Publications by authors named "Cleora J D'Arcy"

Soybean dwarf virus (SbDV), which causes an important disease of soybeans in Japan, is persistently transmitted by aphids and is endemic in forage legumes in the United States. To determine the incidence of SbDV in Illinois, we collected clovers and forage legumes in a total of 49 Illinois counties in 2001 and 2002 and tested them for the presence of SbDV by reversetranscription-polymerase chain reaction. SbDV was detected in 43% of red clover (Trifolium pratense), 10% of white clover (T.

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The complete nucleotide sequence of the Bean leafroll virus (BLRV) genomic RNA and the termini of its smallest subgenomic RNAs were determined to better understand its mechanisms of gene expression and replication and its phylogenetic position within the Luteoviridae: The number and placement of open reading frames (ORFs) within the BLRV genome was Luteovirus-like. The nucleotide and predicted amino acid sequences of BLRV were most similar to those of Soybean dwarf virus (SbDV). Phylogenetic analyses employing the neighbour-joining method and sister-scanning analysis indicated that the BLRV nonstructural proteins were closely related to those of Barley yellow dwarf virus-PAV (BYDV-PAV), a luteovirus: The region surrounding the frameshift at the junction between ORFs 1 and 2 also contained sequences very similar to those of BYDV-PAV and a Dianthovirus, Red clover necrotic mosaic virus.

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Infection of sweet corn (Zea mays L.) by barley yellow dwarf viruses (BYDVs) caused different symptoms on hybrids with shrunken-2 (sh-2) when compared with hybrids with sugary-1 (su-1) endosperm mutations. Sweet corn hybrids inoculated with BYDV-RMV in Urbana, IL, developed either yellow or red-purple leaf symptoms similar to those caused by phosphorus and/or potash deficiency (1).

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The reaction of five sweet corn hybrids to barley yellow dwarf virus (BYDV-RMV-IL) was determined in 1992 and 1993. In 1992, symptoms were observed in three of the five hybrids planted 20 May and four of the five hybrids planted 20 June. No symptoms were observed in hybrids planted June or July 1993.

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Detection of barley yellow dwarf virus (BYDV)-PAV-IL by an improved nucleic acid hybridization technique, using a nonradioactive probe with chromogenic and chemiluminescent substrates, was compared with detection by polymerase chain reaction (PCR), double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) with polyclonal antibodies, and triple antibody sandwich ELISA with polyclonal and monoclonal antibodies. Each method was used to detect purified virus and virus in sap extracts from infected oat leaves. The detection limits for both ELISA procedures were 1 ng of purified BYDV-PAV-IL and the equivalent of 78 ng of infected tissue.

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