Disease Suppressive Soils: Fact or Fiction

1 / 51
About This Presentation
Title:

Disease Suppressive Soils: Fact or Fiction

Description:

Only with high level of Mycorrhiza colonization ... Competition between the pathogenic and non-pathogenic strains did not limit establishment ... – PowerPoint PPT presentation

Number of Views:1175
Avg rating:1.0/5.0
Slides: 52
Provided by: umch

less

Transcript and Presenter's Notes

Title: Disease Suppressive Soils: Fact or Fiction


1
Disease Suppressive Soils Fact or Fiction?
  • Hida Manns
  • March 26, 2007

2
OUTLINE
  • Definition
  • Natural controls on plant pathogens
  • General Suppression
  • Organic Matter
  • Microbial Biomass
  • Actinomycetes
  • Specific Suppression
  • SAR/ISR
  • Antagonism
  • Example Systems
  • Potato Common scab
  • Fusarium in France
  • Take-all of Wheat
  • Sugar beet cyst nematode in California
  • Steps to building suppressive soils
  • Composted Bark
  • Ecological Equilibrium

3
DEFINITION
  • Disease suppressive soils
  • Pathogen is added to soil but does not persist
  • Pathogen exists in soil but does not establish in
    plants or does not produce disease
  • There is a decline in disease severity over time
  • (Lyda, 1982, Weller et al., 2002).

4
Disease Suppression
  • General Disease Suppression
  • Controls levels of most plant pathogens
  • Increased microbial activity
  • Greater microbial diversity
  • Exists over time, regardless of crop
  • Fungistasis
  • Inhibition of germination or growth of fungi
  • Lyda, 1982

5
General Suppression
  • Abiotic
  • pH
  • N, C, Mg, K
  • Sand/clay
  • CEC (Cation Exchange Capacity)
  • Organic matter
  • Biotic
  • Microbial biomass
  • Actinomycetes

6
Management
  • When chemicals are substituted for organic matter
    in agriculture, plant diseases soon develop
  • Bailey Lazarovits, 2003
  • Biologic Vacuum
  • Reduce disease in crops from
  • cover crops
  • compost
  • tillage
  • crop rotation
  • Garbeva et al., 2004

7
Organic Matter
  • Organic matter associated with higher
  • Cation exchange (CEC)
  • Soil moisture
  • Available nutrients (e.g. nitrogen)
  • Activity and diversity of soil microorganisms
  • Bailey Lazarovits, 2003

8
Biological stresses
  • Diversity of organisms
  • Degradation of plant residues and also resting
    propagules
  • Releasing different products into soil solution
  • Antibiotics
  • Fungistatic/biostatic compounds (2nd metabolites)
  • Competition for nutrients
  • Competition for space
  • Predation

9
Fungi
  • Celluloytic activity of Fungi (enzymes)
  • ß glucosidase and Cellobiohydrolase
  • Correlated with carbon and CEC
  • Seedling blight of barley
  • Ratio of oligotrophic/copiotrophic species
  • Mycorrhiza
  • Diversity
  • Janvier et al. 2007

10
Mycorrhiza
  • Mycorrhiza reduced the negative effect of
    take-all on plant growth of wheat at 5 weeks.
  • (Khaosaad 2007)
  • AMF was found to actively reduce pathogen
    infections in plant roots
  • Only with high level of Mycorrhiza colonization
  • Substitution of P fertilizer for mycorrhiza did
    not exhibit disease resistance
  • (Fritz, 2006)

11
Actinomycetes
  • Large, diverse group, active residue decomposers
  • Streptomyces produce anti-fungal compounds
  • Mazzola, 2002
  • Non-Streptomyces
  • Endophytes
  • Rhizosphere competent
  • Slower growing in culture
  • Cell wall-degrading enzymes
  • El-Tarabily Sivasithamparam, 2006

12
Specific Disease Suppression
  • Individual, rather than most pathogens do not
    produce disease
  • Often, antagonism by a certain species of
    organisms is the reason
  • These can be tested and utilized by inoculation
  • eg. Flourescent Pseudomonads (Mazzola, 2002)
  • Does not exist without specific crop host
  • Agrawal et al., 1999

13
Specific Suppression
  • Antagonistic bacteria
  • Non-pathogens the same species as pathogen
  • SAR Systematic Acquired Resistance
  • Activated by biotic and abiotic agents
  • Signal molecule salicylic acid or
  • Jasmonic acid or ethylene
  • Pathogen itself
  • ISR Induced Systemic Resistance
  • Hypersensitivity response
  • Requires salicylic acid in process
  • Agrawal et al., 1999

14
Fo47 Experiment
  • F. oxysporum strain Fo47 isolated from
    Chateaurenard by Alabouvette antagonist
  • F. oxysporum f.sp. Lycopersici Fo18 pathogenic
  • Tomato plants (Bonny Best)
  • susceptible to Fusarium
  • Tested with hydroponic, potting mix, sterile soil
  • One side subjected to pathogen, other to
    antagonist
  • Fuchs et al., 1997

15
Split-root system
  • Split root system
  • Roots grown in 2 parts
  • 1 side inoculated with Fo47
  • 10 days later, plant exposed to Fo18

Fucks et al., 1997
16
ISR
  • Results
  • Inoculation with Fo47 reduced Fusarium wilt from
    37-54 at 4 weeks
  • Fo47 was not found
  • Protective effect disappeared after 2 weeks
  • Fucks et al., 1997
  • Plant responded to both stimulus on both sides.
  • Antagonist Pathogen
  • ISR small volume
    large response (1000 x)
  • Competition large volume (10-100x)
    small response
  • Fravel et al., 2003

17
Examples
  • Potato Wheat
    Sugar Beets
  • Common scab Fusarium
    Take-all Cyst Nematode
  • General
  • Suppression
  • Abiotic
  • Biotic
  • Specific
  • Suppression
  • Antagonist
  • SAR
  • ISR

18
Potato Common Scab
Cornell University Vegetable MD Online Potato
Common Scab http//vegetabledonline.ppath.edu/phot
opages/impt_Diseases/potato/pot_scab.htm
19
Common Scab
  • Potato scab (Streptomyces scabies)
  • 1950 old potato fields scab free
  • new potato fields, scab existed
  • Tested old and virgin soil
  • Scab developed in all soils in the first year
  • Increased in virgin soil suppressed in old
    fields
  • Weller et al., 2002
  • Actinomycetes (Non-streptomycetes) produce
    antibiotics
  • Present in scab free soil, and form inoculation
    at 1
  • Weller et al., 2002
  • Soybean cover crop incorporation prevented scab
    in virgin soil

    Weinhold, 1970
  • OM additives dung, wheat straw, saw dust,
    soybean
  • Mishra Srivastava, 2004

20
Fusarium Wilt
Fusarium http//ecoport.org/ep?SearchTypepdbPdb
ID3593
Hwang, S.C., Ko,W.H., Plant Disease cover Images.
http//www.apsnet.org/online/Archive/PDCoverImage
s/2004V88/jun_I.asp
21
Fusarium
  • Chateaurenard Valley in France
  • Soils suppressive to Fusarium (1800s)
  • Melons grown for centuries
  • 2 km away, no effect of soil
  • Only vegetables grown there
  • Cook, 1982

22
Soil suppressive to Fusarium
  • Fusarium live saprophytically, and persists as
    chlamydospores
  • Exudates from plant roots overcome fungistasis
  • Interaction of species exerts control (Alabouvett
    e, 1986)
  • Chateaurenard soils
  • high populations of F. oxysporum and F. solani
  • especially non-pathogenic strains (Fravel et
    al., 2003)
  • Soils tested for Non-pathogenic Fusarium using
    Kochs Postulates
  • Heat destroyed suppressive effect
    (microbiological)
  • Restored with inoculation (Fravel et al., 2003)

23
F. oxysporum
  • Series of elimination tests
  • soils inhibit all formae speciales of F.
    oxysporum, but allow other soil-borne disease
  • Competition between the pathogenic and
    non-pathogenic strains did not limit
    establishment
  • independent of the ability of the soil to support
    populations
  • colonization on the root surface was not
    inhibited by non-pathogenic Fusarium
  • Alabouvette, 1986

24
Mechanism
  • Intrageneric competition
  • Occurs in the soil
  • In the immediate vicinity of the roots
  • During saprophytic development that
  • Precedes the establishment of F. oxysporum
  • at the root surface
  • (Alabouvette, 1986)

25
Take-all of Wheat
Take-all of Wheat http//scarab.msu.montana.edu/Di
sease/DiseaseGuidewebpics/Petewebpics61-70Img0065.
jpg Also 0066 and 0067
26
Take-all (Ggt)
  • (Gaeumannomyces graminis var. tritici) (pathogen
    of wheat)
  • Take-all decline only in presence of pathogen
  • Transferrable suppression with 1 soil
  • Affected by biotic and abiotic factors in the
    environment
  • Flourescent Pseudomonads (Siderophores)
  • Trichoderma koningii
  • Simon Sivasithamparam, 1989

27
Antagonist Cause of Disease Decline
Weller et al., 2002
28
Pseudomonas fluoresens and Ggt
Weller Cook, 1983
29
Trichoderma koningii
  • T. koningii vs Ggt
  • Seeds grown in tubes
  • 8 different soils
  • 2 replications
  • 2 trials
  • Measured degree of color on roots by PCF
  • T. koningii reduced disease suppression
  • Affect varied with soils
  • Supportiveness of soil to T. koningii
  • Principal components analysis
  • Soil factors -pH, -Phosphorous, NO3,
    Fe
  • Chemical effects Copper, magnesium
  • Clay effects Boron, clay

Duffy et al.,1997
30
Principal Components Analysis
Influence of soil factors on disease reduction by
T. koningii
Duffy et al., 1997
31
Specific effects of soil
  • NH4 decreases pH
  • Increases antagonistic bacteria
  • Trichoderma koningii
  • Production of antibiotics
  • Pseudomonads
  • Production of antibiotics Duffy et al., 1997
  • Phl (DAPG) 2,4-diacetylphloroglucinol
  • PH1C phenazine-1-carboxylate
  • Fe chelated by Siderophores
  • Used in production of H2O2 by bacteria
  • Zn used for production of antibiotics
  • High diversity is suppressive soil, Increased by
    clay
  • Raaijmakers et al., 1999

32
Heterodera schachtii
33
Sugar Beet cyst nematode
  • The sugar beet cyst nematode (Heterodera
    schachtii) was first identified in Utah and
    California in 1907 in areas of intensive
    cultivation of sugar beets
  • In the Imperial Valley, sugar beets were first
    grown in 1938, and the nematode detected in 1957
  • Within 3 years, the nematode was widespread, as
    it can complete up to 5 generations per year
  • As of 1983, 11 of the total cultivated acreage
    in the valley was infested
  • Caswell Thomason, 1985

34
Geographic distribution of H. schachtii
Cumulative geographic distribution of sugar beet
fields in the Imperial Valley of California that
have not been found to be infested with the sugar
beet cyst nematode during 1961-1983. Major
cities and railroad lines are indicated. Caswell
Thomason, 1985
35
Defense
  • Efforts sought to quarantine the disease
  • The number of fields infected slowly spread to
    the function of planted fields infested
  • 13.12 (0.583 x number of years)
  • Solution cleanliness
  • isolate specific antidote
  • Caswell Thomason, 1985

36
Fungal parasitism
  • Acremonium strictum Gams and
  • F. oxysporum Schlecht were tested for
  • active parasitic activity on H. schachtii eggs
  • activity of the fungus in females
  • relative plant parasitic activity
  • Nigh et al., 1980

37
Fusarium on H. schachtii eggs
Nigh et al., 1980
38
Effects of soil on H. schachtii egg survival
Greenhouse Experiment Suppressive and conducive
soils With swiss chard
Westphal Becker, 1999
39
Creating suppressive soil
  • Composted Bark
  • Peat /Composted Bark
  • suppresses disease in seedling
  • extensively used in greenhouse/nursery
  • Replaced Peat
  • Sterilization, fungicides, isolation
  • Aeration, antagonists, phagous fugicidal
    properties of composted Bark gave suppressiveness
  • Hoitink, 1980

40
Microbial Diversity
  • Pythium
  • Rests in low volume in soil
  • Increased disease only with high moisture and
    carbon
  • Pythium in soil with peat alone (conducive) and
    mature compost mix (suppressive)
  • Increased OM decomposition and microflora
    sustained disease suppression
  • Conducive peat Composted peat
  • Bacteria species that
  • induced suppression 1 23
  • Pseudomonads 0 25-45
  • Arthrobacter 30 3-15
  • Anaerobic bacteria predominant Yes No

Boehm et al., 1993
41
Change in colonization species with decomposition

Hoitink Boehm, 1999
42
Soil Food Web
  • Trophic levels
  • Microorganism (Producers)
  • Nematodes (Consumers)
  • Predaceous Nematodes (Predators)

43
Trophic Forces
  • Bottom-up control (restricted by resource
    limitscarrying capacity)
  • organic matter
  • nutrients
  • microbial processes
  • Top-down control (restriction by consumers)
  • predation

44
Trophic levels
  • Microcosms 3 trophic levels
  • 10 species bacteria 10 species fungi
  • Microbes bacterial and fungal nematode
  • Microbes microbivores predatory nematode
  • Results
  • 3rd trophic level decreased 2nd trophic level
  • gt Top down control
  • Abundance of bacteria, not affected by food chain
  • Abundance of fungi increased with predation
  • Mikola Satala, 1998

45
Trophic Cascades vs Bottom up control
  • No evidence of trophic cascades (top-down
    control) that interactions between trophic levels
    regulates microbial biomass and productivity in
    soil food webs
  • Microbial community adjusts growth rate and
    turnover rate
  • Microbial community growth not differentiated by
    trophic level
  • Competition between species with environmental
    conditions and plant exudates determines species
    composition (bottom-up control)
  • Mikola Satala, 1998

46
Summary of factors
  • General Suppression
  • Species number and diversity
  • Abiotic factors
  • Soil moisture
  • H2O2
  • Specific factors
  • Cultivar specific
  • Antibiotics (Phl)
  • SAR/ISR

47
Biological control
  • Attributes for Biocontrol
  • Non-Streptomycete actinomycetes
  • Antibiosis
  • Hyperparasitic
  • Cell-wall degrading enzymes
  • Plant growth promotant
  • El-Tarabily Sivasithamparam, 2006
  • General Biocontrol agents
  • Active suppression
  • Population density
  • Transferable (inoculation)
  • Functional activity
  • Weller,et al., 2002

48
Barriers to development of suppressive soil
  • Host-pathogen specificity
  • Soil variables
  • Climate variables
  • Nutrient inputs
  • Crop rotations

49
Conclusions
  • Multiple methods of control by suppressive soil
  • Biological Interaction between control and
    pathogen
  • Competition for nutrients (Fe)
  • Competition for colonization
  • Production of specific inhibitors (H2O2,
    Antibiotics)
  • SAR/ISR
  • Driven by cultivar exudates and response
  • Species specific
  • Modified by environment
  • Organic matter
  • pH
  • Nitrogen form (NH4)
  • Sand/clay

50
  • References
  • Alabouvette, C., 1986. Fusarium-wilt supp soils
    from the Chateaurrenard region review of 10
    year study.
  • Agronomie 6 273-284.
  • Agrawal, A., Tuzun, S., Bent, E., 1999. Induced
    plant defenses against pathogens and herbivores
    biochemistry, ecology and agriculture. APS
    Press, St. Paul.
  • Bailey, K.L., Lazarovits, 2003. Suppressing
    soil-borne diseases with residue management and
    organic amendments. Soil Tillage Research 72
    169-180.
  • Boehm, M.J., Madden, L.V., Hoitink, H.A.J., 1993.
    Effect of organic matter decomposition level on
    bacterial species diversity and composition in
    relatinship to Pythium damping-off severity.
    Applied and Environmental Microbiology 59
    4171-4179.
  • Caswell, E.P., Thomason, I.J., 1985. Geographic
    distribution of Heterodera schachtii in the
    Imprerial Valley of California from 1961 to1983.
    Plant Disease 69 1075-1077.
  • Cook, R.J., 1982. Use of pathogen-suppressive
    soils for disease control. pp 51-65. In
    Schneider, R.W., Suppressive soils and plant
    disease. The American Phythological Society.
    St. Paul.
  • Duffy, B.K., Ownley, B.H. Weller, D.M. 1997.
    Soil chemical and physical properties associated
    with suppression of take-all of wheat by
    Trichoderma koningii. Phtopathology 87
    1118-1124.
  • El-Tarabily, K.A., Sivasithamparam, K., 2006.
    Non-Streptomycete actinomycetes as biocontrol
    agents of soil borne fungal plant pathogens and
    as plant growth promoters. Soil Biology an
    Biochemistry 38 1505- 1520.
  • Fuchs, J.G., Moenne-Loccoz, Y., Defago, G., 1997.
    Nonpathogenic Fusarium oxysporum strain Fo47
    induces resistance to Fusarium wilt in Tomato.
    Plant Disease 81 492-496.
  • Fritz, M., Jakobsen, I., Foged Lyngkjaer, M.,
    Thordal-Christensen, H. Pons-Kuhnemann, J. 2006.
    Arbuscular mycorrhiza reduces susceptibility of
    tomato to Alternaria solani. Mycorrhiza 16
    413-419.
  • Fravel, D., Olivain, C., Alabouvette, C., 2003.
    Fusarium oxysporum and its biocontrol. New
    Phytologist 157 493- 502.
  • Garbeva, P., vanVeen, J.A., van Elsas, J.D.,
    2004. Microbial Diversity in Soil Selection of
    Microbial populations by plant and soil type and
    implications for disease suppressiveness.
    Annual Review of Phytopathology 42 243-270.
  • Hoitink, H.A.J., 1980. Composted Bark, A
    lightweight growth medium. Plant Disease 64
    142-147.
  • Hoitink, H.A.J., Boehm, M.J., 1999. Biocontrol
    within the context of soil microbial communities
    A substrate- dependent phenomenon. Annual
    Review of Phytopathology 37 427-426.

51
  • Janvier, C., Villeneuve, F., Alabouvette, C.,
    Edel-Hermann, V., Mateille, T., Steinberg, C.,
    2007. Soil health through soil disease
    suppression Which strategy from descriptors to
    indicators. Soil Biology and Biochemistry 39
    1-23.
  • Khaosaad, T., Garcia-Garrido, J.M., Steinkellner,
    S., Vierheilig. 2007. Take-all disease is
    systemically reduced in roots of mycorrhizal
    barley plants. Soil Biology and Biochemistry 39
    727-734.
  • Lyda, S.D., 1982. Physical and chemical
    properties of suppressive soil. pp 9-22 In
    Schneider, R.W., Suppressive soils and plant
    disease. The American Phythological Society.
    St. Paul.
  • Mazzola, M., 2002. Mechanisms of natural soil
    suppressiveness to soilborne diseases. Antonie
    van Leeuwenhoek 81 557-564.
  • McCann, K., Hastings, A., Huxel, G.R., 1998.
    Weak trophic interactions and the balance of
    nature. Nature 395 794-798.
  • Mikola, J., Setala, H., 1998. No evidence of
    trophic cascades in an experimental
    microbial-based soil food web. Ecology 79
    153-164.
  • Mishra, K.K., Srivastava, J.S., 2004. Soil
    amendments to control common scab of potato.
    Potato Research 47 101-109.
  • Nigh, E.A., Thomason, I., van Gundy, S.D., 1980.
    Identification and Distribution of fungal
    parasites of Heterodera schachtii eggs in
    California. Phytopathology 70 884-889.
  • Pimm, S.L., 1982. Food Webs. Chapman Hall,
    London.
  • Raaijmakers, J.M., Bonsall, R.F., Weller, D.M.,
    1999. Effect of population density of
    Pseudomonas fluourescense on production of
    2,4-diacetylphloroglucinal in the rhizosphere of
    wheat. Phytopathology 89 470-475.
  • Simon, A., Sivasithamparam, K., 1989.
    Pathogen-suppression A case study in biological
    suppression of Gaeumannomyces graminis var.
    tritici in soil. Soil Biology Biochemistry 21
    333-337.
  • Weinhold, A.R., 1970. Significance of
    populations of major plant pathogens in soils.
    pp 22-27 In Toussoun, T.A., Bega, R.V., Nelson,
    P.E. Root disease and soil-borne pathogens.
    2nd int. symposium on factors determining the
    behaviour of plant pathology in soil. University
    of California Press, Berkley.
  • Weller, D.M., Cook, R.J., 1983. Suppression of
    Take-all of wheat by seed treatments with
    fluorescent Pseudomonads. Phytopathology 73
    463-469.
  • Weller, D.M., Raaijmakers, J.M., McSpadden
    Gardener, B.B., Thomashow, L.S., 2002. Microbial
    populations responsible for specific soil
    suppressiveness to plant pathogens. Annual
    Review Phytopathology 40 309-348.
  • Westphal, A., Becker, J.O., 1999. Biological
    suppression and natural population decline of
    Heterodera schachtii in a California Field.
    Phytopathology 89 434-440.
Write a Comment
User Comments (0)