Title: Disease Suppressive Soils: Fact or Fiction
1Disease Suppressive Soils Fact or Fiction?
- Hida Manns
- March 26, 2007
2OUTLINE
- 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
3DEFINITION
- 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).
4Disease 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
5General Suppression
- Abiotic
- pH
- N, C, Mg, K
- Sand/clay
- CEC (Cation Exchange Capacity)
- Organic matter
-
- Biotic
- Microbial biomass
- Actinomycetes
-
6Management
- 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
7Organic 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
8Biological 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
9Fungi
- 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
10Mycorrhiza
- 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)
11Actinomycetes
- 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
12Specific 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
13Specific 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
14Fo47 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
15Split-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
16ISR
- 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
17Examples
- Potato Wheat
Sugar Beets - Common scab Fusarium
Take-all Cyst Nematode - General
- Suppression
- Abiotic
- Biotic
- Specific
- Suppression
- Antagonist
- SAR
- ISR
18Potato Common Scab
Cornell University Vegetable MD Online Potato
Common Scab http//vegetabledonline.ppath.edu/phot
opages/impt_Diseases/potato/pot_scab.htm
19Common 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
20Fusarium 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
21Fusarium
- 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
22Soil 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)
23F. 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
-
24Mechanism
- 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)
25Take-all of Wheat
Take-all of Wheat http//scarab.msu.montana.edu/Di
sease/DiseaseGuidewebpics/Petewebpics61-70Img0065.
jpg Also 0066 and 0067
26Take-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
27Antagonist Cause of Disease Decline
Weller et al., 2002
28Pseudomonas fluoresens and Ggt
Weller Cook, 1983
29Trichoderma 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
30Principal Components Analysis
Influence of soil factors on disease reduction by
T. koningii
Duffy et al., 1997
31Specific 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
32Heterodera schachtii
33Sugar 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
34Geographic 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
35Defense
- 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
36Fungal 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
37Fusarium on H. schachtii eggs
Nigh et al., 1980
38Effects of soil on H. schachtii egg survival
Greenhouse Experiment Suppressive and conducive
soils With swiss chard
Westphal Becker, 1999
39Creating 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
40Microbial 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
41Change in colonization species with decomposition
Hoitink Boehm, 1999
42Soil Food Web
- Trophic levels
- Microorganism (Producers)
- Nematodes (Consumers)
- Predaceous Nematodes (Predators)
43Trophic Forces
- Bottom-up control (restricted by resource
limitscarrying capacity) - organic matter
- nutrients
- microbial processes
- Top-down control (restriction by consumers)
- predation
-
44Trophic 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
-
45Trophic 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
46Summary of factors
- General Suppression
- Species number and diversity
- Abiotic factors
- Soil moisture
- H2O2
- Specific factors
- Cultivar specific
- Antibiotics (Phl)
- SAR/ISR
47Biological 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
48Barriers to development of suppressive soil
- Host-pathogen specificity
- Soil variables
- Climate variables
- Nutrient inputs
- Crop rotations
49Conclusions
- 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.