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The American Phytopathological Society
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First Report of Beet black scorch virus in the United States. J.
J. Weiland, USDA-ARS, Red River Valley Agricultural Research Center, Fargo, ND
58105; R. L. Larson, USDA-ARS, Sugarbeet Production Lab, Fort Collins, CO 80526;
T. P. Freeman, North Dakota State University, Fargo, ND, 58105 and M. C.
Edwards, USDA-ARS, Red River Valley Agricultural Research Center, Fargo, ND
58105. Plant Dis. 90:828, 2006; published on-line as DOI: 10.1094/PD-90-0828B.
Accepted for publication 18 March 2006.
In October of 2005, sugar beet (Beta vulgaris L.) plants exhibiting
symptoms of rhizomania caused by Beet necrotic yellow vein virus (BNYVV)
(3) were observed in a production field near Greeley, CO. The roots of seven
plants exhibiting moderate to severe symptoms characteristic of this disease
were tested using double-antibody sandwich enzyme-linked immunosorbent assay
with anti-BNYVV antiserum from rabbits. Of these, only two roots exhibiting the
mildest symptoms tested positive for BNYVV (all roots tested negative for the
presence of the related Beet soilborne mosaic virus (BSBMV). ‘Hairy’
lateral roots characteristic of the disease were combined from the remaining
five roots, ground in phosphate buffer, and the supernatant from the suspension
was mechanically applied to leaves of Chenopodium quinoa in an effort to
isolate an infectious agent. Five days postinoculation (dpi), yellow lesions
with necrotic centers were visible on inoculated leaves, well in advance of
those typically observed for BNYVV or BSBMV. Lesions exhibiting a similar rate
of development on C. quinoa subsequently were induced from extracts of
root vascular tissue prepared from four of seven additional beet roots tested
from this location. Transfer of the infection from the C. quinoa lesions
to 32 healthy C. quinoa and 10 sugar beet plants (hybrid ACH9369;
American Crystal Sugar Co., Moorhead MN) resulted in 100% infection. Inoculated
leaves of C. quinoa exhibited a high density of necrotic local lesions
within 3 dpi, whereas inoculated leaves of sugar beet exhibited pinpoint,
necrotic to diffuse, chlorotic local lesions evident by 5 dpi. Electron
microscopic examination of fixed, ultra-thin sections of symptomatic C.
quinoa leaf tissue revealed aggregates of virus-like particles of
icosahedral symmetry within the cell cytoplasm. Following a virus
minipreparation procedure, nucleic acid extracted from the partially purified
virus was found to be single-stranded RNA by ribonuclease digestion and alone
was infectious when inoculated to C. quinoa leaves. The apparently
monopartite RNA genome was 3.5 kb long and a candidate for the single coat
protein (CP) had a mass of ~25 kDa. The sole reference set found in the
literature for a virus naturally occurring on sugar beet with similar
characteristics was that for Beet black scorch virus (BBSV), a virus
recently accepted by the ICTV into the genus Necrovirus within the family
Tombusviridae (2). Prior to this communication, BBSV has only been
reported in China where it was first documented affecting sugar beet in the late
1980s (1). Using the published sequence of BBSV (Genbank Accession No.
AY626780), DNA primers directed to the 3(prime) half of the BBSV genome were used in
reverse transcription-polymerase chain reaction to produce an amplicon from the
unknown virus. Sequencing the amplicon revealed 88.8% nucleotide sequence
identity to the BBSV CP gene and 97% amino acid sequence identity to the
predicted CP gene product. Combined, the nucleotide sequence and physical
characteristics confirm the presence of BBSV in a U.S. sugarbeet field for the
first time. To our knowledge, this is the first report of the occurrence of BBSV
outside of China.
References: (1) Y. Cao et al. Arch. Virol. 147:2431, 2002. (2) C. M.
Fauquet et al. Eighth Report of the International Committee on the Taxonomy of
Viruses. Academic Press, New York, 2005. (3) C. M. Rush. Ann. Rev. Phytopathol.
41:567, 2003.
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