[1] Scholthof, K. B. G., Adkins, S., Czosnek, H., Palukaitis, P., Jacquot, E., Hohn, T., et al. (2011). Top 10 plant viruses in molecular plant pathology. Mol. Plant. Pathol. 12, 938–954.
[2] Feschotte, C., and Gilbert, C. (2012). Endogenous viruses: insights into viral evolution and impact on host biology. Nat. Rev. Genet. 13, 283.
[3] Wylie, S. J., Adams, M., Chalam, C., Kreuze, J., López-Moya, J. J., Ohshima, K., et al. (2017). ICTV virus taxonomy profile: Potyviridae. J. Gen. Virol. 98, 352.
[4] Liu, J., Liu, Y., Donkersley, P., Dong, Y., Chen, X., Zang, Y., et al. (2019). Preference of the aphid Myzus persicae (Hemiptera: Aphididae) for tobacco plants at specific stages of potato virus Y infection. Arch. Virol. 164, 1567–1573.
[5] Quenouille, J., Vassilakos, N., and Moury, B. (2013). Potato virus Y: a major crop pathogen that has provided major insights into the evolution of viral pathogenicity. Mol. Plant. Patho.14, 439–452.
[6] Lacroix, C., Glais, L., Kerlan, C., Verrier, J. L., and Jacquot, E. (2010). Biological characterization of French Potato virus Y (PVY) isolates collected from PVY-susceptible or-resistant tobacco plants possessing the recessive resistance gene va. Plant Pathol. 59, 1133–1143.
[7] Joshi, R. K., and Nayak, S. (2010). Gene pyramiding-A broad spectrum technique for developing durable stress resistance in crops. Biotechnol. Mol. Biol. Rev.,, 5, 51–60.
[8] Scott, J. M. (2006). Breeding for resistance to viral pathogens. Genetic improvement of solanaceous crops, 2, 457–485.
[9] Peleg, Z., and Blumwald, E. (2011). Hormone balance and abiotic stress tolerance in crop plants. Curr. Opin. Plant Biol. 14, 290–295.
[10] Van Wees, S. C., De Swart, E. A., Van Pelt, J. A., Van Loon, L. C., and Pieterse, C. M. (2000). Enhancement of induced disease resistance by simultaneous activation of salicylate-and jasmonate-dependent defense pathways in Arabidopsis thaliana. P. Natl. A Sci. India. B. 97, 8711–8716.
[11] Ryu, C. M., Murphy, J. F., Mysore, K. S., and Kloepper, J. W. (2004). Plant growth-promoting rhizobacteria systemically protect Arabidopsis thaliana against Cucumber mosaic virus by a salicylic acid and NPR1-independent and jasmonic acid-dependent signaling pathway. Plant J. 39, 381–392.
[12] Zhu, F., Xi, D. H., Yuan, S., Xu, F., Zhang, D. W., and Lin, H. H. (2014). Salicylic acid and jasmonic acid are essential for systemic resistance against tobacco mosaic virus in Nicotiana benthamiana. Mol. Plant Microbe. In. 27, 567–577.
[13] Nessler, C. L., Kurz, W. G., and Pelcher, L. E. (1990). Isolation and analysis of the major latex protein genes of opium poppy. Plant Mol. Biol. 15, 951–953.
[14] Nessler, C. L., & Burnett, R. J. (1992). Organization of the major latex protein gene family in opium poppy. Plant Mol. Biol. 20, 749–752.
[15] Radauer, C., Lackner, P., and Breiteneder, H. (2008). The Bet v 1 fold: an ancient, versatile scaffold for binding of large, hydrophobic ligands. BMC Evol. Biol. 8, 286.
[16] Aggelis, A., John, I., Karvouni, Z., and Grierson, D. (1997). Characterization of two cDNA clones for mRNAs expressed during ripening of melon (Cucumis melo L.) fruits. Plant Mol. Biol. 33, 313–322.
[17] Wu, F. Z., Lu, T. C., Shen, Z., Wang, B.C., and Wang, H. X. (2008). N-terminal acetylation of two major latex proteins from Arabidopsis thaliana using electrospray ionization tandem mass spectrometry.Plant Mol. Biol. Rep. 26, 88–97.
[18] Nam, Y. W., Tichit, L., Leperlier, M., Cuerq, B., Marty, I., and Lelièvre, J. M. (1999). Isolation and characterization of mRNAs differentially expressed during ripening of wild strawberry (Fragaria vesca L.) fruits. Plant Mol. Biol. 39, 629–636.
[19] Suyama, T., Yamada, K., Mori, H., Takeno, K., and Yamaki, S. (1999). Cloning cDNAs for genes preferentially expressed during fruit growth in cucumber. J Am. Soc. Hortic. Sci. 124, 136–139.
[20] Pozueta-Romero, J., Klein, M., Houlné, G., Schantz, M. L., Meyer, B., and Schantz, R. (1995). Characterization of a family of genes encoding a fruit-specific wound-stimulated protein of bell pepper (Capsicum annuum): identification of a new family of transposable elements. Plant Mol. Biol, 28, 1011–1025.
[21] Stanley Kim, H., Yu, Y., Snesrud, E. C., Moy, L. P., Linford, L. D., Haas, B. J., et al. (2005). Transcriptional divergence of the duplicated oxidative stress-responsive genes in the Arabidopsis genome. Plant J. 41, 212–220.
[22] Schenk, P.M., Kazan, K., Wilson, I., Anderson, J. P., Richmond, T., Somerville, S. C., et al. (2000). Coordinated plant defense responses in Arabidopsis revealed by microarray analysis. P. Natl. A. Sci. 97, 11655–11660.
[23] Siemens, J., Keller, I., Sarx, J., Kunz, S., Schuller, A., Nagel, W., et al. (2006). Transcriptome analysis of Arabidopsis clubroots indicate a key role for cytokinins in disease development. Mol. Plant Microbe. In. 19, 480–494.
[24] Malter, D., and Wolf, S. (2011). Melon phloem-sap proteome: developmental control and response to viral infection.Protoplasma. 248, 217–224.
[25] Guex, N., and Peitsch, M. C. (1997). SWISS-MODEL and the Swiss-Pdb Viewer: an environment for comparative protein modeling. Electrophoresis. 18, 2714–2723.
[26] Kumar, S., Stecher, G., and Tamura, K. (2016). MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol 33(7), 1870–1874.
[27] Liu, Y., Schiff, M., and Dinesh-Kumar, S. P. (2002). Virus-induced gene silencing in tomato. Plant J. 31, 777–786.
[28] Sun, H., Shen, L., Qin, Y., Liu, X., Hao, K., Li, Y., et al. (2018). CLC-Nt1 affects Potato Virus Y infection via regulation of endoplasmic reticulum luminal Ph. New Phytol. 220, 539–552.
[29] Livak, K. J., and Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2 − CT method. Methods. 25,402–408.
[30] Chen, J. Y., and Dai, X. F. (2010). Cloning and characterization of the Gossypium hirsutum major latex protein gene and functional analysis in Arabidopsis thaliana. Planta. 231, 861–873.
[31] Kunkel, B. N., and Brooks, D. M. (2002). Cross talk between signaling pathways in pathogen defense. Curr. Opin. Plant. Biol. 5, 325–331.
[32] Zhu, F., Xi, D. H., Deng, X. G., Peng, X. J., Tang, H., Chen, Y. J., et al. (2014). The chilli veinal mottle virus regulates expression of the tobacco mosaic virus resistance gene N and jasmonic acid/ethylene signaling is essential for systemic resistance against chilli veinal mottle virus in tobacco. Plant Mol. Biol. Rep. 32, 382–394.
[33] Heberle-Bors, E., and Vicente, O. (1996). Bet v 1 proteins, the major birch pollen allergens and members of a family of conserved pathogenesis-related proteins, show ribonuclease activity in vitro. Physiol. Plantarum.96, 433–438.
[34] Liu, J. J., and Ekramoddoullah, A. K. (2006). The family 10 of plant pathogenesis-related proteins: their structure, regulation, and function in response to biotic and abiotic stresses. Physiol. Mol. Plant P. 68, 3–13.
[35] Swoboda, I., Hoffmann-Sommergruber, K., O’Ríordáin, G., Scheiner, O., Jain, S., and Kumar, A. (2015). The pathogenesis related class 10 proteins in plant defense against biotic and abiotic stresses. Adv Plants Agric Res. 3, 00077.
[36] Babu, M., Griffiths, J. S., Huang, T. S., & Wang, A. (2008). Altered gene expression changes in Arabidopsis leaf tissues and protoplasts in response to Plum pox virus infection. BMC GENOMICS. 9(1), 325.
[37] Qu, Z. L., Wang, H. Y., and Xia, G. X. (2005). GhHb1: a nonsymbiotic hemoglobin gene of cotton responsive to infection by Verticillium dahliae. Biochimica et Biophysica Acta (BBA)-Gene Structure and Expression. 1730, 103–113.
[38] Wang, F. X., Ma, Y. P., Yang, C. L., Zhao, P.M., Yao, Y., Jian, G. L., et al. (2011). Proteomic analysis of the sea-island cotton roots infected by wilt pathogen Verticillium dahliae. Proteomics. 11 4296–4309.
[39] Zhang, W. W., Jian, G. L., Jiang, T. F., Wang, S. Z., Qi, F. J., and Xu, S. C. (2012). Cotton gene expression profiles in resistant Gossypium hirsutum cv. Zhongzhimian KV1 responding to Verticillium dahliae strain V991 infection. Mol. Biol. Rep. 39, 9765–9774.
[40] Yang, C. L., Liang, S., Wang, H. Y., Han, L. B., Wang, F. X., Cheng, H. Q., et al. (2015). Cotton major latex protein 28 functions as a positive regulator of the ethylene responsive factor 6 in defense against Verticillium dahliae. Mol. Plant. 8, 399–411.
[41] Wang, Y., Yang, L., Chen, X., Ye, T., Zhong, B., Liu, R., et al. (2015). Major latex protein-like protein 43 (MLP43) functions as a positive regulator during abscisic acid responses and confers drought tolerance in Arabidopsis thaliana. J Exp Bot. 67, 421–434.
[42] Ruperti, B., Bonghi, C., Ziliotto, F., Pagni, S., Rasori, A., Varotto, S., et al. (2002). Characterization of a major latex protein (MLP) gene down-regulated by ethylene during peach fruitlet abscission. Plant Sci. 163, 265–272.
[43] Chruszcz, M., Ciardiello, M. A., Osinski, T., Majorek, K. A., Giangrieco, I., Font, J., et al. (2013). Structural and bioinformatic analysis of the kiwifruit allergen Act d 11, a member of the family of ripening-related proteins. Mol. Immunol, 56, 794–803.