P. Cournoyer and S. P. Dineskumar, NB-LRR Immune receptors in plant virus defence, Recent advances in plant virology, pp.149-176, 2011.

V. Truniger and M. A. Aranda, Recessive resistance to plant viruses, Adv Virus Res, vol.75, pp.119-159, 2009.
URL : https://hal.archives-ouvertes.fr/hal-02682496

L. Fernandez-calvino, L. Donaire, and C. Lliave, RNA silencing and the interplay between plants and viruses, Recent advances in plant virology, pp.121-136, 2011.

C. Robaglia and C. Caranta, Translation initiation factors: a weak link in plant RNA virus infection, Trends Plant Sci, vol.11, pp.40-45, 2006.
URL : https://hal.archives-ouvertes.fr/hal-02666136

K. S. Browning, The plant translational apparatus, Plant Mol Biol, vol.32, pp.107-144, 1996.

J. P. Combe, M. E. Petracek, G. Van-eldik, and F. Meulewaeter, Translation initiation factors eIF4E and eIFiso4E are required for polysome formation and regulate plant growth in tobacco, Plant Mol Biol, vol.57, pp.749-760, 2005.

D. R. Gallie and K. S. Browning, eIF4G functionally differs from eIFiso4G in promoting internal initiation, cap-independent translation, and translation of structured mRNAs, J Biol Chem, vol.276, pp.36951-36960, 2001.

C. M. Rodriguez, M. A. Freire, C. Camilleri, and C. Robaglia, The Arabidopsis thaliana cDNAs coding for eIF4E and eIF(iso)4E are not functionally equivalent for yeast complementation and are differentially expressed during plant development, Plant J, vol.13, pp.465-473, 1998.

F. Piron, M. Nicolaï, S. Minoïa, E. Piednoir, and A. Moretti, An induced mutation in tomato eIF4E leads to immunity to two potyviruses, PLoS ONE, vol.5, issue.6, pp.11313-11314, 2010.
URL : https://hal.archives-ouvertes.fr/hal-02658059

N. Stein, D. Perovic, J. Kumlehn, B. Pellio, and S. Stracke, The eukaryotic translation initiation factor 4E confers multiallelic recessive Bymovirus resistance in Hordeum vulgare (L.), Plant J, vol.42, pp.912-922, 2005.

C. Nieto, M. Morales, G. Orjeda, C. Clepet, and A. Montfart, An eIF4E allele confers resistance to an uncapped and non-polyadenylated RNA virus in melon, Plant J, vol.48, pp.452-462, 2006.
URL : https://hal.archives-ouvertes.fr/hal-02662906

L. Gall, O. Aranda, M. Caranta, and C. , Plant resistance to viruses mediated by translation initiation factors, Recent advances in plant virology, pp.177-194, 2011.

I. Yeam, J. R. Cavatorta, D. R. Ripoll, B. Kang, and M. M. Jahn, Functional dissection of naturally occurring amino acid substitutions in eIF4E that confers recessive potyvirus resistance in plants, Plant Cell, vol.19, pp.2913-2928, 2007.

C. Charron, M. Nicolaï, J. L. Gallois, C. Robaglia, and B. Moury, Natural variation and functional analyses provide evidence for co-evolution between plant eIF4E and potyviral VPg, Plant J, vol.54, pp.56-68, 2008.
URL : https://hal.archives-ouvertes.fr/hal-02667924

S. P. Rodrigues, G. G. Lindsey, and P. Fernandes, Biotechnological approaches for plant viruses resistance: from general to the modern RNA silencing pathway, Braz Arch Biol Technol, vol.52, pp.795-808, 2009.

A. Frizzi and S. Huang, Trapping RNA silencing pathways for plant biotechnology, Plant Biotech J, vol.8, pp.655-677, 2010.

S. H. Wani, G. S. Sanghera, and N. Singh, Biotechnology and plant disease control -role of RNA interference, American Journal of Plant Sciences, vol.1, pp.55-68, 2010.

M. Asano, R. Satoh, A. Mochizuki, S. Tsuda, and T. Yamanaka, Tobamovirus-resistant tobacco generated by RNA interference directed against host genes, FEBS Letters, vol.579, pp.4479-4484, 2005.

C. M. Mccallum, L. Comai, E. A. Greene, and S. Henikoff, Targeting induced local lesions in genomes (TILLING) for plant functional genomics, Plant Physiol, vol.123, pp.439-442, 2000.

S. Ruffel, J. L. Gallois, M. L. Lesage, and C. Caranta, The recessive potyvirus resistance gene pot-1 is the tomato orthologue of the pepper pvr2-eIF4E gene, Mol Genet Genomics, vol.274, pp.346-353, 2005.
URL : https://hal.archives-ouvertes.fr/hal-02678329

S. Ruffel, J. L. Gallois, B. Moury, C. Robaglia, and A. Palloix, Simultaneous mutations in translation initiation factors eIF4E and eIF(iso)4E are required to prevent Pepper veinal mottle virus infection in pepper, J Gen Virol, vol.87, pp.2089-2098, 2006.

J. N. Hwang, J. Li, W. Liu, A. Cho, and H. , Double mutations in eIF4E and eIFiso4E confer recessive resistance to Chilli veinal mottle virus in pepper, Mol Cells, vol.27, pp.329-336, 2009.

C. E. Jenner, C. F. Nellist, G. C. Barker, and J. A. Walsh, Turnip mosaic virus (TuMV) is able to use alleles of both eIF4E and eIF(iso)4E from multiple loci of the diploid Brassica rapa, Mol Plant-Microbe Int, vol.23, pp.1498-1505, 2010.

A. Duprat, C. Caranta, F. Revers, B. Menand, and K. S. Browning, The Arabidopsis eukaryotic initiation factor (iso)4E is dispensable for plant growth but required for susceptibility to potyviruses, Plant J, vol.32, pp.927-934, 2002.
URL : https://hal.archives-ouvertes.fr/hal-02673279

M. Karimi, D. Inzé, and A. Depicker, GATEWAY TM vectors for Agrobacteriummediated plant transformation, TRENDS Plant Sci, vol.7, pp.193-195, 2002.

S. Hamza and Y. Chupeau, Re-evaluation of conditions for plant regeneration and Agrobacterium-mediated transformation from tomato (Lycopersicon esculentum), J Exp Bot, vol.44, pp.1837-1845, 1993.
URL : https://hal.archives-ouvertes.fr/hal-02708063

S. Mccormick, J. Niedermeyer, J. Fry, A. Barnason, and R. Horsch, Leaf disc transformation of cultivated tomato (L. esculentum) using Agrobacterium tumefaciens, Plant Cell Rep, vol.5, pp.81-84, 1986.

R. Bernatzky and S. D. Tanksley, Genetics of actin-related sequences in tomato, Theor Appl Genet, vol.72, pp.314-315, 1986.

V. Dubois, E. Botton, C. Meyer, A. Rieu, and M. Bedu, Systematic silencing of a tobacco nitrate reductase transgene in lettuce (Lactuca sativa L.), J Exp Bot, vol.56, pp.2379-2388, 2005.
URL : https://hal.archives-ouvertes.fr/hal-02679777

P. Dunoyer, C. Lecellier, E. A. Parizotto, C. Himber, and O. Voinnet, Probing the microRNA and small interfering RNA pathways with virus-encoded suppressors of RNA silencing, Plant Cell, vol.16, pp.1235-1250, 2004.

G. Selassié, K. Marchoux, G. Delecolle, B. Pochard, and E. , Variabilité naturelle des souches du virus Y de la pomme de terre dans les cultures de piment du sud-est de la France, Caractérisation et classification en pathotypes. Agronomie, vol.5, pp.621-630, 1985.

B. Moury, C. Morel, E. Johansen, L. Guilbaud, and S. Souche, Mutations in Potato virus Y genome-linked protein determine virulence toward recessive resistances in Capsicum annuum and Lycopersicon hirsutum, Plant-Microbe Int, vol.17, pp.322-329, 2004.
URL : https://hal.archives-ouvertes.fr/hal-02682733

R. Allison, R. E. Johnston, and W. G. Dougherty, The nucleotide sequence of the coding region of tobacco etch virus genomic RNA: Evidence for the synthesis of a single polyprotein, Virology, vol.154, pp.9-20, 1986.

B. Janzac, M. Fabre, A. Palloix, and B. Moury, Characterization of a new potyvirus infecting pepper crops in Ecuador, Arch Virol, vol.153, pp.1543-1548, 2008.
URL : https://hal.archives-ouvertes.fr/hal-02662692

J. M. Feldman and O. Garcia, Pepper severe mosaic virus: a new potyvirus from pepper in Argentina, Phytopathol, vol.73, pp.115-122, 1977.

A. K. Inoue-nagata, M. Fonseca, R. O. Resende, L. S. Boiteux, and D. C. Monte, Pepper yellow mosaic virus, a new potyvirus in sweet pepper, Capsicum annuum, Arch Virol, vol.147, pp.849-855, 2002.

V. Vance, D. Moore, T. Turpen, A. Bracker, and V. Hollowell, The complete nucleotide sequence of pepper mottle virus genomic RNA: comparison of the encoded polyprotein with those of other sequenced potyviruses, Virology, vol.191, pp.19-30, 1992.

C. Spetz, A. M. Taboada, S. Darwich, J. Ramsell, and L. F. Salazar, Molecular resolution of a complex of potyviruses infecting solanaceous crops at the centre of origin in Peru, J Gen Virol, vol.84, pp.2565-2578, 2003.

H. Kruskal and W. A. Wallis, Use of ranks in one-criterion variance analysis, J Am Stat Ass, vol.47, pp.583-621, 1952.