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The genomes of four novel begomoviruses and a new Sida micrantha mosaic virus strain from Bolivian weeds

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Abstract

Begomovirus is the largest genus within the family Geminiviridae and includes economically important plant DNA viruses infecting a broad range of plant species and causing devastating crop diseases, mainly in subtropical and tropical countries. Besides cultivated plants, many weeds act as virus reservoirs. Eight begomovirus isolates from Bolivian weeds were examined using rolling-circle amplification (RCA) and restriction fragment length polymorphism (RFLP). An efficient, novel cloning strategy using limited Sau3A digestion to obtain tandem-repeat inserts allowed the sequencing of the complete genomes. The viruses were classified by phylogenetic analysis as typical bipartite New World begomoviruses. Four of them represented distinct new virus species, for which the names Solanum mosaic Bolivia virus, Sida mosaic Bolivia virus 1, Sida mosaic Bolivia virus 2, and Abutilon mosaic Bolivia virus are proposed. Three were variants of a new strain of Sida micrantha mosaic virus (SimMV), SimMV-rho[BoVi07], SimMV-rho[Bo:CF1:07] and SimMV-rho[Bo:CF2:07], and one was a new variant of a previously described SimMV, SimMV-MGS2:07-Bo.

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References

  1. Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25:3389–3402

    Article  CAS  PubMed  Google Scholar 

  2. Anonymous (2009) The World Factbook, vol 2010

  3. Arguello-Astorga G, Ascencio-Ibáñez JT, Dallas MB, Orozco BM, Hanley-Bowdoin L (2007) High-frequency reversion of geminivirus replication protein mutants during infection. J Virol 81:11005–11015

    Article  CAS  PubMed  Google Scholar 

  4. Argüello-Astorga GR, Guevara-González RG, Herrera-Estrella LR, Rivera-Bustamante RF (1994) Geminivirus replication origins have a group-specific organization of iterative elements: a model for replication. Virology 203:90–100

    Article  PubMed  Google Scholar 

  5. Argüello-Astorga GR, Ruiz-Medrano R (2001) An iteron-related domain is associated to Motif 1 in the replication proteins of geminiviruses: identification of potential interacting amino acid-base pairs by a comparative approach. Arch Virol 146:1465–1485

    Article  PubMed  Google Scholar 

  6. Assunção IP, Listik AF, Barros MCS, Amorim EPR, Silva SJC, Izael OS, Ramalho-Neto CE, Lima GSA (2006) Genetic diversity of begomovirus infecting weeds in Northeastern Brazil. Planta Daninha 24:239–244

    Article  Google Scholar 

  7. Blanco L, Bernad A, Lazaro JM, Martin G, Garmendia C, Salas M (1989) Highly efficient DNA synthesis by the phage phi 29 DNA polymerase. Symmetrical mode of DNA replication. J Biol Chem 264:8935–8940

    CAS  PubMed  Google Scholar 

  8. Dean FB, Nelson JR, Giesler TL, Lasken RS (2001) Rapid amplification of plasmid and phage DNA using Phi 29 DNA polymerase and multiply-primed rolling circle amplification. Genome Res 11:1095–1099

    Article  CAS  PubMed  Google Scholar 

  9. Fauquet CM, Briddon RW, Brown JK, Moriones E, Stanley J, Zerbini M, Zhou X (2008) Geminivirus strain demarcation and nomenclature. Arch Virol 153:783–821

    Article  CAS  PubMed  Google Scholar 

  10. Fernandes FR, Cruz ARR, Faria JC, Zerbini FM, Aragao JL (2009) Three distinct begomoviruses associated with soybean in central Brazil. Arch Virol 154:1567–1570

    Article  CAS  PubMed  Google Scholar 

  11. Frischmuth T, Engel M, Lauster S, Jeske H (1997) Nucleotide sequence evidence for the occurrence of three distinct whitefly-transmitted, Sida-infecting bipartite geminiviruses in Central America. J Gen Virol 78:2675–2682

    CAS  PubMed  Google Scholar 

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

    Article  CAS  PubMed  Google Scholar 

  13. Hall TA (1999) BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser 41:95–98

  14. Hellens RP, Edwards EA, Leyland NR, Bean S, Mullineaux PM (2000) pGreen: a versatile and flexible binary Ti vector for Agrobacterium-mediated plant transformation. Plant Mol Biol 42:819–832

    Article  CAS  PubMed  Google Scholar 

  15. Jeske H, Gotthardt D, Kober S (2010) In planta cloning of geminiviral DNA: the true Sida micrantha mosaic virus. J Virol Methods 163:301–308

    Article  CAS  PubMed  Google Scholar 

  16. Jovel J, Preiß W, Jeske H (2007) Characterization of DNA intermediates of an arising geminivirus. Virus Res 130:63–70

    Article  CAS  PubMed  Google Scholar 

  17. Kleinow T, Nischang M, Beck A, Kratzer U, Tanwir F, Preiss W, Kepp G, Jeske H (2009) Three C-terminal phosphorylation sites in the Abutilon mosaic virus movement protein affect symptom development and viral DNA accumulation. Virology 390:89–101

    Article  CAS  PubMed  Google Scholar 

  18. Lizardi PM, Huang X, Zhu Z, Bray-Ward P, Thomas DC, Ward DC (1998) Mutation detection and single-molecule counting using isothermal rolling-circle amplification. Nat Genet 19:225–232

    Article  CAS  PubMed  Google Scholar 

  19. Mansoor S, Briddon RW, Zafar Y, Stanley J (2003) Geminivirus disease complexes: an emerging threat. Trends Plant Sci 8:128–134

    Article  CAS  PubMed  Google Scholar 

  20. Milne I, Wright F, Rowe G, Marshal DF, Husmeier D, McGuire G (2004) TOPALi: software for automatic identification of recombinant sequences within DNA multiple alignments. Bioinformatics 20:1806–1807

    Article  CAS  PubMed  Google Scholar 

  21. Moffat AS (1999) Geminiviruses emerge as serious crop threat. Science 286:1835

    Article  CAS  Google Scholar 

  22. Morales FJ, Anderson PK (2001) The emergence and dissemination of whitefly-transmitted geminiviruses in Latin America. Arch Virol 146:415–441

    Article  CAS  PubMed  Google Scholar 

  23. Paprotka T, Boiteux LS, Fonseca MEN, Resende RO, Jeske H, Faria JC, Ribeiro SG (2010) Genomic diversity of sweet potato geminiviruses in a Brazilian germplasm bank. Virus Res 149:224–233

    Article  CAS  PubMed  Google Scholar 

  24. Stanley J, Bisaro DM, Briddon RW, Brown JK, Fauquet CM, Harrison BD, Rybicki EP, Stenger DC (2005) Geminiviridae. In: Fauquet CM, Mayo MA, Maniloff J, Desselberger U, Ball LA (eds) Virus taxonomy. VIIIth report of the international committee on taxonomy of viruses. Elsevier/Academic Press, London, pp 301–326

  25. Stocsits RR, Hofacker IL, Fried C, Stadler PF (2005) Multiple sequence alignments of partially coding nucleic acid sequences. BMC Bioinformatics 6:160

    Article  PubMed  Google Scholar 

  26. Tamura K, Dudley J, Nei M, Kumar S (2007) MEGA4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol Biol Evol 24:1596–1599

    Article  CAS  PubMed  Google Scholar 

  27. Vincze T, Posfai J, Roberts RJ (2003) NEBcutter: a program to cleave DNA with restriction enzymes. Nucleic Acids Res 31:3688–3691

    Article  CAS  PubMed  Google Scholar 

  28. Zhang DY, Brandwein M, Hsuih TC, Li H (1998) Amplification of target-specific, ligation-dependent circular probe. Gene 211:277–285

    Article  CAS  PubMed  Google Scholar 

  29. Zhang DY, Zhang W, Li X, Konomi Y (2001) Detection of rare DNA targets by isothermal ramification amplification. Gene 274:209–216

    Article  CAS  PubMed  Google Scholar 

  30. Zhang Z, Schwartz S, Lukas W, Web M (2000) A greedy algorithm for aligning DNA sequences. J Comput Biol 7:203–214

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

We like to thank Christina Wege for critically reading the manuscript, Gaus S. A. Lima and Ulrich Kull for help with the taxonomy of host plants, and the members of the ICTV study group for intense discussions. This work was supported by a trilateral ERA-PG/BMBF project (BMBF 0313986).

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Correspondence to Holger Jeske.

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Wyant, P.S., Gotthardt, D., Schäfer, B. et al. The genomes of four novel begomoviruses and a new Sida micrantha mosaic virus strain from Bolivian weeds. Arch Virol 156, 347–352 (2011). https://doi.org/10.1007/s00705-010-0876-9

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  • DOI: https://doi.org/10.1007/s00705-010-0876-9

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