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• Álvarez, C., García, I., Moreno, I., Pérez-Pérez, M.E., Crespo, J.L., Romero, L.C., Gotor, C., Cysteine-generated sulfide in the cytosol negatively regulates autophagy and modulates the transcriptional profile in Arabidopsis (2012) Plant Cell, 24, pp. 4621-4634
• Bethke, G., Grundman, R.E., Sreekanta, S., Truman, W., Katagiri, F., Glazebrook, J., Arabidopsis pectin methylesterases contribute to immunity against Pseudomonas syringae (2014) Plant Physiol., 164, pp. 1093-1107
• Bilgin, D.D., Zavala, J.A., Zhu, J., Clough, S.J., Ort, D.R., De Lucia, E.H., Biotic stress globally downregulates photosynthesis genes (2010) Plant Cell Environ., 33, pp. 1597-1613
• Castillo, P., Escalante, M., Gallardo, M., Alemano, S., Abdala, G., Effects of bacterial single inoculation and co-inoculation on growth and phytohormone production of sunflower seedlings under water stress (2013) Acta Physiol. Plant., 35, pp. 2299-2309
• Cernadas, R.A., Camillo, L.R., Benedetti, C.E., Transcriptional analysis of the sweet orange interaction with the citrus canker pathogens Xanthomonas axonopodis pv. citri and Xanthomonas axonopodis pv. aurantifolii (2008) Mol. Plant Pathol., 9, pp. 609-631
• Chen, P.S., Wang, L.Y., Chen, Y.J., Tzeng, K.C., Chang, S.C., Chung, K.R., Lee, M.H., Understanding cellular defence in kumquat and calamondin to citrus canker caused by Xanthomonas citri subsp. citri (2012) Physiol. Mol. Plant Pathol., 79, pp. 1-12
• Chi, Y.H., Paeng, S.K., Kim, M.J., Hwang, G.Y., Melencion, S.M.B., Oh, H.T., Lee, S.Y., Redox-dependent functional switching of plant proteins accompanying with their structural changes (2013) Front. Plant Sci., 4, p. 277
• Chiesa, M.A., Siciliano, M.F., Ornella, L., Roeschlin, R.A., Favaro, M.A., Delgado, N.P., Sendín, L.N., Marano, M.R., Characterization of a variant of Xanthomonas citri subsp. citri that triggers a host-specific defense response (2013) Phytopathology, 103, pp. 555-564
• Deng, Z.N., Xu, L., Li, D.Z., Long, G.Y., Liu, L.P., Fang, F., Shu, G.P., Screening citrus genotypes for resistance to canker disease (Xanthomonas axonopodis pv. citri) (2010) Plant Breeding, 129, pp. 341-345
• van Doorn, W.G., Beers, E.P., Dangl, J.L., Franklin-Tong, V.E., Gallois, P., Hara-Nishimura, I., Jones, A.M., Bozhkov, P.V., Morphological classification of plant cell deaths (2011) Cell Death Differ., 18, pp. 1241-1246
• Duan, Y.P., Castaneda, A., Zhao, G., Erdos, G., Gabriel, D.W., Expression of a single, host-specific, bacterial pathogenicity gene in plant cells elicits division, enlargement, and cell death (1999) Mol. Plant–Microbe Interact., 12, pp. 556-560
• Durgbanshi, A., Arbona, V., Pozo, O., Miersch, O., Sancho, J.V., Gomez-Cadenas, A., Simultaneous determination of multiple phytohormones in plant extracts by liquid chromatography-electrospray tandem mass spectrometry (2005) J. Agric. Food Chem., 53, pp. 8437-8442
• Enrique, R., Siciliano, F., Favaro, M.A., Gerhardt, N., Roeschlin, R., Rigano, L., Sendín, L., Marano, M.R., Novel demonstration of RNAi in citrus reveals importance of citrus callose synthase in defence against Xanthomonas citri subsp. citri (2011) Plant Biotechnol. J., 9, pp. 394-407
• Escalon, A., Javegny, S., Vernière, C., Noel, L.D., Vital, K., Poussier, S., Hajri, A., Gagnevin, L., Variations in type III effector repertoires, pathological phenotypes and host range of Xanthomonas citri pv. citri pathotypes (2013) Mol. Plant Pathol., 14, pp. 483-496
• Falcone, M.L.F., Rius, S., Emiliani, J., Pourcel, L., Feller, A.J., Morohashi, K., Casati, P., Grotewold, E., Cloning and characterization of an UV-B-inducible maize flavonol synthase (2010) Plant J., 62, pp. 77-91
• Falcone, M.L.F., Emiliani, J., Rodriguez, E.J., Campos-Bermudez, V.A., Grotewold, E., Casati, P., The identification of maize and Arabidopsis type I flavone synthases links flavones with hormones and biotic interactions (2015) Plant Physiol., 169, pp. 1090-1107
• Favaro, M.A., Micheloud, N.G., Roeschlin, R.A., Chiesa, M.A., Castagnaro, A.P., Vojnov, A.A., Gmitter, F.G., Jr., Marano, M.R., Surface barriers of mandarin ‘Okitsu’ leaves make a major contribution to canker disease resistance (2014) Phytopathology, 104, pp. 970-976
• Febres, V.J., Khalaf, A., Gmitter, F.G., Jr., Moore, G.A., Evaluating gene expression responses of citrus to two types of defense inducers using a newly developed citrus Agilent microarray (2012) Acta Hortic., 929, pp. 59-64
• Fu, X.Z., Gong, X.Q., Zhang, Y.X., Wang, Y., Liu, J.H., Different transcriptional response to Xanthomonas citri subsp. citri between kumquat and sweet orange with contrasting canker tolerance (2012) PLoS One, 7
• Fu, Z.Q., Dong, X., Systemic acquired resistance: turning local infection into global defense (2013) Annu. Rev. Plant Biol., 64, pp. 839-863
• Graham, J.H., Gottwald, T.R., Cubero, J., Achor, D.S., Xanthomonas axonopodis pv. citri: factors affecting successful eradication of citrus canker (2004) Mol. Plant Pathol., 1, pp. 1-15
• Hatsugai, N., Iwasaki, S., Tamura, K., Kondo, M., Fuji, K., Ogasawara, K., Nishimura, M., Hara-Nishimura, I., A novel membrane fusion-mediated plant immunity against bacterial pathogens (2009) Genes Dev., 23, pp. 2496-2506
• Hauck, P., Thilmony, R., He, S.Y., A Pseudomonas syringae type III effector suppresses cell wall-based extracellular defense in susceptible Arabidopsis plants (2003) Proc. Natl. Acad. Sci. USA, 100, pp. 8577-8582
• Hernandez-Blanco, C., Feng, D.X., Hu, J., Sanchez-Vallet, A., Deslandes, L., Llorente, F., Berrocal-Lobo, M., Molina, A., Impairment of cellulose synthases required for Arabidopsis secondary cell wall formation enhances disease resistance (2007) Plant Cell, 19, pp. 890-903
• Hofius, D., Schultz-Larsen, T., Joensen, J., Tsitsigiannis, D.I., Petersen, N.H.T., Mattsson, O., Jørgensen, L.B., Petersen, M., Autophagic components contribute to hypersensitive cell death in Arabidopsis (2009) Cell, 37, pp. 773-783
• Hofius, D., Munch, D., Bressendorff, S., Mundy, J., Petersen, M., Role of autophagy in disease resistance and hypersensitive response-associated cell death (2011) Cell Death Differ., 18, pp. 1257-1262
• Jones, J.D., Dangl, J.L., The plant immune system (2006) Nature, 444, pp. 323-329
• Kabbage, M., Williams, B., Dickman, M.B., Cell death control: the interplay of apoptosis and autophagy in the pathogenicity of Sclerotinia sclerotiorum (2013) PLoS Pathog., 9
• Kadota, Y., Sklenar, J., Derbyshire, P., Stransfeld, L., Asai, S., Ntoukakis, V., Jones, J.D., Zipfel, C., Direct regulation of the NADPH oxidase RBOHD by the PRR-associated kinase BIK1 during plant immunity (2014) Mol. Cell, 54, pp. 43-55
• Karpinski, S., Szechynska-Hebda, M., Wituszynska, W., Burdiak, P., Light acclimation, retrograde signalling, cell death and immune defences in plants (2013) Plant Cell Environ., 36, pp. 736-744
• Kazan, K., Lyons, R., Intervention of phytohormone pathways by pathogen effectors (2014) Plant Cell, 26, pp. 2285-2309
• Khalaf, A.A., Gmitter, F.G., Jr., Conesa, A., Dopazo, J., Moore, G.A., Fortunella margarita transcriptional reprogramming triggered by Xanthomonas citri subsp. citri (2011) BMC Plant Biol., 159
• Koch, E., Slusarenko, A., Arabidopsis is susceptible to infection by a downy mildew fungus (1990) Plant Cell, 2, pp. 437-445
• Lee, I.J., Kim, K.W., Hyun, J.W., Lee, Y.H., Park, E.W., Comparative ultrastructure of nonwounded Mexican lime and Yuzu leaves infected with the citrus canker bacterium Xanthomonas citri pv. citri (2009) Microsci. Res. Technol., 72, pp. 507-516
• Lenz, H.D., Haller, E., Melzer, E., Kober, K., Wurster, K., Stahl, M., Bassham, D.C., Nürnberger, T., Autophagy differentially controls plant basal immunity to biotrophic and necrotrophic pathogens (2011) Plant J., 66, pp. 818-830
• Liu, Y., Schiff, M., Czymmek, K., Talloczy, Z., Levine, B., Dinesh-Kumar, S.P., Autophagy regulates programmed cell death during the plant innate immune response (2005) Cell, 121, pp. 567-577
• Liu, Y., Ren, D., Pike, S., Pallardy, S., Gassmann, W., Zhang, S., Chloroplast-generated reactive oxygen species are involved in hypersensitive response-like cell death mediated by a mitogen-activated protein kinase cascade (2007) Plant J., 51, pp. 941-954
• Livak, K.J., Schmittgen, T.D., Analysis of relative gene expression data using real-time quantitative PCR and the 2(–Delta Delta C(T)) method (2001) Methods, 25, pp. 402-408
• Lux, A., Morita, S., Abe, J., Ito, K., An improved method for clearing and staining free-hand sections and whole-mount samples (2005) Ann. Bot., 96, pp. 989-996
• Macho, A.P., Zipfel, C., Targeting of plant pattern recognition receptor-triggered immunity by bacterial type-III secretion system effectors (2015) Curr. Opin. Microbiol., 23, pp. 14-22
• Mafra, V., Kubo, K.S., Alves-Ferreira, M., Ribeiro-Alves, M., Stuart, R.M., Boava, L.P., Rodrigues, C.M., Machado, M.A., Reference genes for accurate transcript normalization in citrus genotypes under different experimental conditions (2012) PLoS One, 7
• Malamud, F., Homem, R.A., Conforte, V.P., Yaryura, P.M., Castagnaro, A.P., Marano, M.R., do Amaral, A.M., Vojnov, A.A., Identification and characterization of biofilm formation-defective mutants of Xanthomonas citri subsp. citri (2013) Microbiology, 157, pp. 819-829
• Mammarella, N.D., Cheng, Z., Fu, Z.Q., Daudi, A., Bolwell, G.P., Dong, X., Ausubel, F.M., Apoplastic peroxidases are required for salicylic acid-mediated defense against Pseudomonas syringae (2014) Phytochemistry, 112, pp. 110-121
• Marano, M.R., Carrillo, N., Constitutive transcription and stable RNA accumulation in plastids during the conversion of chloroplasts to chromoplasts in ripening tomato fruits (1992) Plant Physiol., 100, pp. 1103-1113
• Martinez-Godoy, M.A., Mauri, N., Juarez, J., Marques, M.C., Santiago, J., Forment, J., Gadea, J., A genome-wide 20 K citrus microarray for gene expression analysis (2008) BMC Genomics, 9, p. 318
• Mazza, C.A., Boccalandro, H.E., Giordano, C.V., Battista, D., Scopel, A.L., Ballare, C.L., Functional significance and induction by solar radiation of ultraviolet-absorbing sunscreens in field-grown soybean crops (2000) Plant Physiol., 122, pp. 117-126
• Medina, I., Carbonell, J., Pulido, L., Madeira, S.C., Goetz, S., Conesa, A., Tarraga, J., Dopazo, J., Babelomics: an integrative platform for the analysis of transcriptomics, proteomics and genomic data with advanced functional profiling (2010) Nucleic Acids Res., 38, pp. W210-213
• Pourcel, L., Irani, N.G., Koo, A.J.K., Bohorquez-Restrepo, A., Howe, G.A., Grotewold, E., A chemical complementation approach reveals genes and interactions of flavonoids with other pathways (2013) Plant J., 74, pp. 383-397
• Rigano, L.A., Siciliano, F., Enrique, R., Sendín, L., Filippone, P., Torres, P.S., Qüesta, J., Marano, M.R., Biofilm formation, epiphytic fitness, and canker development in Xanthomonas axonopodis pv. citri (2007) Mol. Plant–Microbe Interact., 20, pp. 1222-1230
• Rojo, E., Martin, R., Carter, C., Zouhar, J., Pan, S., Plotnikova, J., Jin, H., Raikhel, N.V., VPEgamma exhibits a caspase-like activity that contributes to defense against pathogens (2004) Curr. Biol., 14, pp. 1897-1906
• Rybak, M., Minsavage, G.V., Stall, R.E., Jones, J.B., Identification of Xanthomonas citri ssp. citri host specificity genes in a heterologous expression host (2009) Mol. Plant Pathol., 10, pp. 249-262
• Schaad, N.C., Postnikova, E., Lacy, G.H., Sechler, A., Agarkova, I., Stromberg, P.E., Stromberg, V.K., Vidaver, A.K., Emended classification of xanthomonad pathogens on citrus (2006) Syst. Appl. Microbiol., 29, pp. 690-695
• Schaad, N.W., Postnikova, E., Lacy, G.H., Sechler, A., Agarkova, I., Stromberg, P.E., Stromberg, V.K., Vidaver, A.K., Reclassification of Xanthomonas campestris pv. citri (ex Hasse 1915) Dye 1978 forms A, B/C/D, and E as X. smithii ssp. citri (ex Hasse) sp. nov. nom. rev. comb. nov., X. fuscans ssp. aurantifolii (ex Gabriel 1989) sp. nov. nom. rev. comb. nov., and X. alfalfae ssp. citrumelo (ex Riker and Jones) Gabriel 1989 sp. nov. nom. rev. comb. nov.; X. campestris pv. malvacearum (ex Smith 1901) Dye 1978 as X. smithii ssp. smithii nov. comb. nov. nom. nov.; X. campestris pv. alfalfae (ex Riker and Jones, 1935) dye 1978 as X. alfalfae ssp. alfalfae (ex Riker et al., 1935) sp. nov. nom. rev.; and “var. fuscans” of X. campestris pv. phaseoli (ex Smith, 1987) Dye 1978 as X. fuscans ssp. fuscans sp. nov (2005) Syst. Appl. Microbiol., 28, pp. 494-518
• Seay, M.D., Dinesh-Kumar, S.P., Life after death: are autophagy genes involved in cell death and survival during plant innate immune responses? (2005) Autophagy, 1, pp. 185-186
• Shapiguzov, A., Vainonen, J.P., Wrzaczek, M., Kangasjarvi, J., ROS-talk-how the apoplast, the chloroplast, and the nucleus get the message through (2012) Front. Plant Sci., 3, p. 292
• Shiotani, H., Fujikawa, T., Ishihara, H., Tsuyumu, S., Ozaki, K., A pthA homolog from Xanthomonas axonopodis pv. citri responsible for host-specific suppression of virulence (2007) J. Bacteriol., 189, pp. 3271-3279
• Soprano, A.S., Abe, V.Y., Smetana, J.H., Benedetti, C.E., Citrus MAF1, a repressor of RNA polymerase III, binds the Xanthomonas citri canker elicitor PthA4 and suppresses citrus canker development (2013) Plant Physiol., 163, pp. 232-242
• Sun, X., Stall, R.E., Jones, J.B., Cubero, J., Gottwald, T.R., Graham, J.H., Dixon, W.N., Stromberg, V.K., Detection and characterization of a new strain of citrus canker bacteria from Key/Mexican lime and alemow in South Florida (2004) Plant Dis., 88, pp. 1179-1188
• Supek, F., Bošnjakn, M., Škunca, N., Šmuc, T., REVIGO summarizes and visualizes long lists of Gene Ontology terms (2011) PLoS One, 6
• Teh, O.K., Hofius, D., Membrane trafficking and autophagy in pathogen-triggered cell death and immunity (2014) J. Exp. Bot., 65, pp. 1297-1312
• Tusher, V.G., Tibshirani, R., Chu, G., Significance analysis of microarrays applied to the ionizing radiation response (2001) Proc. Natl. Acad. Sci. USA, 98, pp. 5116-5121
• Vanholme, R., Storme, V., Vanholme, B., Sundin, L., Christensen, J.H., Goeminne, G., Halpin, C., Boerjan, W., A systems biology view of responses to lignin biosynthesis perturbations in Arabidopsis (2012) Plant Cell, 24, pp. 3506-3529
• Vernière, C., Hartung, J.S., Pruvost, O.P., Civerolo, E.L., Alvarez, A.M., Maestri, P., Luisetti, J., Characterization of phenotypically distinct strains of Xanthomonas axonopodis pv. citri from Southwest Asia (1998) Eur. J. Plant Pathol., 104, pp. 477-487
• Voigt, C.A., Callose-mediated resistance to pathogenic intruders in plant defense-related papillae (2014) Front. Plant Sci., 5, p. 168
• Vojnov, A., Marano, M.R., Biofilm formation and virulence in bacterial plant pathogens (2015) Virulence Mechanisms of Plant-Pathogenic Bacteria, pp. 21-34. , In, Wang, N., Jones, J.B., Sundin, G.W., White, F.F., Hogenhout, S.A., Roper, C., De la Fuente, L., Ham, J.H., eds), St. Paul, Minnesota, The American Phytopathological Society APS Press
• Vojnov, A.A., do Amaral, A.M., Dow, J.M., Castagnaro, A.P., Marano, M.R., Bacteria causing important diseases of citrus utilise distinct modes of pathogenesis to attack a common host (2010) Appl. Microbiol. Biotechnol., 87, pp. 467-477
• Wrzaczek, M., Brosché, M., Kangasjärvi, J., ROS signaling loops—production, perception, regulation (2013) Curr. Opin. Plant Biol., 16, pp. 575-582
• Xia, P., Wang, S., Du, Y., Xhao, Z., Shi, L., Sun, L., Huang, G., Fan, Z., WASH inhibits autophagy through suppression of Beclin 1 ubiquitination (2013) EMBO J., 32, pp. 2685-2696
• Yoshimoto, K., Hanaoka, H., Sato, S., Kato, T., Tabata, S., Noda, T., Ohsumia, Y., Processing of ATG8s, ubiquitin-like proteins, and their deconjugation by ATG4s are essential for plant autophagy (2004) Plant Cell, 16, pp. 2967-2983
• Yoshimoto, K., Jikumaru, Y., Kamiya, Y., Kusano, M., Consonni, C., Panstruga, R., Ohsumi, Y., Shirasu, K., Autophagy negatively regulates cell death by controlling NPR1-dependent salicylic acid signaling during senescence and the innate immune response in Arabidopsis (2009) Plant Cell, 21, pp. 2914-2927
• Yun, M.H., Torres, P.S., El Oirdi, M., Rigano, L.A., Gonzalez-Lamothe, R., Marano, M.R., Castagnaro, A.P., Vojnov, A.A., Xanthan induces plant susceptibility by suppressing callose deposition (2006) Plant Physiol., 141, pp. 178-187
• Zhou, J., Yu, J.Q., Chen, Z., The perplexing role of autophagy in plant innate immune responses (2014) Mol. Plant Pathol., 15, pp. 637-645

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