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Virus-Encoded MicroRNAs Reveal How Ranavirus Interacts with Amphibian Immune Defense

DOI: 10.4236/jbise.2024.1710014, PP. 179-184

Keywords: Ranaviruses, Amphibians, Virus-Encoded MicroRNA, Frog Virus 3, Virus-Host Interaction

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Abstract:

Ranaviruses are harmful viruses that infect amphibians, fish, and reptiles, and have caused particularly devastating declines in amphibian populations. One particular type of ranavirus, called Frog Virus 3 (FV3), has been extensively studied due to its prevalence and impact on amphibians. Previous research has primarily focused on the virus’s genes, but little attention has been given to the non-coding regions of its genome. This article reviews recent studies that reveal the ability of ranaviruses, including FV3, to encode microRNA (miRNA), a type of regulatory RNA. These viral miRNAs play a crucial role in suppressing frog immune genes, modulating the virus-host interaction, and promoting viral infection. Understanding how ranaviruses use miRNAs to control disease progression is essential for addressing the health threat they pose to wildlife and ecosystems.

References

[1]  Chinchar, V.G., Yu, K.H. and Jancovich, J.K. (2011) The Molecular Biology of Frog Virus 3 and Other Iridoviruses Infecting Cold-Blooded Vertebrates. Viruses, 3, 1959-1985.
https://doi.org/10.3390/v3101959
[2]  Miller, R.E., Lamberski, N. and Calle, P.P. (2019) Fowler’s Zoo and Wild Animal Medicine Current Therapy. W.B. Saunders, W.B. Amphibians and Reptiles, Vol. 9, 356-432.
[3]  Miller, D., Gray, M. and Storfer, A. (2011) Ecopathology of Ranaviruses Infecting Amphibians. Viruses, 3, 2351-2373.
https://doi.org/10.3390/v3112351
[4]  Courtney, E.P., Goldenberg, J.L. and Boyd, P. (2020) The Contagion of Mortality: A Terror Management Health Model for Pandemics. British Journal of Social Psychology, 59, 607-617.
https://doi.org/10.1111/bjso.12392
[5]  Collins, J. (2010) Amphibian Decline and Extinction: What We Know and What We Need to Learn. Diseases of Aquatic Organisms, 92, 93-99.
https://doi.org/10.3354/dao02307
[6]  Alan Pounds, J., Bustamante, M.R., Coloma, L.A., Consuegra, J.A., Fogden, M.P.L., Foster, P.N., et al. (2006) Widespread Amphibian Extinctions from Epidemic Disease Driven by Global Warming. Nature, 439, 161-167.
https://doi.org/10.1038/nature04246
[7]  Green, D.E., Converse, K.A. and Schrader, A.K. (2002) Epizootiology of Sixty-Four Amphibian Morbidity and Mortality Events in the USA, 1996-2001. Annals of the New York Academy of Sciences, 969, 323-339.
https://doi.org/10.1111/j.1749-6632.2002.tb04400.x
[8]  Mishra, R., Kumar, A., Ingle, H. and Kumar, H. (2020) The Interplay between Viral-Derived miRNAs and Host Immunity during Infection. Frontiers in Immunology, 10, Article No. 3079.
https://doi.org/10.3389/fimmu.2019.03079
[9]  Ahmad, I., Valverde, A., Siddiqui, H., Schaller, S. and Naqvi, A.R. (2020) Viral MicroRNAs: Interfering the Interferon Signaling. Current Pharmaceutical Design, 26, 446-454.
https://doi.org/10.2174/1381612826666200109181238
[10]  Tian, Y., Khwatenge, C.N., Li, J., De Jesus Andino, F., Robert, J. and Sang, Y. (2021) Virus-Targeted Transcriptomic Analyses in Frog Virus 3-Infected Frog Tissues Reveal Non-Coding Regulatory Elements in Intergenic Regions of Ranaviral Genome and Their Molecular Interaction with Host Immune Response. Frontiers in Immunology, 12, Article ID: 705253.
[11]  Vilaça, S.T., Bienentreu, J., Brunetti, C.R., Lesbarrères, D., Murray, D.L. and Kyle, C.J. (2019) Frog Virus 3 Genomes Reveal Prevalent Recombination between Ranavirus Lineages and Their Origins in Canada. Journal of Virology, 93, e00765-19.
https://doi.org/10.1128/jvi.00765-19
[12]  Saucedo, B., Garner, T.W.J., Kruithof, N., Allain, S.J.R., Goodman, M.J., Cranfield, R.J., et al. (2019) Common Midwife Toad Ranaviruses Replicate First in the Oral Cavity of Smooth Newts (Lissotriton vulgaris) and Show Distinct Strain-Associated Pathogenicity. Scientific Reports, 9, Article No. 4453.
https://doi.org/10.1038/s41598-019-41214-0
[13]  Goorha, R. (1982) Frog Virus 3 DNA Replication Occurs in Two Stages. Journal of Virology, 43, 519-528.
https://doi.org/10.1128/jvi.43.2.519-528.1982
[14]  Willis, D.B., Goorha, R., Miles, M. and Granoff, A. (1977) Macromolecular Synthesis in Cells Infected by Frog Virus 3. VII. Transcriptional and Post-Transcriptional Regulation of Virus Gene Expression. Journal of Virology, 24, 326-342.
https://doi.org/10.1128/jvi.24.1.326-342.1977
[15]  Goorha, R., Willis, D.B. and Granoff, A. (1979) Macromolecular Synthesis in Cells Infected by Frog Virus 3 XII. Viral Regulatory Proteins in Transcriptional and Post-Transcriptional Controls. Journal of Virology, 32, 442-448.
https://doi.org/10.1128/jvi.32.2.442-448.1979
[16]  Grayfer, L., De Jesús Andino, F. and Robert, J. (2014) The Amphibian (Xenopus laevis) Type I Interferon Response to Frog Virus 3: New Insight into Ranavirus Pathogenicity. Journal of Virology, 88, 5766-5777.
https://doi.org/10.1128/jvi.00223-14
[17]  Tian, Y., DeJesus, F.A., Robert, J. and Sang, Y. (2021) Virus-Targeted Transcriptomic and Functional Analyses Implicate Ranaviral Interaction with Host Interferon Response in Frog Virus 3-Infected Frog Tissues. Journal of Virology, 13, 1325.
https://doi.org/10.3390/v13071325
[18]  Sang, Y., Liu, Q., Lee, J., Ma, W., McVey, D.S. and Blecha, F. (2016) Expansion of Amphibian Intronless Interferons Revises the Paradigm for Interferon Evolution and Functional Diversity. Scientific Reports, 6, Article No. 29072.
https://doi.org/10.1038/srep29072
[19]  Tian, Y., Jennings, J., Gong, Y. and Sang, Y. (2019) Xenopus Interferon Complex: Inscribing the Amphibiotic Adaption and Species-Specific Pathogenic Pressure in Vertebrate Evolution? Cells, 9, Article No. 67.
https://doi.org/10.3390/cells9010067

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