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Rolling circle amplification-based analysis of Sri Lankan cassava mosaic virus isolates from Tamil Nadu, India, suggests a low level of genetic variability

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Abstract

Cassava mosaic disease is a widespread disease of cassava in south Asia and the African continent. In India, CMD is known to be caused by two single-stranded DNA viruses (geminiviruses), Indian cassava mosaic virus (ICMV) and Sri Lankan cassava mosdaic virus (SLCMV). Previously, the diversity of ICMV and SLCMV in India has been studied using PCR, a sequence-dependent method. To have a more in-depth study of the variability of the above viruses and to detect any novel geminiviruses associated with CMD, sequence-independent amplification using rolling circle amplification (RCA)-based methods were used. CMD affected cassava plants were sampled across eighty locations in nine districts of the southern Indian state of Tamil Nadu. Twelve complete sequence of coat protein genes of the resident geminiviruses, comprising 256 amino acid residues were generated from the above samples, which indicated changes at only six positions. RCA followed by RFLP of the 80 samples indicated that most samples (47) contained only SLCMV, followed by 8, which were infected jointly with ICMV and SLCMV. In 11 samples, the pattern did not match the expected patterns from either of the two viruses and hence, were variants. Sequence analysis of an average of 700 nucleotides from 31 RCA-generated fragments of the variants indicated identities of 97–99% with the sequence of a previously reported infectious clone of SLCMV. The evidence suggests low levels of genetic variability in the begomoviruses infecting cassava, mainly in the form of scattered single nucleotide changes.

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References

  1. Thresh JM, Otim-Nape GW, Legg JP, Fargette D. African cassava mosaic disease: the magnitude of problem? Afr J Root Tuber Crops. 1997;2:13–9.

    Google Scholar 

  2. Patil BL, Fauquet CM. Cassava mosaic geminiviruses: actual knowledge and perspectives. Mol Plant Pathol. 2009;10:685–701.

    Article  CAS  PubMed  Google Scholar 

  3. Navas-Castillo J, Fiallo-Olive E, Sanchez-Campos S. Emerging virus diseases transmitted by whiteflies. Annu Rev Phytopathol. 2011;49:219–48.

    Article  CAS  PubMed  Google Scholar 

  4. Lozano-Duran R. Geminiviruses for biotechnology: the art of parasite taming. New Phytol. 2016;210:58–64.

    Article  CAS  PubMed  Google Scholar 

  5. Sanderfoot AA, Lazarowitz SG. Getting it together in plant virus movement: cooperative interactions between bipartite geminivirus movement proteins. Trends Cell Biol. 1996;6:353–8.

    Article  CAS  PubMed  Google Scholar 

  6. Abraham A. Farm Bulletin No 17. New Delhi: Indian Council of Agricultural Research; 1956.

    Google Scholar 

  7. Alagianagalingam MN, Ramakrishnan K. Cassava mosaic in India. South Indian Hortic. 1966;14:71–2.

    Google Scholar 

  8. Hong YG, Robinson DJ, Harrison BD. Nucleotide sequence evidence for the occurrence of three distinct whitefly-transmitted geminiviruses in cassava. J Gen Virol. 1993;74(Pt 11):2437–43.

    Article  CAS  PubMed  Google Scholar 

  9. Saunders K, Salim N, Mali VR, Malathi VG, Briddon R, Markham PG, Stanley J. Characterisation of Sri Lankan cassava mosaic virus and Indian cassava mosaic virus: evidence for acquisition of a DNA B component by a monopartite begomovirus. Virology. 2002;293:63–74.

    Article  CAS  PubMed  Google Scholar 

  10. Dutt N, Briddon RW, Dasgupta I. Identification of a second begomovirus, Sri Lankan cassava mosaic virus, causing cassava mosaic disease in India. Arch Virol. 2005;150:2101–8.

    Article  CAS  PubMed  Google Scholar 

  11. Patil BL, Rajasubramaniam S, Bagchi C, Dasgupta I. Both Indian cassava mosaic virus and Sri Lankan cassava mosaic virus are found in India and exhibit high variability as assessed by PCR-RFLP. Arch Virol. 2005;150:389–97.

    Article  CAS  PubMed  Google Scholar 

  12. Rothenstein D, Briddon RW, Haible D, Stanley J, Frischmuth T, Jeske H. Biolistic infection of cassava using cloned components of Indian cassava mosaic virus. Arch Virol. 2005;150:1669–75.

    Article  CAS  PubMed  Google Scholar 

  13. Borah BK, Dasgupta I. PCR-RFLP analysis indicates that recombination might be a common occurrence among the cassava infecting begomoviruses in India. Virus Genes. 2012;45:327–32.

    Article  CAS  PubMed  Google Scholar 

  14. Kushawaha AK, Rabindran R, Dasgupta I. Phylogenetic analysis and biolistic infectivity of a cloned Sri Lankan cassava mosaic virus DNA-A from Tamil Nadu, India on Nicotiana benthamiana. Acta Virol. 2015;59:57–63.

    Article  CAS  PubMed  Google Scholar 

  15. Elena SF, Sanjuan R. Adaptive value of high mutation rates of RNA viruses: separating causes from consequences. J Virol. 2005;79:11555–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Kirthi N, Maiya SP, Murthy MR, Savithri HS. Evidence for recombination among the tomato leaf curl virus strains/species from Bangalore, India. Arch Virol. 2002;147:255–72.

    Article  CAS  PubMed  Google Scholar 

  17. Ndunguru J, Legg JP, Aveling TA, Thompson G, Fauquet CM. Molecular biodiversity of cassava begomoviruses in Tanzania: evolution of cassava geminiviruses in Africa and evidence for East Africa being a center of diversity of cassava geminiviruses. Virol J. 2005;2:21.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Sharma S, Rabindran R, Robin S, Dasgupta I. Analysis of the complete DNA sequence of rice tungro bacilliform virus from southern India indicates it to be a product of recombination. Arch Virol. 2011;156:2257–62.

    Article  CAS  PubMed  Google Scholar 

  19. Rishishwar R, Mazumdar B, Dasgupta I. Diverse and recombinant begomoviruses and various satellites are associated with Bhendi yellow vein mosaic disease of okra in India. J Plant Biochem Biotechnol. 2015;24(4):470–5.

    Article  Google Scholar 

  20. Hou YM, Gilbertson RL. Increased pathogenicity in a pseudorecombinant bipartite geminivirus correlates with intermolecular recombination. J Virol. 1996;70:5430–6.

    CAS  PubMed  PubMed Central  Google Scholar 

  21. Pita JS, Fondong VN, Sangare A, Otim-Nape GW, Ogwal S, Fauquet CM. Recombination, pseudorecombination and synergism of geminiviruses are determinant keys to the epidemic of severe cassava mosaic disease in Uganda. J Gen Virol. 2001;82:655–65.

    Article  CAS  PubMed  Google Scholar 

  22. Martin DP, van der Walt E, Posada D, Rybicki EP. The evolutionary value of recombination is constrained by genome modularity. PLoS Genet. 2005;1:e51.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Lima AT, Sobrinho RR, Gonzalez-Aguilera J, Rocha CS, Silva SJ, Xavier CA, Silva FN, Duffy S, Zerbini FM. Synonymous site variation due to recombination explains higher genetic variability in begomovirus populations infecting non-cultivated hosts. J Gen Virol. 2013;94:418–31.

    Article  CAS  PubMed  Google Scholar 

  24. Sobrinho RR, Xavier CA, Pereira HM, Lima GS, Assuncao IP, Mizubuti ES, Duffy S, Zerbini FM. Contrasting genetic structure between two begomoviruses infecting the same leguminous hosts. J Gen Virol. 2014;95:2540–52.

    Article  PubMed  Google Scholar 

  25. Haible D, Kober S, Jeske H. Rolling circle amplification revolutionizes diagnosis and genomics of geminiviruses. J Virol Methods. 2006;135:9–16.

    Article  CAS  PubMed  Google Scholar 

  26. Varsani A, Roumagnac P, Fuchs M, Navas-Castillo J, Moriones E, Idris A, Briddon RW, Rivera-Bustamante R, Murilo Zerbini F, Martin DP. Capulavirus and Grablovirus: two new genera in the family Geminiviridae. Arch Virol. 2017;162:1819–31.

    Article  CAS  PubMed  Google Scholar 

  27. Dellaporta S, Wood J, Hicks JB. A plant DNA minipreparartion: version II. Plant Mol Biol Report. 1983;1:19–21.

    Article  CAS  Google Scholar 

  28. Homs M, Kober S, Kepp G, Jeske H. Mitochondrial plasmids of sugar beet amplified via rolling circle method detected during curtovirus screening. Virus Res. 2008;136:124–9.

    Article  CAS  PubMed  Google Scholar 

  29. Thompson JD, Higgins DG, Gibson TJ. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 1994;22:4673–80.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Wieczorek P, Obrepalska-Steplowska A. The N-terminal fragment of the tomato torrado virus RNA1-encoded polyprotein induces a hypersensitive response (HR)-like reaction in Nicotiana benthamiana. Arch Virol. 2016;161:1849–58.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Garcia-Boronat M, Diez-Rivero CM, Reinherz EL, Reche PA. PVS: a web server for protein sequence variability analysis tuned to facilitate conserved epitope discovery. Nucleic Acids Res. 2008;36:W35–41.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Karthikeyan C, Patil BL, Borah BK, Resmi TR, Turco S, Pooggin MM, Hohn T, Veluthambi K. Emergence of a latent Indian cassava mosaic virus from cassava which recovered from infection by a non-persistent Sri Lankan cassava mosaic virus. Viruses. 2016;8:264.

    Article  PubMed Central  Google Scholar 

  33. Kumar V, Singh D, Singh AK, Chakraborty S. Molecular diversity, recombination and population structure of alphasatellites associated with begomovirus disease complexes. Infect Genet Evol. 2017;49:39–47.

    Article  Google Scholar 

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Acknowledgements

AKK gratefully acknowledges fellowships from University of Delhi and Department of Biotechnology, Government of India. This work was funded by the Grant Number BT/PR/13094/PBD/16/866/2005 by Department of Biotechnology, Government of India to ID.

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Correspondence to Indranil Dasgupta.

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Kushawaha, A.K., Rabindran, R. & Dasgupta, I. Rolling circle amplification-based analysis of Sri Lankan cassava mosaic virus isolates from Tamil Nadu, India, suggests a low level of genetic variability. VirusDis. 29, 61–67 (2018). https://doi.org/10.1007/s13337-018-0432-x

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