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2000 North Central Division Meeting Abstracts
June 18-20, 2000 - Columbus, Ohio
Posted online October 4, 2000
A summary of 1999 growth chamber and field trial laboratory assays and
1998 and 1999 field trial disease control results after lactofen
application to soybean. T. G. BEAN (1) and T. L. Graham (2). (1) Field
Development Scientist, Valent USA Corporation, Franklin, PA 16323; (2)
Dept. of Plant Pathology, Ohio State University, Columbus, OH 43210.
Publication no. P-2000-0001-NCA.
Cobra 2 EC plus adjuvant applications were made to soybeans at the V3
and R1 growth stage in 1998 and at the R1 growth stage in 1999. Cobra
provided significant Sclerotinia sclerotiorum control in a 1998
field trial and significant Phytophthora sojae control in two 1999
field trials. The R1 growth stage application provided better Sclerotinia
sclerotiorum control than did the V3 stage applications. Laboratory
cotyledon assay results indicate that lactofen is a strong inducer of
soybean isoflavones and glyceollin elicitation competency. Analysis of
lactofen field treated trifoliate leaves in 1999 also revealed increased
isoflavone levels compared to the control plots.
Effects of inoculum dilutions on wheat streak mosaic tritimovirus
disease expression in winter wheat. C. I. BERGMAN (1), M. A. C.
Langham (1), and S. D. Haley (2). (1) Plant Science Dept., South Dakota State
University, Brookings, SD 57007; (2) Dept. Soil and Crop Sciences,
Colorado State University, Ft. Collins, CO 80523. Publication no.
P-2000-0002-NCA.
Ten lines of winter wheat (Triticum aestivum) in four
replications were mechanically inoculated in the fall two weeks after
emergence with wheat streak mosaic tritimovirus (WSMV). Sap inoculum from
infected plants was applied with a high pressure sprayer to each line at
dilutions of 1:5, 1:10, or 1:20 (weight:volume). Significant effects were
exhibited for plant height, total yield, test weight, and protein. Yields
of Arapaho, SD92107, TAM107, Vista, Jagger, SD93267, Sage, and Dawn were
all reduced at the 1:20 dilution compared to the 1:5. Yield of KS95-H102
was the lowest at the 1:5 dilution, and higher than the controls at the
1:20. The yield of KS96HW10-1 increased at the 1:5 dilution, was reduced
at the 1:10, and was not affected at the 1:20.
New methods for producing, recovering, storing and delivering
ascospores of Sclerotinia sclerotiorum and other fungal propagules.
M. G. Boosalis, J. R. STEADMAN, K. Powers, and B. Higgins. Dept. Plant
Pathology, University of Nebraska, Lincoln. Publication no.
P-2000-0003-NCA.
Ascospores of Sclerotinia sclerotiorum are used to test
management strategies of diseases caused by this fungus. In lieu of filter
membranes for the deposition of ejected ascospores we use silica sand,
calcimate clay mineral particles, petroleum jelly, plastic disks (PD) cut
from plastic food bags and aluminum foil disks (AD). Spores on petroleum
jelly, silica sand and clay were viable and virulent for over 30 months,
whereas viability and virulence was retained for over 6 months on PD and
AD. Conidia of Alternaria spp. and Bipolaris sorokinia and
chlamydospores of Ustilago tritici stored on petroleum jelly were
viable for 24 months while urediospores of wheat leaf rust lost viability
after several months. Rinsing ascospores off PD and AD did not inhibit
their germination or pathogenicity. Silica sand and clay particles with
ascospores intact are used as inoculum. This would retain the gelatinous
matrix that is associated with freshly ejected ascospores.
Greenhouse evaluation of commercial and public soybean cultivars for
resistance to rhizoctonia root and crown rot. C. A. Bradley, G. L.
Hartman, D. S. Mueller, and W. L. Pedersen. Dept. of Crop Sciences,
University of Illinois, Urbana, IL 61801. Publication no. P-2000-0004-NCA.
Rhizoctonia root and crown rot of soybean, caused by Rhizoctonia
solani, can be a problem wherever soybean is grown, and there are no
known commercial soybean cultivars released for resistance. Seven hundred
soybean cultivars were evaluated for resistance to Rhizoctonia solani
(root and crown rot) in the greenhouse. Cultivars were planted into trays
containing a 2:1 sand:soil mix. Each tray also had cultivars Bedford or
Jack (susceptible) or Centennial or Savoy (resistant). Plants were
inoculated at their bases with a mycelial suspension of Rhizoctonia
solani (AG-2) at the VE growth stage and were rated for disease
severity using a 0 to 5 scale after 21 days. One hundred forty cultivars
had disease ratings one standard deviation below the mean (<2.5 disease
rating) and were reevaluated in a replicated trial. Twenty of the 140
cultivars had disease ratings of <2.5 in this test and were reevaluated
in another replicated trial. In this final trial, cultivars Savoy, Asgrow
2601, and Asgrow 3701 had the lower disease ratings and were classified as
moderately resistant to infection by Rhizoctonia solani.
Control of Rhizoctonia root and crown rot of sugar beet with
azoxystrobin. J. R. BRANTNER and C. E. Windels. Univ. Minn., NW
Research & Outreach Center, Crookston, 56716. Publication no.
P-2000-0005-NCA.
Azoxystrobin was tested for control of early- and late-season root and
crown rot of sugar beet caused by R. solani AG-2-2. Plants were
inoculated with R. solani 5 wk after planting. Azoxystrobin (13.9 g
a.i./1000 m row) was applied in an 18-cm band after inoculation and again
2 and 4 wk later. After 2½ wk, inoculated plots treated with
azoxystrobin had greater (P=0.05) plant stand than untreated plots
(75% vs 30%, respectively); stand in noninoculated, no fungicide plots was
97%. At harvest, inoculated plots treated with azoxystrobin had higher (P=0.05)
stand than untreated plots (29% vs 3%, respectively); stand in
noninoculated, no fungicide plots was 87%. In a late season trial, plants
were inoculated with R. solani at row closure. Azoxystrobin was
broadcast-applied (0.168 kg a.i./ha) after inoculation and again 3 wk
later. At harvest, plant stand in inoculated plots treated with
azoxystrobin and in noninoculated, no fungicide plots (86% and 95%,
respectively) was (P=0.05) greater than in inoculated plots with no
fungicide (63%). Azoxystrobin is more effective in controlling late- than
early-season Rhizoctonia root and crown rot of sugar beet.
Evaluation of Burkard cyclonic spore sampler efficiency. C. BUTTKE
and L. Francl. Dept. of Plant Pathology, North Dakota State University,
Fargo, ND 58105. Publication no. P-2000-0006-NCA.
The Burkard cyclonic sampler takes in air volumetrically, creates a
vortex in an aluminum cylinder, and deposits particulates in an eppendorf
vial. Sampling efficiency was determined for ascospores of Sordaria
fimicola and Gibberella zeae under variable power and with and
without a surfactant. Results showed an average of 78% of the S.
fimicola ascospores entered the vial, while 22% lodged inside the
cylinder. G. zeae ascospores were tested identically, but only 25%
entered the vial, while 75% remained lodged inside the cylinder. When
testing a liquid silicone product (Sigmacote) on the cylinder wall,
approximately 17% of the S. fimicola spores entered the vial. The
aluminum collecting cylinder should be rinsed thoroughly when collecting
samples. Tests of Sigmacote with G. zeae had 99.7% of the spores
lodged inside the cylinder. When the power supply was decreased from 200mA
to 140mA, spore counts decreased, indicating that the Burkard needs full
power to run efficiently. A 38 amp hour battery maintained greater than
150mA to the Burkard for four days. A solar panel 10W or greater powering
a battery should maintain the amperage needed for the Burkard to function
properly.
Introduction to the late wilt disease of maize. L. M. BUTTONOW (1)
and A. H. Ellingboe (1). (1) Dept. Plant Pathology, University of
Wisconsin, Madison, WI 53706. Publication no. P-2000-0007-NCA.
For the past five decades, late wilt disease, causal agent Cephalosporium
maydis, has been an economically important disease of maize in Egypt;
it is considered one of the most significant factors reducing maize yield.
When one considers the high economic and agricultural importance of this
disease, research progress is extremely slow. Maize lines resistant to
late wilt disease have been found, however, these lines have been low
yielding, resulting in poor acceptance and use by producers. Other means
of control in the field have not been found. The literature on late wilt
disease contains contradictory reports, a lack of consensus as to
inoculation and screening techniques, an incomplete understanding of the
field epidemiology and the genetics of the pathogen, and a lack of
communication between workers. The focus of this paper is the comparison
of four greenhouse-inoculation systems commonly used by workers: root
inoculation at planting with grain-grown pathogen, root inoculation at 3
weeks after planting with cut roots, stem injection of conidia, and stem
toothpick inoculation at 3 weeks after planting. We found that disease
progress was dependent on the inoculation system used. This result may
explain part of the contradictions in the literature and argues for
increased focus on the basic biology of the pathogen.
Identification of resistance to soybean cyst nematode in Glycine
tomentella. R. J. CAMPBELL, G. L. Hartman, G. R. Noel, and T.
Hymowitz. Dept. Crop Sciences, University of Illinois, Urbana, IL 61801.
Publication no. P-2000-0008-NCA.
Transfer of soybean cyst nematode (SCN) resistance to soybean from a
wild perennial relative of soybean (Glycine tomentella) has been
reported. Our research objective is to determine SCN resistance levels in
all 328 known accessions of G. tomentella. In our initial study, 12
accessions representing all four chromosome levels (2n=38,40,78,80) within
G. tomentella were screened for resistance to SCN races 1, 3, and
4. Resistant, susceptible and intermediate plants were found between and
within accessions. Susceptibility appears to be correlated with chromosome
number. All 328 accessions will be tested in year 2000. We will begin to
study the mode of inheritance of this SCN resistance, and ultimately
transfer new sources of genetic resistance to SCN into soybean.
Developing microsatellite markers for the soybean brown stem rot
pathogen Phialophora gregata. W. CHEN and X. Shi. Illinois
Natural History Survey, and University of Illinois at Urbana-Champaign,
Champaign, 61820. Publication no. P-2000-0009-NCA.
Isolates of P. gregata from soybean were separated into two
distinct genotypes (A & B). The two genotypes showed
cultivar-preferential infection under field conditions. In order to study
gene flow between the two genotypes and variation within genotypes, we
have developed several microsatellite markers for P. gregata. Total
genomic DNA was digested with two four-basepair recognition enzymes, and
the digested DNA fragments ranging from 300 to 600 bps were isolated and
used to construct a DNA library. The DNA library was further enriched for
microsatellites by producing single stranded DNA followed by selective
second strand extension with microsatellite oligonucleotides as primers.
After sequencing selected clones and confirming microsatellite sequences,
specific primers were designed to flank the microsatellite repeats. Among
three microsatellites tested so far, two microsatellites produced
monomorphic bands for P. gregata from soybean. One microsatellite
consisting of ACGA repeats produced two alleles which correspond to the
separation of the genotypes A and B.
Multiple infection of soybean by the brown stem rot pathogen Phialophora
gregata. Y.-C. CHEN (1), C. R. Grau (2), and W. Chen (1). (1)
Illinois Natural History Survey, 607 E. Peabody Drive, Champaign, 61820;
(2) Dept. of Plant Pathology, University of Wisconsin, Madison, WI 53706.
Publication no. P-2000-0010-NCA.
In a previous study we discovered that soybean isolates of P.
gregata are characterized as either genotype A or genotype B, and the
two genotypes preferentially infect susceptible and resistant cultivars
under field conditions, respectively. Most infected plants in field
environments are colonized by one pathogen genotype if assayed by PCR
using primers specific for the two genotypes. In these same studies,
however, a few plants exhibited DNA bands characteristic of both genotypes
A and B. Studies were designed to determine whether those plants were
infected by a new genotype of the pathogen or the plants were co-infected
by both genotypes. Seven isolates of P. gregata were recovered from
a single soybean plant that showed DNA bands of both genotypes collected
from Arlington, Wisconsin. Six of the seven strains were genotype A, and
one strain was genotype B. Results show that the plants exhibited DNA
bands of both genotypes were infected by both A and B genotypes and not by
a new genotype of P. gregata.
Maize dwarf mosaic virus movement in resistant and susceptible maize.
Z. B. CHEN (1), T. Meulia (2), M. G. Redinbaugh (1,3), S. A. Hogenhout (4),
and D. T. Gordon (1). (1) The Department of Plant Pathology; (2) Molecular
and Cellular Imaging Center and (4) Department of Entomology, The Ohio
State University and (3) USDA, ARS Corn and Soybean Research, OARDC,
Wooster, OH 44691. Publication no. P-2000-0011-NCA.
Maize dwarf mosaic potyvirus (MDMV) causes an important disease in corn
worldwide. The disease is controlled primarily through use of resistant
hybrids. The maize inbred, Pa405 has a high level resistance to MDMV
conferred by a single dominant gene on chromosome 6. To develop an
understanding of the resistance mechanism, the distribution of MDMV-A coat
protein and RNA in vascular puncture inoculated Pa405 and a susceptible
inbred (Oh28) were compared. After inoculation, the viral coat protein and
RNA were found in the scutellum and embryo of both inbreds, demonstrating
that MDMV-A entered and replicated in Pa405 cells. However, the virus was
more invasive in Oh28 suggesting that virus movement was limited in the
resistant line. To further characterize limitations to virus movement in
Pa405, the MDMV-A genome was cloned, and a full-length cDNA construct was
inserted downstream of a T3 promoter. Sequence analysis of the genome
revealed a polyprotein sequence with similarity to other potyviruses.
Transcripts, synthesized from the clone, are being tested for their
infectivity in maize. To identify maize proteins involved in the
resistance response, a "virus overlay" assay was used to
identify several MDMV-binding proteins in both Pa405 and Oh28. Work to
identify, characterize and isolate these maize proteins is ongoing.
Petiole inoculation as a tool to screen soybean germplasm for
resistance to Sclerotinia sclerotiorum. L. DEL RIO, N. C.
Kurtzweil, and C. R. Grau. Dept. Plant Pathology, University of
Wisconsin-Madison, Madison, WI 53706. Publication no. P-2000-0012-NCA.
A petiole inoculation technique was used to evaluate soybean germplasm
for resistance to Sclerotinia sclerotiorum in a controlled
environment. Plastic drinking straws (2.5 cm length) were used to cut and
retain mycelium plugs from the leading edge of two-day-old colonies of S.
sclerotiorum. The petiole of the first trifoliate leaf was cut 2.5 cm
from the stem when the second leaf was fully open and capped with the
straw containing inoculum. Wilt and plant mortality were rated multiple
times during the incubation period and were used to calculate wilt and
resistance indices. A negative correlation was detected between the
resistance index and disease incidence in field experiments for nine
(r=-0.55, P<0.08), and six (r=-0.64, P<0.06) cultivars. Soybean PIs
548-625, 547-799, 547-803 (MG I), and 507-803 (MG 0) expressed a higher
resistance index (P<0.05) than the commercial cultivar S19-90.
Occurrence of soybean viruses and association with green stem of
soybean in Wisconsin. D. M. DOUGHTY (1), M. E. Lee (1), N. C. Kurtzweil
(1), C. M. Boerboom (2), and C. R. Grau (1). Department of Plant
Pathology; (2) Department of Agronomy, University of Wisconsin, Madison,
Wisconsin 53706. Publication no. P-2000-0013-NCA.
Green stem syndrome (GSS) of soybeans has been observed for years and
while incidence of GSS is usually 1-5%, in recent years fields have been
observed with 50-75% incidence. Plants retain green stems, leaves and
petioles well past the point of normal maturity and may have symptoms
including leaf distortion similar to herbicide injury, mosaic patterns,
leaf rugosity, and mottled seed. Because soybean viruses are often
implicated as causal agents of GSS, a virus survey was initiated in 1999
to determine incidence. Soybean cultivars common to 13 statewide
evaluation trials were sampled by collecting a leaf from five plants per
replicate plot, and were assayed using ELISA. Percent incidence was based
on the number of plots positive for a specific virus. Statewide incidence
for alfalfa mosaic virus was 28%, soybean mosaic virus 27%, tobacco streak
virus 17%, bean yellow mosaic virus 6%, tobacco ringspot virus 6% and bean
pod mottle virus 2%. Tobacco ringspot virus, soybean mosaic virus and bean
pod mottle virus were associated with plants expressing GSS.
Managing Fusarium head blight (scab) with fungicides. M. A. DRAPER.
Plant Science Dept., South Dakota State University, Brookings, SD 57007.
Publication no. P-2000-0014-NCA.
Fusarium head blight (scab) has been a problem in South Dakota wheat
since 1993, particularly on spring wheat in the northeastern quarter of
the state. Fungicides have been a proven element in effective scab
management. Ten treatments were evaluated during 1999 in South Dakota as a
part of a thirteen-state, uniform regional trial to evaluate fungicide
suppression of scab under different environments. Scab suppression can be
achieved with several fungicide products, but Folicur has provided the
best return on yield. Folicur treatment resulted in about a 60% reduction
in leaf disease and a 30-60% reduction in scab in 1999, but no significant
reduction in vomitoxin levels. New strobilurin chemistry fungicides,
Quadris, Stratego, and BAS 500, showed increased levels of vomitoxin and
are being monitored closely. All three of the new fungicides showed great
promise in suppressing leaf diseases and scab. BAS 500 was similar to
Folicur in both disease suppression and increased yield. Overall, Folicur
continues to provide the best performance against scab and the greatest
potential for full Section 3 labeling from EPA in the near future.
Relative titer of PVY in three inoculated potato cultivars over time.
M. A. DRAPER (1) and N. C. Gudmestad (2). (1) Plant Science Dept., South
Dakota State University, Brookings, SD 57007; (2) Dept. Plant Pathology,
North Dakota State University, Fargo, ND 58103. Publication no.
P-2000-0015-NCA.
Mosaic, caused by potato virus Y (PVY), has been a problem in US-grown
potatoes since the mid-1980s. Cultivars Shepody and Russet Norkotah,
express mosaic symptoms poorly when infected by PVY. These cultivars and
Red La Soda, a cultivar that expresses mosaic, were grown from single eye
seed pieces and inoculated with a local strain of PVY(^O),
transmitted to the plants by green peach aphids (Myzus persicae).
The aphids acquired PVY from detached PVY-infected potato leaves and were
transfered to the first leaves, soon after emergence. PVY replicated at
similar rates in the three potato cultivars. Over a four-week period of
time, there was no significant difference in rate or distance of virus
movement with all cultivars. No cultivar showed impaired PVY movement.
Following inoculation of a basal leaf, PVY was detected by ELISA in upper,
middle, or basal leaves within two weeks of inoculation. The relative
virus titer, as measured by ELISA, was not significantly different among
the three cultivars. These factors together indicate a susceptible
response in all three cultivars.
Risk factors associated with Stewart’s disease of corn. P. D.
ESKER and F. W. Nutter, Jr. Department of Plant Pathology, Iowa State
University, Ames, IA 50011. Publication no. P-2000-0016-NCA.
Accurate prediction of the risk for Stewart’s disease of corn would
help seed corn producers to select low-disease-risk sites and use
insecticide sprays in a cost-effective manner. Factors important in
estimating risks for this disease include: (i) mean monthly temperatures
during Dec, Jan, and Feb, (ii) prevalence of the disease the previous
season, (iii) population dynamics of the corn flea beetle (Chaetocnema
pulicaria) (vector), and (iv) the proportion of beetles infested with Pantoea
stewartii. In 1999, Stewart’s disease occurred in 58% of 1317 Iowa
fields inspected, and large populations of the corn flea beetle were found
in the southern 2/3 of Iowa. ELISA tests found that 50 to 70% of the
beetles sampled from mid- to late season were infested with P.
stewartii. The Stewart’s disease risk for Iowa in 2000 is predicted
to be moderate- to high based on geospatially referenced mean monthly air
temperatures. However, considering all four risk factors, we predict that
Stewart’s disease will be high throughout Iowa. Thus, seed and foliar
applications of insecticide will be needed to reduce disease risk in 2000.
Susceptibility of soybeans and dry beans to root rot pathogens in
Minnesota. C. ESTEVEZ DE JENSEN, M. ElAraby, J. A. Percich, and J. E.
Kurle. Dept. of Plant Pathology, University of MN, St. Paul, MN 55108.
Publication no. P-2000-0017-NCA.
Susceptibilities of dry bean (Phaseolus vulgaris) ‘Montcalm’
and soybean (Glycine max) ‘Sturdy’ to infection by Fusarium
solani f. sp phaseoli (Fsp) F. solani (Fs), and Rhizoctonia
solani (Rs) were determined in growth chamber studies. Five-day-old
seedlings germinated from disinfected seed of both crops were established
in growth pouches. They were then inoculated with isolates of Fsp or Fs (1
× 10(^6) macroconidia / ml) or with 1 cm disks of PDA supporting actively
growing cultures of Rs. Fusarium solani f. sp. phaseoli was
pathogenic to bean and soybean resulting in root disease severity (DS) of
7.5 (dry bean) and 3.2 (soybean) (1-9 scale). Fusarium solani
infected both dry bean and soybean resulting in a DS of 2.5 and 3.2
respectively. Plant biomass was decreased for bean (65%) and soybean (4%)
when infected with Fsp when compared with noninfected plants. Rhizoctonia
solani caused severe root rot and decreased plant biomass of infected
dry bean (42%) and soybean (19%). The results suggest that crop sequences
containing either of these crops may increase the risk of these root rots
in Minnesota.
Monitoring Fusarium head blight temporal progress. L. J. FRANCL.
Dept. of Plant Pathol., North Dak. State Univ., Fargo, ND 58105.
Publication no. P-2000-0018-NCA.
A method was developed to measure Fusarium head blight (FHB)
progression in field-grown spring wheat. Wheat susceptible to FHB was
planted in one-year old wheat stubble in replicated blocks on three dates
and soil was mulched with plastic to accelerate maturation of the first
planting. A weather station and Burkard air sampler were placed on-site.
Every day from heading until the milk stage, culms were cut at the first
node and collected. Five heads per replicate were shaken in water to
dislodge inoculum, which was assayed on selective medium. Twelve culms per
replicate were inserted directly into a floral preservative solution,
while 12 others were first misted for 24 h to promote disease expression.
Culms then were kept in a growth chamber at 22 C with a 12 h photoperiod
for 14 days. FHB intensity was evaluated before heads senesced. Under
these conditions, FHB severity in 1999 ranged from 0 to 100% and
sporodochia could sometimes be seen. This data series can be related to
time, environment, spore dispersal, inoculum level, and plant growth
stage. Once it is conducted in multiple environments, this approach should
lead to a greater understanding of FHB epidemiology and development of a
forecasting model.
Foliar-applied calcium sulfate increased yield and reduced white mold
in dry bean. P. L. GROSS, J. R. Venette, and R. S. Lamppa. Dept. Plant
Pathology, North Dakota State University, Fargo, ND 58105-5012.
Publication no. P-2000-0019-NCA.
Dry bean Phaseolus vulgaris L. is an important crop in North
Dakota and white mold Sclerotinia sclerotiorum is the worst disease
problem. Five grower fields in three North Dakota counties were chosen for
white mold strip trials in 1999. Five treatments (Thiophanate methyl or
benomyl at 1.7 and 0.56 kg/ha, calcium sulfate liquid at 9.4 L/ha plus
thiophanate methyl or benomyl at 0.56 kg/ha, calcium sulfate liquid at 9.4
L/ha) were arranged so that each treated strip was adjacent to an
untreated strip. White mold incidence and severity was determined at 8
paired sites 80 m apart in each treated and untreated strip. Incidence was
reduced by 13% and 15% with fungicides alone at 0.56 kg/ha and 1.7 kg/ha
respectively, by 26% with fungicide plus calcium sulfate, and by 2.5% with
calcium sulfate alone, compared to the untreated control. Severity was
reduced by 15% with fungicide treatment applied at 1.7 kg/ha and by 14%
with calcium sulfate. Yields were increased by all treatments. Calcium
sulfate used alone had the highest yield increase of 446 kg/ha compared to
the untreated check.
Fungicide application timing effects on field severity of Fusarium head
blight in wheat and barley. S. Halley (1), M. P. MCMULLEN (1), J.
Pederson (1), and J. Moos (2). (1) Dept. Plant Pathology; (2) Dept.
Agricultural Systems and Engineering, North Dakota State University,
Fargo, ND 58105. Publication no. P-2000-0020-NCA.
Optimum timing of fungicide application for control of Fusarium head
blight (FHB) in spring wheat, durum, and barley was evaluated in a
greenhouse environment. For each crop, 20 plants were planted in each of
five replicate trays per treatment and grown to heading stage. Folicur
(tebuconazole) fungicide (4 fl oz/acre in 9 gpa) was applied at three
separate Feekes growth stages, 10.3, 10.51, or 10.54., using a track
sprayer fitted with forward/backward XR8001 flat fan nozzles. Plants were
inoculated with 5000 spores/ml of Fusarium graminearum at Feekes
10.51 using atomization. FHB field severity (incidence × head severity)
was measured 21 days after inoculation. For each crop, FHB field severity
was lowest when Folicur was applied at Feekes 10.51 and highest when
treatment was delayed to Feekes 10.54. An additional trial on barley
indicated that fungicide application on the day of, or 2 days after,
inoculation to the head gave significantly lower FHB severities compared
to 3 or 4 days after inoculation.
Effect of preharvest benomyl spray on winter storage of carrots. J.
M. HANSEN (1), D. J. Tobias (1), N. F. Balbyshev (1), R. W. Stack (1), and
C. W. Lee (2). (1) Dept. Plant Pathology; (2) Dept. Plant Science, North Dakota
State University, Fargo, ND 58105. Publication no. P-2000-0021-NCA.
A major consideration for carrot production in northern regions is the
necessity to store the crop over the winter. In 1995 and 1996, growers in
North Dakota and Minnesota suffered severe losses of stored carrots due
primarily to white mold (WM) (Sclerotinia sclerotiorum (Lib)
deBary). In 1997 trials, a preharvest application of benomyl reduced WM
storage rot by 50%, but these results could not be repeated in 1998. In
1999, two experiments were done to test the effectiveness of preharvest
benomyl application on the incidence of WM in stored carrots. In trials, a
benomyl spray 10 days prior to harvest resulted in lower WM incidence.
After 4 months of cold storage at 4 C, 9.7% of benomyl-sprayed carrots
were decayed due to WM compared to 18.5% decay in unsprayed checks in one
trial. In the other trial, the WM was 5.2% in the benomyl-sprayed versus
37.6% in the check. It appears that properly timed preharvest application
of benomyl will substantially reduce losses to WM of carrots in storage.
Reaction of soybean germplasm with soybean cyst nematode resistance to
brown stem rot development. T. J. HUGHES, N. C. Kurtzweil, and C. R. Grau.
Dept. of Plant Pathology, University of Wisconsin, Madison, WI 53706.
Publication no. P-2000-0022-NCA.
Field and greenhouse experiments indicate a strong relationship between
some sources of soybean cyst nematode (SCN) resistance and resistance to Phialophora
gregata, causal agent of brown stem rot (BSR). To determine which
sources of SCN resistance conferred resistance to BSR, 10 plant
introductions (PI) with different sources of SCN resistance and 12
varieties representing six of these sources, were root-dip inoculated in
greenhouse assays with isolate H96-5. BSR severity was calculated as the
percentage of symptomatic leaf, stem, and root tissue. PI 209332 was the
only SCN-resistant source with resistance (3%) to BSR development.
Reaction of Peking (50%) and PI 88788 (62%) were higher than two BSR
susceptible checks, Sturdy (19%) and Williams 82 (32%). SCN-resistant
varieties derived from PI 88788 showed varying levels of symptom severity.
Dwight was similar to PI 88788 while Freeborn, Fayette, Jack, and Bell
were similar to varieties with the Rbs 1, 2, and 3 (2-10%) genes
for BSR resistance. Studies are underway to determine the source of BSR
resistance observed in PI 88788 derived soybean varieties.
Genetics of maize resistance to Maize chlorotic dwarf waikivirus.
M. W. JONES (1,2), R. Louie (1,2), R. A. Anderson (1,3), and M. G. Redinbaugh
(1,2). (1) USDA-ARS Corn and Soybean Research, OARDC, Wooster, OH 44691;
(2) Department of Plant Pathology; (3) Department of Entomology, The Ohio
State University. Publication no. P-2000-0023-NCA.
Ineffective screening methods and low levels of disease resistance have
hampered genetic analysis of maize resistance to maize chlorotic dwarf.
This disease is caused by Maize chlorotic dwarf waikivirus, which
is vectored by the leafhopper, Graminella nigrifrons. Germplasm
identified as resistant by one or more screening methods (natural
infection, single inoculation of 14-day old plants, and multiple
inoculation of 3-4 day old seedlings) was re-evaluated with the highly
effective multiple inoculation screening method. In this screen, inbreds
Oh1VI, Mp705, and inbred lines derived from Compuesto Cuba 551 (CC551) and
Dominican Republic (DR) were highly resistant. In contrast, T232, Oh1EP,
Pa11, and CI21, which were resistant to MCDV in the natural infection
and/or single inoculation screens, were susceptible in the multiple
inoculation screen. Tests of F(1) crosses (resistant inbred X susceptible
inbred Va35) and subsequent F(2) populations indicated the MCDV resistance
was quantitative, and AUDPC scores for the F(1) crosses suggested the
inheritance of resistance was polygenic. QTL analyses and ANOVA of 300
F(2) progeny of Oh1VI x Va35 indicated two independent QTLs of equal
strength located on chromosomes three and ten. Experiments to map loci
controlling resistance in Mp705, CC551 and DR are still underway.
Increased susceptibility to Sclerotinia stem rot of soybeans associated
with increased planting density. J. E. Kurle and M. ElAraby. Dept. of
Plant Pathology, University of Minnesota, St. Paul, MN 55108. Publication
no. P-2000-0024-NCA.
The incidence of Sclerotinia stem rot (SSR) or white mold of soybean Glycine
max caused by Sclerotinia sclerotiorum increases when soybeans
are planted in narrow rows or at high plant populations. The increase is
attributed to high humidity and low temperatures in the crop canopy.
Soybean (cvs. Sturdy and S19-90) was planted at five planting rates: 38,
61, 84, 106, and 129 plants/m(^2). At growth stage V4, plants were
inoculated with S. sclerotiorum mycelium by placing plugs of PDA
cut from the edge of growing S. sclerotiorum colonies over the cut
ends of main stems. Susceptibility to SSR was indicated by the length of
the lesion developing from the point of inoculation. Increasing plant
density was correlated with increasing susceptiblity to SSR (r = 0.39, p
< 0.001). The result indicates that increased incidence of SSR
associated with high planting rates or narrow rows may be a result of
physiological or structural changes caused by crowding.
Plant population and row spacing effects on Sclerotinia stem rot
severity in soybean. J. E. Kurle (1) and S. Naeve (2). (1) Dept. of
Plant Pathology, University of Minnesota, St. Paul, MN 55108; (2) Dept. of
Agronomy and Plant Genetics, University of Minnesota, St. Paul, MN 55108.
Publication no. P-2000-0025-NCA.
Sclerotinia stem rot (SSR) or white mold of soybean (Glycine max)
caused by Sclerotinia sclerotiorum is an important disease in the
North Central states. Increased prevalence of SSR in soybean has been
attributed to more frequent use of narrow row spacing and high plant
populations. We examined the effect of three row spacings on SSR incidence
(25 cm, 50 cm and 76 cm) and three plant populations (100,000; 175,000 ,
and 225,000 plants ha(^-1)) planted in a factorial design at
seven locations with a history of SSR occurrence. In 1999 SSR developed at
four locations. Incidence of SSR was affected by the interaction of row
spacing and plant population at one location (P=9.7), by plant population
at two locations (P<=0.01, P=1.5), and was present only in plots
planted at 225,000 plants ha(^-1) at a fourth location where
average incidence was < 5%. The results indicate that plant population
has a greater influence on white mold incidence than row spacing.
Relationship of soil pH and brown stem rot of soybean. N. C. KURTZWEIL
and C. R. Grau. Department of Plant Pathology, University of
Wisconsin, Madison, WI 53706. Publication no. P-2000-0026-NCA.
Brown stem rot (BSR), caused by Phialophora gregata, is commonly
found in Midwest soybean fields, occurring over a range of soil types and
soil pH. While incidence of BSR has increased with shortened crop
rotations and decreased tillage, fields are encountered that remain
relatively free of BSR symptoms despite pathogen presence and management
practices that should favor the pathogen and disease. Although climate,
soil moisture, and cultivar influence BSR severity, results from several
years of small plot and large on-farm trials suggest that symptom severity
is greatest as soil pH approaches 6.0 and severity declines as soil
approaches pH 7.0. A yield difference of 16-19 bu/a between BSR resistant
and BSR susceptible cultivars was obtained at soil pH below 6.0, compared
to a 5 bu/a yield difference for resistant and susceptible cultivars at
soil pH above 6.5. Symptom severity of BSR susceptible cultivars was
inversely correlated with soil pH (r=-0.41, p=0.0001), but not for BSR
resistant cultivars (r=0.08 p=NS). Population density of P. gregata
in host tissue decreased as soil pH increased. Knowledge of soil pH can be
used to tailor BSR management systems for specific fields.
Evaluation of winter wheat cultivars and lines for wheat streak mosaic
tritimovirus resistance or tolerance. M. A. C. LANGHAM (1), S. D.
Haley (2), D. C. Doxtader (1), S. Kalsbeck (1), and R. S. Little (1). (1)
Plant Science Department, South Dakota State University, Brookings, SD
57007; (2) Soil & Crop Sciences, Colorado State University, Fort
Collins, CO 80523. Publication no. P-2000-0027-NCA.
Ninety-six winter wheat (Triticum aestivum) cultivars and lines
in three replications were evaluated for response to wheat streak mosaic
tritimovirus (WSMV) in a field study. Two rows of a four-row plot were
inoculated with infected sap extract using high-pressure spray. The
remaining rows served as uninoculated controls. Disease severity, height,
total yield, test weight, and heading date were recorded. Average disease
severity (scale of 0-5) ranged from 1.9-4.1. Heights ranged from a 30%
increase to 22.7% decrease. The hard red winter wheat cultivars, Alliance,
Crimson, Scout 66, and Tandem had less than 10% yield loss. Yield losses
up to 41.6% were recorded among the remaining cultivars. Among hard red
wheat experimental lines, 12 lines had yield losses under 10%, but other
lines had losses up to 61%. Five hard white winter wheat lines had yield
losses under 10%, and maximum yield loss among these was 63.3%.
Characterization of phytoplasmas detected in Wisconsin. M. E. LEE and
C. R. Grau. University of Wisconsin, Madison, WI 53706. Publication no.
P-2000-0028-NCA.
Phytoplasmas are commonly associated with diverse plant hosts in
Wisconsin. No recent work has been done to characterize the phytoplasmas
present in Wisconsin using molecular methods. We investigated the presence
of phytoplasmas in soybeans and carrots and found aster yellows
phytoplasma subgroups A and B (16SrI-A and 16SrI-B), according to Ing-Ming
Lee’s RFLP classification system. Phylogenetic analysis of the 16S rDNA
gene sequence suggests the phytoplasmas in carrot and soybean differ from
each other. Of 121 soybean leaf samples collected from throughout
Wisconsin, 2 tested positive. These positive samples were located at the
West Madison Agricultural Research Station next to an alfalfa field. The
positive soybean plants could not be distinguished based on symptoms from
the surrounding plants. Of 37 aster yellows symptomatic and asymptomatic
carrots sampled from areas near Hancock and Plover, Wisconsin, only one
carrot plant did not contain phytoplasma in young leaves or root tips.
Phytoplasmas were most frequently detected in the roots (97%) versus the
leaves (73%) of carrots.
Relationships among environmental variables, ascospore dispersal, and
inoculum of Gibberella zeae. S. MARKELL and L. Francl. Dept. of
Plant Pathology, North Dakota State University, Fargo, ND 58105.
Publication no. P-2000-0029-NCA.
Ascospores of Gibberella zeae, thought to be the primary
inoculum for Fusarium head blight, are borne on infested plant residues. A
Burkard 7-day spore sampler was placed in one-year-old wheat stubble left
unplowed and fallow. Greenhouse grown, potted wheat plants were exposed
daily in the stubble field for a 24 h period. Four heads per pot were cut,
shaken in a solution of distilled water and Tween20, and 0.5 ml was spread
on Komada’s medium to determine colony forming units per head per day. A
Campbell weather station was also on the site. Environmental variables
were correlated with spores collected in the sampler and inoculum
recovered from the heads. Six of seven major spore dispersal events
occurred within 2 h of rain. Daily inoculum levels peaked when rainfall
occurred within the previous 24 or 48 h. Time of day, relative humidity,
and wind speed affected spore dispersal. Further research and analysis may
provide a prediction model of inoculum level based on environmental
variables.
Effect of Sclerotinia stem rot on seed yield of two soybean cultivars
inoculated at two growth stages. G. A. MARS (1), B. D. Nelson (1), and
T. C. Helms (2). (1) Depts. Plant Pathology and (2) Plant Sciences, North
Dakota State University, Fargo, 58105. Publication no. P-2000-0030-NCA.
Sclerotinia stem rot, caused by Sclerotinia sclerotiorum, is an
important soybean disease in the Northern Plains. Seed yield loss
(measured as total seed weight) due to Sclerotinia stem rot was evaluated
in two cultivars, Traill (less susceptible) and M301 (highly susceptible),
inoculated at two growth stages (R-3 and R-5; 15 days apart) in the field
using two inoculation methods. One method was infested tissue paper
appressed to the stem and the other was infested ground wheat grain
sprinkled over the top of the plants. Following inoculation, an irrigation
system maintained high humidity for 30 days. Both types of inoculations at
R-3 resulted in significant seed weight reductions on individual plants of
both cultivars. Although plants inoculated at the R-5 stage were diseased,
there was no significant reduction in seed weight. The mean seed weight
reduction per diseased plant was 50% for the tissue paper method and 42%
and 45% for Traill and M301, respectively, for the grain inoculum method.
The two cultivars did not significantly differ in seed weights,
irrespective of the inoculation method.
Preferential infection of soybean cultivars by genotypes of the brown
stem rot pathogen Phialophora gregata. X. Q. MENG (1), C. R.
Grau (2), and W. Chen (1). (1) Dept. of Crop Sciences, Univ. of Illinois,
and Ill. Nat. Hist. Surv., Champaign; (2) Dept. of Plant Pathology, Univ.
of Wisconsin-Madison. Publication no. P-2000-0031-NCA.
Isolates of P. gregata from soybean were separated into two
distinct genotypes (A and B). The two genotypes showed
cultivar-preferential infection in field environments. An experiment was
designed to study the cultivar-preferential infection in a controlled
environment. Four isolates each of the two genotypes were used
individually or in combination to inoculate resistant (Bell) and
susceptible (Sturdy) cultivars. When the isolates were used individually,
all isolates of both genotypes infected both cultivars. Genotype A
isolates caused both stem discoloration and defoliation on cv. Sturdy,
whereas genotype B isolates caused stem discoloration only. Bell expressed
mild symptoms to most of the isolates. When the two genotypes were mixed
in 1:1 ratio, genotype A isolates preferentially infected cv. Sturdy,
whereas genotype B isolates preferentially infected cv. Bell. The results
confirm field observations and also support the concept that P. gregata
is composed of defoliating and non-defoliating strains.
A computer program to quantify the "just noticeable
difference" when assessing disease severity. F W. NUTTER, Jr.
(1), P. D. Esker (1), J. Guan (1), and C. Conover. (1) Dept. Plant
Pathology, Iowa State University, Ames, IA 50011. Publication no.
P-2000-0032-NCA.
Psychophysical laws (e.g., Weber’s Law and Fechner’s Law) that have
been proposed as the basis for the development and use of nonlinear
disease rating scales (e.g., Horsfall-Barrett scale) have recently been
called into question (Can. J. Plant Pathology 17:174-185). A new computer
program "Disease Comparison" was developed to measure the
"just noticeable difference" (JND) in disease severity when
raters were asked to compare images of diseased leaves (grape downy
mildew) to the level of a known standard (e.g., 25, 37, and 50%).
Preliminary studies were performed with nine raters, who recorded whether
each of 150 images was < , >, or = to the comparison stimulus
(image). All raters could correctly identify that images were not equal
with a JND of + 5 to 6%. The JND was not significantly (P <= 0.05)
affected by the disease severity of the comparison levels (25, 37, 50%).
The results of this study suggest that a linear disease rating scale is
more appropriate than the Horsfall-Barrett scale which apparently has no
psychophysical basis for assessing the severity of at least some plant
diseases.
Mapping the temporal and spatial spread of gray leaf spot of corn in
Iowa using GIS. F.W. NUTTER, Jr. (1), P. D. Esker (1), and R. Rubsam
(1). (1) Dept. Plant Pathology, Iowa State University, Ames, IA 50011.
Publication no. P-2000-0033-NCA.
Geographic Information Systems (GIS) is a powerful tool that can be
used to geospatially reference disease and/or pathogen information over
time to assess the risk for diseases in specific years and fields. We
geospatially referenced the spread of Cercospora zeae-maydis
(casual agent of gray leaf spot) in Iowa from 1981 to 1997 by
obtaining the original hard copies of corn inspection data from the Iowa
Dept. of Ag. and Land Stewardship, Des Moines, IA. A GIS database was
created using ArcView GIS software (ESRI Inc., Redlands, CA, USA).
Prevalence data was mapped by county and year for C. zeae-maydis,
using ArcView. In 1981, gray leaf spot was reported in 4 out of 28
counties inspected. By 1997, however, gray leaf spot was reported in 44
out of 46 counties inspected. Prevalence based on the percentage of fields
with gray leaf spot disease increased from 8% in 1981 to 95% in 1997. The
disease prevalence maps for gray leaf spot clearly indicate that farmers
should place greater emphasis through the use of resistant hybrids and/or
the application of fungicides and not rely solely on practices that reduce
initial inoculum.
Quantifying the effect of prescribed burning on disease dynamics in
tallgrass prairies. R. J. PERCIFIELD (1), T. Rosburg (2), and F. W.
Nutter, Jr. (1). (1) Dept. Plant Pathology, Iowa State University, Ames,
IA 50011; (2) Dept. Biology, Drake University, Des Moines, IA 50311.
Publication no. P-2000-0034-NCA.
The management program most utilized to maintain the health and
diversity of prairie "remnants" is prescribed burning. However,
optimal seasonal timing and frequency of burning for managing plant
diseases is unknown. The objective of this study was to quantify the
impact of spring burning on disease dynamics in 3 Iowa tallgrass prairies.
Disease incidence and severity were visually assessed at Cayler,
Doolittle, and Sheeder Prairies in Iowa from sections burned in April 1999
and from sections burned in prior years. Four prairie species (Helianthus
rigidus, Desmodium canadense, Andropogon gerardii,
Sorghastrum nutans) were assessed for disease incidence and severity
at 2-wk intervals from late May to mid-September. Predominant pathogens
were: Puccinia andropogonis on A. gerardii, Stagnospora
simplicior on S. nutans, and Puccinia helianthi on H.
rigidus. Prescribed burning significantly reduced initial inoculum,
which delayed the onset of disease epidemics at all 3 locations by up to
29 days, but had no effect on the rate of epidemics.
Fusarium head blight reaction in F2 and F3 generations of a spring
wheat recombinant population. R. W. Stack (1), R. C. Frohberg (2), J.
Mitchell-Fetch (1), and J. M. HANSEN (1). (1) Dept. of Plant Pathology; (2)
Dept. of Plant Sciences, North Dakota State Univ., Fargo, ND 58105.
Publication no. P-2000-0035-NCA.
From the spring wheat cross ND2709/ND688, 107 individual F2 plants and
F3 families were screened for Fusarium head blight (FHB) reaction in
greenhouse tests. ND2709 is resistant and ND688 is susceptible to FHB. On
each individual F2 plant 3-5 heads were inoculated at anthesis by spikelet
injection with F. graminearum. Seed was saved from non-inoculated
heads of the F2 plants. Fifteen F2:3 seeds were planted in three
replicates. Wheat heads were inoculated at anthesis as before. In both
experiments, individual heads were scored for FHB symptoms on a 0-100%
scale at 3.5 weeks postinoculation. Both the F2 and F3 generations showed
highly significant differences in FHB, but the correlation between
generations was low (r = 0.37). Selecting the "best" and
"worst" of the F2 plants did result in population shifts in the
F3, but F2 selection would have neither retained the most resistant F3
lines nor discarded the most susceptible ones. Phenotypic selection for
FHB resistance in spring wheat should be deferred until at least the F3
generation.
Internal stem browning can be an unreliable indicator of colonization
of soybean stems by Phialophora gregata. G. M. TABOR, G. L.
Tylka, and C. R. Bronson. Dept. of Plant Pathology, Iowa State University,
Ames, Iowa 50011. Publication no. P-2000-0036-NCA.
Growth chamber experiments were conducted to assess the relationship
between internal stem browning and colonization of soybean stems by Phialophora
gregata, the causal agent of soybean brown stem rot (BSR). P.
gregata (10(^8) spores/plant) was added to soil at the base of
2-week-old susceptible (Sturdy) and resistant (BSR101) cultivars. Internal
stem browning and presence of P. gregata were assessed over 12
weeks. Stems of Sturdy were colonized earlier than stems of BSR101;
however, the fungus had colonized the full length of the stems of all
infected plants by 12 weeks. All Sturdy and 75% of BSR101 plants were
infected; yet, 59% of infected Sturdy plants and 67% of infected BSR101
plants had no internal stem browning. These results indicate that both
resistant and susceptible varieties can be colonized extensively by P.
gregata without detectable stem browning. The possibility of
asymptomatic P. gregata infections should be considered when
breeding and selecting for BSR resistance.
Soybean cyst nematode increases colonization of soybean stems by Phialophora
gregata. G. M. TABOR, G. L. Tylka, and C. R. Bronson. Dept. of
Plant Pathology, Iowa State University, Ames, Iowa 50011. Publication no.
P-2000-0037-NCA.
Two growth chamber experiments were conducted to test if Heterodera
glycines, the soybean cyst nematode, increases susceptibility of
soybeans to Phialophora gregata, causal agent of brown stem rot
(BSR) of soybeans. Four cultivars with various combinations of resistance
or susceptibility to both pathogens were planted in soil mix with four
pathogen treatment combinations. H. glycines was applied as eggs
(1,600/plant), and P. gregata was applied as artificially infested
soybean straw (7.5 × 10(^8) cfu/plant). After 10 weeks, presence of P.
gregata was assessed by plating stem pieces on a semi-selective
medium. In the presence of H. glycines, incidence of stem
colonization by P. gregata was 38 to 79% for BSR-resistant
cultivars which was significantly greater than the 13 to 33% in the
absence of H. glycines. For these cultivars, stem length colonized
was 22 to 39% with H. glycines, versus 6 to 13% without H.
glycines. Incidence and colonization were 90 to 100% with or without H.
glycines for a BSR-susceptible cultivar. Our findings suggest that H.
glycines infection increases colonization of soybean stems by P.
gregata.
Genetic variation of Monilinia vaccinii-corymbosi populations
determined with amplified fragment-length polymorphic DNA markers. T.
R. Thompson (1), J. S. LEHMAN (1), L. A. Wasilwa (2), and P. V. Oudemans
(2). (1) Otterbein College, Westerville, OH 43081; (2) Rutgers University,
Chatsworth, NJ 08019. Publication no. P-2000-0038-NCA.
Genetic variation of Monilinia vaccinii-corymbosi (Mvc)
populations was examined with AFLPs. Isolates of Mvc were collected from
Nova Scotia (NS) and New Jersey (NJ). Variation in allelic frequencies was
calculated for AFLP loci in 16 isolates from each population. Allelic
variation was partitioned into within- and between-population components
(Nei’s Gst). Linkage disequilibrium was calculated among all pairs of
loci. Nine bands were identified. Seven of the bands were found in both
populations while two were found only in the NS population. A Gst value of
0.10 indicated that 10% of the allelic variation was due to
differentiation between populations, while 90% was due to
within-population variation. Linkage disequilibrium was present to a
greater extent in the NS population. We conclude that NJ and NS
populations share the same alleles and exhibit little differentiation
between populations. Based on disequilibrium values, NJ and NS populations
may differentially emphasize sexual and asexual reproduction.
Soil moisture and air temperature effects on Rhizoctonia solani
infection of soybean. N. T. TUTTLE (1), A. E. Dorrance (1), and M.
Kleinhenz (2). (1) Dept. of Plant Pathology, and (2) Dept. of Hort. and
Crop Science, The Ohio State University OARDC, Wooster, OH 44691.
Publication no. P-2000-0039-NCA.
Reports on environmental conditions favoring Rhizoctonia solani damping-off,
root and stem rot of soybean are conflicting. To determine soil moisture
and air temperature limits for infection, inoculum of sterile oat kernels
colonized by R. solani isolate 91-1 AG (UNK) was used. A 1:1 v/v
mixture of Wooster silt loam and silica sand and vermiculite only were
used for soil moisture and air temperature studies respectively. Soil
moisture was maintained at 25, 50, 75, or 100 percent (%) of moisture
holding capacity (MHC) in a greenhouse. Air temperature studies were in
growth chambers maintained at 20, 25, 30, or 35°C. Emergence, plant
height, top weight, disease incidence and severity, and root health were
recorded on the soybean cultivar Resnik. Disease incidence and severity
were greatest at 75(%)MHC and 25°C for this isolate. Disease incidence
tended to increase with increases in soil moisture and was greatest at air
temperatures of 25°C. Infections occurred, albeit at a lower incidence,
at 25 and 100(%) MHC as well as 20 and 35°C.
Osmolytes enhance room temperature shelf-life of freeze-dried, cells of
the biocontrol agent Enterobacter cloacae S11:T:07( NRRL 21050).
J. E. VanCauwenberge, D. A. Schisler, and P. J. Slininger. USDA-ARS,
NCAUR, Peoria, IL 61604. Publication no. P-2000-0040-NCA.
Enterobacter cloacae S11:T:07 (NRRL 21050) has been identified as
an antagonist effective against the causative agent of potato dry rot (Gibberella
pulicaris) during tuber storage. In an effort to improve the shelf
life of cells stored at room temperature, 15 osmolytes at 4 concentrations
were added to individual E. cloacae cultures at initial inoculation
or after 72 hours of incubation. Cultures were harvested at 96 hours
incubation, freeze dried, stored at room temperature, and tested for
culture viability over 21 days. Five osmolytes were identified that
improved the shelf life of E. cloacae. Cell counts for control
samples decreased from 10(^10) to 10(^1) CFU/ml by day 5 and approached 0 by day
7. In comparison, day 7 cultures which had turanose or arginine added at
initial inoculation were at 10(^8) CFU/ml and 10(^5) CFU/ml, respectively. Day
seven cultures which had proline, maltose or sucrose added at 72 hours
were at 10(^5) CFU/ml, 10(^4) CFU/ml, or 10(^6) CFU/ml, respectively. Further
experimentation will be conducted to optimize product shelf life and
determine the influence of osmolytes on cell efficacy.
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