequential white mold screening

34
Results

Mean white mold score of selected IBL
35
Comparison with known resistant sources

36
Small seed upright architecture late maturity,
but different flower and seed coat color
37
Summary
  • First successful introgression of white mold
    resistance from P. costaricensis and P.
    polyanthus into common bean.
  • Three of five IBL were developed using the
    congruity backcross method between ICA Pijao and
    P. coccineus.
  • The use of congruity backcrosses to introgress
    white mold resistance from related species
    resulted in the most resistance phenotypes
    compared to other types of crosses.



38
Future Studies
  • Determine the effectiveness of IBL for
    controlling WM without chemicals and management
    practices across different environments.
  • Study the inheritance with molecular mapping of
    WM resistance in these IBL.
  • Transfer the highest levels of introgressed WM
    resistance into pinto and great northern bean
    cultivars for Idaho bean producers.



39
Acknowledgments
  • This research was funded by the USDA Sclerotinia
  • Initiative since 2002.
  • Dr. S. Singh, University of Idaho
  • Dr. B. Zemetra, Univesity of idaho
  • Dr. C. Mohan, Univesity of idaho
  • Dr. H. Schwartz, Colorado State University
  • Dr. P. Miklas USDA-ARS-Prosser, Washington
  • Dr. M. Lema, visiting scientist, Spain
  • R. Hayes, manager, Kimberly RE Center
  • C. Robinson, manager, Parma RE Center
  • Julia Piaskowski, and Karen Laitala

40
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