Genomic heterogeneity in the pol region of ovine lentiviruses obtained from bronchoalveolar cells of infected sheep from France

References

1. Alizon M., Wain Hobson S., Montagnier L., Sonigo P. 1986; Genetic variability of the AIDS virus: nucleotide sequence analysis of two isolates from African patients. Cell 46:63–74
   [Google Scholar]
2. Cheevers W., McGuire T., Norton L., Cordery-Cotter R., Knowles D. 1993; Failure of neutralizing antibodies to regulate CAE lentivirus expression in vivo. Virology 196:835–839
   [Google Scholar]
3. Chomczynski P., Sacchi N. 1987; Single-step method of RNA isolation by acid guanidium thiocyanate-phenol-chloroform extraction. Analytical Biochemistry 162:156–159
   [Google Scholar]
4. Cordier G., Cozon G., Greenland T., Rocher F., Guiguen F., Guerret S., Brune J., Mornex J. F. 1990; In vivo activation of alveolar macrophages in ovine lentivirus infection. Clinical Immunology and Immunopathology 55:355–367
   [Google Scholar]
5. Fitzgibbon J., Mazar S., Dubin D. 1993; A new type of G-A hypermutation affecting human immunodeficiency virus. AIDS Research and Human Retroviruses 9:833–838
   [Google Scholar]
6. Goodenow M., Huet T., Saurin W., Kwok S., Sninsky J., Wain-Hobson S. 1989; HIV-1 isolates are rapidly evolving quasispecies: evidence for viral mixtures and preferred nucleotide substitution.. Journal of Acquired ImmunoDeficiency Syndrome 2:344–352
   [Google Scholar]
7. Lutley R., Petursson G., Palsson P. A., Georgsson G., Klein J., Nathanson N. 1983; Antigenic drift in visna: virus variation during long-term infection of Icelandic sheep. Journal of General Virology 64:1433–1440
   [Google Scholar]
8. McClure M. A., Johnson M. S., Feng D. F., Doolittle R. F. 1988; Sequence comparisons of retroviral proteins: relative rates of change and general phylogeny. Proceedings of the National Academy of Sciences, USA 85:2469–2473
   [Google Scholar]
9. Meyerhans A., Cheynier R., Albert J., Seth M., Kwok S., Sninsky J., Morfeldt-Manson L., Asko B., Wain-Hobson S. 1988; Temporal fluctuation in HIV quasispecies in vivo are not reflected by sequential HIV isolation. Cell 58:901–910
   [Google Scholar]
10. Mornex J. F., Lena P., Loire R., Cozon G., Greenland T., Guiguen F., Jacquier M. F., Cordier G. 1994; Lentivirus-induced interstitial lung disease: pulmonary pathology in sheep naturally infected by the visna-maedi virus. Veterinary Research 25:478–488
    [Google Scholar]
11. Preston B. D., Poiesz B. J., Loeb L. A. 1988; Fidelity of HIV-1 reverse transcriptase. Science 242:1168–1171
    [Google Scholar]
12. Querat G., Audoly G., Sonigo P., & Vigne R. 1990; Nucleotide sequence analysis of SA-OMVV, a visna-related ovine lentivirus: phylogenetic history of lentiviruses. Virology 175:434–447
    [Google Scholar]
13. Roberts J. D., Bebnek K., Kunkel T. A. 1988; The accuracy of reverse transcriptase from HIV-1. Science 242:1171–1173
    [Google Scholar]
14. Saltarelli M., Querat G., Konings D. A., Vigne R., Clements J. E. 1990; Nucleotide sequence and transcriptional analysis of molecular clones of CAEV which generate infectious virus. Virology 179:347–364
    [Google Scholar]
15. Sargan D. R., Bennet I. D., Cousens C., Roy D. J., Blacklaws B. A., Dalziel R. G., Watt N. J., McConnell I. 1991; Nucleotide sequence of EVI, a British isolate of maedi-visna virus. Journal of General Virology 72:1893–1903
    [Google Scholar]
16. Sonigo P., Alizon M., Staskus K., Klatzmann D., Cole S., Danos O., Retzel E., Tiollais P., Haase P., Wain-Hobson S. 1985; Nucleotide sequence of the visna lentivirus: relationship to the AIDS virus. Cell 42:369–382
    [Google Scholar]
17. Ward C. W. 1993; Progress toward a higher taxonomy of viruses. Research in Virology 144:419–453
    [Google Scholar]
18. Zanoni R. G., Nauta I. M., Kuhnert P., Pauli U., Pohl B., Peterhans E. 1992; Genomic heterogeneity of small ruminant lentiviruses detected by PCR. Veterinary Microbiology 33:341–351
    [Google Scholar]