2,374
Views
5
CrossRef citations to date
0
Altmetric
Research Articles

Screening of Endophytic Fungal Isolates Against Raffaelea quercus-mongolicae Causing Oak Wilt Disease in Korea

, , & ORCID Icon
Pages 484-494 | Received 11 May 2020, Accepted 21 Sep 2020, Published online: 23 Oct 2020

References

  • Nixon KC. An overview of Quercus: classification and phylogenetics with comments on differences in wood anatomy. In: Appel DN, Billings RF, editors. Proceedings of the 2nd National Oak Wilt Symposium. Texas, USA: International Society of Arboriculture – Texas Chapter; 2007. p. 13–25.
  • Johnson PS, Shifley SR, Rogers R (eds.). The ecology and silviculture of oaks. New York, NY: CABI Publishing; 2002.
  • Juzwik J, Appel DN, MacDonald WL, et al. Challenges and successes in managing oak wilt in the United States. Plant Dis. 2011;95(8):888–900.
  • Kim KH, Choi YJ, Seo ST, et al. Raffaelea quercus-mongolicae sp. Nov. associated with Platypus koryoensis on oak in Korea. Mycotaxon. 2009;110(1):189–197.
  • Kubono T, Ito S. Raffaelea quercivora sp. Nov. associated with mass mortality of Japanese oak, and the ambrosia beetle (Platypus quercivorus). Mycoscience. 2002;43(3):255–260.
  • Yi SH, Lee JH, Seo ST, et al. In vivo pathogenicity test of oak wilt fungus (Raffaelea quercus-mongolicae) on oriental chestnut oak (Quercus acutissima). J For Environ Sci. 2017;33(4):342–347.
  • Kim MS, Hohenlohe PA, Kim KH, et al. Genetic diversity and population structure of Raffaelea quercus-mongolicae, a fungus associated with oak mortality in South Korea. For Pathol. 2016;46(2):164–167.
  • Jeon J, Kim KT, Song H, et al. Draft genome sequence of the fungus associated with oak wilt mortality in South Korea, Raffaelea quercus-mongolicae KACC44405. Genome Announc. 2017;5(34):e00797.
  • Kim SW, Kim KS, Lamsal K, et al. An in vitro study of the antifungal effect of silver nanoparticles on oak wilt pathogen Raffaelea sp. J Microbiol Biotechnol. 2009;19(8):760–764.
  • Park IK, Nam Y, Seo ST, et al. Development of a mass trapping device for the ambrosia beetle, Platypus koryoensis, an insect vector of oak wilt disease in Korea. J Asia-Pac Entomol. 2016;19(1):39–43.
  • Lee JH, Hong AR, Yun JH, et al. Prevention of oak wilt by tree injection of culture suspension of an antifungal microorganism, Streptomyces blastmyceticus against oak wilt fungus, Raffaelea quercus-mongolicae. J For Environ Sci. 2018;34(5):376–381.
  • Nair DN, Padmavathy S. Impact of endophytic microorganisms on plants, environment and humans. Sci World J. 2014;2014:1–11.
  • Posada F, Vega FE. Inoculation and colonization of coffee seedlings (Coffea arabica L.) with the fungal entomopathogen Beauveria bassiana (Ascomycota: Hypocreales). Mycoscience. 2006;47(5):284–289.
  • Zou WX, Meng JC, Lu H, et al. Metabolites of Colletotrichum gloeosporioides, an endophytic fungus in Artemisia mongolica. J Nat Prod. 2000;63(11):1529–1530.
  • Jeon YT, Ryu KH, Kang MK, et al. Alternariol monomethyl ether and α, β-dehydrocurvularin from endophytic fungi Alternaria spp. inhibit appressorium formation of Magnaporthe grisea. J Kor Soc Appl Biol Chem. 2009;53(1):39–42.
  • Suryanarayanan TS. Endophyte research: going beyond isolation and metabolite documentation. Fungal Ecol. 2013;6(6):561–568.
  • Masi M, Maddau L, Linaldeddu BT, et al. Bioactive metabolites from pathogenic and endophytic fungi of forest trees. Curr Med Chem. 2018;25(2):208–252.
  • Xie J, Strobel GA, Mends MT, et al. Collophora aceris, a novel antimycotic producing endophyte associated with douglas maple. Microb Ecol. 2013;66(4):784–795.
  • McMullin DR, Green BD, Miller JD. Antifungal sesquiterpenoids and macrolides from an endophytic lophodermium species of Pinus strobus. Phytochem Lett. 2015;14:148–152.
  • Shiono Y, Koyama H, Murayama T, et al. New sesquiterpenes from the endophyte Microdiplodia sp. TT-12 and their antimicrobial activity. Phytochem Lett. 2015;14:143–147.
  • Lee SH, Lee SK, Kim JY, et al. Antifungal property of microorganisms against Korea oak wilt pathogen, Raffaelea quercus-mongolicae. Kor J Microbiol Biotechnol. 2012;40(1):66–69.
  • Hong AR, Yun JH, Yi SH, et al. Screening of antifungal microorganisms with strong biological activity against oak wilt fungus, Raffaelea quercus-mongolicae. J For Environ Sci. 2018;34(5):395–404.
  • Yong JH. Diversity analysis of endophytic fungi isolated from pine and oak trees in Korea [Master Thesis]. Korea: Kangwon National University; 2019.
  • Al-Reza SM, Rahman A, Ahmed Y, et al. Inhibition of plant pathogens in vitro and in vivo with essential oil and organic extracts of Cestrum nocturnum L. Pestic Biochem Physiol. 2010;96(2):86–92.
  • Jung SJ, Kim NK, Lee DH, et al. Screening and evaluation of Streptomyces species as a potential biocontrol agent against a wood decay fungus, Gloeophyllum trabeum. Mycobiology. 2018;46(2):138–146.
  • Xiao Y, Li HX, Li C, et al. Antifungal screening of endophytic fungi from Ginkgo biloba for discovery of potent anti-phytopathogenic fungicides. FEMS Microbiol Lett. 2013;339(2):130–136.
  • Bae H, Roberts DP, Lim HS, et al. Endophytic Trichoderma isolates from tropical environments delay disease onset and induce resistance against Phytophthora capsici in hot pepper using multiple mechanisms. Mol Plant Microbe Interact. 2011;24(3):336–351.
  • Saxena A, Raghuwanshi R, Singh HB. Elevation of defense network in chilli against Colletotrichum capsici by phyllospheric Trichoderma strain. J Plant Growth Regul. 2016;35(2):377–389.
  • Šišić A, Baćanović J, Finckh MR. Endophytic Fusarium equiseti stimulates plant growth and reduces root rot disease of pea (Pisum sativum L.) caused by Fusarium avenaceum and Peyronellaea pinodella. Eur J Plant Pathol. 2017;148(2):271–282.
  • Velmurugan N, Han SS, Sa DM, et al. Consideration of Daldinia childiae as a new record in Korea, based on morphological characteristics of Korea collections. Appl Microsc. 2007;37(4):289–295.
  • Hirooka Y, Rossman AY, Samuels GJ, et al. A monograph of Allantonectria, Nectria, and Pleonectria (Nectriaceae, Hypocreales, Ascomycota) and their pycnidial, sporodochial, and synnematous anamorphs. Stud Mycol. 2012;71(1):1–210.
  • Damm U, Cannon PF, Woudenberg JHC, et al. The Colletotrichum acutatum species complex. Stud Mycol. 2012;73(1):37–113.
  • Basım E, Basım H, Abdulai M, et al. Identification and characterization of Alternaria alternata causing leaf spot of olive tree (Olea europaea) in Turkey. Crop Prot. 2017;92:79–88.
  • Garrido C, Carbú M, Javier FAF, et al. Phylogenetic relationships and genome organisation of Colletotrichum acutatum causing anthracnose in strawberry. Eur J Plant Pathol. 2009;125(3):397–411.
  • Peres NA, MacKenzie SJ, Peever TL, et al. Postbloom fruit drop of citrus and key lime anthracnose are caused by distinct phylogenetic lineages of Colletotrichum acutatum. Phytopathology. 2008;98(3):345–352.
  • Lee DH, Kim DH, Jeon YA, et al. Molecular and cultural characterization of Colletotrichum spp. causing bitter rot of apples in Korea. Plant Pathol J. 2007;23(2):37–44.
  • Abbas HK, Tanaka T, Duke SO, et al. Susceptibility of various crop and weed species to AAL-toxin, a natural herbicide. Weed Technol. 1995;9(1):125–130.
  • Cannon PF, Damm U, Johnston PR, et al. Colletotrichum - current status and future directions. Stud Mycol. 2012;73(1):181–213.
  • Vasundhara M, Reddy MS, Kumar A. Secondary metabolites from endophytic fungi and their biological activities. In: Gupta VK, Pandey A, editors. New and future developments in microbial biotechnology and bioengineering. Microbial secondary metabolites biochemistry and application. Amsterdam: Elsevier; 2019. p. 237–258.
  • Jeon YT, Jun EM, Oh KB, et al. Identification of 12-methyltetradecanoic acid from endophytic Senotrophomonas maltophilia as inhibitor of appressorium formation of Magnaporthe oryzae. J Kor Soc Appl Biol Chem. 2010;53(5):578–583.
  • Gunatilaka AAL. Natural products from plant-associated microorganisms: distribution, structural diversity, bioactivity, and implications of their occurrence. J Nat Prod. 2006;69(3):509–526.
  • Kamlesh K, Sivakumar T, Afroze A. Antimicrobial activity of flavone analogues. J Appl Pharm. 2017;09(01):1000232.
  • Wicklow DT, Jordan AM, Gloer JB. Antifungal metabolites (Monorden, Monocillins I, II, III) from Colletotrichum graminicola, a systemic vascular pathogen of maize. Mycol Res. 2009;113(Pt 12):1433–1442.
  • Brooks DS, Gonzalez CF, Appel DN, et al. Evaluation of endophytic bacteria as potential biological-control agents for oak wilt. Biol Control. 1994;4(4):373–381.
  • Maria GL, Sridhar KR. Endophytic fungal assemblage of two halophytes from west coast mangrove habitats, India. Czech Mycol. 2003;55(3-4):241–251.
  • Park YH, Lee SG, Ahn DJ, et al. Diversity of fungal endophytes in various tissues of Panax ginseng Meyer cultivated in Korea. J Ginseng Res. 2012;36(2):211–217.
  • Kurandawad JM, Lakshman HC. Diversity of the endophytic fungi isolated from Acalypha indica Linn - a promising medicinal plant. Int J Sci Res Publ. 2014;4(4):1–7.
  • Yadav M, Yadav A, Kumar S, et al. Spatial and seasonal influences on culturable endophytic mycobiota associated with different tissues of Eugenia jambolana Lam. and their antibacterial activity against MDR strains. BMC Microbiol. 2016;16(1):44.
  • Mishra A, Gond SK, Kumar A, et al. Season and tissue type affect fungal endophyte communities of the Indian medicinal plant Tinospora cordifolia more strongly than geographic location. Microb Ecol. 2012;64(2):388–398.
  • Chareprasert S, Piapukiew J, Thienhirun S, et al. Endophytic fungi of teak leaves Tectona grandis L. and rain tree leaves Samanea saman Merr. World J Microbiol Biotechnol. 2006;22(5):481–486.
  • Huang WY, Cai YZ, Hyde KD, et al. Biodiversity of endophytic fungi associated with 29 traditional Chinese medicinal plants. Fungal Divers. 2008;33(33):61–75.