Volume 7, Issue 1 (3-2018)
Plant Pathol. Sci. 2018, 7(1): 51-62 |
Back to browse issues page
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
MOHAMMADI M, HOSSEINI A, SEDAGHATI E, HOSSEINI S. (2018). Mycoviruses Application in Biocontrol of Fugal Pathogens. Plant Pathol. Sci.. 7(1), 51-62. doi:10.29252/pps.7.1.51
URL: http://yujs.yu.ac.ir/pps/article-1-143-en.html
URL: http://yujs.yu.ac.ir/pps/article-1-143-en.html
Department of Plant Protection, Vali-e-Asr University of Rafsanjan, Iran , Hosseini@vru.ac.ir
Abstract: (7450 Views)
Mohammadi M., Hosseini A., Sedaghati E. and Hosseini S. 2018. Mycoviruses application in biocontrol of fugal pathogens. Plant Pathology Science 7(1):51-62.
Mycoviruses or fungal parasitic viruses have dsDNA, dsRNA or ssRNA genome. Some of these viruses have a restricted host range and can infect certain strains of host species. In contrast, some other viruses have wider host range and can infect different species of a fungal family. In most cases these viruses are transmitted by anastomosis of mycelium. In a phenomenon called hypovirulence, most of these viruses decrease the virulence of their host fungus. Discovery of hypovirulence revealed the biocontrol ability of mycoviruses. In summary, mycoviruses could be implemented as powerful agents for biocontrol of fungal pathogens and induction of resistance in plants.
Mycoviruses or fungal parasitic viruses have dsDNA, dsRNA or ssRNA genome. Some of these viruses have a restricted host range and can infect certain strains of host species. In contrast, some other viruses have wider host range and can infect different species of a fungal family. In most cases these viruses are transmitted by anastomosis of mycelium. In a phenomenon called hypovirulence, most of these viruses decrease the virulence of their host fungus. Discovery of hypovirulence revealed the biocontrol ability of mycoviruses. In summary, mycoviruses could be implemented as powerful agents for biocontrol of fungal pathogens and induction of resistance in plants.
References
1. Alfen N. K. V. and Kazmierczak P. 2008. Hypovirulence. Pp. 574-580. In: B. W. J. Mahy and M. H. V. V. Regenmortel(ed). Encyclopedia of Virology. Academic Press, USA. [DOI:10.1016/B978-012374410-4.00564-1]
2. Aoki N., Moriyama H., Kodama M., Arie T., Teraoka T. and Fukuhara T. 2009. A novel mycovirus associated with four double-stranded RNAs affects host fungal growth in Alternaria alternata. Virus Research 140:179-187. [DOI:10.1016/j.virusres.2008.12.003]
3. Boine B., Kingston R. L. and Pearson M. N. 2012. Recombinant expression of the coat protein of Botrytis virus X and development of an immunofluorescence detection method to study its intracellular distribution in Botrytis cinerea. Journal of General Virology 93:2502-2511. [DOI:10.1099/vir.0.043869-0]
4. Botella L., Tuomivirta T. T., Kaitera J., Carrasco Navarro V., Diez J. J., and Hantula J. 2010. Spanish population of Gremmeniella abietina is genetically unique but related to type A in Europe. Fungal Biology 114:778–789. [DOI:10.1016/j.funbio.2010.07.003]
5. Brasier C. M. 2000. Viruses as biological control agents of the Dutch elm disease fungus Ophiostoma novo-ulmi. Pp. 201-212. In: C.P. Dunne (ed.). The Elms: Breeding, Conservation and Disease Management. Kluwer Academic Publishers, USA. [DOI:10.1007/978-1-4615-4507-1_12]
6. Chiba S., Salaipeth L., Lin Y.-H., Sasaki A., Kanematsu S. and Suzuki N. 2009. A novel bipartite double-stranded RNA mycovirus from the white root rot fungus Rosellinia necatrix: molecular and biological characterization, taxonomic considerations, and potential for biological control. Journal of Virology 83:12801-12812. [DOI:10.1128/JVI.01830-09]
7. Choi G. H., Dawe A. L., Churbanov A., Smith M. L., Milgroom M. G. and Nuss D. L. 2012. Molecular characterization of vegetative incompatibility genes that restrict hypovirus transmission in the chestnut blight fungus Cryphonectria parasitica. Genetics 190:113-127. [DOI:10.1534/genetics.111.133983]
8. Chun S. J. and Lee Y. H. 1997. Inheritance of dsRNAs in the rice blast fungus, Magnaporthe grisea. FEMS Microbiology Letters 148:159-162. [DOI:10.1111/j.1574-6968.1997.tb10282.x]
9. Deng F., Xu R. and Boland G. 2003. Hypovirulence-associated double-stranded RNA from Sclerotinia homoeocarpa is conspecific with Ophiostoma novo-ulmi mitovirus 3a-Ld. Phytopathology 93:1407-1414. [DOI:10.1094/PHYTO.2003.93.11.1407]
10. Ganley, R. J., and L. S. Bulman. 2016. Dutch elm disease in New Zealand: impacts from eradication and management programmes. Plant Pathology 65:1047-1055. [DOI:10.1111/ppa.12527]
11. Ghabrial S. A. 1998. Origin, adaptation and evolutionary pathways of fungal viruses. Virus Genes 16:119-131. [DOI:10.1023/A:1007966229595]
12. Ghabrial S. A. and Suzuki N. 2008. Fungal Viruses. Pp. 284-291. In: B. W. J. Mahy and M. H. V. v. Regenmortel(ed). Encyclopedia of Virology. Academic Press, USA. [DOI:10.1016/B978-012374410-4.00563-X]
13. Ghabrial S. A. and Nibert M. L. 2009. Victorivirus, a new genus of fungal viruses in the family Totiviridae. Archives of Virology 154:373-379. [DOI:10.1007/s00705-008-0272-x]
14. Ghabrial S. A. and Suzuki N. 2009. Viruses of plant pathogenic fungi. Annual Review of Phytopathology 47:353-384. [DOI:10.1146/annurev-phyto-080508-081932]
15. Heiniger U. and Rigling D. 1994. Biological control of chestnut blight in Europe. Annual Review of Phytopathology 32:581-599. [DOI:10.1146/annurev.py.32.090194.003053]
16. Hutchison E., Brown S., Tian C. and Glass NL. 2005. Transcriptional profiling and functional analysis of heterokaryon incompatibility in Neurospora crassa reveals that reactive oxygen species, but not metacaspases, are associated with programmed cell death. Microbiology 155:3957–3970. [DOI:10.1099/mic.0.032284-0]
17. Ikeda K., Inoue K., Kida C., Uwamori T., Sasaki A., Kanematsu S. and Park P. 2013. Potentiation of mycovirus transmission by zinc compounds via attenuation of heterogenic incompatibility in Rosellinia necatrix. Applied and Environmental Microbiology 79:3684-3691. [DOI:10.1128/AEM.00426-13]
18. King A. M., Adams M. J., Lefkowitz E. J. and Carstens E. B. 2012. Virus Taxonomy: Classification and Nomenclature of Viruses. Elsevier, USA, 1272p.
19. Liu H., Fu Y., Jiang D., Li G., Xie J., Peng Y., Yi X. and Ghabrial S. A. 2009. A novel mycovirus that is related to the human pathogen hepatitis E virus and rubi-like viruses. Journal of Virology 83:1981-1991. [DOI:10.1128/JVI.01897-08]
20. Liu L., Xie J., Cheng J., Fu Y., Li G., Yi X. and Jiang D. 2014. Fungal negative-stranded RNA virus that is related to Bornaviruses and Nyaviruses. Proceedings of the National Academy of Sciences 111:12205-12210. [DOI:10.1073/pnas.1401786111]
21. Milgroom M. G. and Cortesi P. 2004. Biological control of chestnut blight with hypovirulence: a critical analysis. Annual review of phytopathology 42:311-338. [DOI:10.1146/annurev.phyto.42.040803.140325]
22. Mu-oz-Adalia E. J., Fernández M. M. and Diez J. J. 2016. The use of mycoviruses in the control of forest diseases. Biocontrol Science and Technology 26:577-604. [DOI:10.1080/09583157.2015.1135877]
23. Pearson M. N., Beever R. E., Boine B., Arthur K. 2009. Mycoviruses of filamentous fungi and their relevance to plant pathology. Molecular Plant Pathology 10:115–128. [DOI:10.1111/j.1364-3703.2008.00503.x]
24. Regenmortel M. H. and Mahy B. W. 2009. Desk Encyclopedia of Plant and Fungal Virology. Academic Press, USA, 613p.
25. Tavantzis S. 2008. Partitiviruses of fungi. Pp. 63-68. In: B. W. J. Mahy and M. H. V. Regenmortel(ed). Encyclopedia of Virology. Academic Press, USA. [DOI:10.1016/B978-012374410-4.00405-2]
26. Webber J. F., Sticklen M. B. and Sherald J. L. 1993. D factors and their potential for controlling Dutch elm disease. Pp. 322-332. In: M. B. Sticklen, J. L. Sherald (ed.). Dutch Elm Disease Research: Cellular and Molecular Approaches. Springer, USA. [DOI:10.1007/978-1-4615-6872-8_24]
27. Wickner R. B. 1996. Double-stranded RNA viruses of Saccharomyces cerevisiae. Microbiological Reviews 60:250.
28. Wu M., Zhang J., Yang L. and Li G. 2016. RNA mycoviruses and their role in Botrytis biology. Pp. 71-90. In: S. Fillinger, Y. Elad (ed.). Botrytis–the Fungus, the Pathogen and its Management in Agricultural Systems. Springer International Publishing, Switzerland. [DOI:10.1007/978-3-319-23371-0_5]
29. Xie J., Xiao X., Fu Y., Liu H., Cheng J., Ghabrial S. A., Li G. and Jiang D. 2011. A novel mycovirus closely related to hypoviruses that infects the plant pathogenic fungus Sclerotinia sclerotiorum. Virology 418:49-56. [DOI:10.1016/j.virol.2011.07.008]
30. Xie J. and Jiang D. 2014. New insights into mycoviruses and exploration for biological control of crop fungal diseases. Annual Review of Phytopathology 52:45-68. [DOI:10.1146/annurev-phyto-102313-050222]
31. Yu X., Li B., Fu Y., Xie J., Cheng J., Ghabrial S. A., Li G., Yi X. and Jiang D. 2013. Extracellular transmission of a DNA mycovirus and its use as a natural fungicide. Proceedings of the National Academy of Sciences 110:1452-1457. [DOI:10.1073/pnas.1213755110]
32. Zhang L., Fu Y., Xie J., Jiang D., Li G. and Yi X. 2009. A novel virus that infecting hypovirulent strain XG36-1 of plant fungal pathogen Sclerotinia sclerotiorum. Virology journal 6:96-105. [DOI:10.1186/1743-422X-6-96]
Send email to the article author
| Rights and permissions | |
 |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
