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Avian leukosis virus – new mutations: a threat for the upcoming century

Published online by Cambridge University Press:  18 September 2007

L.N. Payne
Affiliation:
Institute for Animal Health, Compton, Newbury, Berkshire RG20 7NN, UK
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Abstract

New strains of avian leukosis virus (ALV) and new threats to the poultry industry such as the appearance of subgroup J ALV arise as a result of virus mutation. Avian retroviruses are classified as exogenous (transmitted as infectious virus) and endogenous (transmitted genetically). Exogenous species are the avian leukosis-sarcoma viruses, reticuloendotheliosis virus, and lymphoproliferative disease virus of turkeys. Endogenous virus families include the ev loci, EAV, ART-CH and CR 1. Evolutionary relationships between different species of retrovirus are determined from their nucleotide sequences and construction of phylogenetic trees. Similar analyses are conducted to determine the relationships between endogenous and exogenous retroviruses and the various retroelements from which retroviruses are believed to have evolved. Retroviruses are subject to several types of mutation. Point mutations are the most common and occur mainly because of errors during reverse transcription. The frequency of point mutations is of the order of one mutation per virion per replicative cycle. Point mutations occur most frequently in the env gene of ALVs resulting in changes in antigenicity and host range. Antigenic variation enables mutant viruses to avoid the host immune response. Mutation also occurs from genetic recombination among exogenous and endogenous ALVs, and between exogenous ALVs and non-retroviral host genes such as cellular oncogenes, giving rise to acute avian leukaemia and sarcoma viruses. Thus, continuing viral mutation will result in the appearance of ALVs with new disease producing properties.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2001

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References

Bai, J., Howes, K., Payne, L.N. and Skinner, M.A. (1995a) Sequence of host-range determinants in the env gene of a full-length infectious proviral clone of exogenous avian leukosis virus HPRS-103 confirms that it represents a new subgroup (designated J). Journal of General Virology 76: 181187CrossRefGoogle ScholarPubMed
Bai, J., Payne, L.N. and Skinner, M.A. (1995b) HPRS-103 (exogenous avian leukosis virus, subgroup J) has an env gene related to those of endogenous elements EAV-0 and E51 and an E element found previously only in sarcoma viruses. Journal of Virology 69: 779784CrossRefGoogle Scholar
Best, S., Le Tissier, P.R. and Stoye, J.P. (1997) Endogenous retroviruses and the evolution of resistance to retroviral infection. Trends in Microbiology 5: 315318CrossRefGoogle ScholarPubMed
Bova, C.A., Manfredi, J.P. and Swanstrom, R. (1986) Env genes of avian retroviruses: nucleotide sequence and molecular recombinants define host rang: determinants. Virology 152: 343354CrossRefGoogle Scholar
Chesters, P., Howes, K., Mckay, J.C., Payne, L.N. and Venugopal, K. (2001) Acutely transforming avian leukosis virus subgroup J strain 996: defective genome encodes a 72-kDa gag-myc fusion protein. Journal of Virology 75: 42194225CrossRefGoogle Scholar
Crittenden, L.B. (1991) Retroviral elements in the genome of the chicken: implications for poultry genetics and breeding. Critical Reviews in Poultry Biology 3: 73109Google Scholar
Dimcheff, D.E., Drovetski, S.V., Krishnan, M. and Mindell, D.P. (2000) Cospeciation and horizontal transmission of ASLV gag genes and galliform birds. Journal of Virology 74: 39843995CrossRefGoogle ScholarPubMed
Doolittle, R.F., Feng, D.-F., Johnson, M.S. and Mcclure, M.A. (1989) Origins and evolutionary relationships of retroviruses. Quarterly Revim of Biology 64: 130CrossRefGoogle ScholarPubMed
Doolittle, R.F., Feng, D.-F., Mcclure, M.A. and Johnson, M.S. (1990) Retrovirus phylogeny and evolution. Current Topics in Microbiology and Immunology 157: 118Google ScholarPubMed
LÖwer, R. (1999) The pathogenic potential of endogenous retroviruses: facts and fantasies. Trends in Microbiology 7: 350356CrossRefGoogle ScholarPubMed
Mansky, L.M. (1998) Retrovirus mutation rates and their role in genetic variation. Journal of General Virology 79: 13371345CrossRefGoogle ScholarPubMed
Maynard Smith, J.H. (1998) Evolutionary Genetics. 2nd Edition, Oxford University Press, OxfordGoogle Scholar
Mcclure, M.A., Johnson, M.S., Feng, D.-F. and Doolittle, R.F. (1988) Sequence comparisons of retroviral proteins: relative rates of change and general phylogeny. Proceedings of the National Academy of Sciences USA 85: 24692473CrossRefGoogle ScholarPubMed
Nikiforov, M.A. and Gudkov, A.V. (1994) ART-CH a VL30 in chickens? Journal of Virology 68: 846853CrossRefGoogle ScholarPubMed
Page, R.D.M. and Holmes, E.C. (1998) Molecular Evolution. A Phylogenetic Approach. Blackwell Science, OxfordGoogle Scholar
Payne, L.N. (1992) Biology of avian retroviruses. In: The Retroviridae (Levy, J., Ed.), Volume 1. Plenum Press, New York, pp. 299404CrossRefGoogle Scholar
Payne, L.N., Gillespie, A.M. and Howes, K. (1993) Recovery of acutely transforming viruses from myeloid leukosis induced by the HPRS-103 strain of avian leukosis virus. Avian Diseases 37: 438–350CrossRefGoogle ScholarPubMed
Preston, B.D. and Dougherty, J.P. (1996) Mechanisms of retroviral mutation. Trends in Microbiology 4: 1621CrossRefGoogle ScholarPubMed
Sacco, M.A., Flannery, D.M.J., Howes, K. and Venugopal, K. (2000) Avian endogenous retrovirus EAV-HP shares regions of identity with avian leukosis virus subgroup J and the avian retrotransposon ART-CH. Journal of Virology 74: 12961306CrossRefGoogle ScholarPubMed
Smith, L.M., Toye, A.A., Howes, K., Bumstead, N., Payne, L.N. and Venugopal, K. (1999) Novel endogenous retroviral sequences in the chicken genome closely related to HPRS-103 (subgroup J) avian leukosis virus. Journal of General Virology 80: 261268CrossRefGoogle ScholarPubMed
Taplitz, R.A. and Coffin, J.M. (1997) Selection of an avian retrovirus mutant with extended receptor usage. Journal of Virology 71: 78147819CrossRefGoogle ScholarPubMed
Temin, H.M. (1985) Reverse transcription in the eukaryotic genome: retroviruses, pararetroviruses, retrotransposons and retrotranscripts. Molecular Biology and Evolution 2: 455468Google ScholarPubMed
Vandergon, T.L. and Reitman, M. (1994) Evolution of chicken repeat 1 (CR 1) elements: evidence for ancient subfamilies and multiple progenitors. Molecular Biology and Evolution 11: 886898Google Scholar
Venugopal, K. (1999) Avian leukosis virus subgroup J: a rapidly evolving group of oncogenic retroviruses. Research in Veterinary Science 67: 113119CrossRefGoogle Scholar
Venugopal, K., Smith, L.M., Howes, K. and Payne, L.N. (1998a) Antigenic variants of J subgroup avian leukosis virus: sequence analysis reveals multiple changes in the env gene. Journal of General Virology 79: 757766CrossRefGoogle ScholarPubMed
Venugopal, K., Spackman, D., Smith, L.M., Howes, K. and Payne, L.N. (1998b) Characteristics of an avian retrovirus isolated from an outbreak of haemangioma among layers. Avian Pathology 27: S91 (abstract)Google Scholar
Venugopal, K., Howes, K., Flannery, D.M.J. and Payne, L.N. (2000) Isolation of acutely transforming subgroup J avian leukosis viruses that induce erythroblastosis and myelocytomatosis. Avian Pathology 29: 327332CrossRefGoogle ScholarPubMed
Wain-Hobson, S. (1996) Running the gamut of retroviral variation. Trends in Microbiology 4: 135141CrossRefGoogle ScholarPubMed
Weissmahr, R.N., Schupbach, J. and Boni, J. (1997) Reverse transcriptase activity in chicken embryo fibroblast culture supernatants is associated with particles containing endogenous avian retrovirus EAV-0 RNA. Journal of Virology 71: 30053012CrossRefGoogle ScholarPubMed
Wyke, J.A. and Beamand, J.A. (1979) Genetic recombination in Rous sarcoma virus: the genesis of recombinants and lack of evidence for linkage between pol, env and src genes in three factor crosses. Journal of General Virology 43: 349364CrossRefGoogle ScholarPubMed