Skip to main content
Log in

Diversity and prevalence of Brazilian bipartite begomovirus species associated to tomatoes

  • Published:
Virus Genes Aims and scope Submit manuscript

Abstract

Information on the distribution and prevalence of the economically destructive Begomovirus species and recombinant forms infecting fresh-market and processing tomato crops in Brazil is crucial in guiding breeding programs and also to understand the evolutionary mechanisms associated with the upsurge of so many species and quasi-species comprising this unique disease complex. An extensive survey was carried out over 3 years (between 2002 and 2004) aiming to study the diversity of begomoviruses in tomato plants, predominantly collected in central Brazil. Polymerase chain reaction (PCR) with degenerated primers was used to detect the begomoviruses in tomato leaf samples showing virus-like symptoms in commercial fields. Seven hundred and seventeen out of 2,295 samples were found to be PCR positive for a begomovirus infection. High quality sequences were obtained from a fragment encompassing the 5′ region of the coat protein (CP) gene and a segment of the intergenic region for 295 isolates from distinct geographic regions. Comparison analyses with those available in public databases enabled preliminary classification of the isolates into four previously described and/or proposed species: Tomato severe rugose virus (61%), Tomato golden vein virus (29.8%), Tomato mottle leaf curl virus (7.1%), Tomato yellow vein streak virus (0.7%), and two putative new species (1.4% of isolates). Within the prevailing species, we noted a relatively low degree of diversity, possibly indicating the existence of recent population founder effects and/or recent selective sweeps.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. E. Flores, K. Silberschmidt, M. Kramer, Biológico 26, 65–69 (1960)

    Google Scholar 

  2. A.S. Costa, Fitopatologia 9, 47 (1974)

    Google Scholar 

  3. A.S. Costa, A.R. Oliveira, D.M. Silva, Braz. Phytopatol. 6, 147 (1975)

    Google Scholar 

  4. J.C. Matyis, D.M. Silva, A.R. Oliveira, A.S. Costa, Summa Phytopathol. 1, 267–275 (1975)

    Google Scholar 

  5. W.D.O. Hamilton, R.C. Sanders, R.H.A. Coutts, K.W. Buck, FEMS Microbiol. Lett. 11, 263–267 (1981)

    Article  CAS  Google Scholar 

  6. L.P. Ambrozevícius, R.F. Calegário, E.P.B. Fontes, M.G. Carvalho, F.M. Zerbini, Braz. Phytopatol. 27, 372–377 (2002)

    Google Scholar 

  7. S.G. Ribeiro, L.P. Ambrozevícius, A.C. Ávila, R.F. Calegario, J.J. Fernandes, M.F. Lima, R.N. Mello, H. Rocha, F.M. Zerbini, Arch. Virol. 148, 281–295 (2003)

    Article  PubMed  CAS  Google Scholar 

  8. S.G. Ribeiro, D.P. Martin, C. Lacorte, I.C. Simões, D.R.S. Orlandini, A.K. Inoue-Nagata, Phytopathology 97, 702–711 (2007)

    Article  CAS  PubMed  Google Scholar 

  9. A.K. Inoue-Nagata, D.P. Martin, L.S. Boiteux, L.B. Giordano, I.C. Bezerra, A.C. Ávila, Pesqui. Agropecu. Bras. 41, 1329–1332 (2006)

    Google Scholar 

  10. E.C. Andrade, G.G. Manhani, P.F. Alfenas, R.F. Calegario, E.P.B. Fontes, F.M. Zerbini, J. Gen. Virol. 87, 3687–3696 (2006)

    Article  PubMed  CAS  Google Scholar 

  11. R.F. Calegario, S.S. Ferreira, E.C. Andrade, F.M. Zerbini, Pesqui. Agropecu. Bras. 42, 1335–1347 (2007)

    Google Scholar 

  12. F.A. Albuquerque, L.M. Borges, E. Betioli Junior, Cultivar HF 38, 8–14 (2006)

  13. J.J. Doyle, J.L. Doyle, Phytochem. Bull. 19, 11–15 (1987)

    Google Scholar 

  14. M.R. Rojas, R.L. Gilbertson, D.R. Russell, D.P. Maxwell, Plant Dis. 77, 340–347 (1993)

    Article  CAS  Google Scholar 

  15. S.F. Altschul, T.L. Madden, A.A. Schäffer, J. Zhang, Z. Zhang, W. Miller, D.J. Lipman, Nucleic Acids Res. 25, 3389–3402 (1997)

    Article  PubMed  CAS  Google Scholar 

  16. J.D. Thompson, D.G. Higgins, T.J. Gibson, Nucleic Acids Res. 22, 4673–4680 (1994)

    Article  PubMed  CAS  Google Scholar 

  17. S. Kumar, K. Tamura, M. Nei, Brief. Bioinform. 5, 150–163 (2004)

    Article  PubMed  CAS  Google Scholar 

  18. J. Stanley, D.M. Bisaro, R.W. Briddon, J.K. Brown, C.M. Fauquet, B.D. Harrison, E.P. Rybicki, D.C. Stenger, in Virus Taxonomy. Eighth Report of the International Committee on Taxonomy of Viruses, ed. by C.M. Fauquet, M.A. Mayo, J. Maniloff, U. Desselberger, L.A. Ball (Elsevier Academic Press, San Diego, 2005), pp. 301–326

  19. M. Padidam, R.N. Beachy, C.M. Fauquet, J. Gen. Virol. 76, 249–263 (1995)

    Article  PubMed  CAS  Google Scholar 

  20. J.J. Fernandes, M.G. Carvalho, E.C. Andrade, S.H. Brommonschenkel, E.P.B. Fontes, F.M. Zerbini, Plant Pathol. 55, 513–522 (2006)

    Article  CAS  Google Scholar 

  21. A.R. Nava, C.P. Patte, E. Hiebert, J.E. Polston, Plant Dis. 90, 61–66 (2006)

    Article  CAS  Google Scholar 

  22. M. Padidam, S. Sawyer, C.M. Fauquet, Virology 265, 218–225 (1999)

    Article  PubMed  CAS  Google Scholar 

  23. J.C. Faria, J.A.C. Souza-Dias, S. Slack, D.P.A. Maxwell, Plant Dis. 81, 423–423 (1997)

    Article  Google Scholar 

  24. C.D.G. Santos, A.C. Ávila, A.K. Inoue-Nagata, R.O. Resende, Braz. Phytopatol. 29, 450–455 (2004)

    Google Scholar 

  25. R.M. Galvão, A.C. Mariano, D.F. Luz, P.C. Alfenas, E.C. Andrade, M.R. Almeida, F.M. Zerbini, E.P.B. Fontes, J. Gen. Virol. 84, 715–726 (2003)

    Article  PubMed  CAS  Google Scholar 

  26. F.J. Morales, P.K. Anderson, Arch. Virol. 146, 415–441 (2001)

    Article  PubMed  CAS  Google Scholar 

  27. Z.H. Li, X.P. Zhou, X. Zhang, Y. Xie, Arch. Virol. 149, 1721–1732 (2004)

    PubMed  CAS  Google Scholar 

  28. J. Ndunguru, J.P. Legg, T.A.S. Aveling, G. Thompson, C.M. Fauquet, Virol. J. 2, 1–23 (2005)

    Article  CAS  Google Scholar 

  29. G.B. Ferreira, A.C. Ávila, A.K. Inoue-Nagata, Braz. Phytopatol. 29, S202 (2004)

    Google Scholar 

  30. I.C. Bezerra-Agasie, G.B. Ferreira, A.C. Ávila, A.K. Inoue-Nagata, Plant Dis. 90, 114 (2006)

    Article  Google Scholar 

  31. S.G. Ribeiro, L.V. Melo, L.S. Boiteux, E.W. Kitajima, J.C. Faria, Braz. Phytopatol. 19, 330 (1994)

    Google Scholar 

  32. S.G. Ribeiro, A.C. Ávila, I.C. Bezerra, J.J. Fernandes, J.C. Faria, M.F. Lima, R.L. Gilbertson, E. Maciel-Zambolim, F.M. Zerbini, Plant Dis. 82, 830 (1998)

    Article  Google Scholar 

  33. L.S. Boiteux, V.R. Oliveira, C.S. Silva, N. Makishima, A.K. Inoue-Nagata, M.E.N. Fonseca, L.B. Giordano, Hort. Bras. 25, 20–23 (2007)

    Google Scholar 

  34. A.K. Inoue-Nagata, J. Navas-Castillo, P.C.T. Melo, A.C. Ávila, Hort. Bras. 22, 799–800 (2004)

    Google Scholar 

Download references

Acknowledgments

We are grateful to Élcio Vieira da Silva (in Memorian) for his technical assistance, and Darren Patrick Martin and Arvind Varsani for helpful discussion and critically reading the manuscript. This study was sponsored by Embrapa, CNPq, Unilever Bestfoods Brasil and IFS (Sweden).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Alice Kazuko Inoue-Nagata.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Fernandes, F.R., de Albuquerque, L.C., de Britto Giordano, L. et al. Diversity and prevalence of Brazilian bipartite begomovirus species associated to tomatoes. Virus Genes 36, 251–258 (2008). https://doi.org/10.1007/s11262-007-0184-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11262-007-0184-y

Keywords

Navigation