DOI QR코드

DOI QR Code

Screening and Evaluation of Streptomyces Species as a Potential Biocontrol Agent against a Wood Decay Fungus, Gloeophyllum trabeum

  • Jung, Su Jung (Tree Pathology and Mycology Laboratory, College of Forest and Environmental Sciences, Kangwon National University) ;
  • Kim, Nam Kyu (Korea National Arboretum) ;
  • Lee, Dong-Hyeon (Division of Forest Diseases and Insect Pests, National Institute of Forest Science) ;
  • Hong, Soon Il (Forest Biomaterials Engineering, College of Forest and Environmental Sciences, Kangwon National University) ;
  • Lee, Jong Kyu (Tree Pathology and Mycology Laboratory, College of Forest and Environmental Sciences, Kangwon National University)
  • Received : 2018.03.14
  • Accepted : 2018.03.23
  • Published : 2018.06.01

Abstract

Two-hundred and fifty-five strains of actinomycetes isolated from soil samples were screened for their antagonistic activities against four well-known wood decay fungi (WDF), including a brown rot fungus, Gloeophyllum trabeum and three white rot fungi Donkioporia expansa, Trametes versicolor, and Schizophyllum commune. A dual culture assay using culture media supplemented with heated or unheated culture filtrates of selected bacterial strains was used for the detection of their antimicrobial activity against four WDF. It was shown that Streptomyces atratus, S. tsukiyonensis, and Streptomyces sp. greatly inhibited the mycelial growth of the WDF tested compared with the control. To evaluate the biocontrol efficacy of S. atratus, S. tsukiyonensis, and Streptomyces sp., wood blocks of Pinus densiflora inoculated with three selected Streptomyces isolates were tested for weight loss, compression strength (perpendicular or parallel to the grain), bending strength, and chemical component changes. Of these three isolates used, Streptomyces sp. exhibited higher inhibitory activity against WDF, especially G. trabeum, as observed in mechanical and chemical change analyses. Scanning electron microscopy showed that cell walls of the wood block treated with Streptomyces strains were thicker and collapsed to a lesser extent than those of the non-treated control. Taken together, our findings indicate that Streptomyces sp. exhibits the potential to be used as a biocontrol agent for wood decay brown rot fungus that causes severe damage to coniferous woods.

Keywords

References

  1. Wellman RH. Problems in development, registration, and use of fungicides. Annu Rev Phytopathol. 1977;15:153-163. https://doi.org/10.1146/annurev.py.15.090177.001101
  2. Spadaro D, Gullino ML. Improving the efficacy of biocontrol agents against soilborne pathogens. Crop Prot. 2005;24:601-613. https://doi.org/10.1016/j.cropro.2004.11.003
  3. Lechevalier MP. Actinomycetes in agriculture and forestry. In: Goodfellow M, Williams ST, Mordarski M, editors. Actinomycetes in biotechnology. New York: Academic Press; 1989. p. 327-358.
  4. Srnivasan MC, Laxman RS, Despharde MV. Physiology and nutritional aspects of actinomycetes:an overview. World J Microbiol Biotechnol. 1991;7:171-184. https://doi.org/10.1007/BF00328987
  5. Zimmerman W. Degradation of lignin by bacteria. J Biotechnol. 1990;13:199-130. https://doi.org/10.1016/0168-1656(90)90105-K
  6. Franklin TJ, Snow GA, Barrett-Bee KJ, et al., editors. Antifungal, antiprotozoal and antiviral agents. 4th ed. Biochemistry of antimicrobial action. New York: Chapman & Hall Ltd; 1989. p. 137-161.
  7. Waksman SA, Lechevalier HA. The actinomycetes. Vol. III, Antibiotics of actinomycetes. Baltimore:The Williams & Wilkins Co; 1962. p. 248-252.
  8. Lechevalier MP. Actinomycetes in agriculture and forestry. In: Goodfellow M, Williams ST, Mordarski M, editors. Actinomycetes in biotechnology. New York: Academic Press; 1989. p. 327-358.
  9. Miller JJ, Liljeroth E, Henken G, et al. Fluctuations in the fluorescent pseudomonad and actinomycete populations of rhizosphere and rhizoplane during the growth of spring wheat. Can J Microbiol. 1990;36:389-391.
  10. Miller JJ, Liljeroth E, Willemsen-de Klein MJEIM, et al. The dynamics of actinomycetes and fluorescent pseudomonads in wheat rhizoplane and rhizosphere. Symbiosis. 1990;9:389-391.
  11. Blanchette R. Degradation of the lignocellulose complex in wood. Can J Bot. 1995;73:999-1010. https://doi.org/10.1139/b95-350
  12. Worrall JJ, Anagnost SE, Zabel RA. Comparison of wood decay among diverse lignicolous fungi. Mycologia. 1997;89:199-219. https://doi.org/10.1080/00275514.1997.12026772
  13. Yelle DJ, Ralph J, Lu F, et al. Evidence for cleavage of lignin by a brown rot basidiomycete. Environ Microbiol. 2008;10:1844-1849. https://doi.org/10.1111/j.1462-2920.2008.01605.x
  14. Niemenmaa O, Uusi-Rauva A, Hatakka A. Demethoxylation of [$O_{14}CH_3$]-labelled lignin model compounds by the brown-rot fungi Gloeophyllum trabeum and Poria (Postia) placenta. Biodegradation. 2008;19:555-565. https://doi.org/10.1007/s10532-007-9161-3
  15. Martinez D, Challacombe J, Morgenstern I, et al. Genome, transcriptome, and secretome analysis of wood decay fungus Postia placenta supports unique mechanisms of lignocellulose conversion. Proc Natl Acad Sci USA. 2009;106:1954-1959. https://doi.org/10.1073/pnas.0809575106
  16. Gilbertson RL. Wood-rotting fungi of North America. Mycologia. 1980;72:1-49. https://doi.org/10.1080/00275514.1980.12021153
  17. Rayner AD, Boddy L. Fungal decomposition of wood. Its biology and ecology. Wiley: John Wiley & Sons; 1988.
  18. Paterson RR. Ganoderma disease of oil palm - a white rot perspective necessary for integrated control. Crop Prot. 2007;9:1369-1376.
  19. Schmidt O. Indoor wood-decay basidiomycetes:damage, causal fungi, physiology, identification and characterization, prevention and control. Mycol Progress. 2007;6:261-279. https://doi.org/10.1007/s11557-007-0534-0
  20. Butt TM, Copping LG. Fungal biological control agents. Pestic Outlook. 2000;11:186-191. https://doi.org/10.1039/b008009h
  21. Ashwini N, Srividya S. Potentiality of Bacillus subtilis as biocontrol agent for management of anthracnose disease of chilli caused by Colletotrichum gloeosporioides OGC1. 3 Biotech. 2014;4:127-136.
  22. Solanki MK, Kumar S, Pandey AK, et al. Diversity and antagonistic potential of Bacillus spp. associated to the rhizosphere of tomato for the management of Rhizoctonia solani. Biocontrol Sci Techn. 2012;22:203-117. https://doi.org/10.1080/09583157.2011.649713
  23. Kobayashi DY, Guglielmoni M, Clarke BB. Isolation of the chitinolytic bacteria Xanthomonas maltophilia and Serratia marcescens as biological control agents for summer patch disease of turfgrass. Soil Biol Biochem. 1995;27:1479-1487. https://doi.org/10.1016/0038-0717(95)00062-J
  24. Howell CR. Mechanisms employed by Trichoderma species in the biological control of plant diseases:the history and evolution of current concepts. Plant Dis. 2003;7:4-10.
  25. Yuan WM, Crawford DL. Characterization of Streptomyces lydicus WYEC108 as a potential biocontrol agent against fungal root and seed rots. Appl Environ Microbiol. 1995;61:3119-3128.
  26. Trejo-Estrada SR, Sepulveda IR, Crawford DL. In vivo antagonism of Streptomyces violaceusniger YCED9 a fungal pathogen of turfgrass. World J Microbiol Biotechnol. 1998;14:865-872. https://doi.org/10.1023/A:1008877224089
  27. Crawford DL, Lynch JM, Whipps JM, et al. Isolation and characterization of actinomycete antagonists of a fungal root pathogen. Appl Environ Microbiol. 1993;59:3899-3905.
  28. El-Abyad MS, El-Sayed MA, El-Shanshoury AR, et al. Towards the biological control of fungal and bacterial diseases of tomato using antagonistic Streptomyces spp. Plant Soil. 1993;149:185-193. https://doi.org/10.1007/BF00016608
  29. Trejo-Estrada SR, Paszczynski A, Crawford DL. Antibiotics and enzymes produced by biocontrol agent Streptomyces violaceusniger YCED9. J Ind Microbiol Biotechnol. 1998;21:81-90. https://doi.org/10.1038/sj.jim.2900549
  30. Hayakawa M, Nonomura H. Humic acid-vitamin agar, a new medium for the selective isolation of soil actinomycetes. J Ferment Tech. 1987;65:501-509. https://doi.org/10.1016/0385-6380(87)90108-7
  31. Shirling ET, Gottlieb D. Methods for characterization of Streptomyces species. Int J Syst Evol Microbiol. 1966;16:313-340.
  32. Lane DJ. 16S/23S rRNA sequencing. In:Stackebrandt E, Goodfellow M, editors. Nucleic acid techniques in bacterial systematics. Chichester:Wiley; 1991. p. 115-175.
  33. Lee DH, Lee SK, Lee SH, et al. Accurate detection of chestnut ink disease causing Phytophthora katsurae by nested PCR. Australasian Plant Pathol. 2012;41:535-539. https://doi.org/10.1007/s13313-012-0154-2
  34. Wise LE, Murphy M, D Adieco AA. A chlorite holocellulose, its fractionation and bearing on summative wood analysis and studies on the hemicelluloses. Paper Trade J. 1946;122:35-43.
  35. R Core Team. 2014. R: a language and environment for statistical computing. 2012.
  36. Kumar D, Gupta RK. Biocontrol of wood-rotting fungi. Indian J. Biotechnol. 2006;5:20-25.
  37. Susi P, Aktuganov G, Himanen J, et al. Biological control of wood decay against fungal infection. J. Environ Manage. 2011;92:1681-1689. https://doi.org/10.1016/j.jenvman.2011.03.004
  38. Li Q, Jiang Y, Ning P, et al. Suppression of Magnaporthe oryzae by culture filtrates of Streptomyces globisporus JK-1. Biol Control. 2011;58:139-148. https://doi.org/10.1016/j.biocontrol.2011.04.013
  39. Aldesuquy HS, Mansour FA, Abo-Hamed SA. Effect of the culture filtrates of Streptomyces on growth and productivity of wheat plants. Folia Microbiol. 1998;43:465-470. https://doi.org/10.1007/BF02820792
  40. Prapagdee B, Kuekulvong C, Mongkolsuk S. Antifungal potential of extracellular metabolites produced by Streptomyces hygroscopicus against phytopathogenic fungi. Int J Biol Sci. 2008;4:330-337.
  41. Bruce A, Highley TL. Control of growth of wood decay Basidiomycetes by Trichoderma spp. and other potentially antagonistic fungi. Forest Prod J. 1991;41:63-67.
  42. Pellegrini A, Prodorutti D, Pertot I. Use of bark mulch pre-inoculated with Trichoderma atroviride to control Armillaria root rot. Crop Prot. 2014;64:104-109. https://doi.org/10.1016/j.cropro.2014.06.007
  43. Gilbertson RL, Ryvarden L. North American polypores. Vol. 1 and 2. Oslo, Norway: Fungiflora; 1986.
  44. McFee WW, Stone EL. The persistence of decaying wood in the humus layers of northern forests. Soil Sci Soc Am J. 1966;30:513-516. https://doi.org/10.2136/sssaj1966.03615995003000040032x
  45. Morrell JJ, Zabel RA. Wood microbiology: decay and its prevention. San Diego: Academic Press;1992.

Cited by

  1. Screening of Antifungal Microorganisms with Strong Biological Activity against Oak Wilt Fungus, Raffaelea quercus-mongolicae vol.34, pp.5, 2018, https://doi.org/10.7747/jfes.2018.34.5.395
  2. Draft Genomic Sequences of Streptomyces misionensis ACT66 and Streptomyces albidoflavus ACT77, Bacteria with Potential Application for Phytopathogen Biocontrol vol.8, pp.36, 2018, https://doi.org/10.1128/mra.00949-19
  3. Antagonistic Potential of Endophytic Bacteria Against Phytophthora palmivora Causing Black Pod Rot Disease on Cacao (Theobroma cacao L.) In Indonesia vol.19, pp.1, 2018, https://doi.org/10.3923/ppj.2020.22.41
  4. Microbial remediation for the removal of inorganic contaminants from treated wood: Recent trends and challenges vol.258, pp.None, 2018, https://doi.org/10.1016/j.chemosphere.2020.127429
  5. A novel streptomyces rhizobacteria from desert soil with diverse anti-fungal properties vol.16, pp.None, 2020, https://doi.org/10.1016/j.rhisph.2020.100243
  6. Screening of Endophytic Fungal Isolates Against Raffaelea quercus-mongolicae Causing Oak Wilt Disease in Korea vol.48, pp.6, 2018, https://doi.org/10.1080/12298093.2020.1830486
  7. Identification, Enzymatic Activity, and Decay Ability of Basidiomycetous Fungi Isolated from the Decayed Bark of Mongolian Oak (Quercus mongolica Fisch. ex Ledeb.) vol.37, pp.1, 2021, https://doi.org/10.7747/jfes.2021.37.1.52
  8. Enhancing pomegranate (Punica granatum L.) plant health through the intervention of a Streptomyces consortium vol.31, pp.4, 2018, https://doi.org/10.1080/09583157.2020.1859095
  9. The Threat of Pests and Pathogens and the Potential for Biological Control in Forest Ecosystems vol.12, pp.11, 2018, https://doi.org/10.3390/f12111579