Education
Ph.D. in Molecular Biology, University of Konstanz, Germany, 1992
Current position
Tenured Scientist, Departamento de Biología del Estrés y Patología, Centro de Edafología y Biología Aplicada del Segura (CEBAS), Consejo Superior de Investigaciones Científicas (CSIC), Murcia, Spain
Publications
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Miras, M., Sempere, R. N., Kraft, J. J., Miller, W. A., Aranda, M. A. and Truniger, V. (2014). Interfamilial recombination between viruses led to acquisition of a novel translation-enhancing RNA element that allows resistance breaking. New Phytol 202(1): 233-246.
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Juarez, M., Legua, P., Mengual, C. M., Kassem, M. A., Sempere, R. N., Gómez, P., Truniger, V., and Aranda, M. A. (2013). Relative incidence, spatial distribution and genetic diversity of cucurbit viruses in eastern Spain. Ann Appl Biol 162(3): 362-370.
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Rodriguez-Hernandez, A. M., Gosalvez, B., Sempere, R. N., Burgos, L., Aranda, M. A. and Truniger, V. (2012). Melon RNA interference (RNAi) lines silenced for Cm-eIF4E show broad virus resistance. Mol Plant Pathol 13(7): 755-763.
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Gonzalez-Ibeas, D., Blanca, J., Cañizares, J., Blanca, V., Truniger and Aranda, M. A. (2012). A cost-effective double-stranded cDNA synthesis for plant microarrays. Plant Mol Biol Rep 30(5): 1276-1282.
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Clepet, C., Joobeur, T., Zheng, Y., Jublot, D., Huang, M., Truniger, V., Boualem, A., Hernandez-Gonzalez, M. E., Dolcet-Sanjuan, R., Portnoy, V., Mascarell-Creus, A., Cano-Delgado, A. I., Katzir, N., Bendahmane, A., Giovannoni, J. J., Aranda, M. A., Garcia-Mas, J. and Fei, Z. (2011). Analysis of expressed sequence tags generated from full-length enriched cDNA libraries of melon. BMC Genomics 12: 252.
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Sempere, R. N., Gomez, P., Truniger, V. and Aranda, M. A. (2011). Development of expression vectors based on pepino mosaic virus. Plant Methods 7: 6.
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Nieto, C., Rodriguez-Moreno, L., Rodriguez-Hernandez, A. M., Aranda, M. A. and Truniger, V. (2011). Nicotiana benthamiana resistance to non-adapted Melon necrotic spot virus results from an incompatible interaction between virus RNA and translation initiation factor 4E. Plant J 66(3): 492-501.
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Truniger, V., Aranda, M. A. (2009). Recessive resistance to plant viruses. Adv Virus Res 75: 119-231.
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Truniger, V., Nieto, C., Gonzalez-Ibeas, D. and Aranda, M. (2008). Mechanism of plant eIF4E-mediated resistance against a Carmovirus (Tombusviridae): cap-independent translation of a viral RNA controlled in cis by an (a)virulence determinant. Plant J 56(5): 716-727.
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Gonzalez-Ibeas, D., Blanca, J., Roig, C., Gonzalez-To, M., Pico, B., Truniger, V., Gomez, P., Deleu, W., Cano-Delgado, A., Arus, P., Nuez, F., Garcia-Mas, J., Puigdomenech, P. and Aranda, M. A. (2007). MELOGEN: an EST database for melon functional genomics. BMC Genomics 8: 306.
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Kassem, M. A., Sempere, R. N., Juárez, M., Aranda, M. A. and Truniger, V. (2007). Cucurbit aphid-borne yellows virus is prevalent in field-grown cucurbit crops of southeastern Spain. Plant Disease 91(3): 232-238.
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Nieto, C., Piron, F., Dalmais, M., Marco, C. F., Moriones, E., Gomez-Guillamon, M. L., Truniger, V., Gomez, P., Garcia-Mas, J., Aranda, M. A. and Bendahmane, A. (2007). EcoTILLING for the identification of allelic variants of melon eIF4E, a factor that controls virus susceptibility. BMC Plant Biol 7: 34.
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Trunige, V., Kassem, M. and Aranda, M. A. (2006). Cucurbit yellow stunting disorder virus (CYSDV). In: Rao, G., Kumar, L. and Holguín-Peña, R. (eds). Characterization, diagnosis and manegement of plant viruses. Studium Press, 283-301.
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Truniger, V., Bonnin, A., Lazaro, J. M., de Vega, M. and Salas, M. (2005). Involvement of the "linker" region between the exonuclease and polymerization domains of phi29 DNA polymerase in DNA and TP binding. Gene 348: 89-99.
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Juarez, M., Truniger, V. and Aranda, M. A. (2004). First report of Cucurbit aphid-borne yellows virus in Spain. Plant Disease 88(8): 907-907.
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Truniger, V., Nieto, C., Juan A. D. and Aranda, M. A. (2004). A Melon necrotic spot virus untranslated RNA sequence is the genetic avirulence determinant for both cultivar and non-host resistances. Int Proc. 2nd European Congress of Virology 7-10.
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Diaz-Pendon, J. A., Truniger, V., Nieto, C., Garcia-Mas, J., Bendahmane, A. and Aranda, M. A. (2004). Advances in understanding recessive resistance to plant viruses. Mol Plant Pathol 5(3): 223-233.
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Diaz, J. A., Nieto, C., Moriones, E., Truniger, V. and Aranda, M. A. (2004). Molecular characterization of a Melon necrotic spot virus strain that overcomes the resistance in melon and nonhost plants. Mol Plant Microbe Interact 17(6): 668-675.
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Truniger, V., Lázaro, J. M. and Salas, M. (2004). Two positively charged residues of ø 29 DNA polymerase, conserved in protein-primed DNA polymerases are involved in stabilization of the incoming nucleotide. J Mol Biol 335: 481-494.
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Truniger, V., Lazaro, J. M. and Salas, M. (2004). Function of the C-terminus of phi29 DNA polymerase in DNA and terminal protein binding. Nucleic Acids Res 32(1): 361-370.
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Truniger, V., Lázaro, J. M., de Vega, M., Blanco, L. and Salas, M. (2003). ϕ29 DNA polymerase residue Leu384, highly conserved in motif B of eukaryotic type DNA replicases, is involved in nucleotide insertion fidelity. J Biol Chem 278(35): 33482-33491.
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Aguilar, J. M., Franco, M., Marco, C. F., Berdiales, B., Rodriguez-Cerezo, E., Truniger, V. and Aranda, M. A. (2003). Further variability within the genus Crinivirus, as revealed by determination of the complete RNA genome sequence of Cucurbit yellow stunting disorder virus. J Gen Virol 84(Pt 9): 2555-2564.
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Truniger, V., Lazaro, J. M., Esteban, F. J., Blanco, L. and Salas, M. (2002). A positively charged residue of phi29 DNA polymerase, highly conserved in DNA polymerases from families A and B, is involved in binding the incoming nucleotide. Nucleic Acids Res 30(7): 1483-1492.
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Truniger, V., Lazaro, J. M., Blanco, L. and Salas, M. (2002). A highly conserved lysine residue in phi29 DNA polymerase is important for correct binding of the templating nucleotide during initiation of phi29 DNA replication. J Mol Biol 318(1): 83-96.
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Brenkman, A. B., Heideman, M. R., Truniger, V., Salas, M. and van der Vliet, P. C. (2001). The (I/Y)XGG motif of adenovirus DNA polymerase affects template DNA binding and the transition from initiation to elongation. J Biol Chem 276(32): 29846-29853.
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Truniger, V., Blanco, L. and Salas, M. (2000). Analysis of O29 DNA polymerase by partial proteolysis: binding of terminal protein in the double-stranded DNA channel. J Mol Biol 295(3): 441-453.
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Truniger, V., Blanco, L. and Salas, M. (1999). Role of the "YxGG/A" motif of Phi29 DNA polymerase in protein-primed replication. J Mol Biol 286(1): 57-69.
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Truniger, V., Lazaro, J. M., Salas, M. and Blanco, L. (1998). Phi 29 DNA polymerase requires the N-terminal domain to bind terminal protein and DNA primer substrates. J Mol Biol 278(4): 741-755.
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Truniger, V., Lazaro, J. M., Salas, M. and Blanco, L. (1996). A DNA binding motif coordinating synthesis and degradation in proofreading DNA polymerases. EMBO J 15(13): 3430-3441.
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Truniger, V. and Boos, W. (1994). Mapping and cloning of gldA, the structural gene of the Escherichia coli glycerol dehydrogenase. J Bacteriol 176(6): 1796-1800.
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Truniger, V. and Boos, W. (1993). Glycerol uptake in Escherichia coli is sensitive to membrane lipid composition. Res Microbiol 144(7): 565-574.
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Truniger, V., Boos, W. and Sweet, G. (1992). Molecular analysis of the glpFKX regions of Escherichia coli and Shigella flexneri. J Bacteriol 174(21): 6981-6991.
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Sweet, G., Gandor, C., Voegele, R., Wittekindt, N., Beuerle, J., Truniger, V., Lin, E. C. and Boos, W. (1990). Glycerol facilitator of Escherichia coli: cloning of glpF and identification of the glpF product. J Bacteriol 172(1): 424-430.