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Genetic variation of coat protein gene among the isolates of Rice tungro spherical virus from tungro-endemic states of the India

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Abstract

Rice tungro disease, one of the major constraints to rice production in South and Southeast Asia, is caused by a combination of two viruses: Rice tungro spherical virus (RTSV) and Rice tungro bacilliform virus (RTBV). The present study was undertaken to determine the genetic variation of RTSV population present in tungro endemic states of Indian subcontinent. Phylogenetic analysis based on coat protein sequences showed distinct divergence of Indian RTSV isolates into two groups; one consisted isolates from Hyderabad (Andhra Pradesh), Cuttack (Orissa), and Puducherry and another from West Bengal, Coimbatore (Tamil Nadu), and Kanyakumari (Tamil Nadu). The results obtained from phylogenetic study were further supported with the SNPs (single nucleotide polymorphism), INDELs (insertion and deletion) and evolutionary distance analysis. In addition, sequence difference count matrix revealed 2–68 nucleotides differences among all the Indian RTSV isolates taken in this study. However, at the protein level these differences were not significant as revealed by Ka/Ks ratio calculation. Sequence identity at nucleotide and amino acid level was 92–100% and 97–100%, respectively, among Indian isolates of RTSV. Understanding of the population structure of RTSV from tungro endemic regions of India would potentially provide insights into the molecular diversification of this virus.

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References

  1. K. Muralidharan, D. Krishnaveni, N.V.L. Rajarajeshwari, A.S.R. Prasad, Curr Sci 85, 1143 (2003)

    Google Scholar 

  2. M. Periasamy, F.R. Niazi, V.G. Malathi, J. Virol. Methods 134, 230 (2006)

    Article  CAS  Google Scholar 

  3. R. Hull, Annu. Rev. Phytopathol 34, 275 (1996)

    Article  PubMed  CAS  Google Scholar 

  4. H. Hibino, Plant Dis 67, 774 (1983)

    Article  Google Scholar 

  5. M.C. Jones, K. Gough, I. Dasgupta, B.L. Subba Rao, J. Cliffe, R. Qu, P. Shen, M. Kaniewska, M. Blakebrough, J.W. Davies, R.N. Beachy, R. Hull, J. Gen. Virol 72, 757 (1991)

    Article  PubMed  CAS  Google Scholar 

  6. P. Shen, M. Kaniewska, C. Smith, R.N. Beachy, Virology 193, 621 (1993)

    Article  PubMed  CAS  Google Scholar 

  7. A. Druka, T. Burns, S. Zhang, R. Hull, J. Gen. Virol 77, 1975 (1996)

    Article  PubMed  CAS  Google Scholar 

  8. R. Joshi, V. Kumar, I. Dasgupta, J. Virol. Methods 109, 89 (2003)

    Article  CAS  Google Scholar 

  9. A. Banerjee, S. Roy, J. Tarafdar, Virus Genes 43, 398 (2011)

    Article  PubMed  CAS  Google Scholar 

  10. A. Banerjee, S. Roy, J. Tarafdar, Virus Genes. (2011) doi:10.1007/s11262-011-0680-y

  11. Y.P. Tian, J.L. Liu, X.Q. Yu, L.P. Lei, X.P. Zhu, J.P.T. Valkonen, X.D. Li, Arch. Virol. 152, 191 (2007)

    Article  Google Scholar 

  12. J.D. Thompson, T.J. Gibson, F. Plewniak, F. Jeanmougin, D.G. Higgins, Nucleic Acids Res. 24, 4876 (1997)

    Article  Google Scholar 

  13. T.A. Hall, Nucleic Acids Symp. Ser 41, 95 (1999)

    CAS  Google Scholar 

  14. K. Tamura, D. Peterson, N. Peterson, G. Stecher, M. Nei, S. Kumar, Mol. Biol. Evol 28, 2731 (2011)

    Article  PubMed  CAS  Google Scholar 

  15. O. Azzam, M. Arboleda, K.M. Umadhay, J.B. DeLos Reyes, F.S. Cruz, A. Mackenzie, K.L. McNally, Arch. Virol 145, 2657 (2000)

    Google Scholar 

  16. S.K. Mangrauthia, P. Malathi, S.M. Balachandran, C.S. Reddy, B.C. Viraktamath, J Plant Biochem Biotech 19, 263 (2010)

    Google Scholar 

  17. M.S. Rosenberg, BMC Bioinformatics 6, 102 (2005)

    Article  Google Scholar 

  18. D. Krishnaveni, C.S. Reddy, G.S. Laha, C.N. Neeraja, G.S.V. Prasad, M.S. Prasad, S.K. Mangrauthia, K. Muralidharan, B.C. Viraktamath, Technical bulletin No. 43 Directorate of Rice Research (ICAR) Rajendranagar, Hyderabad, (2009)

  19. Z. Fan, G. Dahal, I. Dasgupta, J. Hay, R. Hull, J. Gen. Virol 77, 847 (1996)

    Article  PubMed  CAS  Google Scholar 

  20. S. Zhang, J.W. Davies, R. Hull, Virus Genes 15, 61 (1997)

    Article  PubMed  Google Scholar 

  21. S. Zhang, G. Lee, J.W. Davies, R. Hull, Arch. Virol 142, 1873 (1997)

    Article  PubMed  CAS  Google Scholar 

  22. D. Posada, K.A. Crandall, E.C. Holmes, Annu. Rev. Genet 36, 75 (2002)

    Article  PubMed  CAS  Google Scholar 

  23. S.K. Mangrauthia, B. Parameswari, R.K. Jain, S. Praveen, Biochem. Genet 46, 835 (2008)

    Article  PubMed  CAS  Google Scholar 

  24. C. Roth, D.A. Liberles, BMC Plant Biol 6, 12 (2006)

    Article  PubMed  Google Scholar 

  25. L. Duret, Trends Genet 16, 287 (2000)

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

Authors are highly thankful to Dr. R.M. Sundaram (Senior Scientist, Directorate of Rice Research, Hyderabad) for providing the tungro infected rice samples of Puducherry. Financial support obtained under the SERC fast track scheme of Department of Science and Technology (DST), Govt. of India is highly acknowledged.

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Correspondence to Satendra K. Mangrauthia.

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Mangrauthia, S.K., Malathi, P., Agarwal, S. et al. Genetic variation of coat protein gene among the isolates of Rice tungro spherical virus from tungro-endemic states of the India. Virus Genes 44, 482–487 (2012). https://doi.org/10.1007/s11262-011-0708-3

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  • DOI: https://doi.org/10.1007/s11262-011-0708-3

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