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First Report of Northern Stem Canker of Soybean Caused by Diaporthe
phaseolorum var. caulivora in North Dakota. C. A. Bradley,
Department of Plant Pathology, North Dakota State University, Fargo, 58105; and
S. Li, Department of Crop Sciences, University of Illinois, Urbana 61801. Plant
Dis. 90:687, 2006; published on-line as DOI: 10.1094/PD-90-0687A. Accepted for
publication 10 February 2006.
In early September 2003, patches of soybean (Glycine max) plants in a
field in Foster County, ND had dead branches with reddish brown cankers at the
nodes. Stem tissue with cankers from two plants were excised and immersed in a
0.5% NaOCl solution for 1 min, rinsed with sterilized distilled water, and
placed into Petri dishes containing potato dextrose agar (PDA) amended with
streptomycin sulfate (200 mg/liter). Four fungi were hyphal tipped and grown on
PDA, acidified PDA, or water agar (WA) with soybean stem pieces incubated at
21°C with 24-h light and identified by culture and spore morphology after 3 to 4
weeks. Cultures were identified as Diaporthe phaseolorum var.
caulivora that produced white colonies with interspersed cottony tufts of
mycelium on PDA (1). Stromata were small and scattered irregulary on the plate.
Perithecia of the D. phaseolorum var. caulivora isolates
were black and globose with eight-spored asci formed on soybean stem pieces on
WA. To confirm pathogenicity of the D. phaseolorum var.
caulivora isolates, soybean plants (cv. NuTech 0606) were grown in the
greenhouse and inoculated with recovered D. phaseolorum var.
caulivora isolates. The stems of soybean plants at the V3 stage were excised
just below the fourth node. Mycelia plugs of the four different 1-week-old
cultures of D. phaseolorum var. caulivora were placed into
the large end of disposable micropipette tips (200 µl). The micropipette tip
containing a D. phaseolorum var. caulivora culture was
subsequently placed over a cut soybean stem. The four D. phaseolorum
var. caulivora isolates were used to inoculate 10 stems apiece. To serve
as controls, 10 cut soybean stems were inoculated with micropipette tips
containing plugs of noninfested PDA and 10 cut stems were not inoculated. Ten
days after inoculation, micropipette tips were removed and lesions that had
developed on the stem were measured. The mean lesion lengths of the D.
phaseolorum var. caulivora inoculated stems ranged from 48 to 82 mm
and were significantly (P < 0.05) greater than the lesion lengths of the
noninfested PDA (3 mm) and no PDA (1 mm) controls. Northern stem canker was only
observed in the one field; however, surveys were not conducted to determine the
prevalence of the disease throughout the soybean-production area of North
Dakota. To our knowledge, this is the first report of northern stem canker on
soybean in North Dakota.
Reference: (1) F. A. Fernandez et al. Stem canker. Pages 33-35 in:
Compendium of Soybean Diseases. 4th ed. The American Phytopathological Society,
St. Paul, MN, 1999.
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