scholarly journals A note on the detection of bean yellow mosaic virus infecting white lupine in Canada

2005 ◽  
Vol 74 (3) ◽  
pp. 153-155 ◽  
Author(s):  
C. Piché ◽  
J. Peterson ◽  
M.G. Fortin
Keyword(s):  
Mosaic Virus ◽  
Growth Habit ◽  
Lupinus Albus ◽  
Viral Disease ◽  
Bean Yellow Mosaic Virus ◽  
Yellow Mosaic Virus ◽  
Enzyme Linked Immunosorbent Assay ◽  
Mechanical Inoculation ◽  
Eastern Canada ◽  
White Lupine

Virus-like symptoms were observed in fields of white lupine (Lupinus albus) in Eastern Canada. Affected plants displayed mosaic, leaf stunting and deformation, and bunchy growth habit. The disease was successfully reproduced in greenhouse by mechanical inoculation of white lupine cv. Ultra. The causal virus was identified as bean yellow mosaic virus (BYMV) by symptomatology on diagnostic species, electron microscopy, enzyme linked immunosorbent assay (ELISA) and immunodetection after Western blotting. This is the first report of a viral disease of lupine in Canada. BYMV may represent a significant limitation to lupine culture since it is transmitted by aphids and through infected seed.

scholarly journals Characteristics of a Potyvirus of the Bean Yellow Mosaic Virus Subgroup in Sesbania speciosa Germ Plasm

Plant Disease ◽  
1998 ◽  
Vol 82 (7) ◽  
pp. 807-810 ◽  
Author(s):  
A. G. Gillaspie ◽  
M. S. Hopkins ◽  
D. L. Pinnow ◽  
R. L. Jordan
Keyword(s):  
Monoclonal Antibody ◽  
Mosaic Virus ◽  
Germ Plasm ◽  
Lupinus Albus ◽  
Yellow Mosaic Virus ◽  
Enzyme Linked Immunosorbent Assay ◽  
Green Beans ◽  
White Lupine ◽  
Polyclonal Antisera ◽  
Sesbania Spp

A plant of Sesbania speciosa with leaf mosaic and distortion symptoms was identified in a germ plasm regeneration plot at Griffin, Georgia. The Sesbania virus produced mild or moderate mosaic symptoms on Glycine max cvs. Bragg and Tracy M, Lupinus albus, Nicotiana benthamiana, Pisum sativum cv. Perfected Wales, Phaseolus vulgaris cvs. Black Turtle, Bountiful, and Pinto, and did not infect N. tabacum. Bean yellow mosaic potyvirus (BYMV) and pea mosaic potyvirus (PMV) do not infect Perfected Wales pea and they produce mosaic, distortion, and necrosis on white lupine. The PMV strain tested produced much more severe symptoms on the three green beans, with top necrosis on Pinto. BYMV produced local latent infection of N. tabacum and BYMV and PMV produced mosaic with distortion on N. benthamiana. The Sesbania virus was seed-transmitted at a low rate in S. speciosa. Indirect-enzyme-linked immunosorbent assay tests with a general potyvirus monoclonal antibody and BYMV and white lupine mosaic virus (WLMV) polyclonal antisera were strongly positive. Tests of the Sesbania virus against a monoclonal antibody panel suggests that it is not BYMV or any of the previously described subgroup members, but is a member of the BYMV subgroup. This is the first report of a seedborne BYMV-like virus of Sesbania spp.

scholarly journals First Report of Bean yellow mosaic virus (Pea Mosaic Strain) in Verbena × hybrida

Plant Disease ◽  
2004 ◽  
Vol 88 (5) ◽  
pp. 574-574 ◽  
Author(s):  
M. A. Guaragna ◽  
R. L. Jordan ◽  
M. L. Putnam
Keyword(s):  
Amino Acid ◽  
Coat Protein ◽  
Mosaic Virus ◽  
Plant Viruses ◽  
Bean Yellow Mosaic Virus ◽  
Yellow Mosaic Virus ◽  
Enzyme Linked Immunosorbent Assay ◽  
Pairwise Comparisons ◽  
Putative Coat Protein ◽  
On Line

Verbena × hybrida is an ornamental annual used in rock gardens as an edging plant and hanging baskets. It comes in a variety of colors and grows approximately 1.5 to 2.5 cm (6 to 10 inches) high. In the spring of 2002, verbena cv. Lavender Shades plants from California showing leaf mosaic symptoms tested positive for potyvirus using an antigen-coated plate enzyme-linked immunosorbent assay with our genus Potyvirus broad spectrum reacting PTY-1 monoclonal as the detecting antibody (3). The virus was transmitted mechanically to Nicotiana benthamiana by sap inoculation from infected verbena plants. Infected tobacco showed systemic mild mosaic symptoms. Total RNA extractions from infected verbena and tobacco leaves were used in reverse transcription-polymerase chain reaction (RT-PCR) assays with generic potyvirus-specific primers that amplify highly conserved 700-bp or 1,600-bp fragments from the 3′ terminus of most potyviruses. This region includes the 3′ noncoding region (3′NCR) and the potyviral coat protein (CP). The PCR-amplified fragments were cloned by using standard TA cloning procedures and sequenced using dye-terminator chemistry. The cloned nucleotide and putative coat protein amino acid sequences from the infected verbena and tobacco plants were compared with the corresponding regions of other potyviruses. Amino acid comparison of the CP region of the verbena po-tyvirus showed 95 to 96% identity to four pea mosaic strains (PMV) of Bean yellow mosaic virus (BYMV), 85 to 89% identity to 20 other strains of BYMV, 74 to 76% identity with six strains of Clover yellow vein virus (CYVV), and only 50 to 64% identity with 28 other potyviruses. Pairwise comparisons among and between the CP sequences of PMV, BYMV, CYVV, and other potyviruses revealed identities of 92 to 99% for BYMV∷ BYMV, PMV∷PMV, and CYVV∷CYVV; 84 to 89% for BYMV∷ PMV, 69 to 78% for BYMV∷CYVV and PMV∷CYVV, and 50 to 64% for all other potyvirus combinations. Additionally, similar pairwise analysis of the 3′NCR of the verbena potyvirus revealed 98 to 99% identity to PMV strains, 81 to 94% to other BYMVs, 68 to 75% to CYVVs, and 52 to 64% with other potyviruses. Other 3′NCR pairwise comparisons generally revealed the same identity trend as described for the CP. Further serological analysis with our panel of BYMV-specific, BYMV-subgroup, and potyvirus cross-reactive monoclonal antibodies (3) confirmed the designation of the verbena potyvirus isolate as a pea mosaic strain of BYMV. To our knowledge this is the first confirmed report of BYMV-pea mosaic strain in Verbena (1,2). References: (1) Agdia, Inc. Positive Ornamental Plant Samples. Agdia On-line Publication, 2003. (2) A. A. Brunt et al. Verbena hybrida. Plant Viruses Online: Descriptions and Lists from the VIDE Database. Version 20. On-line publication, August 1996. (3) R. L. Jordan, and J. Hammond. J. Gen. Virol. 72:1531, 1991.

scholarly journals Affection of Gladiolus plants with Bean Yellow Mosaic Virus, Cucumber Mosaic Virus and Tobacco Ringspot Virus in some Northern and Central regions of Ukraine

2020 ◽  
Vol 81 (2) ◽  
pp. 36-42
Author(s):  
R. Sovinska ◽  
A. Dunich ◽  
L. Mishchenko
Keyword(s):  
Cucumber Mosaic Virus ◽  
Mosaic Virus ◽  
Viral Infections ◽  
Flower Color ◽  
Bean Yellow Mosaic Virus ◽  
Ringspot Virus ◽  
Yellow Mosaic Virus ◽  
Economic Losses ◽  
Enzyme Linked Immunosorbent Assay ◽  
Tobacco Ringspot Virus

Gladioli can be affected with 15 species of viruses, which cause significant economic losses to both floriculture and agriculture. The most prevalent and harmful for gladioli are Bean yellow mosaic virus (BYMV) and Cucumber mosaic virus (CMV), circulating on the territory of Ukraine on vegetable, legume and other crops, and also Tobacco ringspot virus (TRSV), which is included into the List of regulated pests of Ukraine and is the subject to strict control. The aim of the work was to conduct testing of gladiolus plants for the presence of viral infection symptoms and to test them for the affection with the most widespread and dangerous viruses, namely: BYMV, CMV, TRSV. Visual diagnostics, enzyme-linked immunosorbent assay in DAS-ELISA modification, transmission electron microscopy method and statistical data analysis were used in this research. The results of the studies showed absence of TRSV in all tested samples. For the first time in Ukraine, it has been established that gladioli are infected by Bean yellow mosaic virus. Its circulation on gladioli has been registered in Poltava, Kyiv and Sumy regions. Gladioli were also found to be affected by CMV or mixed infection of these pathogens. Gladioli infection by BYMV and CMV in Kyiv region is 88.2% and 93.8%, in Poltava – 69.2% and 55.5%, in Sumy – 66.6% and 0%, respectively. Typical symptoms on gladiolus plants caused by CMV and BYMV isolates are leaf chlorotic stripes and flower color break, less often – spotting on the leaves and plant stunting. It has been revealed that affection of gladioli by CMV and BYMV can be asymptomatic. The diversity, nature and course of viral infections in gladioli demonstrate the relevance of further research and their monitoring in Ukraine.

scholarly journals Black Pod Syndrome of Lupinus angustifolius Is Caused by Late Infection with Bean yellow mosaic virus

Plant Disease ◽  
2014 ◽  
Vol 98 (6) ◽  
pp. 739-745 ◽  
Author(s):  
M. A. Kehoe ◽  
B. J. Buirchell ◽  
B. A. Coutts ◽  
R. A. C. Jones
Keyword(s):  
Mosaic Virus ◽  
Lupinus Angustifolius ◽  
Bean Yellow Mosaic Virus ◽  
Yellow Mosaic Virus ◽  
Enzyme Linked Immunosorbent Assay ◽  
Growth Stages ◽  
Late Infection ◽  
Rt Pcr ◽  
Tissue Samples ◽  
Black Pod

Black pod syndrome (BPS) causes devastating losses in Lupinus angustifolius (narrow-leafed lupin) crops in Australia, and infection with Bean yellow mosaic virus (BYMV) was suggested as a possible cause. In 2011, an end-of-growing-season survey in which L. angustifolius plants with BPS were collected from six locations in southwestern Australia was done. Tissue samples from different positions on each of these symptomatic plants were tested for BYMV and generic potyvirus by enzyme-linked immunosorbent assay and reverse-transcription polymerase chain reaction (RT-PCR). Detection was most reliable when RT-PCR with generic potyvirus primers was used on tissue taken from the main stem of the plant just below the black pods. Partial coat protein nucleotide sequences from eight isolates from BPS-symptomatic L. angustifolius plants all belonged to the BYMV general phylogenetic group. An initial glasshouse experiment revealed that mechanical inoculation of L. angustifolius plants with BYMV after pods had formed caused pods to turn black. This did not occur when the plants were inoculated before this growth stage (at first flowering) because BYMV infection caused plant death. A subsequent experiment in which plants were inoculated at eight different growth stages confirmed that BPS was only induced when L. angustifolius plants were inoculated after first flowering, when pods had formed. Thus, BYMV was isolated from symptomatic L. angustifolius survey samples, inoculated to and maintained in culture hosts, inoculated to healthy L. angustifolius test plants inducing BPS, and then successfully reisolated from them. As such, Koch's postulates were fulfilled for the hypothesis that late infection with BYMV causes BPS in L. angustifolius plants.

scholarly journals The Complete Nucleotide Sequence of Bean Yellow Mosaic Virus Genomic RNA.

1996 ◽  
Vol 62 (5) ◽  
pp. 472-477 ◽  
Author(s):  
Shigeo NAKAMURA ◽  
Ryoso HONKURA ◽  
Takayoshi IWAI ◽  
Masashi UGAKI ◽  
Yuko OHASHI
Keyword(s):  
Nucleotide Sequence ◽  
Mosaic Virus ◽  
Complete Nucleotide Sequence ◽  
Bean Yellow Mosaic Virus ◽  
Yellow Mosaic Virus ◽  
Genomic Rna

scholarly journals PCNA Interacts with Indian Mung Bean Yellow Mosaic Virus Rep and Downregulates Rep Activity

2004 ◽  
Vol 78 (21) ◽  
pp. 11890-11903 ◽  
Author(s):  
Basavaraj Bagewadi ◽  
Shoajiang Chen ◽  
Sunil K. Lal ◽  
Nirupam Roy Choudhury ◽  
Sunil K. Mukherjee
Keyword(s):  
Mosaic Virus ◽  
Mung Bean ◽  
Bean Yellow Mosaic Virus ◽  
Yellow Mosaic Virus ◽  
Nuclear Antigen ◽  
Resting Cells ◽  
Rolling Circle Replication ◽  
Proliferative Cell Nuclear Antigen ◽  
Bipartite Genome

ABSTRACT Proliferative cell nuclear antigen (PCNA), a conserved plant protein as well as an important replication factor, is induced in response to geminivirus infection in the resting cells of the phloem tissues. The biochemical role of PCNA in rolling circle replication (RCR) of geminivirus DNA has not been explored in detail. The initiation of RCR of the bipartite genome of a geminivirus, Indian mung bean yellow mosaic virus (IMYMV), is mainly controlled by viral protein Rep (or AL1 or AC1). The role of host PCNA in RCR of IMYMV was revealed by studying the physical and functional interactions between recombinant PCNA and recombinant IMYMV Rep. Pea nuclear PCNA as well as recombinant pea PCNA showed binding to recombinant Rep in experiments involving both affinity chromatography and yeast two-hybrid approaches. The contacting amino acid residues of PCNA seemed to be present throughout a wide region of the trimeric protein, while those of Rep appeared to be localized only in the middle part of the protein. The site-specific nicking-closing activity and the ATPase function of IMYMV Rep were impaired by PCNA. These observations lead to interesting speculations about the control of viral RCR and dynamic profiles of protein-protein interactions at the RCR origin of the geminiviruses.

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