Evaluation of germ plasm for resistant to Soybean mosaic virus (SMV)

2020 ◽  
Vol 21 (1) ◽  
pp. 6-9
Author(s):  
Wuye Ria Andayanie

Soybean superior varieties with high yields and are resistant to abiotic stress have been largely released, although some varieties grown in the field are not resistant to SMV. In addition, the opportunity to obtain lines of hope as prospective varieties with high yield and resistance to SMV is very small. The method for evaluating soybean germplasm is based on serological observations of 98 accessions of leaf samples from SMV inoculation with T isolate. The evaluation results of 98 accessions based on visual observations showed 31 genotypes reacting very resistant or healthy to mild resistant category to SMV T isolate  with a percentage of symptom severity of 0 −30 %. Among 31 genotypes there are 2 genotypes (PI 200485; M8Grb 44; Mlg 3288) with the category of visually very resistant and resistant, respectively and  Mlg 3288  with the category of mild resistant.  They have a good agronomic appearance with a weight of 100 seeds (˃10 g) and react negatively with polyclonal antibodies to SMV, except Mlg 3288 reaction is not consistent, despite the weight of 100 seeds (˃ 10 g). Leaf samples from 98 accessions revealed various symptoms of SMV infection in the field. This diversity of symptoms is caused by susceptibility to accession, when infection occurs, and environmental factors. Keywords—: soybean; genotipe; Soybean mosaic virus (SMV); disease severity; polyclonal  antibody

2014 ◽  
Vol 14 (2) ◽  
pp. 152-159
Author(s):  
Wuye Ria Andayanie ◽  
Praptiningsih Gamawati Adinurani

Soybean lines selection of F4 population resistant  to soybean mosaic disease (Soybean mosaic virus) with high yield.  The soybean breeding program is usually not purposedly done for resistance to Soybean mosaic virus (SMV) but rather for crop yields. The experiment was aimed to obtain soybean lines of F4 population resistant to soybean mosaic disease with high yield.  F2-F4 plants that have been inoculated with the T isolate of SMV one week after planting were selected by the pedigree  in the screen house. The result indicated eight  F4 populations (Wilis x L. Temanggung; Wilis x L. Jombang; Wilis x Pangrango; Wilis x PI 200485;  Gepak Kuning x L. Jombang; Gepak Kuning x L. Temanggung; Gepak Kuning x Malabar; Gepak Kuning x PI 200485) produced medium seed size (from 9.84-10.26 g 100/seeds).  Gepak Kuning x Mlg 3288  showed more resistant than Gepak Kuning x PI 200485. The seed produced by Gepak Kuning x PI 200485 was 1.97 ton/ha. There were no F4 populations that had higher yield and bigger seed size than Gepak Kuning x PI 200485 even though they were  moderately resistant to SMV. Therefore, these lines of Gepak Kuning x Mlg 3288 and Gepak  Kuning x  PI 200485 might provide exellent sources to develop a new variety that resistant to SMV and of high yield.


Plant Disease ◽  
2009 ◽  
Vol 93 (12) ◽  
pp. 1259-1264 ◽  
Author(s):  
M. Malapi-Nelson ◽  
R.-H. Wen ◽  
B. H. Ownley ◽  
M. R. Hajimorad

Co-infection of potyviruses with taxonomically diverse plant viruses results in disease synergism and elevation in the level of accumulation of non-potyviruses involved. In the majority of cases, however, the accumulation level of potyviruses remains essentially unaltered. A few potyviruses, such as Soybean mosaic virus (SMV), naturally infect soybean (Glycine max). Soybean is also a natural host to a number of non-potyviruses including Alfalfa mosaic virus (AMV), which causes mild symptoms often associated with symptom remission. We have now studied the interactions between AMV and SMV on symptom severity and accumulation level of each of the two viruses in soybean. Co-infection of soybean with AMV and SMV was established following mechanical inoculation, irrespective of simultaneous or sequential introduction of the two viruses. In multiple experiments, co-infection of soybean resulted in severe symptoms in doubly infected plants in a strain-independent manner, with enhancement in the level of AMV indicating that the interaction of AMV with SMV is synergistic. Conversely, the level of SMV accumulation was reduced. This suggests that in co-infection with AMV, SMV interacts antagonistically. The observation that co-infection of AMV and SMV results in disease synergism suggests enhancement of potential that AMV may become a serious viral disease of soybean.


1984 ◽  
Vol 160 (6) ◽  
pp. 1767-1781 ◽  
Author(s):  
A Donohue-Rolfe ◽  
G T Keusch ◽  
C Edson ◽  
D Thorley-Lawson ◽  
M Jacewicz

A simple purification scheme for shigella cytotoxin was devised, resulting in high yields (approximately 50%) and a 1,300-fold increase in specific activity compared with the initial crude bacterial cell lysate. The purified toxin was enterotoxic in ligated rabbit ileal loops and neurotoxic when injected into the peritoneal cavity of mice. Measurement of specific activity of cytotoxin and enterotoxin demonstrated that these two toxicities copurify during the fractionation procedure. On sodium dodecyl sulfate gel electrophoresis, the toxin migrated as two polypeptide subunits, an A subunit of 32,000 mol wt and a B subunit of 6,500 mol wt. Chemical cross-linking experiments demonstrate that the toxin is a complex consisting of one A and five B subunits with a molecular weight of 64,000. Polyclonal rabbit anti-toxin and anti-subunit B antisera were produced as well as subunit-specific mouse monoclonal antibodies. All antibodies preincubated with toxin neutralized cytotoxic effects in HeLa cell monolayers. In contrast, only A subunit-specific antibodies were able to neutralize toxin prebound to the HeLa cell surface. Antibody to the B subunit also inhibited binding of 125I-labeled toxin to these cells by 94% or more. These data demonstrate that the B subunit is involved in shigella toxin binding to the cell surface.


2017 ◽  
Vol 19 (02) ◽  
pp. 226-232 ◽  
Author(s):  
Wuye Ria Andayanie ◽  
Venny Santosa ◽  
Muji Rahayu

2010 ◽  
Vol 36 (4) ◽  
pp. 549-554
Author(s):  
Rong-Xia GUAN ◽  
Yu-Bo CHEN ◽  
Hong-Liang FANG ◽  
Shuo LIU ◽  
Wei-Li TENG ◽  
...  

Crop Science ◽  
1989 ◽  
Vol 29 (6) ◽  
pp. 1439-1441 ◽  
Author(s):  
G. R. Buss ◽  
C. W. Roane ◽  
S. A. Tolin ◽  
P. Chen

2019 ◽  
Vol 13 (1) ◽  
pp. 137-145 ◽  
Author(s):  
Tzonka Godjevargova ◽  
Zlatina Becheva ◽  
Yavor Ivanov ◽  
Andrey Tchorbanov

Objectives: Staphylococcus aureus is a Gram-positive microorganism. S. aureus can grow in various foods and cause food poisoning by secreting enterotoxins. The most common enterotoxins involved in food poisoning are staphylococcal enterotoxin A and staphylococcal enterotoxin B, but Staphylococcal Enterotoxin A (SEA) is predominant. The main types of food contaminated with SEs are meat and meat products, poultry and eggs, milk and dairy products. The aim of this study was to develop a rapid and sensitive fluorescence immunoassay for detection of staphylococcal enterotoxin A in milk. Methods: Monoclonal and polyclonal antibodies for SEA were produced and characterized. Competitive fluorescence immunoassay based on Magnetic Nanoparticles (MNPs) was performed and optimized. MNPs were used as a solid carrier of the antibodies. The first step of the assay was immunoreaction between the immobilized antibody onto MNPs and SEA in milk sample. Then the fluorescein-SEA conjugate was added to the sample. Thus, competitive immunoreaction between MNP-mAb/MNP-pAb with SEA and SEA-FITC was performed. These immuno-complexes were separated by a magnetic separator and the obtained supernatants were analyzed. The fluorescent signal from the excess of conjugated SEA was proportional to the SEA contained in the milk. The assay duration was only 30 min. Results: The fluorescence immunoassays performed with polyclonal antibody had linear ranges from 5 pg/mL to 100 ng/mL SEA in a buffer, and from 50 pg/mL to 50 ng/mL SEA in spiked milk samples. While the same assays performed with monoclonal antibody had linear ranges from 1 pg/mL to 20 ng/mL SEA in buffer, and from 10 pg/mL to 10 ng/mL SEA in spiked milk samples. The detection limits of the developed immunoassays performed in milk were: 48 pg/mL with polyclonal antibody and 9 pg/mL with monoclonal antibody. Conclusion: A rapid and sensitive fluorescence immunoassay based on magnetic nanoparticles with a polyclonal and monoclonal antibody for determination of staphylococcal enterotoxin A in milk was developed.


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