DOI QR코드

DOI QR Code

Pathogenicity and Host Range of a Potential Mycoherbicide, Isolate BWC98-105, Causing White Root Rot on Trifoliorum repens

  • Hong, Yeon-Kyu (Plant Environment Division, National Yeongnam Agricultural Experiment Station (NYARI), Rural Development Administration) ;
  • Cho, Jae-Min (Plant Environment Division, National Yeongnam Agricultural Experiment Station (NYARI), Rural Development Administration) ;
  • Lee, Bong-Choon (Plant Environment Division, National Yeongnam Agricultural Experiment Station (NYARI), Rural Development Administration) ;
  • Song, Seok-Bo (Plant Environment Division, National Yeongnam Agricultural Experiment Station (NYARI), Rural Development Administration) ;
  • Park, Sung-Tae (Plant Environment Division, National Yeongnam Agricultural Experiment Station (NYARI), Rural Development Administration)
  • Published : 2004.03.01

Abstract

White root rot of wild white clover (Trifoliorum repens) caused by isolate BWC98-105 has been first reported in Korea. Typical symptoms on root include water-soaked and dark-brown rot, resulting in complete blight of the whole plant. The fungus grew well at $20-28^{\circ}C$ and produced abundant sclerotia at 10-15 days after full mycelial growth on potato dextrose agar. Sclerotia were brown to dark-brown in color and 1-3 mm in length. When white clover plants were inoculated with mycelial suspension ($10^5$ cfu/ml) of isolate BWC98-105, the plant shoots were killed within 4-6 days and the roots were completely blighted. Sclerotia were also formed on the surface of the root covered with whitish mycelia within 10-15 days in the field. All nine isolates developed high incidences of white root rot disease on white clover seedlings, of which the symptoms were similar to those observed in the fields. Hence, their pathogenicity was confirmed on white clover. The infection rate of the fungal isolates varied from 78.5% to 95.2%, among which BWC98-105 was the most virulent isolate. The weeding efficacy of the fungus was maintained until the following year, leading to a significant reduction of reshooting. The fungus was specifically parasitic to white clover, but not to four lawn species including zoysiagrass (Zoysia japonica) under greenhouse test. The fungus also had no response to some Gramineae species including rice, but caused little damage to five species of Leguminosae.

Keywords

References

  1. Aoshima, K., Chubagi, K. and Mirora, K.:函類硏究法, 共立出版, 東京 1983. pp.61
  2. Boyette, C. D. 1991. Host range and virulence of Colletotrichum truncatum, a potential mycoherbicide for hemp sesbania (Sesbania exaltata). Plant Dis. 75: 62-64 https://doi.org/10.1094/PD-75-0062
  3. Boyetchko, S. M. 1997. Principles of biological weed control with microorganism. HortScience 32:201-205
  4. Conway, K E. 1976. Evaluation of Cercospora rodmanii as a biological control of waterhyacinths. Phytopathology 66:914-917 https://doi.org/10.1094/Phyto-66-914
  5. Danial, J. T., Templeton, G. E., Smith, R. J. and Fox, W. T. 1973. Biological control of northern jointvetch in rice with an endemic fungal disease. Weed Sci. 21:303-307
  6. Hong, Y. K., Cho, J. M., Shin, D. B. and Uhm, J. Y. 1998. Pathogenicity to white clover of fungal pathogen YK101 and its host range. Kor. Soc. Weed Sci. Abstr. 18(2)
  7. Hong, Y. K., Cho, J. M., Shin, D. B. and Uhm, J. Y. 1999. Pathogenicity and host range of potential bioherbicide isolate YK101, causing white root rot on white clover (Trifoliorum repens). Kor. Soc. Plant Pathol. Abstr. 4(O-03)
  8. Hong, Y. K., Song, S. B., Shin, D. B., Lee, B. C., Leem, D. C. and Moon, H. P. 2001. Evaluation of mycelium virulence of mycoherbicide agent, fungal isolate, BWC-101 to Aeschynomene indica L. Kor. Soc. Plant Pathol. Abstr. (B-11)
  9. Hong, Y. K., Hyun, J. N., Lee, B. C., Lee, D. C. and Kim, S. C. 2002. Weeding efficacy of phytotoxin extracted from Sclerotinia sp. (BWC98-105) on the white clover Trifolium repens. Kor. Soc. Plant Pathol. Abstr. (B-26)
  10. Hong, Y. K., Hyun, J. N., Song, S. B., Lee, B. C., Lee, D. C. and Kim, S. C. 2002. The antibiotic effect of the secondary product purified from Sclerotinia sp. (BWC98-105) on the plant pathogenic bacteria. Kor. Soc. Plant Pathol. Abstr. (B-32)
  11. Ormeno-Nunez, J., Reeleder, F. D. and Watson, A. K. 1988. A foliar disease of field bindweed (Convolvulus arvensis) caused by Phomopsis convolvulus. Plant Disease. 72:338-342 https://doi.org/10.1094/PD-72-0338
  12. Reuveni, M., Tuzun, S., Cole, J. S., Siegel, M. R. and Kuc, J. 1986. The effects of plant age and leaf position on the susceptibility of tobacco to blue mold caused by Peronospora tabacina. Phytopathology 76:455-458 https://doi.org/10.1094/Phyto-76-455
  13. Rosskopf, E. N., Charudattan, R. and Kadir, J. B. 1999. Use of plant pathens in weed control. In: Handbook of biological control. Academic Press, San Diego, CA. pp. 891-918
  14. TeBeest, D. O. 1988. Additions to the host range of Colletotrichum gloeosporiodes f. sp. aeschynomene Plant Disease 72: 16-18 https://doi.org/10.1094/PD-72-0016
  15. Walker, H. L. 1981. Factors affecting biological control of spurred anoda (Anoda cristata) with Altemaria macrospora. Weed Sci. 29:505-507
  16. Walker, H. L. 1981. Fusarium lateritium: A pathogen of spurred anoda (Anoda cristata), prickly sida (Sida spinosa), and velvetleaf (Abutilon theophrasti). Weed Sci. 20:629-631
  17. Weidemann, G. J., TeBeest, D. O. and Cartwright, R. D. 1988. Host specificity of Colletotrichum gloeosporiodes f. sp. aeschynomene and C. truncatum in the Leguminosae. Phytopathology 66:914-917 https://doi.org/10.1094/Phyto-66-914

Cited by

  1. The occurrence of Sclerotium rot on white clover (Trifolium repens L.) caused by Sclerotium rolfsii in Korea vol.8, pp.1, 2013, https://doi.org/10.1007/s13314-013-0103-0