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Virions of "Sclerotinia sclerotiorum negative-stranded RNA virus 1" (SsNSRV-1), a mycovirus of family "Mymonaviridae".

Mycoviruses (Ancient Greek: μύκης mykes ("fungus") + Latin virus), also known as mycophages, are viruses that infect fungi. The majority of mycoviruses have double-stranded RNA (dsRNA) genomes and isometric particles, but approximately 30% have positive-sense, single-stranded RNA (+ssRNA) genomes.[1][2]

True mycoviruses demonstrate an ability to be transmitted to infect other healthy fungi. Many double-stranded RNA elements that have been described in fungi do not fit this description, and in these cases they are referred to as virus-like particles or VLPs. Preliminary results indicate that most mycoviruses co-diverge with their hosts, i.e. their phylogeny is largely congruent with that of their primary hosts.[3] However, many virus families containing mycoviruses have only sparsely been sampled. Mycovirology[4] is the study of mycoviruses. It is a special subdivision of virology and seeks to understand and describe the taxonomy, host range, origin and evolution, transmission and movement of mycoviruses and their impact on host phenotype.


The first record of an economic impact of mycoviruses on fungi was recorded in cultivated mushrooms (Agaricus bisporus) in the late 1940s and was called the La France disease.[5] Hollings found more than three different types of viruses in the abnormal sporophores. This report essentially marks the beginning of mycovirology.[4]

The La France Disease is also known as X disease, watery stripe, dieback and brown disease. Symptoms include:

Mushrooms have shown no resistance to the virus, and so control has been limited to hygienic practises to stop the spread of the virus.

Perhaps the best known mycovirus is Cryphonectria parasitica hypovirus 1 (CHV1). CHV1 is exceptional within mycoviral research for its success as a biocontrol agent against the fungus C. parasitica, the causative agent of chestnut blight, in Europe, but also because it is a model organism for studying hypovirulence in fungi. However, this system is only being used in Europe routinely because of the relatively small number of vegetative compatibility groups (VCGs) on the continent. By contrast, in North America the distribution of the hypovirulent phenotype is often prevented because an incompatibility reaction prevents fungal hyphae from fusing and exchanging their cytoplasmic content. In the United States, at least 35 VCGs were found.[7] A similar situation seems to be present in China and Japan, where 71 VCGs have been identified so far.[8]


The majority of mycoviruses have double-stranded RNA (dsRNA) genomes and isometric particles, but approximately 30% have positive-sense, single-stranded RNA (+ssRNA) genomes.[1][2] However, negative single-stranded RNA viruses and single-stranded DNA viruses have also been described.[9][10][11] The updated 9th ICTV report on virus taxonomy[12] lists over 90 mycovirus species covering 10 viral families, of which 20% were not assigned to a genus or, in some cases, not even to a family.

Isometric forms predominate mycoviral morphologies in comparison to rigid rods, flexuous rods, club-shaped particles, enveloped bacilliform particles, and Herpesvirus-like viruses.[13] The lack of genomic data often hampers a conclusive assignment to already established groups of viruses or makes it impossible to erect new families and genera. The latter is true for many unencapsidated dsRNA viruses, which are assumed to be viral, but missing sequence data has prevented their classification so far.[1] So far, viruses of the families Partitiviridae, Totiviridae, and Narnaviridae are dominating the "mycovirus sphere".[4]

Listing of all formally named and recognised mycoviruses summarised from “Virus Taxonomy: The Ninth Report of the International Committee on Taxonomy of Viruses”[12]

Host range and incidence[edit]

Mycoviruses are common in fungi (Herrero et al., 2009) and are found in all four phyla of the true fungi: Chytridiomycota, Zygomycota, Ascomycota and Basidiomycota. Fungi are frequently infected with two or more unrelated viruses and also with defective dsRNA and/or satellite dsRNA.[14][15] There are also viruses that simply use fungi as vectors and are distinct from mycoviruses because they cannot reproduce in the fungal cytoplasm.[16]

It is generally assumed that the natural host range of mycoviruses is confined to closely related vegetability compatibility groups or VCGs which allow for cytoplasmic fusion,[17] but some mycoviruses can replicate in taxonomically different fungal hosts.[4] Good examples are mitoviruses found in the two fungal species S. homoeocarpa and Ophiostoma novo-ulmi.[18] Nuss et al. (2005) described that it is possible to extend the natural host range of C. parasitica hypovirus 1 (CHV1) to several fungal species that are closely related to C. parasitica using in vitro virus transfection techniques.[19] CHV1 can also propagate in the genera Endothia and Valsa,[14] which belong to the two distinct families Cryphonectriaceae and Diaporthaceae, respectively. Furthermore, some human pathogenic fungi are also found to be naturally infected with mycoviruses, including AfuPmV-1 of Aspergillus fumigatus[20] and TmPV1 of Talaromyces marneffei[21] (formerly Penicillium marneffei).

In one study, forty patients with acute lymphoblastic leukemia were found to have antibodies to a mycovirus-containing Aspergillus flavus.In another research report, exposure of mononuclear cells from patients with acute lymphoblastic leukemia in full remission resulted in the re-development of the genetic and cell surface phenotypes characteristic of acute lymphoblastic leukemia

Origin and evolution[edit]

Viruses consisting of dsRNA as well as ssRNA are assumed to be very ancient and presumably originated from the "RNA world" as both types of RNA viruses infect bacteria as well as eukaryotes.[22] Although the origin of viruses is still not well understood,[23] recently presented data suggest that viruses may have invaded the emerging "supergroups" of eukaryotes from an ancestral pool during a very early stage of life on earth. According to Koonin,[23] RNA viruses colonized eukaryotes first and subsequently co-evolved with their hosts. This concept fits well with the proposed "ancient co-evolution hypothesis", which also assumes a long co-evolution of viruses and fungi.[1][13] The "ancient co-evolution hypothesis" could explain why mycoviruses are so diverse.[13][24]

It has also been suggested that it is very likely that plant viruses containing a movement protein evolved from mycoviruses by introducing an extracellular phase into their life cycle rather than eliminating it. Furthermore, the recent discovery of an ssDNA mycovirus has tempted some researchers[10] to suggest that RNA and DNA viruses might have common evolutionary mechanisms. However, there are many cases where mycoviruses are grouped together with plant viruses. For example, CHV1 showed phylogenetic relatedness to the ssRNA genus Potyvirus,[25] and some ssRNA viruses, which were assumed to confer hypovirulence or debilitation, were often found to be more closely related to plant viruses than to other mycoviruses.[1] Therefore, another theory arose that these viruses moved from a plant host to a plant pathogenic fungal host or vice versa. This "plant virus hypothesis" may not explain how mycoviruses developed originally, but it could help to understand how they evolved further.[citation needed]


A significant difference between the genomes of mycoviruses to other viruses is the absence of genes for ‘cell-to-cell movement’ proteins. It is therefore assumed that mycoviruses only move intercellularly during cell division (e.g. sporogenesis) or via hyphal fusion.[14][26] Mycoviruses might simply not need an external route of infection as they have many means of transmission and spread due to their fungal host’s life style:

  • Plasmogamy and cytoplasmic exchange over extended periods of time
  • Production of vast amounts of asexual spores
  • Overwintering via sclerotia[27]
  • More or less effective transmission into sexual spores

However, there are potential barriers to mycovirus spread due to vegetative incompatibility and variable transmission to sexual spores. Transmission to sexually produced spores can range from 0% to 100% depending on the virus-host combination.[14] Transmission between species of the same genus sharing the same habitat has also been reported including Cryphonectria (C. parasitica and C. sp), Sclerotinia (Sclerotinia sclerotiorum and S. minor), and Ophiostoma (O. ulmi and O. novo-ulmi).[28][29] Intraspecies transmission has also been reported[30] between Fusarium poae and black Aspergillus isolates. However, it is not known how fungi overcome the genetic barrier; whether there is some form of recognition process during physical contact or some other means of exchange, such as vectors. Research[31] using Aspergillus species indicated that transmission efficiencies might depend on the hosts viral infection status (infected with no, different, or same virus), and that mycoviruses might play a role in the regulation of secondary mycoviral infection. Whether this is also true for other fungi is not yet known. In contrast to acquiring mycoviruses spontaneously, the loss of mycoviruses seems very infrequent[31] and suggests that either viruses actively moved into spores and new hyphal tips, or the fungus might facilitate the mycoviral transport in some other way.

Movement of mycoviruses within fungi[edit]

Although it is not known yet whether viral transport is an active or passive process, it is generally assumed that fungal viruses move forward by plasma streaming.[32] Theoretically they could drift with the cytoplasm as it extends into new hyphae, or attach to the web of microtubuli, which would drag them through the internal cytoplasmic space. That might explain how they pass through septa and bypass woronin bodies. However, some researchers have found them located next to septum walls,[2][33] which could imply that they ‘got stuck’ and were not able to move actively forward themselves. Others have suggested that the transmission of viral mitochondrial dsRNA may play an important role in the movement of mitoviruses found in Botrytis cinerea.[34]

Impact on host phenotype[edit]

Phenotypic effects of mycoviral infections can vary from advantageous to deleterious, but most of them are asymptomatic or cryptic. The connection between phenotype and mycovirus presence is not always straight forward. Several reasons may account for this. First, the lack of appropriate infectivity assays often hindered the researcher from reaching a coherent conclusion.[35] Secondly, mixed infection or unknown numbers of infecting viruses make it very difficult to associate a particular phenotypic change with the investigated virus.[citation needed]

Although most mycoviruses often do not seem to disturb their host’s fitness, this does not necessarily mean they are living unrecognized by their hosts. A neutral co-existence might just be the result of a long co-evolutionary process.[36][37] Accordingly, symptoms may only appear when certain conditions of the virus-fungus-system change and get out of balance. This could be external (environmental) as well as internal (cytoplasmic). It is not known yet why some mycoviruses-fungus-combinations are typically detrimental while others are asymptomatic or even beneficial. Nevertheless, harmful effects of mycoviruses are economically interesting, especially if the fungal host is a phytopathogen and the mycovirus could be exploited as biocontrol agent. The best example is represented by the case of CHV1 and C. parasitica.[14] Other examples of deleterious effects of mycoviruses are the ‘La France’ disease of A. bisporus[5][38] and the mushroom diseases caused by Oyster mushroom spherical virus[39] and Oyster mushroom isometric virus.[38]

In summary, the main negative effects of mycoviruses are:

Hypovirulent phenotypes do not appear to correlate with specific genome features and it seems there is not one particular metabolic pathway causing hypovirulence but several.[44] In addition to negative effects, beneficial interactions do also occur. Well described examples are the killer phenotypes in yeasts[45] and Ustilago.[46] Killer isolates secrete proteins that are toxic to sensitive cells of the same or closely related species while the producing cells themselves are immune. Most of these toxins degrade the cell membrane.[45] There are potentially interesting applications of killer isolates in medicine, food industry, and agriculture.[24][45] A three-part system involving a mycovirus of an endophytic fungus (Curvularia protuberata) of the grass Dichanthelium lanuginosum has been described, which provides a thermal tolerance to the plant, enabling it to inhabit adverse environmental niches.[47] In medically important fungi, an uncharacterized A78 virus of A. fumigatus causes mild hypervirulent effect on pathogenicity when tested on Galleria mellonella (Greater wax moth).[42] Furthermore, TmPV1, a dsRNA partitivirus, of Talaromyces marneffei (formerly Penicillium marneffei) was found to cause hypervirulence phenotype on T. marneffei when tested on a mouse model.[21] These could imply mycoviruses may play important roles in the pathogensis of human pathogenic fungi.[citation needed]


Most fungal viruses belong to double-stranded RNA viruses, but about 30% belong to positive-strand RNA virus.[1] However, negative single-stranded RNA viruses and single-stranded DNA viruses have also been described.[9][11][48][10] The ninth edition of the report of the International Committee on Taxonomy of Viruses lists more than 90 fungal viruses belonging to 10 families, of which about 20% of the viruses have not been incertae sedis due to insufficient sequence data and have not yet been determined.[12] The shape of most fungal viruses is isometric.[13]


49.Tebbi CK, Badiga A, Sahakian E, Arora AI, Nair S, Powers JJ, Achille AN, Jaglal MV, Patel S, Migone F. Plasma of Acute Lymphoblastic Leukemia Patients React to the Culture of a Mycovirus Containing Aspergillus flavus. J Pediatr Hematol Oncol. 2020 Jul;42(5):350-358. doi: 10.1097/MPH.0000000000001845. PMID: 32576782. 50. Tebbi CK, Badiga A, Sahakian E, Powers JJ, Achille AN, Patel S, Migone F. Exposure to a mycovirus containing Aspergillus Flavus reproduces acute lymphoblastic leukemia cell surface and genetic markers in cells from patients in remission and not controls. Cancer Treat Res Commun. 2021;26:100279. doi: 10.1016/j.ctarc.2020.100279. Epub 2020 Dec 11. PMID: 33348275.

  1. ^ a b c d e f Pearson MN, Beever RE, Boine B, Arthur K (January 2009). "Mycoviruses of filamentous fungi and their relevance to plant pathology". Molecular Plant Pathology. 10 (1): 115–28. doi:10.1111/j.1364-3703.2008.00503.x. PMC 6640375. PMID 19161358.
  2. ^ a b c Bozarth RF (October 1972). "Mycoviruses: a new dimension in microbiology". Environmental Health Perspectives. 2 (1): 23–39. doi:10.1289/ehp.720223. PMC 1474899. PMID 4628853.
  3. ^ Göker M, Scheuner C, Klenk HP, Stielow JB, Menzel W (2011). "Codivergence of mycoviruses with their hosts". PLOS ONE. 6 (7): e22252. Bibcode:2011PLoSO...622252G. doi:10.1371/journal.pone.0022252. PMC 3146478. PMID 21829452.
  4. ^ a b c d Ghabrial SA, Suzuki N (2009). "Viruses of plant pathogenic fungi". Annual Review of Phytopathology. 47: 353–84. doi:10.1146/annurev-phyto-080508-081932. PMID 19400634.
  5. ^ a b Hollings M (1962). "Viruses Associated with A Die-Back Disease of Cultivated Mushroom". Nature. 196 (4858): 962–965. Bibcode:1962Natur.196..962H. doi:10.1038/196962a0. S2CID 28710444.
  6. ^ Romaine CP, Schlagnhaufer B (June 1995). "PCR analysis of the viral complex associated with La France disease of Agaricus bisporus". Applied and Environmental Microbiology. 61 (6): 2322–5. Bibcode:1995ApEnM..61.2322R. doi:10.1128/AEM.61.6.2322-2325.1995. PMC 167503. PMID 7793952.
  7. ^ Anagnostakis SL, Chen B, Geletka LM, Nuss DL (July 1998). "Hypovirus Transmission to Ascospore Progeny by Field-Released Transgenic Hypovirulent Strains of Cryphonectria parasitica". Phytopathology. 88 (7): 598–604. doi:10.1094/PHYTO.1998.88.7.598. PMID 18944931.
  8. ^ Liu YC, Milgroom MG (2007). "High diversity of vegetative compatibility types in Cryphonectria parasitica in Japan and China". Mycologia. 99 (2): 279–84. doi:10.3852/mycologia.99.2.279. PMID 17682780.
  9. ^ a b Li, P; Wang, S; Zhang, L; Qiu, D; Zhou, X; Guo, L (2020). "A tripartite ssDNA mycovirus from a plant pathogenic fungus is infectious as cloned DNA and purified virions". Science Advances. 6 (14): eaay9634. Bibcode:2020SciA....6.9634L. doi:10.1126/sciadv.aay9634. PMC 7138691. PMID 32284975. S2CID 215746433.
  10. ^ a b c Yu, X.; Li, B.; Fu, Y.; Jiang, D.; Ghabrial, S. A.; Li, G.; Peng, Y.; Xie, J.; Cheng, J.; Huang, J.; Yi, X. (2010). "A geminivirus-related DNA mycovirus that confers hypovirulence to a plant pathogenic fungus". Proceedings of the National Academy of Sciences of the United States of America. 107 (18): 8387–8392. Bibcode:2010PNAS..107.8387Y. doi:10.1073/pnas.0913535107. PMC 2889581. PMID 20404139.
  11. ^ a b Liu, Lijiang; Xie, Jiatao; Cheng, Jiasen; Fu, Yanping; Li, Guoqing; Yi, Xianhong; Jiang, Daohong (2014-08-19). "Fungal negative-stranded RNA virus that is related to bornaviruses and nyaviruses". Proceedings of the National Academy of Sciences of the United States of America. 111 (33): 12205–12210. Bibcode:2014PNAS..11112205L. doi:10.1073/pnas.1401786111. ISSN 1091-6490. PMC 4143027. PMID 25092337.
  12. ^ a b c King, A. M. Q., Lefkowitz E. M., Adams, J., Carstens, E. B. (2011). "Virus Taxonomy: Ninth Report of the International Committee on Taxonomy of Viruses (ICTV)". San Diego, USA: Elsevier Academic. Archived from the original on 2017-02-03. Retrieved 2018-09-01.{{cite web}}: CS1 maint: multiple names: authors list (link) CS1 maint: numeric names: authors list (link)
  13. ^ a b c d Varga, J.; Tóth, B.; Vágvölgyi, C. (2003). "Recent advances in mycovirus research" (PDF). Acta Microbiologica et Immunologica Hungarica. 50 (1): 77–94. doi:10.1556/AMicr.50.2003.1.8. PMID 12793203.
  14. ^ a b c d e Ghabrial, S. A., Suzuki, N. (2008). Fungal Viruses. In B. W. J. Mahy and M. H. V. Van Regenmortel (ed.), Encyclopedia of Virology, 3rd ed., vol. 2. Elsevier, Oxford, United Kingdom. p. 284-291.
  15. ^ Howitt RL, Beever RE, Pearson MN, Forster RL (March 2006). "Genome characterization of a flexuous rod-shaped mycovirus, Botrytis virus X, reveals high amino acid identity to genes from plant 'potex-like' viruses". Archives of Virology. 151 (3): 563–79. doi:10.1007/s00705-005-0621-y. PMID 16172841. S2CID 6741139.
  16. ^ Adams, M. J. (1991). "Transmission of plant viruses by fungi". Annals of Applied Biology. 118 (2): 479–492. doi:10.1111/j.1744-7348.1991.tb05649.x.
  17. ^ Buck, K. W. (1986). Fungal Virology- An overview', in K. Buck (ed.), Fungal Virology (Boca Raton: CRC Press): 1-84.
  18. ^ Deng F, Xu R, Boland GJ (November 2003). "Hypovirulence-Associated Double-Stranded RNA from Sclerotinia homoeocarpa Is Conspecific with Ophiostoma novo-ulmi Mitovirus 3a-Ld". Phytopathology. 93 (11): 1407–14. doi:10.1094/PHYTO.2003.93.11.1407. PMID 18944069.
  19. ^ Chen B, Choi GH, Nuss DL (June 1994). "Attenuation of fungal virulence by synthetic infectious hypovirus transcripts". Science. 264 (5166): 1762–4. Bibcode:1994Sci...264.1762C. doi:10.1126/science.8209256. PMID 8209256.
  20. ^ Kotta-Loizou I, Coutts RH (2017). "Aspergilli: A Comprehensive Review". Frontiers in Microbiology. 8: 1699. doi:10.3389/fmicb.2017.01699. PMC 5592211. PMID 28932216.
  21. ^ a b c Lau SK, Lo GC, Chow FW, Fan RY, Cai JJ, Yuen KY, Woo PC (June 2018). "Novel Partitivirus Enhances Virulence of and Causes Aberrant Gene Expression in Talaromyces marneffei". mBio. 9 (3): e00947–18. doi:10.1128/mBio.00947-18. PMC 6016240. PMID 29895639.
  22. ^ Forterre P (April 2006). "The origin of viruses and their possible roles in major evolutionary transitions". Virus Research. 117 (1): 5–16. doi:10.1016/j.virusres.2006.01.010. PMID 16476498.
  23. ^ a b Koonin EV, Wolf YI (December 2008). "Genomics of bacteria and archaea: the emerging dynamic view of the prokaryotic world". Nucleic Acids Research. 36 (21): 6688–719. doi:10.1093/nar/gkn668. PMC 2588523. PMID 18948295.
  24. ^ a b Dawe AL, Nuss DL (2001). "Hypoviruses and chestnut blight: exploiting viruses to understand and modulate fungal pathogenesis". Annual Review of Genetics. 35: 1–29. doi:10.1146/annurev.genet.35.102401.085929. PMID 11700275.
  25. ^ Fauquet CM, Mayo MA, Maniloff J (2005). Virus Taxonomy: Classification and Nomenclature of Viruses: The Eighth Report of the International Committee on the Taxonomy of Viruses. San Diego, CA: Elsevier Academic.
  26. ^ Ghabrial SA (1994). "New Developments in Fungal Virology". In Murphy FA, Maramorosch K, Aaron JS (eds.). Advances in Virus Research. Vol. 43. Academic Press. pp. 303–388.
  27. ^ Liu H, Fu Y, Jiang D, Li G, Xie J, Peng Y, Yi X, Ghabrial SA (February 2009). "A novel mycovirus that is related to the human pathogen hepatitis E virus and rubi-like viruses". Journal of Virology. 83 (4): 1981–91. doi:10.1128/JVI.01897-08. PMC 2643757. PMID 19073734.
  28. ^ Liu YC, Linder-Basso D, Hillman BI, Kaneko S, Milgroom MG (June 2003). "Evidence for interspecies transmission of viruses in natural populations of filamentous fungi in the genus Cryphonectria". Molecular Ecology. 12 (6): 1619–28. doi:10.1046/j.1365-294x.2003.01847.x. PMID 12755889. S2CID 31537342.
  29. ^ Melzer MS, Deng F, Boland GJ (December 2005). "Asymptomatic infection, and distribution of Ophiostoma mitovirus 3a (OMV3a), in populations of Sclerotinia homoeocarpa". Canadian Journal of Plant Pathology. 27 (4): 610–5. doi:10.1080/07060660509507262. S2CID 84507238.
  30. ^ Van Diepeningen AD, Debets AJ, Slakhorst SM, Fekete C, Hornok L, Hoekstra RF (2000). "Interspecies virus transfer via protoplast fusions between Fusarium poae and black Aspergillus strains". Fungal Genetics Newsletter. 47: 99–100. doi:10.4148/1941-4765.1216.
  31. ^ a b van Diepeningen AD, Debets AJ, Hoekstra RF (June 2006). "Dynamics of dsRNA mycoviruses in black Aspergillus populations". Fungal Genetics and Biology. 43 (6): 446–52. doi:10.1016/j.fgb.2006.01.014. PMID 16546419.
  32. ^ Sasaki A, Kanematsu S, Onoue M, Oyama Y, Yoshida K (April 2006). "Infection of Rosellinia necatrix with purified viral particles of a member of Partitiviridae (RnPV1-W8)". Archives of Virology. 151 (4): 697–707. doi:10.1007/s00705-005-0662-2. PMID 16307176. S2CID 13393656.
  33. ^ Vilches S, Castillo A (October 1997). "A double-stranded RNA mycovirus in Botrytis cinerea". FEMS Microbiology Letters. 155 (1): 125–30. doi:10.1016/S0378-1097(97)00377-7. PMID 9345772.
  34. ^ Wu M, Zhang L, Li G, Jiang D, Ghabrial SA (October 2010). "Genome characterization of a debilitation-associated mitovirus infecting the phytopathogenic fungus Botrytis cinerea". Virology. 406 (1): 117–26. doi:10.1016/j.virol.2010.07.010. PMID 20674953.
  35. ^ McCabe PM, Pfeiffer P, Van Alfen NK (September 1999). "The influence of dsRNA viruses on the biology of plant pathogenic fungi". Trends in Microbiology. 7 (9): 377–81. doi:10.1016/S0966-842X(99)01568-1. PMID 10470047.
  36. ^ May RM, Nowak MA (August 1995). "Coinfection and the evolution of parasite virulence" (PDF). Proceedings. Biological Sciences. 261 (1361): 209–15. Bibcode:1995RSPSB.261..209M. doi:10.1098/rspb.1995.0138. PMID 7568274. S2CID 202574889.
  37. ^ Araújo, A., Jansen, A. M., Bouchet, F., Reinhard, K., Ferreira, L. F. (2003). Parasitism, the Diversity of Life, and Paleoparasitology. Memórias do Instituto Oswaldo Cruz, 98 (SUPPL. 1): 5-11.
  38. ^ a b Ro HS, Lee NJ, Lee CW, Lee HS (December 2006). "Isolation of a novel mycovirus OMIV in Pleurotus ostreatus and its detection using a triple antibody sandwich-ELISA". Journal of Virological Methods. 138 (1–2): 24–9. doi:10.1016/j.jviromet.2006.07.016. PMID 16930731.
  39. ^ Yu HJ, Lim D, Lee HS (September 2003). "Characterization of a novel single-stranded RNA mycovirus in Pleurotus ostreatus". Virology. 314 (1): 9–15. doi:10.1016/S0042-6822(03)00382-9. PMID 14517055.
  40. ^ a b Moleleki N, van Heerden SW, Wingfield MJ, Wingfield BD, Preisig O (July 2003). "Transfection of Diaporthe perjuncta with Diaporthe RNA virus". Applied and Environmental Microbiology. 69 (7): 3952–6. Bibcode:2003ApEnM..69.3952M. doi:10.1128/AEM.69.7.3952-3956.2003. PMC 165159. PMID 12839766.
  41. ^ Suzaki K, Ikeda KI, Sasaki A, Kanematsu S, Matsumoto N, Yoshida K (June 2005). "Horizontal transmission and host-virulence attenuation of totivirus in violet root rot fungus Helicobasidium mompa". Journal of General Plant Pathology. 71 (3): 161–168. doi:10.1007/s10327-005-0181-8. S2CID 32799546.
  42. ^ a b Özkan S, Coutts RH (March 2015). "Aspergillus fumigatus mycovirus causes mild hypervirulent effect on pathogenicity when tested on Galleria mellonella". Fungal Genetics and Biology. 76: 20–6. doi:10.1016/j.fgb.2015.01.003. hdl:2299/16060. PMID 25626171.
  43. ^ Ihrmark K, Stenström E, Stenlid J (February 2004). "Double-stranded RNA transmission through basidiospores of Heterobasidion annosum". Mycological Research. 108 (Pt 2): 149–53. doi:10.1017/S0953756203008839. PMID 15119351.
  44. ^ Xie J, Wei D, Jiang D, Fu Y, Li G, Ghabrial S, Peng Y (January 2006). "Characterization of debilitation-associated mycovirus infecting the plant-pathogenic fungus Sclerotinia sclerotiorum". The Journal of General Virology. 87 (Pt 1): 241–9. doi:10.1099/vir.0.81522-0. PMID 16361437.
  45. ^ a b c Schmitt MJ, Breinig F (August 2002). "The viral killer system in yeast: from molecular biology to application". FEMS Microbiology Reviews. 26 (3): 257–76. doi:10.1016/S0168-6445(02)00099-2. PMID 12165427.
  46. ^ Marquina D, Santos A, Peinado JM (June 2002). "Biology of killer yeasts" (PDF). International Microbiology. 5 (2): 65–71. doi:10.1007/s10123-002-0066-z. PMID 12180782. S2CID 3056365.
  47. ^ Márquez LM, Redman RS, Rodriguez RJ, Roossinck MJ (January 2007). "A virus in a fungus in a plant: three-way symbiosis required for thermal tolerance". Science. 315 (5811): 513–5. Bibcode:2007Sci...315..513M. doi:10.1126/science.1136237. PMID 17255511. S2CID 220420.
  48. ^ Kondo H, Chiba S, Toyoda K, Suzuki N (2013). "Evidence for negative-strand RNA virus infection in fungi". Virology. 435 (2): 201–209. doi:10.1016/j.virol.2012.10.002. PMID 23099204.{{cite journal}}: CS1 maint: multiple names: authors list (link)

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External links[edit]