참고문헌
- Savary S, Teng PS, Willocquet L, et al. Quantification and modeling of crop losses: a review of purposes. Annu Rev Phytopathol. 2006; 44:89-112. https://doi.org/10.1146/annurev.phyto.44.070505.143342
- Strange RN, Scott PR. Plant disease: a threat to global food security. Annu Rev Phytopathol. 2005; 43:83-116. https://doi.org/10.1146/annurev.phyto.43.113004.133839
- Makovitzki A, Viterbo A, Brotman Y, et al. Inhibition of fungal and bacterial plant pathogens in vitro and in planta with ultrashort cationic lipopeptides. Appl Environ Microbiol. 2007;73: 6629-6636. https://doi.org/10.1128/AEM.01334-07
- Boyraz N, Ozcan M. Inhibition of phytopathogenic fungi by essential oil, hydrosol, ground material and extract of summer savory (Satureja hortensis L.) growing wild in Turkey. Int J Food Microbiol. 2006;107:238-242. https://doi.org/10.1016/j.ijfoodmicro.2005.10.002
- Rahman M, Punja ZK. Factors influencing development of root rot on ginseng caused by Cylindrocarpon destructans. Phytopathology. 2005; 95:1381-1390. https://doi.org/10.1094/PHYTO-95-1381
- Denny TP. Plant pathogenic Ralstonia species. In: Gnanamanickam SS, editor. Plant-associated bacteria. Dordrecht: Springer; 2007. p. 573-644.
- Ham JH, Melanson RA, Rush MC. Burkholderia glumae: next major pathogen of rice? Mol Plant Pathol. 2011;12:329-339. https://doi.org/10.1111/j.1364-3703.2010.00676.x
- Lemanceau P. Beneficial effects of rhizobacteria on plants: example of fluorescent Pseudomonas spp. [plant growth promoting rhizobacteria, PGPR, microbial antagonism, siderophore, bacterial inoculation]. Agronomie. 1992;12:413-437. https://doi.org/10.1051/agro:19920601
- Jung B, Park J, Kim N, et al. Cooperative interactions between seed-borne bacterial and air-borne fungal pathogens on rice. Nat Commun. 2018;9:31. https://doi.org/10.1038/s41467-017-02430-2
-
Daoubi M, Hernandez-Galan R, Benharref A, et al. Screening study of lead compounds for natural product-based fungicides: antifungal activity and biotransformation of
$6{\alpha}$ ,$7{\alpha}$ -dihydroxy-${\beta}$ -himachalene by Botrytis cinerea. J Agric Food Chem. 2005; 53:6673-6677. https://doi.org/10.1021/jf050697d - Russell P. Fungicide resistance: occurrence and management. J Agric Sci. 1995;124:317-323. https://doi.org/10.1017/S0021859600073275
- Knight S, Anthony V, Brady A, et al. Rationale and perspectives on the development of fungicides. Annu Rev Phytopathol. 1997;35:349-372. https://doi.org/10.1146/annurev.phyto.35.1.349
- Brent KJ, Hollomon DW. Fungicide resistance in crop pathogens: how can it be managed? GIFAP Brussels; 1995.
- Walsh T, Viviani M-A, Arathoon E, et al. New targets and delivery systems for antifungal therapy. Med Mycol. 2000;38:335-347. https://doi.org/10.1080/mmy.38.s1.335.347
- Pirgozliev SR, Edwards SG, Hare MC, et al. Strategies for the control of Fusarium head blight in cereals. Eur J Plant Pathol. 2003;109:731-742. https://doi.org/10.1023/A:1026034509247
- Park SE, Song JD, Kim KM, et al. Diphenyleneiodonium induces ROS-independent p53 expression and apoptosis in human RPE cells. FEBS Lett. 2007;581:180-186. https://doi.org/10.1016/j.febslet.2006.12.006
- Dodd -o. JM, Zheng G, Silverman HS, et al. Endothelium-independent relaxation of aortic rings by the nitric oxide synthase inhibitor diphenyleneiodonium. Br J Pharmacol. 1997;120: 857-864. https://doi.org/10.1038/sj.bjp.0701014
- Sanders SA, Eisenthal R, Harrison R. NADH oxidase activity of human xanthine oxidoreductasegeneration of superoxide anion. Eur J Biochem. 1997;245:541-548. https://doi.org/10.1111/j.1432-1033.1997.00541.x
- Suzuki H, Hatano N, Muraki Y, et al. The NADPH oxidase inhibitor diphenyleneiodonium activates the human TRPA1 nociceptor. Am J Physiol Cell Physiol. 2014;307:C384-C394. https://doi.org/10.1152/ajpcell.00182.2013
- Pandey M, Singh AK, Thakare R, et al. Diphenyleneiodonium chloride (DPIC) displays broad-spectrum bactericidal activity. Sci Rep. 2017; 7:11521. https://doi.org/10.1038/s41598-017-11575-5
- Ogasawara MA, Zhang H. Redox regulation and its emerging roles in stem cells and stem-like cancer cells. Antioxid Redox Signal. 2009;11: 1107-1122. https://doi.org/10.1089/ars.2008.2308
- Jacobo-Velazquez DA, Martinez-Hernandez GB, del C. Rodriguez S, et al. Plants as biofactories: physiological role of reactive oxygen species on the accumulation of phenolic antioxidants in carrot tissue under wounding and hyperoxia stress. J Agric Food Chem. 2011;59:6583-6593. https://doi.org/10.1021/jf2006529
- Bernards MA, Razem FA. The poly(phenolic) domain of potato suberin: a non-lignin cell wall bio-polymer. Phytochemistry. 2001;57:1115-1122. https://doi.org/10.1016/S0031-9422(01)00046-2
- Razem FA, Bernards MA. Reactive oxygen species production in association with suberization: evidence for an NADPH-dependent oxidase. J Exp Bot. 2003;54:935-941. https://doi.org/10.1093/jxb/erg094
- Cappellini R, Peterson J. Macroconidium formation in submerged cultures by a non-sporulating strain of Gibberella zeae. Mycologia. 1965;57: 962-966. https://doi.org/10.2307/3756895
- Leslie JF, Summerell BA. The Fusarium laboratory manual. Hoboken (NJ): John Wiley & Sons; 2008.
- Maniatis T, Fritsch EF, Sambrook J. Molecular cloning: a laboratory manual. Vol. 545. Cold spring harbor laboratory Cold Spring Harbor, NY; 1982.
- Kang Y, Kim MR, Kim KH, et al. Chlamydospore induction from conidia of Cylindrocarpon destructans isolated from ginseng in Korea. Mycobiology. 2016;44:63-65. https://doi.org/10.5941/MYCO.2016.44.1.63
- Takemoto D, Tanaka A, Scott B. NADPH oxidases in fungi: diverse roles of reactive oxygen species in fungal cellular differentiation. Fungal Genet Biol. 2007;44:1065-1076. https://doi.org/10.1016/j.fgb.2007.04.011
- Hajjar C, Cherrier MV, Mirandela GD, et al. The NOX family of proteins is also present in bacteria. mBio. 2017;8:e01487.
- Cano-Dominguez N, Alvarez-Delfin K, Hansberg W, et al. NADPH oxidases NOX-1 and NOX-2 require the regulatory subunit NOR-1 to control cell differentiation and growth in Neurospora crassa. Eukaryot Cell. 2008;7:1352-1361. https://doi.org/10.1128/EC.00137-08
- Kashmiri Z, Mankar S. Free radicals and oxidative stress in bacteria. Int J Curr Microbiol App Sci. 2014;3:34-40.
- Vaughan M, Backhouse D, Ponte ED. Climate change impacts on the ecology of Fusarium graminearum species complex and susceptibility of wheat to Fusarium head blight: a review. World Mycotoxin J. 2016;9:685-700. https://doi.org/10.3920/WMJ2016.2053
- Schaad NW. Emerging plant pathogenic bacteria and global warming. In: Fatmi M et al., editors. Pseudomonas syringae pathovars and related pathogens- identification, epidemiology and genomics. Dordrecht: Springer; 2008. p. 369-379.
- Kim K, Lee Y, Ha A, et al. Chemosensitization of Fusarium graminearum to chemical fungicides using cyclic lipopeptides produced by Bacillus amyloliquefaciens strain JCK-12. Front Plant Sci. 2017;8:2010. https://doi.org/10.3389/fpls.2017.02010
- Sarkar DJ, Mukherjee I, Shakil NA, et al. Antibiotics in agriculture: use and impact. Ind J Ethnophytopharm. 2018;4:4-19.
- Hollomon D. Does agricultural use of azole fungicides contribute to resistance in the human pathogen Aspergillus fumigatus? Pest Manag Sci. 2017; 73:1987-1993. https://doi.org/10.1002/ps.4607
- Becher R, Hettwer U, Karlovsky P, et al. Adaptation of Fusarium graminearum to tebuconazole yielded descendants diverging for levels of fitness, fungicide resistance, virulence, and mycotoxin production. Phytopathology. 2010;100: 444-453. https://doi.org/10.1094/PHYTO-100-5-0444
피인용 문헌
- Carrier-Mediated Drug Uptake in Fungal Pathogens vol.11, pp.11, 2020, https://doi.org/10.3390/genes11111324