scholarly journals Induction of Systemic Resistance to Bean yellow mosaic virus (BYMV) Infecting Bean Plants Using Plant Extracts and Salicylic Acid

2017 ◽  
Vol 8 (7) ◽  
pp. 361-370
Author(s):  
H. Awad ◽  
Sahar El-Helaly
2019 ◽  
Author(s):  
Patricia Rodríguez Pardina ◽  
Claudia Nome ◽  
Pablo Reyna ◽  
Nacira Muñoz ◽  
Evangelina Argüello Caro ◽  
...  

AbstractBroad bean (Vicia faba L) is the fourth most important pulse crop in the world. In Argentina, broad bean production was of 1,841 hectares and 16,500 tons during the 2017 growing season. Broad bean is commonly used in rotations; especially by farmers located in “green belts” that are peri-urban areas surrounding large cities that include horticultural family farms. Plants showing marked foliar mosaic symptoms, typical of viral infection, were collected during the 2015 growing season in the green belt of Córdoba city, Argentina. Preparations of symptomatic tissues were mechanically inoculated onto healthy broad bean plants in the greenhouse, which developed symptoms similar to those observed in the field. In addition, symptomatic samples were positive when tested by indirect ELISA with the anti-potyvirus group monoclonal antibody. Further, flexuous filamentous particles typical of potyviruses were observed under the electronic microscope on dip preparations. Lastly, total RNA was extracted from a symptomatic leaf and high-throughput sequenced, which allowed the assembly of a single virus sequence corresponding to a new highly divergent strain of Bean yellow mosaic virus (BYMV). Phylogenetic insights clustered this Argentinean broad bean isolate (BYMV-ARGbb) within group IX of BYMV. Given the economical importance of this virus and its associated disease, the results presented here are a pivotal first step oriented to explore the eventual incidence and epidemiological parameters of BYMV in broad bean in Argentina.


1993 ◽  
Vol 2 (1) ◽  
pp. 41-49
Author(s):  
Jari P. T. Valkonen

A pea mosaic strain and a bean strain of bean yellow mosaic virus (BYMV) were isolated from naturally infected pea and broad bean plants and named BYMV-Ps and BYMV-Vf, respectively. A third strain of BYMV isolated from Gladiolus (BYMV-G) was obtained from Denmark which was distinguished from the two above strains serologically and by its symptoms in test plants. BYMV-Ps and BYMV-Vf caused yellow mosaic symptoms and green mosaic symptoms, respectively, in eight pea cultivars tested, but the concentration of BYMV varied among the cultivars. BYMV-G caused mild mosaic or vein clearing in peas. A need to improve resistance to BYMV in the Finnish pea varieties was recognized.


2008 ◽  
Vol 165 (8) ◽  
pp. 845-857 ◽  
Author(s):  
Deya Eldeen Mohammed Radwan ◽  
Guoquan Lu ◽  
Khalaf Ali Fayez ◽  
Sabry Younis Mahmoud

2021 ◽  
Vol 790 (1) ◽  
pp. 012058
Author(s):  
Shrooq Zagier ◽  
Fadhal Al Fadhal ◽  
Osamah Alisawi

1996 ◽  
Vol 62 (5) ◽  
pp. 472-477 ◽  
Author(s):  
Shigeo NAKAMURA ◽  
Ryoso HONKURA ◽  
Takayoshi IWAI ◽  
Masashi UGAKI ◽  
Yuko OHASHI

2004 ◽  
Vol 78 (21) ◽  
pp. 11890-11903 ◽  
Author(s):  
Basavaraj Bagewadi ◽  
Shoajiang Chen ◽  
Sunil K. Lal ◽  
Nirupam Roy Choudhury ◽  
Sunil K. Mukherjee

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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