DOI QR코드

DOI QR Code

An investigation of Panax ginseng Meyer growth promotion and the biocontrol potential of antagonistic bacteria against ginseng black spot

  • Sun, Zhuo (Cultivation Base of State Key Laboratory for Ecological Restoration and Ecosystem Management of JL Province and MOST, College of Chinese Medicinal Materials, Jilin Agricultural University) ;
  • Yang, Limin (College of Chinese Medicinal Materials, Jilin Agriculture University) ;
  • Zhang, Lianxue (College of Chinese Medicinal Materials, Jilin Agriculture University) ;
  • Han, Mei (College of Chinese Medicinal Materials, Jilin Agriculture University)
  • 투고 : 2016.10.11
  • 심사 : 2017.03.31
  • 발행 : 2018.07.15

초록

Background: Ginseng black spot disease resulting from Alternaria panax Whuetz is a common soil-borne disease, with an annual incidence rate higher than 20-30%. In this study, the bacterial strains with good antagonistic effect against A. panax are screened. Methods: A total of 285 bacterial strains isolated from ginseng rhizosphere soils were screened using the Kirby-Bauer disk diffusion method and the Oxford cup plate assay. We analyzed the antifungal spectrum of SZ-22 by confronting incubation. To evaluate the efficacy of biocontrol against ginseng black spot and for growth promotion by SZ-22, we performed pot experiments in a plastic greenhouse. Taxonomic position of SZ-22 was identified using morphology, physiological, and biochemical characteristics, 16S ribosomal DNA, and gyrB sequences. Results: SZ-22 (which was identified as Brevundimonas terrae) showed the strongest inhibition rate against A. panax, which showed 83.70% inhibition, and it also provided broad-spectrum antifungal effects. The inhibition efficacies of the SZ-22 bacterial suspension against ginseng black spot reached 82.47% inhibition, which is significantly higher than that of the 25% suspension concentrate azoxystrobin fungicide treatment (p < 0.05). Moreover, the SZ-22 bacterial suspension also caused ginseng plant growth promotion as well as root enhancement. Conclusion: Although the results of the outdoor pot-culture method were influenced by the pathogen inoculum density, the cropping history of the field site, and the weather conditions, B. terrae SZ-22 controlled ginseng black spot and promoted ginseng growth successfully. This study provides resource for the biocontrol of ginseng black spot.

키워드

참고문헌

  1. Jung J, Kim KH, Yang K, Bang KH, Yang TJ. Practical application of DNA markers for high-throughput authentication of Panax ginseng and Panax quinquefolius from commercial ginseng products. J Ginseng Res 2014;38:123-9. https://doi.org/10.1016/j.jgr.2013.11.017
  2. Zhao YF, Zhu GX, Wang S, Wu LJ, Yang YJ. Studies on the integrated control of ginseng black spot (Alternaria panax Whuetz) in China. Acta Phytophy Sin 1990;17:123-6 [in Chinese].
  3. Yu SH, Nishimura S, Hirosawa T. Morphology and pathogenicity of Alternaria panax isolated from Panax schinseng in Japan and Korea. Ann. Phytopathol Soc Jpn 1984;50:313-21. https://doi.org/10.3186/jjphytopath.50.313
  4. Wang X, Wang XW, Gao J, Xu HY, Ma DY, Song HM, Feng ZW. Toxicity test and field control effects of different fungicides against Alternaria panax. Agrochemicals 2011;50:841-4 [in Chinese].
  5. Kalia A, Gosal SK. Effect of pesticide application on soil microorganisms. Arch Agron Soil Sci 2011;57:569-96. https://doi.org/10.1080/03650341003787582
  6. Emmert EA, Handelsman J. Biocontrol of plant disease: a (grame) positive perspective. FEMS Microbiol Lett 1999;171:1-9. https://doi.org/10.1111/j.1574-6968.1999.tb13405.x
  7. Wood RKS, Tveit M. Control of plant diseases by use of antagonistic organisms. Bot Rev 1955;1:441-92.
  8. Kim SG, Jang Y, Kim HY, Koh YJ, Kim YH. Comparison of microbial fungicides in antagonistic activities related to the biological control of phytophthora blight in chili pepper caused by Phytophthora capsici. Plant Pathol J 2010;26:340-5. https://doi.org/10.5423/PPJ.2010.26.4.340
  9. Young SK, Balaraju K, Young HK, Yongho J. Biological characteristics of Paenibacillus polymyxa GBR-1 involved in root rot of stored Korean ginseng. J Ginseng Res 2016;40:43-61.
  10. Joy A, Parke JL. Biocontrol of Alternaria leaf blight on America ginseng by Burkholderia cepacia AMMD. In: Bailey WG, Whitehead C, Proctor JTA, Kyle JT, editors. The challenges of the 21st century - Proc. Int. Ginseng Conf., Vancouver, 1994. Burnaby, Canada: Simon Fraser University; 1995. p. 93-100.
  11. Cardinale BJ, Harvey CT, Gross K, Ives AR. Biodiversity and biocontrol: emergent impacts of a multi-enemy assemblage on pest suppression and crop yield. Ecol Lett 2003;6:857-65. https://doi.org/10.1046/j.1461-0248.2003.00508.x
  12. Toal ME, Yeomans C, Killham K, Mecharg AA. A review of rhizosphere carbon flow modeling. Plant Soil 2000;222:263-81. https://doi.org/10.1023/A:1004736021965
  13. Krzyzanowska DM, Potrykus M, Golanowska M, Polonis K, Gwizdek- Wisniewska A, Lojkowska E, Jafra S. Rhizosphere bacteria as potential biocontrol agents against soft rot caused by various Pectobacterium and Dickeya spp. strains. J Plant Pathol 2012;94:367-72.
  14. Whipps JM. Microbial interactions and biocontrol in the rhizosphere. J Exp Bot 2001;52:487-511. https://doi.org/10.1093/jxb/52.suppl_1.487
  15. Bloemberg GV, Lugtenberg BJJ. Molecular basis of plant growth promotion and biocontrol by rhizobacteria. Curr Opin Plant Biol 2001;4:343-50. https://doi.org/10.1016/S1369-5266(00)00183-7
  16. Ma Y, Prasad MN, Rajkumar M, Freitas H. Plant growth promoting rhizobacteria and endophytes accelerate phytoremediation of metalliferous soils. Biotechnol Adv 2011;29:248-58. https://doi.org/10.1016/j.biotechadv.2010.12.001
  17. Shaikh SS, Sayyed RZ. Role of plant growth-promoting rhizobacteria and their formulation in biocontrol of plant diseases. In: Arora NK, editor. Plant microbes symbiosis: applied facets. Maharashtra, IA: Springer India; 2015. p. 337-51.
  18. Fang ZD. Study methods of plant pathology. 3rd ed. Beijing: China Agriculture Press; 2007. p. 137-8 [in Chinese].
  19. Sun Z, Yang LM. The screening and identification of the antagonistic strain against Cylindrocarpon destructans. J China Agro Univ 2016;21:773-81 [in Chinese].
  20. Shapiro MF, Greenfield S. The complete blood count and leukocyte differential count. An approach to their rational application. Ann Intern Med 1987;106:65-74. https://doi.org/10.7326/0003-4819-106-1-65
  21. Jones RN, Ballow CH, Biedenbach DJ. Multi-laboratory assessment of the linezolid spectrum of activity using the KirbyeBauer disk diffusion method: report of the Zyvox Antimicrobial Potency Study (ZAPS) in the United States. Diagn Microbiol Infect Dis 2001;40:59-66. https://doi.org/10.1016/S0732-8893(01)00235-8
  22. Kishore GK, Pande S, Podile AR. Biological control of collar rot disease with broad-spectrum antifungal bacteria associated with groundnut. Can J Microbiol 2005;51:123-32. https://doi.org/10.1139/w04-119
  23. Hessenmuller A, Zeller W. Biological control of soilborne Phytophthora species on strawberry with bacterial antagonists: I. Antagonistic effect and colonization of rhizoplane. J Plant Dis Prot 1996;103:602-9.
  24. Yang XD, Gao J, Ma GL, Zhang JH. Improvement on the calculation formula of plant disease control effect. J Jilin Agro Univ 1999;21:46-8 [in Chinese].
  25. George G. Bergey's manual of systematic bacteriology. In: Volume 2: The Proteobacteria. 2nd ed. Berlin: Springer-Verlag; 2005. p. 735-69.
  26. Marshall SM, Melito PL, Woodward DL, Johnson WM, Rodgers FG, Mulvey MR. Rapid identification of Campylobacter, Arcobacter, and Helicobacter isolates by PCR-restriction fragment length polymorphism analysis of the 16S rRNA gene. J Clin Microbiol 1999;37:4158-60.
  27. Lim CY, Lee KH, Cho MJ, Chang MW, Kim SY, Myong NH, Lee WK, Rhee KH, Kook YH. Detection of Helicobacter pylori in gastric mucosa of patients with gastroduodenal diseases by PCR-restriction analysis using the RNA polymerase gene (rpoB). J Clin Microbiol 2003;41:3387-91. https://doi.org/10.1128/JCM.41.7.3387-3391.2003
  28. Liu WQ, Mao ZC, Yang YH, Xie BY. Analysis of soil bacterial diversity by using the 16S rRNA gene library. Acta Microbiol Sin 2008;48:1344-50 [in Chinese].
  29. Tayeb LA, Lefevre M, Passet V, Diancourt L, Brisse S, Grimont PA. Comparative phylogenies of Burkholeria, Ralstonia, Comamonas, Brevundimonas and related organisms derived from rpoB, gyrB and rrs gene sequences. Res Microbol 2008;159:169-77. https://doi.org/10.1016/j.resmic.2007.12.005
  30. Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG. The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 1997;25:4876-82. https://doi.org/10.1093/nar/25.24.4876
  31. Ramadan EM, AbdelHafez AA, Hassan EA, Saber FM. Plant growth promoting rhizobacteria and their potential for biocontrol of phytopathogens. Afr J Microbiol Res 2016;10:486-504. https://doi.org/10.5897/AJMR2015.7714
  32. Bhattacharyya PN, Jha DK. Plant growth-promoting rhizobacteria (PGPR): emergence in agriculture. World J Microbiol Biotechnol 2012;28:1327-50. https://doi.org/10.1007/s11274-011-0979-9
  33. Velusamy P, Immanuel JE, Gnanamanickam SS. Rhizosphere bacteria for biocontrol of bacterial blight and growth promotion of rice. Rice Sci 2013;20:356-62. https://doi.org/10.1016/S1672-6308(13)60143-2
  34. Zhang SP, Kuang J, Wang JX, Chen CJ, Zhou MG. Identification of biocontrol bacterial strain N J-18 and its antagonistic activity to several phytopathogenic fungi. Chin Agro Sci Bull 2009;25:213-7 [in Chinese].
  35. Garbeva P, van Veen JA, van Elsas JD. Assessment of the diversity, and antagonism towards Rhizoctonia solani AG3, of Pseudomonas species in soil from different agricultural regimes. FEMS Microbiol Ecol 2004;47:51-64. https://doi.org/10.1016/S0168-6496(03)00234-4
  36. Haas D, Keel C. Regulation of antibiotic production in root-colonized Pseudomonas spp., and relevance for biological control of plant disease. Annu Rev Phytopathol 2003;41:117-53. https://doi.org/10.1146/annurev.phyto.41.052002.095656
  37. Lee JY, Moon SS, Hwang BK. Isolation and antifungal and antioomycete activities of aerugine produced by Pseudomonas fluorescens strain MM-B16. Appl Environ Microbiol 2003;69:2023-31. https://doi.org/10.1128/AEM.69.4.2023-2031.2003
  38. Zeng QG, Zhu D, Yan RM, Zhu F, Wang ZX. Isolation and identification of Endophytic bacteria H-6 with high antifungal activity from Huperzia serrata. Microbiol China 2008;35:512-8 [in Chinese].
  39. Mishra S, Arora NK. Evaluation of rhizospheric Pseudomonas and Bacillus as biocontrol tool for Xanthomonas campestris pv campestris. World J Microbiol Biotechnol 2012;28:693-702. https://doi.org/10.1007/s11274-011-0865-5
  40. Broadbent P, Baker KF, Waterworth Y. Bacteria and actinomycetes antagonistic to fungal root pathogens in Australian soils. Aust J Biol Sci 1971;24:925-44. https://doi.org/10.1071/BI9710925
  41. Weller DM. Biological control of soilborne plant pathogens in the rhizosphere with bacteria. Annu Rev Phytopathol 1988;26:379-407. https://doi.org/10.1146/annurev.py.26.090188.002115
  42. Bae YS, Park K, Kim CH. Bacillus spp. as biocontrol agents of root rot and Phytophthora blight on ginseng. Plant Pathol J 2004;20:63-6. https://doi.org/10.5423/PPJ.2004.20.1.063
  43. Jang YL, Kim SG, Kim YH. Biocontrol efficacies of Bacillus species against Cylindrocarpon destructans causing ginseng root rot. Plant Pathol J 2011;27:333-41. https://doi.org/10.5423/PPJ.2011.27.4.333
  44. Shanmugam V, Gupta S, Dohroo NP. Selection of a compatible biocontrol strain mixture based on co-cultivation to control rhizome rot of ginger. Crop Prot 2013;43:119-27. https://doi.org/10.1016/j.cropro.2012.08.012
  45. Liu DQ, Anderson NA, Kinkel LL. Field evaluation of antagonistic Streptomyces strains on biocontrol of potato scab. Acta Phytopathol Sin 2000;30:237-44 [in Chinese].

피인용 문헌

  1. Inhibitory Effects of Black Ginseng on Particulate Matter-Induced Pulmonary Injury vol.47, pp.6, 2018, https://doi.org/10.1142/s0192415x19500630
  2. An LCI‐like protein APC2 protects ginseng root from Fusarium solani infection vol.130, pp.1, 2018, https://doi.org/10.1111/jam.14771
  3. A Novel Biocontrol Strain Bacillus amyloliquefaciens FS6 for Excellent Control of Gray Mold and Seedling Diseases of Ginseng vol.105, pp.7, 2018, https://doi.org/10.1094/pdis-07-20-1593-re
  4. Long‐term fertilisation regimes influence the diversity and community of wheat leaf bacterial endophytes vol.179, pp.2, 2018, https://doi.org/10.1111/aab.12689