Distribution and localization of bean common mosaic virus and bean black root virus in stems of doubly infected bean plants

1994 ◽  
Vol 138 (1-2) ◽  
pp. 95-104 ◽  
Author(s):  
J. A. Khan ◽  
H. Lohuis ◽  
R. W. Goldbach ◽  
J. Dijkstra
2000 ◽  
Vol 13 (11) ◽  
pp. 1266-1270 ◽  
Author(s):  
Candace Whitmer Collmer ◽  
Marcia Fisher Marston ◽  
Jessica C. Taylor ◽  
Molly Jahn

The resistance to the potyvirus Bean common mosaic virus (BCMV) conferred by the I allele in cultivars of Phaseolus vulgaris has been characterized as dominant, and it has been associated with both immunity and a systemic vascular necrosis in infected bean plants under field, as well as controlled, conditions. In our attempts to understand more fully the nature of the interaction between bean with the I resistance allele and the pathogen BCMV, we carefully varied both I allele dosage and temperature and observed the resulting, varying resistance responses. We report here that the I allele in the bean cultivars we studied is not dominant, but rather incompletely dominant, and that the system can be manipulated to show in plants a continuum of response to BCMV that ranges from immunity or extreme resistance, to hypersensitive resistance, to systemic phloem necrosis (and subsequent plant death). We propose that the particular phenotypic outcome in bean results from a quantitative interaction between viral pathogen and plant host that can be altered to favor one or the other by manipulating I allele dosage, temperature, viral pathogen, or plant cultivar.


2005 ◽  
Vol 95 (9) ◽  
pp. 1037-1042 ◽  
Author(s):  
Richard C. Larsen ◽  
Phillip N. Miklas ◽  
Keri L. Druffel ◽  
Stephen D. Wyatt

A strain of Bean common mosaic necrosis virus (BCMNV) from Idaho was identified by enzyme-linked immunosorbent assay using monoclonal antibodies and determined to be similar to the NL-3 D strain (of Drifjhout) by reaction of differential bean cultivars. However, this BCMNV strain (designated NL-3 K) caused earlier and more severe symptoms on bean plants representing host groups 0, 4, and 5. The nucleotide sequence encoding the predicted polyprotein of NL-3 K was 9,893 nucleotides (nt) in length, yielding a peptide with a molecular size of 362.1 kDa compared with a 9,626-nt, 350.9-kDa polyprotein for NL-3 D. Sequence analysis of the putative P1 protein suggests that the NL-3 K strain is a recombinant between NL-3 D and the Russian strain (RU1) of Bean common mosaic virus. The P1 protein of NL-3 K consisted of 415 amino acids compared with 317 for NL-3 D. The first 114 predicted amino acids of the NL-3 K P1 region were 98% identical with RU1. The remaining 301 amino acids of the protein shared only 34% identity with RU1 but were 98% identical with NL-3 D. Primers were designed that flanked the recombination point in the P1 coding sequence of NL-3 K. An amplicon of the expected size was produced by reverse-transcriptase polymerase chain reaction of total nucleic acid extracts of bean plants inoculated with NL-3 K, but not from those with NL-3 D or RU1. The increased symptom severity on selected common bean lines induced by NL-3 K suggests that the P1 gene may play a significant role in pathogenicity and virulence.


2021 ◽  
Vol 20 (6) ◽  
pp. 7-18
Author(s):  
İlyas Deligoz ◽  
Miray Arlı-Sökmen ◽  
Mucella Tekeoglu

Bean common mosaic virus (BCMV) and bean common mosaic necrosis virus (BCMNV) are among the most economically important virus species infecting common bean. The use of resistant plant cultivars is the most effective way to control these viruses. National dry bean breeding studies have been conducted by seven different governmental agricultural research institutes in Turkey, and advanced breeding lines have been developed by using the selected local dry bean populations and crossing studies. In this study, 204 breeding lines were tested for resistance levels to BCMV and BCMNV. Initially, BCMNV NL-3 and BCMV NL-4 strains were individually sap-inoculated onto the leaves of bean plants belonging to each breeding lines with 10 replications, and the reactions of plants were evaluated for symptomatic appearance of virus infection 21 days after inoculation. Additionally, phenotypic evaluation was confirmed by molecular markers linked to resistance genes. As a result of the study, 153 breeding lines were found to involve the dominant I gene whereas four and five of the tested lines had the recessive genes bc-1² and bc-2², respectively. In conclusion, it was emphasized that these breeding lines could be registered after evaluating them in terms of yield and quality. Also, the use of seeds of the resistant lines to supply the source of virus-resistance in breeding studies and maintaining their seeds at the national genebank were recommended.


Plant Disease ◽  
2004 ◽  
Vol 88 (2) ◽  
pp. 119-124 ◽  
Author(s):  
M. Grisoni ◽  
F. Davidson ◽  
C. Hyrondelle ◽  
K. Farreyrol ◽  
M. L. Caruana ◽  
...  

A survey was carried out to identify the viruses infecting vanilla in French Polynesia and to assess their incidence. Virus identification was based on enzyme-linked immunosorbent assay (ELISA) and, for potyviruses, on the sequence of part of the coat protein and inoculation assays. Between 1998 and 1999, 3,610 vanilla plants from 49 plots in the Society Islands were indexed. Cymbidium mosaic virus (CymMV) was detected in 500 vines from 10 plots in the Leeward Islands. The data suggest that this virus has spread widely since its first detection in French Polynesia in 1986, most likely through the dissemination of symptomless infected cuttings. Viruses belonging to the Potyvirus genus were found in 674 plants from 27 plots in the four islands surveyed. Three distinct potyviruses have been identified: (i) Vanilla mosaic virus, (ii) Watermelon mosaic virus, and (iii) and a virus related to Bean common mosaic virus. The symptoms induced on Vanilla tahitensis by the three potyviruses can be differentiated from each other and from those due to CymMV. A significant proportion of the plants surveyed (97/476) were symptomatic but tested negative by ELISA for CymMV and the Potyvirus group. Odontoglossum ringspot virus was not detected in any sample tested.


2006 ◽  
Vol 22 (1) ◽  
pp. 97-102 ◽  
Author(s):  
Hong-Soo Choi ◽  
Mi-Kyeong Kim ◽  
Jin-Woo Park ◽  
Jeong-Uk Cheon ◽  
Kook-Hyung Kim ◽  
...  

Author(s):  
M.S. Iqbal ◽  
S.A. Hussain ◽  
N. Arshad ◽  
S. Munir ◽  
M.A. Ali ◽  
...  

Background: Cowpea is a major food legume rich in protein but its production has been dwindling by several factors including viral infection due to various virus strains in all agro-ecological zones.Methods: Sixty eight cowpea genotypes were screened against qualitative traits (leaf shape, seed surface, twinning tendency, anthocynin pigment, plant type, fodder type and cream color) and four seed borne viruses viz. cucumber mosaic virus (CMV), cowpea aphid borne mosaic virus (CABMV), black eye cowpea mosaic virus (BlCMV) and bean common mosaic virus (BCMV) under both in situ and laboratory conditions using DAC-ELISA.Result: Based on in situ screening, 16 genotypes were found resistant to all the four viruses, whereas for ELISA, 13 genotypes (27005, 27041, 27075, 27141, 27145, 27146, 27147, 27158, 27160, 27167, 27172, IT85F-1380 and IT86D-719) were found resistant to all. Twelve clusters were obtained from UPGMA based on disease severity. Genotype 27008 (Pakistan) was present in cluster VI and was susceptible to all antisera CMV, CABMV, BICMV and BCMV. Whereas 13 genotypes were present in cluster VIII which were found resistant to all the four antisera applied. Therefore, 13 genotypes suggested for safe use in any breeding program at developing resistant cultivars. First two factors obtained through PCA with eigen-values greater than 1 contributed greater than 80 per cent variability. Twelve distinct groups were observed and these were in coordination with cluster analysis.


1988 ◽  
Vol 54 (1-2) ◽  
pp. 7-10 ◽  
Author(s):  
M. E. Omunyin ◽  
E.M. Gathuru ◽  
D. M. Mukunya

2018 ◽  
Vol 108 (8) ◽  
pp. 1011-1018 ◽  
Author(s):  
Xue Feng ◽  
Gardenia E. Orellana ◽  
James R. Myers ◽  
Alexander V. Karasev

Recessive resistance to Bean common mosaic virus (BCMV) in common bean (Phaseolus vulgaris) is governed by four genes that include one strain-nonspecific helper gene bc-u, and three strain-specific genes bc-1, bc-2, and bc-3. The bc-3 gene was identified as an eIF4E translation initiation factor gene mediating resistance through disruption of the interaction between this protein and the VPg protein of the virus. The mode of action of bc-1 and bc-2 in expression of BCMV resistance is unknown, although bc-1 gene was found to affect systemic spread of a related potyvirus, Bean common mosaic necrosis virus. To investigate the possible role of both bc-1 and bc-2 genes in replication, cell-to-cell, and long-distance movement of BCMV in P. vulgaris, we tested virus spread of eight BCMV isolates representing pathogroups I, IV, VI, VII, and VIII in a set of bean differentials expressing different combinations of six resistance alleles including bc-u, bc-1, bc-12, bc-2, bc-22, and bc-3. All studied BCMV isolates were able to replicate and spread in inoculated leaves of bean cultivars harboring bc-u, bc-1, bc-12, bc-2, and bc-22 alleles and their combinations, while no BCMV replication was found in inoculated leaves of cultivar IVT7214 carrying the bc-u, bc-2, and bc-3 genes, except for isolate 1755a, which was capable of overcoming the resistance conferred by bc-2 and bc-3. In contrast, the systemic spread of all BCMV isolates from pathogroups I, IV, VI, VII, and VIII was impaired in common bean cultivars carrying bc-1, bc-12, bc-2, and bc-22 alleles. The data suggest that bc-1 and bc-2 recessive resistance genes have no effect on the replication and cell-to-cell movement of BCMV, but affect systemic spread of BCMV in common bean. The BCMV resistance conferred by bc-1 and bc-2 and affecting systemic spread was found only partially effective when these two genes were expressed singly. The efficiency of the restriction of the systemic spread of the virus was greatly enhanced when the alleles of bc-1 and bc-2 genes were combined together.


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