References
-
Jones C, Robertson E, Arora V, Friedlingstein P, Shevliakova E, Bopp L, et al. 2016. Twenty-first-century compatible
$CO_2$ emissions and airborne fraction simulated by CMIP5 earth system models under four representative concentration pathways. J. Clinmate. 26: 4398-4413. - Coakley SM, Seherm H, Chakraborty S. 1999. Climate change and plant disease menagement. Annu. Rev. Phytopathol. 37: 399-426. https://doi.org/10.1146/annurev.phyto.37.1.399
-
Manning WJ, Tiedemann AN. 1995. Climate change: Potential effects of increased atmospheric carbon dioxide (
$CO_2$ ), ozone (O3), and ultraviolet (UV-B), radiation on plant diseases. Environ. Pollut. 88: 219-245. https://doi.org/10.1016/0269-7491(95)91446-R - Wells JM. 1974. Grwoth of Erwinia carotovora, E. atroseptica and Pseudomonas fluorescens in low oxygen and high carbon dioxide atmospheres. Phyopathol. 64: 1012-1015. https://doi.org/10.1094/Phyto-64-1012
- Mitchell DJ, Zentmyer GA. 1971. Effect of oxygen and carbon dioxide tensions on gowth of several species of Phytophthora. Phyopathol. 61: 787-791. https://doi.org/10.1094/Phyto-61-787
- Chakraborty S, Luck J, Hollaway G, Freeman A, Norton R, Garrett KA, et al. 2008. Impacts of global change on diseases of agricultural crops and forest trees. CAB Reviews: Perspectives in Agriculture, Veterinary Science, Nutr. Nat. Resour. 3: 1-15.
-
Percy KE, Awmack CS, Lindroth RL, Kubiske ME, Kopper BJ, Isebrands JG, et al. 2002. Altered performance of forest pests under atmospheres enriched by
$CO_2$ and$O_3$ . Nature 420: 403-407. https://doi.org/10.1038/nature01028 - Mesarich CH, Stergiopoulos I, Beenen HG, Cordovez V, Guo Y, Jashni MK, et al. 2016. A conserved proline residue in dothideomycete Avr4 effector proteins is required to trigger a Cf-4- dependent hypersensitive response. Mol. Plant Pathol. 17: 84-95. https://doi.org/10.1111/mpp.12265
- Roeschlin RA, Favaro MA, Chiesa MA, Alemano S, Vojnov AA, Castagnaro AP, et al. 2017. Resistance to citrus canker induced by a variant of Xanthomonas citri ssp. citri is associated with a hypersensitive cell death response involving autophagy-associated vacuolar processes. Mol. Plant Pathol. 18: 1267-1281. https://doi.org/10.1111/mpp.12489
- Hayashi K, Fujita Y, Ashizawa T, Suzuki F, Nagamura Y, Hayano- Saito Y. 2016. Serotonin attenuates biotic stress and leads to lesion browning caused by a hypersensitive response to Magnaporthe oryzae penetration in rice. Plant J. 2016: 46-56.
- Guo A, Salih G, Klessig DF. 2000. Activation of a diverse set of genes during the tobacco resistance response to TMV is independent of salicylic acid; induction of a sibset is also ethylene independent. Plant J. 21: 409-418.
- Nurnberger T, Brunner F, Kemmerling B, Piater L. 2004. Innate immunity in plants and animals: striking similarities and obvious differences. Immunol. Rev. 198: 249-266. https://doi.org/10.1111/j.0105-2896.2004.0119.x
- Stahl E, Bellwon P, Huber S, Schlaeppi K, Bernsdorff F, Vallat- Michel A, et al. 2016. Regulatory and functional aspects of indolic metabolism in plant systemic acquired resistance. Molecular Plant. 9: 662-681. https://doi.org/10.1016/j.molp.2016.01.005
- Niu D, Wang X, Wang Y, Song X, Wang J, Guo J, et al. 2016. Bacillus cereus AR156 activates PAMP-triggered immunity and induces a systemic acquired resistance through NPR1-and SAdependent signaling pathoway. Biochem. Bioph. Res. Co. 469: 120-125.
- Kim DS, Kim NH, Hwang BK. 2015. The Capsicum annuum class IV chitinase ChitIV interacts with receptor-like cytoplasmic protein kinase PIK1 to accelerate PIK1-triggered cell death and defence responses. J. Exp. Bot. 66: 1987-1999. https://doi.org/10.1093/jxb/erv001
- Kim NH, Kim DS, Chung EH, Hwang BK. 2014. Pepper suppressor of the G2 Allele of skp1 interacts with the receptor-like cytoplasmic kinase1 and type III effector AvrBsT and promotes the hypersensitive cell death response in an phosphorylation dependent manner. Plant Physiol. 165: 76-91. https://doi.org/10.1104/pp.114.238840
- Caddell DF, Park C-J, Thomas NC, Canlas PE, Ronald PC. 2017. Silencing of the rice gene LRR1 compromises rice Xa21 transcript accumulation and XA21-mediated immunity. RICE. 10: 1-11. https://doi.org/10.1186/s12284-016-0141-2
- Huang L-F, Lin K-H, He S-L, Chen J-L, Jiang J-Z, Chen B-H, et al. 2016. Multiple patterns of regulation and overexpression of a ribonuclease-like pathogenesis-related protein gene, OsPR10a, conferring disease resistance in rice and Arabidopsis. PLoS One 11: 1-27.
- Qiao Z, Li C-L, Zhang W. 2016. WRKY1 regulates stomatal movement in drought stressed Arabidopsis Thaliana. Plant Mol. Biol. 91: 53-65. https://doi.org/10.1007/s11103-016-0441-3
- Konda AK, Farmer R, Soren KR, S. SP, Setti A. 2017. Structural modelling and molecular dynamics of a multi-stress responsive WRKY TF-DNA complex towards elucidating its role in stress signalling mechanisms in chickpea. J. Biomol. Struct. Dyn. 1-13.
- Park J-H, Park S-J, Kwon O-H, Choi S-Y, Park S-D, Kim J-E. 2015. Effect of mixed treatment of nitrogen fertilizer and zeolite on soil chemical properties and growth of hot pepper. Korean J. Soil Sci. Fert. 48: 44-49. https://doi.org/10.7745/KJSSF.2015.48.1.044
- Minsavage GV, Dahlbeck D, Whalen MC, Kearney B, Bonas U, Staskawicz BJ, et al. 1990. Gene-for-gene relationships specifying disease resistance in Xanthomonas campestris pv. vesicatoria - pepper interactions. Mol. Plant Microbe. Interact. 3: 41-47. https://doi.org/10.1094/MPMI-3-041
- Dangle JL, Jones JDG. 2001. Plant pathogens and intergrated defense response to infection. Nature 411: 826-833. https://doi.org/10.1038/35081161
- Kobe B, Deisenhofer J. 1994. The leucine-rich repeat: a versatile binding motif. Trends Biochem. Sci. 19: 415-421. https://doi.org/10.1016/0968-0004(94)90090-6
- Jung HW, Hwang BK. 2007. The leucine-rich repeat (LRR) protein, CaLRR1, interacts with the hypersensitive induced reaction (HIR) protein, CaHIR1, and suppresses cell death induced by the CaHIR1 protein. Mol. Plant Pathol. 8: 503-514.
- Hong JK, Hwang IS, Hwang BK. 2017. Functional roles of the pepper leucine-rich repeat protein and its interactions with pathogenesis-related and hypersensitive-induced proteins in plant cell death and immunity. Planta 246: 351-364.
- Chen L, Song Y, Li S, Zhang L, Zou C, Yu D. 2012. The role of WRKY transcription factors in plant abiotic stresses. Biochim. Biophys. Acta. 1819: 120-128. https://doi.org/10.1016/j.bbagrm.2011.09.002
- Tang M, Lu S, Jing Y, Shou X, Sun J, Shen S. 2005. Isolation and identification of a cold-inducible gene encoding a putative DRE-binding transcription factor from Festuca arundinacea. Plant Physiol. Biochem. 43: 233-239. https://doi.org/10.1016/j.plaphy.2005.01.015
- Eulgem T. 2006. Dissecting the WRKY web of plant defense regulators. PLos Pathogens. 2: 1028-1030.
- Oh S-K, Baek K-H, Park JM, Yi SY, Yu SH, Kamoun S, et al. 2008. Capsicum annuum WRKY protein CaWRKY1 is a negative regulator of pathogen defense. New Phytol. 177: 177-989.
- Johnson LN, Noble MEM, Owen DJ. 1996. Active and inactive protein kinases: structural basis for regulation. Cell 85: 149-158. https://doi.org/10.1016/S0092-8674(00)81092-2
- Afzal AJ, Wood AJ, Lightfoot DA. 2008. Plant receptor like serine threonine kinase: roles in signaling and plant defense. Mol. Plant Microbe. Interact. 21: 507-517. https://doi.org/10.1094/MPMI-21-5-0507
- Zhang X, Dai Y, Xiong Y, DeFraia C, Li J, Dong X, et al. 2007. Overexpression of Arabidopsis MAP kinase kinase 7 leads to activation of plant basal and systemic acquired resistance. Plant J. 52: 1066-1079. https://doi.org/10.1111/j.1365-313X.2007.03294.x
- Asai T, Tena G, Plotnikova J, Willmann MR, Chiu WL, Gomez- Gomez L, et al. 2002. MAP kinase signalling cascade in Arabidopsis innate immunity. Nature 415: 977-983. https://doi.org/10.1038/415977a
- Kim DS, Hwang BK. 2011. The pepper receptor-like cytoplasmic protein kinase CaPIK1 is involved in plant signaling of defense and cell-death responses. Plant J. 66: 642-655. https://doi.org/10.1111/j.1365-313X.2011.04525.x
- Leon J, Yalpani N, Raskin I, Lawton MA. 1993. Induction of benzoic acid 2-hydroxylase in virus-inoculated tobacco. Plant Physiol. 103: 323-328. https://doi.org/10.1104/pp.103.2.323
- van Loon LC, van Strein EA. 1999. The families of pathogenesisrelated proteins, their activities, and comparative analysis of PR-1 type proteins. Physiol. Mol. Plant P. 55: 85-97.
- Upadhyay P, Rai A, Kumar R, Singh M, Sinha B. 2014. Differential expressiion of pathogenesis related protein genes in tomato during inoculation with A. solani. J. Plant Pathol. Microb. 5: 217.
- Lo S-CC, Hipskind JD, Nicholson RL. 1999. cDNA cloning of sorghum pathogenesis-related protein (PR-10) and differential expression of defense-related genes following inoculation with Cochliobolus heterostrophus or Collectotrichum sublineolum. Mol. Plant Microbe Interact. 12: 479-489. https://doi.org/10.1094/MPMI.1999.12.6.479
- Van Loon LC, Pierpoint WS, Boller TH. 1994. Recommendations for naming plant pathogenesis-related proteins. Plant Mol. Biol. Rep. 12: 245-264. https://doi.org/10.1007/BF02668748
- Guevara-Morato MA, Lacoba MGd, Garcia-Luque I, Serra MT. 2010. Characterization of a pathogenesis-related protein 4 (PR- 4) induced in Capsicum chinense L3 plants with dual RNase and DNase activities. J. Exp. Bot. 61: 3259-3271.
- Park C-J, Kim K-J, Shin R, Park JM, Shin Y-C, Paek K-H. 2004. Pathogenesis-related protein 10 isolated from hot pepper funtion as a ribonuclease in an antiviral pathway. Plant J. 37: 186-198. https://doi.org/10.1046/j.1365-313X.2003.01951.x
- Hwang IS, Choi DS, Kim NH, Kim DS, Hwang BK. 2014. Pathogenesis- related protein 4b interacts with leucine-rich repeat protein 1 to suppress PR4b-triggered cell death and defense response in pepper. Plant J. 77: 521-533. https://doi.org/10.1111/tpj.12400
- Hipskind JD, Nicholson RL, Goldsbrough PB. 1996. Isolation of a cDNA encoding a novel leucine-rich repeat motif from Sorghum bicolor inoculated with fungi. Mol. Plant Microbe. Interact. 9: 819-825. https://doi.org/10.1094/MPMI-9-0819
- Moon J-C, Kim JY, Beak S-B, Kwon Y-U, Song K, Lee B-M. 2014. Transcription factor for gene funtion analysis in maize. Korean J. Crop Sci. 59: 263-281. https://doi.org/10.7740/kjcs.2014.59.3.263
- Eulgem T, Rushton PJ, Robatzek S, Somssich IE. 2000. The WRKY superfamily of plant transcription factors. Trends Plant Sci. 5: 199-206. https://doi.org/10.1016/S1360-1385(00)01600-9
- Oh S-K, Baek K-H, Park JM, Yi SY, Yu SH, Kamoun S, et al. 2008. Capsicum annuum WRKY protein CaWRKY1 is a negative regulator of pathogen defense. New Phytol. 177: 977-989. https://doi.org/10.1111/j.1469-8137.2007.02310.x
- Shiu SH, Bleecker AB. 2003. Expansion of the receptor-like kinase/Pelle gene famil and receptor-like proteins in Arabidopsis. Plant Physiol. 132: 530-543.
- Shiu SH, Bleecker AB. 2001. Receptor-like kinases from Arabidopsis form a nomophyletic gene family elated to animal receptor kinases. Proc. Natl. Acad. Sci. USA 98: 10763-10768. https://doi.org/10.1073/pnas.181141598
- Duner J, Shah J, Klessig DF. 1997. Salicylic acid and disease resistance in plants. Trends Plant Sci. 2: 226-274.
- Ecker JR. 1995. The ethylene signal transduction pathway in plants. Science 268: 667-675. https://doi.org/10.1126/science.7732375
- Ziadi A, Poupard P, Brisset MN, Paulin JP, Simoneau P. 2001. Characterization in apple leaves of two subclasses of PR-10 transcrips inducible by acibenzolar-S-methyl, a functional analogue of salicylic acid Physiol. Mol. Plant P. 59: 33-43. https://doi.org/10.1006/pmpp.2001.0343
- Wang CS, Huang JC, Hu JH. 1999. Characterization of two subclasses of PR-10 transctipts in lily anthers and induction of their genes through separate signal transduction pathways. Plant Mol. Biol. 40: 807-814.
- Jones JB, Stall RE, Bouzar H. 1998. Diversity among xanthomonads pathogenic on pepper and tomato. Annurev. Phyto. 36: 41-58.
- B.Jonesa. J, Lacy GH, Bouzar H, Stall RE, Schaad NW. 2004. Reclassification of the Xanthomonads associated with bacterial spot disease of tomato and pepper. System Appl. Microbiol. 27: 755-762. https://doi.org/10.1078/0723202042369884
- Byeon SE , Abebe AM, Jegal YH, Wai KPP, Siddique MI, Mo HS et al. 2016. Characterization of sources of resistance to bacterial spot in Capsicum peppers. Kor. J. Hort. Sci. Technol. 34: 779-789.
-
Shin J-W, Yun S-C. 2010. Elevated
$CO_2$ and temperature effects on the incidence of four major chili pepper diseases. Plant Pathol. J. 26: 178-184. https://doi.org/10.5423/PPJ.2010.26.2.178 - Silvar C, Merino F, Diaz J. 2008. Differential activation of defense-related genes in susceotible and resistant pepper cultivars infected with Phytophthora capsici. J. Plant Physiol. 165: 1120-1124.
- Liu Z, Shi L, Yang S, Lin Y, Weng Y, Li X, et al. 2017. Functional and promoter analysis of ChiIV3, a chitinase of pepper plant, in response to Phytophthora capsici infection. Int. J. Mol. Sci. 18: 1661. https://doi.org/10.3390/ijms18081661
-
Chakraborty S, Pangga IB, Lupton J, Hart L, Room PM, Yates D. 2000. Production and dispersal of Collectotrichum gloeosporioides spores on Stylosanthes scabra under elevated
$CO_2$ . Environ. Pollut. 108: 381-387. https://doi.org/10.1016/S0269-7491(99)00217-1 -
Hibberd JM, Whitbread R, Farrar JF. 1996. Effect of elevated concentrations of
$CO_2$ on infection of barley by Erysiphe graminis. Physiol. Mol. Plant P. 48: 37-53. https://doi.org/10.1006/pmpp.1996.0004 -
Bettarini I, Vaccari FP, Miglietta F. 1998. Elevated
$CO_2$ concentrations and stomatal density observations from 17 plant species growing in a$CO_2$ spring in central Italy. Glob. Change Biol. 4: 17-22. https://doi.org/10.1046/j.1365-2486.1998.00098.x
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