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Detection of a Phytophthora sp. Causing Asparagus Spear and Root Rot
in Michigan. C. Saude and M. K. Hausbeck, Department of Plant Pathology,
Michigan State University, East Lansing 48824; and O. Hurtado-Gonzales and K. H.
Lamour, Department of Entomology and Plant Pathology, University of Tennessee,
Knoxville 37996. Plant Dis. 89:1011, 2005; published on-line as DOI:
10.1094/PD-89-1011B. Accepted for publication 10 June 2005.
In the spring of 2004, a Phytophthora sp. was isolated from asparagus (Asparagus
officinalis) spears, roots, and dormant crowns from several fields in Oceana
and Ingham counties in Michigan. Symptomatic spears were often curved, had
water-soaked lesions slightly above or below the soil line or were shriveled at
the site of infection or both. Infected storage roots had water-soaked lesions
but were not soft at the lesion site. Infected crowns had fewer roots than
healthy crowns. In the laboratory, plant tissues were rinsed in tap water and
blotted dry. Sections from the edge of lesions were placed aseptically onto BARP
(25 ppm of benomyl, 100 ppm of ampicillin, 30 ppm of rifampicin, and 100 ppm of
pentachloronitrobenzene) amended unclarified V8 juice agar and incubated at
25°C for up to 7 days. Phytophthora sp. isolates recovered from the
infected material produced ovoid, nonpapillate, noncaducous sporangia and
amphigynous oospores on isolation media. Single-sporangium cultures made for
each isolate were stored long term in sterile 2-ml microcentrifuge tubes
containing two 7-mm mycelial plugs, two sterile hemp seeds, and 1 ml of sterile
distilled water. Sporangia produced on dilute V8 juice agar averaged 45 µm
long × 26 µm wide and oospores were 25 to 30 µm in diameter. Chlamydospores
were not observed. Five detached ‘Jersey Knight’ spears were
inoculated with a 7-mm mycelial plug from the edge of actively growing
5-day-old cultures and incubated at 23 to 25°C for 5 to 7 days in a moist
chamber. After 3 days, water-soaked lesions and shriveling and curving of the
spears were visible on all inoculated spears. The pathogen was always reisolated
from the lesion edge. No symptoms were observed when spears were inoculated with
sterile V8 juice agar plugs. DNA was extracted from representative isolates, and
the nuclear ribosomal internal transcribed spacer (ITS) region was amplified
with ITS6 and ITS4 primers and sequenced. A BLAST search of the NCBI database
with the ITS sequence revealed Phytophthora sp. UQ2141, Accession No.
AF266795, as the closest match with 99% sequence similarity. These results,
coupled with the morphological characteristics of the isolates, indicate that
the Phytophthora sp. isolated from asparagus in Michigan is among the
constituents of Phytophthora spp. included in the P. megasperma
clade 6 (2), whose taxa are currently being reevaluated. Although a Phytophthora
sp. has been described previously on asparagus (1,3), this is the first report,
to our knowledge, of a Phytophthora sp. on asparagus in Michigan. The
occurrence of excessive rainfall in the spring of 2004 is likely responsible for
widespread disease and considerable yield losses in production fields.
References: (1) P. A. Ark and J. T. Barrett. Phytopathology 28:754, 1938.
(2) D. E. L. Cooke et al. Fungal Genet. Biol. 30:17, 2000. (3) V. Vujanovic et
al. Plant Dis. 87:447, 2003.
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