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Attenuated mutants of Potato virus Y necrotic strain produced by nitrous acid treatment and mutagenesis-in-tissue culture methods
Authors:Tetsuji Ogawa  Shigeo Nakamura  Mitsuru Sayama  Kazusato Ohshima
Affiliation:1. Laboratory of Plant Virology, Department of Applied Biological Sciences, Faculty of Agriculture, Saga University, 1-banchi, Honjo-machi, Saga, 840-8502, Japan
2. The United Graduate School of Agricultural Sciences, Kagoshima University, 1-21-24, Korimoto, Kagoshima, 890-0065, Japan
3. Potato Laboratory, Agriculture and Forestry Technical Development Center, Nagasaki Prefectural Government, 2777 Otu, Aino, Unzen City, Nagasaki, 854-0302, Japan
4. Food and Biotechnology Department, Industrial Technology Institute, Miyagi Prefectural Government, 2-2, Akedohri, Izumi-ku, Sendai, Miyagi, 981-3206, Japan
5. Agro-environmental Research Division, NARO Hokkaido Agricultural Research Center, 1-Hitsujigaoka, Toyohira, Sapporo, Hokkaido, 062-8555, Japan
Abstract:We produced attenuated mutants of Potato virus Y necrotic strain not only by nitrous acid treatment but also by a novel method, probably unique to plant viruses, which we call the “mutagenesis-in-tissue culture method”. This relies on the natural or experimental generation of virus sequence variants within an infected plant, and then isolating the mutants by serially cloning them in plants. A total of fifteen attenuated mutants were obtained and studied. Nucleotide and amino acid sequences of the genomes of the attenuated mutant populations were compared with those parental severe isolates, and the amino acid changes in relevant genomic regions for viral attenuation were inferred. Many of the mutations were located in the 5’ half of the genome; 65 % were located in the protein 1 (P1) and helper component proteinase protein (HC-Pro) encoding regions. Amino acid changes mostly involved simultaneous changes in two or more protein encoding regions, one of which was often in the HC-Pro encoding region. The attenuated mutants M-MY10 and N-NA10 were effective in cross-protection against the original severe isolate NTND6.
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