DOI QR코드

DOI QR Code

Infection and cox2 sequence of Pythium chondricola (Oomycetes) causing red rot disease in Pyropia yezoensis (Rhodophyta) in Korea

  • Lee, Soon Jeong (Seaweed Research Center, National Institute of Fisheries Science) ;
  • Jee, Bo Young (Aquatic Life Disease Control Division, National Institute of Fisheries Science) ;
  • Son, Maeng-Hyun (Aquatic Life Disease Control Division, National Institute of Fisheries Science) ;
  • Lee, Sang-Rae (Marine Research Institute, Pusan National University)
  • Received : 2017.04.02
  • Accepted : 2017.05.16
  • Published : 2017.06.15

Abstract

Red rot disease has caused a major decline in Pyropia (Nori) crop production in Korea, Japan, and China. To date, only Pythium porphyrae (Pythiales, Oomycetes) has been reported as the pathogen causing red rot disease in Pyropia yezoensis (Rhodophyta, Bangiales). Recently, Pythium chondricola was isolated from the infected blades of Py. yezoensis during molecular analyses using the mitochondrial cox1 region. In this study, we evaluated the pathogenicity of P. chondricola as an algal pathogen of Py. yezoensis. Moreover, a new cox2 marker was developed with high specificity for Pythium species. Subsequent to re-inoculation, P. chondricola successfully infected Py. yezoensis blades, with the infected regions containing symptoms of red rot disease. A novel cox2 marker successfully isolated the cox2 region of Pythium species from the infected blades of Py. yezoensis collected from Pyropia aquaculture farms. cox2 sequences showed 100% identity with that of P. chondricola (KJ595354) and 98% similarity with that of P. porphyrae (KJ595377). The results of the pathogenicity test and molecular analysis confirm that P. chondricola is a new algal pathogen causing red rot disease in Pyropia species. Moreover, it could also suggest the presence of cryptic biodiversity among Korean Pythium species.

Keywords

References

  1. Arasaki, S. 1947. Studies on the rot of Porphyra tenera by Pythium. Nippon Suisan Gakkaishi 13:74-90. https://doi.org/10.2331/suisan.13.74
  2. Arasaki, S., Akino, K. & Tomiyama, T. 1968. A comparison of some physiological aspects in a marine Pythium on the host and on the artificial medium. Bull. Misaki Mar. Biol. Inst. Kyoto Univ. 12:203-206.
  3. Blouin, N. A., Brodie, J. A., Grossman, A. C., Xu, P. & Brawley, S. H. 2011. Porphyra: a marine crop shaped by stress. Trends Plant Sci. 16:29-37. https://doi.org/10.1016/j.tplants.2010.10.004
  4. Choi, Y. -J., Beakes, G., Glockling, S., Kruse, J., Nam, B., Nigrelli, L., Ploch, S., Shin, H. -D., Shivas, R. G., Telle, S., Voglmayr, H. & Thines, M. 2015. Towards a universal barcode of oomycetes: a comparison of the cox1 and cox2 loci. Mol. Ecol. Resour. 15:1275-1288. https://doi.org/10.1111/1755-0998.12398
  5. De Cock, A. W. A. M. 1986. Marine Pythiaceae from decaying seaweeds in the Netherlands. Mycotaxon 25:101-110.
  6. Diehl, N., Kim, G. H. & Zuccarello, G. C. 2017. A pathogen of New Zealand Pyropia plicata (Bangiales, Rhodophyta), Pythium porphyrae (Oomycota). Algae 32:29-39. https://doi.org/10.4490/algae.2017.32.2.25
  7. Hudspeth, D. S. S., Nadler, S. A. & Hudspeth, M. E. S. 2000. A COX2 molecular phylogeny of the Peronosporomycetes. Mycologia 92:674-684. https://doi.org/10.2307/3761425
  8. Kawamura, Y., Yokoo, K., Tojo, M. & Hishiike, M. 2005. Distribution of Pythium porphyrae, the causal agent of red rot disease of Porphyrae spp., in the Ariake Sea, Japan. Plant Dis. 89:1041-1047. https://doi.org/10.1094/PD-89-1041
  9. Kim, G. H., Moon, K. -H., Kim, J. -Y., Shim, J. & Klochkova, T. A. 2014. A revaluation of algal diseases in Korean Pyropia (Porphyra) sea farms and their economic impact. Algae 29:249-265. https://doi.org/10.4490/algae.2014.29.4.249
  10. Klochkova, T. A., Jung, S. & Kim, G. H. 2017. Host range and salinity tolerance of Pythium porphyrae may indicate its terrestrial origin. J. Appl. Phycol. 29:371-379. https://doi.org/10.1007/s10811-016-0947-8
  11. Lee, S. J., Hwang, M. S., Park, M. A., Baek, J. M., Ha, D. -S., Lee, J. -E. & Lee, S. -R. 2015. Molecular identification of the algal pathogen Pythium chondricola (Oomycetes) from Pyropia yezoensis (Rhodophyta) using ITS and cox1 markers. Algae 30:217-222. https://doi.org/10.4490/algae.2015.30.3.217
  12. Levesque, C. A. & De Cock, A. W. A. M. 2004. Molecular phylogeny and taxonomy of the genus Pythium. Mycol. Res. 108:1363-1383. https://doi.org/10.1017/S0953756204001431
  13. Liu, Y. -M., Ma, J. -H. & Wen, Q. 2012. Simultaneous infection by red rot and olpidiops disease in laver Porphyra haitanensis. J. Dalian Ocean Univ. 27:546-550.
  14. Mo, Z., Li, S., Kong, F., Tang, X. & Mao, Y. 2016. Characterization of a novel fungal disease that infects the gametophyte of Pyropia yezoensis (Bangiales, Rhodophyta). J. Appl. Phycol. 28:395-404. https://doi.org/10.1007/s10811-015-0539-z
  15. Park, C. S., Kakinuma, M. & Amano, H. 2006. Forecasting infections of the red rot disease on Porphyra yezoensis Ueda (Rhodophyta) cultivation farms. J. Appl. Phycol. 18:295-299. https://doi.org/10.1007/s10811-006-9031-0
  16. Park, C. S., Kakinuma, M., Sakaguchi, K. & Amano, H. 2003. Genetic variation detected with random amplified polymorphic DNA markers among isolates of the red rot disease fungus Pythium porphyrae isolated from Porphyra yezoensis from Korea and Japan. Fish. Sci. 69:361-368. https://doi.org/10.1046/j.1444-2906.2003.t01-1-00629.x
  17. Robideau, G. P., De Cock, A. W. A. M., Coffey, M. D., Voglmayr, H., Brouwer, H., Bala, K., Chitty, D. W., Desaulniers, N., Eggertson, Q. A., Gachon, C. M. M., Hu, C. -H., Kupper, F. C., Rintoul, T. L., Sarhan, E., Verstappen, E. C. P., Zhang, Y., Bonants, P. J. M., Ristaino, J. B. & Levesque, C. A. 2011. DNA barcoding of oomycetes with cytochrome c oxidase subunit I and internal transcribed spacer. Mol. Ecol. Resour. 11:1002-1011. https://doi.org/10.1111/j.1755-0998.2011.03041.x
  18. Seifert, K. A. 2009. Progress towards DNA barcoding of fungi. Mol. Ecol. Resour. 9:83-89.
  19. Senda, M., Kageyama, K., Suga, H. & Levesque, C. A. 2009. Two new species of Pythium, P. senticosum and P. takayamanum, isolated from cool-temperate forest soil in Japan. Mycologia 101:439-448. https://doi.org/10.3852/08-104
  20. Takahashi, M., Ichitani, T. & Sasaki, M. 1977. Pythium porphyrae Takahashi et Sasaki, sp. nov. causing red rot of marine red algae Porphyra spp. Trans. Mycol. Soc. Jpn. 18:279-285.
  21. Villa, N. O., Kageyama, K., Asano, T. & Suga, H. 2006. Phylogenetic relationships of Pythium and Phytophthora species based on ITS rDNA, cytochrome oxidase II and $\beta$-tubulin gene sequences. Mycologia 98:410-422.

Cited by

  1. Compositional Shifts of Bacterial Communities Associated With Pyropia yezoensis and Surrounding Seawater Co-occurring With Red Rot Disease vol.10, pp.None, 2019, https://doi.org/10.3389/fmicb.2019.01666
  2. Characterization of Pythium chondricola associated with red rot disease of Pyropia yezoensis (Ueda) (Bangiales, Rhodophyta) from Lianyungang, China vol.37, pp.3, 2017, https://doi.org/10.1007/s00343-019-8075-3
  3. 감태(Ecklonia cava Kjellman) 신품종 개발을 위한 양식 개체군과 자연 개체군의 형태 비교 vol.37, pp.4, 2017, https://doi.org/10.11626/kjeb.2019.37.4.707
  4. Occurrence and pathogenicity of Pythium (Oomycota) on Ulva species (Chlorophyta) at different salinities vol.35, pp.1, 2017, https://doi.org/10.4490/algae.2020.35.2.25
  5. The gene repertoire of Pythium porphyrae (Oomycota) suggests an adapted plant pathogen tackling red algae vol.35, pp.2, 2020, https://doi.org/10.4490/algae.2020.35.6.4
  6. A review of reported seaweed diseases and pests in aquaculture in Asia vol.51, pp.4, 2017, https://doi.org/10.1111/jwas.12649