Maedi-Visna virus was detected in association with virally exposed IVF-produced early ewes embryos

Theriogenology

Volumn 74, Issue 4, 2010, Pages 682-690

  Romero, C Cortez ^a   Pellerin, J L ^a   Poulin, N ^c   Cognie Y ^c   Chebloune, Y ^b   Pepin M ^d   Fieni, F ^a  

^a LUNAM UNIVERSITÉ   (France)

^b CNRS   (France)

^c CEMAGREF   (France)

^d VETAGRO SUP   (France)

Author keywords

Embryos; Maedi Visna; Nested PCR; RT PCR; Zona pellucida

Indexed keywords

BOVINAE; CAPRA HIRCUS; OVIS; VISNA/MAEDI VIRUS;

EID: 77955513418     PISSN: 0093691X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.theriogenology.2010.03.020     Document Type: Article

References (48)

1. Frank H. Lentivirinae. Chapter 17C. Nermut/Steven, Animal Virus Structure 1987, 295-304. Elsevier Science Publishers B.V.
2. Carey N., Dalziel R.G. The biology of maedi-visna virus - an overview. Br Vet J 1993, 149:437-454.
3. Greenwood P.L., North R.N., Kirkland P.D. Prevalence, spread and control of caprine arthritis-encephalitis virus in dairy goat herds in New-South-Wales. Aust Vet J 1995, 72:341-345.
4. Radostits O.M., Gay C.C., Blood D.C., Hinchcliff K.W. Ovine progressive pneumonia (Maedi, Maedi-Visna). Veterinary Medecine 2000, 1186-1189. W.B. Saunders Company Ltd, London, United Kingdom. ninth ed.
5. Narayan O., Wolinsky J.S., Clements J.E., Strandberg J.D., Griffin D.E., Cork L.C. Slow viruses replication: the role of macrophages in the persistence and expression of visna viruses of sheep and goat. J Gen Virol 1982, 59:345-356.
6. Brodie S., Pearson L., Zink M., Bickle H., Anderson B., Marcom K., Dematini J. Ovine lentivirus expression and disease. Virus replication, but not entry, is restricted to macrophages of specific tissues. Am J Pathol 1995, 146:250-263.
7. Cortez Romero C., Fieni F., Russo P., Pepin M., Pellerin J.L. Presence of Maedi Visna Virus (MVV)-proviral DNA in female genital tract tissue from naturally infected sheep. Reproduction in Domestic Animals 2010, in press.
8. Cortez Romero C., Fieni F., Roux C., Russo P., Guibert J.M., Guiguen F., Chebloune Y., Pépin M., Pellerin J.L. Detection of ovine lentivirus in the cumulus cells, but not in the oocytes or follicular fluid, of naturally-infected sheep. Theriogenology 2006, 66(5):1131-1139.
9. Cognié Y., Baril G., Poulin N., Mermillod P. Current status of embryo technologies in sheep and goat. Theriogenology 2003, 59:171-188.
10. Baldassare H., Wang B., Kafidi N., Keefer C., Lazaris A., Karatzas C.N. Advances in the production and propagation of transgenic goats using laparoscopic ovum pick-up and in vitro embryo production technologies. Theriogenology 2002, 57:275-284.
11. Eaglesome M.D., Hare W.C.D., Singh E.L. Embryo transfer: discussion on its potential for infectious disease control based on a review of studies on infection of gametes and early embryos by various agents. Can Vet J 1980, 21:106-112.
12. Philipott M. The danger of disease transmission by artificial insemination and embryo transfer. Br Vet J 1993, 149:339-369.
13. Lamara A., Fieni F., Mselli-Lakhal L., Chatagnon G., Bruyas J.F., Tainturier D., Battut I., Fornazero C., Chebloune Y. Early embryonic cells from in vivo-produced goat embryos transmit the caprine arthritis-encephalitis virus (CAEV). Theriogenology 2002, 58(6):1153-1163.
14. Ali Al Ahmad M.Z., Fieni F., Guiguen F., Larrat M., Pellerin J.L., Roux C., Chebloune Y. Cultured goat embryos and cells are susceptible to infection with caprine encephalitis virus. Virology 2006, 353:307-315.
15. Bielanski A., Jordan L. Washing or washing and trypsin treatment is ineffective for removal of noncytopathic bovine viral diarrhea virus from bovine oocytes or embryos after experimental viral contamination of an in vitro fertilization system. Theriogenology 1996, 46:1467-1476.
16. Tsuboi T., Imada T. Noncytopathogenic and cytopathogenic bovine viral diarrhea-mucosal disease viruses do not affect in vitro embryonic development into the blastocyst stage. Vet Microbiol 1996, 49:127-134.
17. Stringfellow D.A., Riddell K.P., Brock K.V., Riddell M.G., Galik P.K., Wright J.C., Hasler J.F. In vitro fertilization and in vitro culture of bovine embryos in the presence of noncytopathic bovine viral diarrhea virus. Theriogenology 1997, 48:171-183.
18. Trachte E., Stringfellow D., Riddell K., Galik P., Riddell M., Wright J. Washing and trypsin treatment of in vitro derived bovine embryos exposed to bovine viral diarrhea virus. Theriogenology 1998, 50:717-726.
19. Booth P.J., Collins M.E., Jenner L., Prentice H., Ross J., Bradsberg J.H., Brownlie J. Association of non-cytopathogenic BVDV with bovine blastocysts: effects of washing, duration of viral exposure and degree of blastocyst expansion. Vet Rec 1999, 144:150-152.
20. Corteel J.M. Viabilité des spermatozoides de bouc conserves et congelés avec ou sans leur plasma seminal: effet du glucose. Annales de Biologie Animale, Biochimie, Biophysique 1974, 14:741-745.
21. Takahashi Y., First N.L. In vitro development of bovine one-cell embryos: influence of glucose, lactate, pyruvate, amino acids and vitamins. Theriogenology 1992, 37:963-978.
22. Narayan O., Clements J.E., Strandberg J.D., Cork L.C., Griffin D.E. Biological characterization of the virus causing leukoencephalitis and arthritis in goats. J Gen Virol 1980, 50:69-79.
23. Sonigo P., Alizon M., Staskus K., Klatzmann D., Cole S., Danos O., Retzel E., Tiollais P., Haase A.T., Wain-Hobson S. Nucleotide sequence of the visna lentivirus: relationship to the AIDS virus. Cell 1985, 42:369-382.
24. Reed L., Muench H. A simple method for estimating fifty per cent points. Am J Hyg 1938, 27:413-497.
25. Guiguen F., Mselli-Lakhal L., Durand J., Du J., Favier C., Fornazero C., Grezel D., Balleydier S., Hausmann E., Chebloune Y. Experimental infection of Mouflon-domestic sheep hybrids with caprine arthritis-encephalitis virus. Am J Vet Res 2000, 61(4, April):456-461.
26. Saltarelli M.J., Querat G., Konings D.A., Vigne R., Clements J.E. Nucleotide sequence and transcriptional analysis of molecular clones of CAEV which generate infectious virus. Virology 1990, 179:347-364.
27. Nakajima-Iijima S., Hamada H., Reddy P., Kakunaga T. Molecular structure of the human cytoplasmic beta-actin gene: Interspecies homology of sequences in the intron. Proc Natl Acad Sci USA 1985, 82:6133-6137.
28. Chebloune Y., Sheffer D., Karr B.M., Stephens E., Narayan O. Restrictive type of replication of ovine/caprine lentiviruses ovine fibroblast cell cultures. Virology 1996, 222:21-30.
29. Leroux C., Cordier G., Mercier I., Chastang J., Lyon M., Quérat G., Greenland T., Vigne R., Mornex J.F. Ovine aortic smooth muscle cells allow the replication of visna-maedi virus in vitro. Arch Virol 1995, 140:1-11.
30. McNemar Q. Note on the sampling error of the difference between correlated proportions or percentages. Psychometrika 1947, 12(2):153-157.
31. Good I.J. Some statistical applications of Poisson's work. Statist. Sci 1986, 1(2):157-180.
32. Cross R.F., Smith C.K., Moorhead P.D. Vertical transmission of progressive pneumonia of sheep. Am J Vet Res 1975, 36:465-468.
33. Cutlip R.C., Lehmkuhl H.D., Jackson T.A. Intrauterine transmission of ovine progressive pneumonia virus. Am J Vet Res 1981, 42(10, October):1795-1797.
34. Brodie S.J., De la Concha-Bermejillo A., Köenig G., Snowder G.D., DeMartini J.C. Maternal factors associated with prenatal transmission of ovine lentivirus. J Infect Dis 1994, 169:653-657.
35. Cavalcante TV, Salles HO, Freitas VJF. Ovulatory response and embryo production after superovulatory treatment in goats seropositive for caprine arthritis-encephalitis virus (CAEV): Preliminary results. 14e meeting of European Embryo transfer association. Venise 11-12 September, 1998;136 (abstract).
36. Booth P.J., Collins M.E., Jenner L., Prentice H., Ross J., Badsberg J.H., Brownlie J. Noncytopathogenic bovine viral diarrhoea virus (BVDV) reduces cleavage but increases blastocyst yield of in vitro produced embryos. Theriogenology 1998, 50(5):769-777.
37. Vanroose G., Nauwynck H., Van Soom A., Vanopdenbosch E., de Kruif A. Replication of cytopathic and noncytopathic bovine viral diarrhea virus in zona-free and zona-intact in vitro-produced bovine embryos and the effect on embryo quality. Biol Reprod 1998, 58(3):857-866.
38. Givens M.D., Galik P.K., Riddell K.P., Brock K.V., Stringfellow D.A. Replication and persistence of different strains of bovine viral diarrhea virus in an in vitro embryo production system. Theriogenology 2000, 54:1093-1107.
39. Stringfellow D.A., Riddell K.P., Galik P.K., Damiani P., Bishop M.D., Wright J.C. Quality controls for bovine viral diarrhea virus-free IVF embryos. Theriogenology 2000, 53:827-839.
40. Vanroose G., Nauwynck H., Van Soom A., Vanopdenbosch E., de Kruif A. Succeptibility of zona-intact and zona-free in vitro-produced bovine embryos at different stages of development to infection with bovine herpesvirus-1. Theriogenology 1997, 47:1389-1402.
41. Ali Al Ahmad M.Z., Chebloune Y., Bouzar B.A., Baril G., Bouvier F., Chatagnon G., Leboeuf B., Pepin M., Guibert J.M., Russo P., Manfredi E., Martin J., Fieni F. Lack of risk of transmission of caprine arthritis-encephalitis virus (CAEV) after an appropriate embryo transfer procedure. Theriogenology 2008, 69:408-415.
42. Riddell K.P., Stringfellow D.A., Gray B.W., Riddell M.G., Wright J.C., Galik P.K. Structural and viral association comparisons of bovine zonae pellucidae from follicular oocytes, day-7 embryos and day-7 degenerated ova. Theriogenology 1993, 40:1281-1291.
43. Bercegeay S., Allaire F., Jean M., Hermite A.L., Bruyas J.F., Renard N., Tainturier D., Barriere P. La zone pellucide bovine: Differences de composition macromoleculaire entre ovocytes, pretraites ou non à l' A23187, et embryons. Reprod Nutr Dev 1993, 33:567-576.
44. Nibart M., Marquant-Le Guienne, Humnlot P. General sanitary procedures associated with in vitro produced embryos. Manual of the International Embryo Transfer Society 1998, IETS, Champaign, IL, Illinois, USA. 3rd. Edition. D.A. Stringfellow, S.M. Seidel (Eds.).
45. Stringfellow D.A. Recomandation for sanitary handling of in-vivo derived embryos. Manual of the International Embryo Transfer Society 1998, 170. IETS, Champaign, IL, Illinois, USA. 3rd. Edition. D.A. Stringfellow, S.M. Seidel (Eds.).
46. Vainas E., Papakostaki D., Christodoulou V., Besenfelder U., Amiridis G.S., Kuehholzer B., Samartzi F., Brem G. Exploitation of embryos collected from Maedi-Visna seropositive ewes during eradication programs. Small Rum Res 2006, 62:129-134.
47. Givens M.D., Galik P.K., Riddell K.P., Stringfellow D.A. Bovine viral diarrhea virus was not detected in association with virally exposed IVF bovine embryos. Theriogenology 1998, 49:252. (abstract).
48. Shisong C., Wrathall A.E. The importance of the zona pellucida for disease control in livestock by embryo transfer. Br Vet J 1989, 145:129-140.