| Autor: |
Yarullina L; Institute of Biochemistry and Genetics, pr. Oktyabrya, 71, 450054 Ufa, Russia., Kalatskaja J; Institute of Experimental Botany Named after V.F. Kuprevich, ul. Akademicheskaya, 27, 220072 Minsk, Belarus., Tsvetkov V; Department of Biochemistry and Biotechnology, Ufa University of Science and Technology, ul. Zaki Validi, 32, 450076 Ufa, Russia., Burkhanova G; Institute of Biochemistry and Genetics, pr. Oktyabrya, 71, 450054 Ufa, Russia., Yalouskaya N; Institute of Experimental Botany Named after V.F. Kuprevich, ul. Akademicheskaya, 27, 220072 Minsk, Belarus., Rybinskaya K; Institute of Experimental Botany Named after V.F. Kuprevich, ul. Akademicheskaya, 27, 220072 Minsk, Belarus., Zaikina E; Institute of Biochemistry and Genetics, pr. Oktyabrya, 71, 450054 Ufa, Russia., Cherepanova E; Institute of Biochemistry and Genetics, pr. Oktyabrya, 71, 450054 Ufa, Russia., Hileuskaya K; Institute of Chemistry of New Materials, The National Academy of Sciences of Belarus, 220141 Minsk, Belarus., Nikalaichuk V; Institute of Chemistry of New Materials, The National Academy of Sciences of Belarus, 220141 Minsk, Belarus. |
| Abstrakt: |
Viral diseases of potatoes are among the main problems causing deterioration in the quality of tubers and loss of yield. The growth and development of potato plants largely depend on soil moisture. Prevention strategies require comprehensive protection against pathogens and abiotic stresses, including modeling the beneficial microbiome of agroecosystems combining microorganisms and immunostimulants. Chitosan and its derivatives have great potential for use in agricultural engineering due to their ability to induce plant immune responses. The effect of chitosan conjugate with caffeic acid (ChCA) in combination with Bacillus subtilis 47 on the transcriptional activity of PR protein genes and changes in the proteome of potato plants during potato virus Y (PVY) infection and drought was studied. The mechanisms of increasing the resistance of potato plants to PVY and lack of moisture are associated with the activation of transcription of genes encoding PR proteins: the main protective protein (PR-1), chitinase (PR-3), thaumatin-like protein (PR-5), protease inhibitor (PR-6), peroxidase (PR-9), and ribonuclease (PR-10), as well as qualitative and quantitative changes in the plant proteome. The revealed activation of the expression of marker genes of systemic acquired resistance and induced systemic resistance under the influence of combined treatment with B. subtilis and chitosan conjugate indicate that, in potato plants, the formation of resistance to viral infection in drought conditions proceeds synergistically. By two-dimensional electrophoresis of S. tuberosum leaf proteins followed by MALDI-TOF analysis, 10 proteins were identified, the content and composition of which differed depending on the experiment variant. In infected plants treated with ChCA, the synthesis of proteinaceous RNase P 1 and oxygen-evolving enhancer protein 2 was enhanced in conditions of normal humidity, and 20 kDa chaperonin and TMV resistance protein N-like was enhanced in conditions of lack of moisture. The virus coat proteins were detected, which intensively accumulated in the leaves of plants infected with potato Y-virus. ChCA treatment reduced the content of these proteins in the leaves, and in plants treated with ChCA in combination with Bacillus subtilis , viral proteins were not detected at all, both in conditions of normal humidity and lack of moisture, which suggests the promising use of chitosan derivatives in combination with B. subtilis bacteria in the regulation of plant resistance. |
