Journals / Uluslararası tarım araştırmalarında yenilikçi yaklaşımlar dergisi (Online) / 2020 / Cilt: 4 - Sayı: 1

Biochemical Alterations in the Leaves of Resistant and Susceptible Mungbean Genotypes Infected with Mungbean Yellow Mosaic India Virus

Pages
99–118
DOI
—
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⚡ TL;DR(Too Long; Didn't Read)

Differential expression of protein phosphatase 2C (PP2C) and Cytochrome b6 (Photosynthesis) in resistant and moderately resistant genotypes; Pectin acetyl esterase and Resistant specific protein-1(4) in resistant genotype and up-regulation of superoxide dismutase [Cu-Zn] and RuBisco by MYMIV may have triggered signal transduction pathway and consequently induced a resistance response against MYMIV in V. radiata by activating PR proteins.

📌 3 Key Takeaways

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Objective & Hypothesis:Mungbean (Vigna radiata), an important leguminous crop, is highly susceptible to yellow mosaic disease (YMD) caused by Mungbean yellow mosaic India virus (MYMIV), resulting in high yield penalty.
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Key Findings & Data:Therefore, in this study using MYMIV-resistant (NM-2016), moderately resistant (NM-2011) and susceptible genotype (VC-1647C), alterations in various biochemical attributes due to MYMIV infection were analysed and compared with healthy non-inoculated control plants for understanding the resistance mechanism.
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Conclusion & Impact:Differential expression of protein phosphatase 2C (PP2C) and Cytochrome b6 (Photosynthesis) in resistant and moderately resistant genotypes; Pectin acetyl esterase and Resistant specific protein-1(4) in resistant genotype and up-regulation of superoxide dismutase [Cu-Zn] and RuBisco by MYMIV may have triggered signal transduction pathway and consequently induced a resistance response against MYMIV in V. radiata by activating PR proteins.
🔬Design:Research Article
📍Scope:2016 Verileri
⚙️Variables:Domain Parameters

Özet

Mungbean (Vigna radiata), an important leguminous crop, is highly susceptible to yellow mosaic disease (YMD) caused by Mungbean yellow mosaic India virus (MYMIV), resulting in high yield penalty. Previously, different varieties of mungbean have been reported possessing resistance/ tolerance against MYMIV. However, the molecular events occurring during compatible and incompatible interactions between mungbean and MYMIV are yet to be explored. Therefore, in this study using MYMIV-resistant (NM-2016), moderately resistant (NM-2011) and susceptible genotype (VC-1647C), alterations in various biochemical attributes due to MYMIV infection were analysed and compared with healthy non-inoculated control plants for understanding the resistance mechanism. After MYMIV inoculation, the level of total phenolic contents (TPC) and total soluble proteins (TSP) increased significantly in the susceptible genotype. However, the level of Malondialdehyde (MDA) and Ascorbate peroxidase (APX) remained same in all the genotypes. Level of superoxide dismutase (SOD) and catalase (CAT) decreased in the susceptible genotype but CAT level increased in the moderately resistant genotype. Protease level decreased significantly in all the genotypes while esterase level increased in moderately resistant and susceptible genotype. Peroxidase (POD) increased only in moderately resistant genotype and Total Oxidant Status (TOS) increased significantly in the susceptible genotype. Due to MYMIV infection the level of all plant pigments decreased in all the genotypes tested. The comparative proteome analysis using SDS-PAGE resolved 22 peptides with molecular weight from 12.5 to 163 kDa. Differential expression of protein phosphatase 2C (PP2C) and Cytochrome b6 (Photosynthesis) in resistant and moderately resistant genotypes; Pectin acetyl esterase and Resistant specific protein-1(4) in resistant genotype and up-regulation of superoxide dismutase [Cu-Zn] and RuBisco by MYMIV may have triggered signal transduction pathway and consequently induced a resistance response against MYMIV in V. radiata by activating PR proteins.

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Cite This Article

SUHAIL, A., AKHTAR, K. P., HAMEED, A., ULLAH, N., AMIN, I., ABBAS, G. (2020). Biochemical Alterations in the Leaves of Resistant and Susceptible Mungbean Genotypes Infected with Mungbean Yellow Mosaic India Virus. Uluslararası tarım araştırmalarında yenilikçi yaklaşımlar dergisi (Online), Cilt: 4 - Sayı: 1, 99–118. https://ajindex.com/articles/339779

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References (13)

  1. Abbas, G., A. Hameed, M. Rizwan, M. Ahsan, M. J. Asghar and N. Iqbal (2015). Genetic Confirmation of mungbean (Vigna radiata) and Mashbean (Vigna mungo) interspecific recombinants using molecular markers. Front. Plant Sci., 6, 1107 Aftab, M., S. Asad, K. Khokhar, M. Ayub and T. Butt T (1993). Effect of Mungbean yellow mosaic virus on the yield and growth components of asparagus bean. Pak. J. Phytopathol., 5, 58-61
  2. Ainsworth, E. A. and K.M. Gillespie (2007). Estimation of total phenolic content and other oxidation substrates in plant tissues using Folin–Ciocalteu reagent. Nat. Protoc., 2, 875-877
  3. Akhtar, K. P., G. Sarwar, G. Abbas, M. J. Asghar, N. Sarwar and T. M. Shah (2011). Screening of mungbean germplasm against Mungbean yellow mosaic India virus and its vector Bemisia tabaci. Crop Protec., 30, 1202-1209
  4. Akhtar, K. P., R. Kitsanachandee, P. Srinives, G. Abbas, M. J. Asghar, T. Shah, B. Atta, O. Chatchawankanphanich, G. Sarwar and M. Ahmad (2009). Field evaluation of mungbean recombinant inbred lines against mungbean yellow mosaic disease using new disease scale in Thailand. Plant Pathol. J., 25, 422-428
  5. Aly, A. A., M. Mansour, H. I. Mohamed and K. A. Abd-Elsalam (2012). Examination of correlations between several biochemical components and powdery mildew resistance of flax cultivars. Plant Pathol. J. 28, 149-155
  6. Bashir, M. and B. A. Malik (1988). Diseases of major pulse crops in Pakistan—a review. Int J Pest Manag., 34, 309-314
  7. Bashir, M., Z. Ahmad and S. Mansoor (2006). Occurrence and distribution of viral diseases of mungbean and mashbean in Punjab, Pakistan. Pak. J. Bot., 38, 1341 Beers, R. F. and I. W. Sizer (1952). A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J. Biol. Chem., 195, 133-140
  8. Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem., 72, 248-254.
  9. Chance, B. and A. Maehly (1955). Assay of catalases and peroxidases. Methods Enzymol., 2, 764-775.
  10. Chatterjee, A. and S.K. Ghosh (2008). Alterations in biochemical components in mesta plants infected with yellow vein mosaic disease. Braz. J. Plant Physiol., 20, 267-275.
  11. Dixit, V., V. Pandey and R. Shyam (2001). Differential antioxidative responses to cadmium in roots and leaves of pea (Pisum sativum L. cv. Azad). J. Exp. Bot., 52, 1101-1109.
  12. Drapeau, G.R. (1976). Protease from Staphyloccus aureus. Methods Enzymol., 45. 469-475.
  13. Erel, O.