<<
>>

OTHER RETROVIRUS INFECTIONS

Bovine leukaemia virus (BLV) is a deltaretrovirus that causes enzootic bovine leucosis, characterized by chronic leukaemia or lymphosarcoma in cattle. Enzootic bovine leucosis is a notifiable disease in the EU and has been eradicated from cattle herds in most western European countries.

In the early 1980s, a free- ranging European bison (Bison bison) bull in Poland was found subclinically infected with BLV(13). Serological studies performed on cervid populations have failed to detect BLV infection in red deer (Cervus elaphus), roe deer (Capreolus capreolus) and fallow deer (Dama dama) populations in Germany1-14) and in chamois (Rupicapra rupicapra) populations in Italy(15). However, lymphosarcoma has been described in red deer, roe deer and brown hare (Lepus europaeus).

Bovine immunodeficiency virus (BIV) is a lentivirus that is associated with leukocytosis, lymphadenopathy and meningoencephalitis in cattle. Seropositive cattle are present in many European countries. There are no known reports of BIV infection in free- ranging wild ungulates, including bison, in Europe.

Small ruminant lentiviruses (SRLV) include Visna/ maedi virus and Caprine arthritis encephalitis virus. These viruses cause interstitial pneumonia and mastitis in sheep, and arthritis and encephalitis in goats. Hybrids of sheep and mouflon ( Ovis aries musimon) have been experimen­tally shown to be susceptible to infection with SRLV(16). Natural SRLV infection has been reported in ibexes ( Capra ibex) in the French Alps(17). Other serological studies have failed to detect SRLV circulation in chamois in Italy(15), in red deer, roe deer and fallow deer in Germany1-18) and in mouflons in central Spain(19).

Jaagsiekte sheep retrovirus (JSRV) and Enzootic nasal tumor virus (ENTV) are betaretroviruses of small rumi­nants.

JSRV causes pulmonary adenocarcinoma in sheep and ENTV causes nasal adenocarcinoma in sheep and goats. Ethmoturbinate adenocarcinoma potentially caused by a lentivirus has been described in a Persian fallow deer(20) and has occurred for many years in moose and roe deer in Scandinavia(21). Endogenous retroviruses related to JSRV have been detected in the genome of many species of ungulates, including mouflon, ibex, European bison, moose, reindeer (Rangifer tarandus) and Przewalskis horse (Equus caballus przewalskif'22'. Their impact on these populations is unknown.

Equine infectious anemia virus (EIAV) is a Ientivirus causing severe anaemia in equids. There are no known reports of EIAV infection in wild or semi-wild equids in Europe.

REFERENCES

1. Fromont, E., Pontier D., Sager A. et al. Prevalence and pathogenicity of retroviruses in wildcats in France. Veterinary Record. 2000;146: 317-9.

2. Meli, M.L., Cattori, V., Martinez, F. et al. Feline leukemia virus infec­tion: a threat for the survival of the critically endangered Iberian lynx (Lynx pardinut). Veterinary Immunology and Immunopathology. 2009;134:61-7.

3. Hoover, E.A. & Mullins, J.I. Feline leukemia virus infection and dis­eases. Journal of the American Veterinary Medical Association. 1991;199: 1287-97.

4. Artois, M. & Remond, M. Viral diseases as a threat to free-living wild cats (Felis silvestris) in continental Europe. Veterinary Record. 1994;134:651-2.

5. Bendinelli, M., Pistello, M., Lombardi, S. et al. Feline immunodefi­ciency virus: an interesting model for AIDS studies and an important cat pathogen. Clinical Microbiology Reviews. 1995;8:87-112.

6. Troyer, J.L., Pecon-Slattery, J., Roelke, M.E. et al. Seroprevalence and genomic divergence of circulating strains of feline immunodeficiency virus among Felidae and Hyaenidae species. Journal of Virology. 2005;79:8282-94.

7. Merza, M., Larsson, E., Steen, M. & Morein, B. Association of a ret­rovirus with a wasting condition in the Swedish moose.

Virology. 1994;202:956-61.

8. Broman, E., Wallin, K., Steen, M. & Cederlund, G. A wasting syn­drome in Swedish moose (Alces alces): background and current hypoth­eses. Ambio. 2002;31:409-16.

9. Drew, M.L. Retroviral infections. In: Thomas, N.J., Hunter, D.B. & Atkinson, C.T., (eds). Infectious Diseases of Wild Birds. Oxford: Black­well Publishing; 2007; pp. 216-35.

10. Wade, L.L., Polack, E.W, O'Connell, P.H., Starrak, G.S., Abou-Madi, N. & Schat, K.A. Multicentric Lymphoma in a European Starling (Sturnus vulgaris). Journal ofAvian Medicine and Surgery. 1999;13:108- 15.

11. Dimcheff, D.E., Drovetski, S.V, Krishnan, M. & Mindell, D.P. Cospe­ciation and horizontal transmission of avian sarcoma and leukosis virus gag genes in galliform birds. Journal of Virology. 2000;74:3984-95.

12. Fadly, A.M. & Payne, L.N. LeukosisZSarcoma group. In: Saif, Y.M., Barnes, H.J., Glissonet, J.R. et al. (eds). Diseases of Poultry. Ames, Iowa: Iowa State Press; 2003; pp. 465-516.

13. Kita, J. & Anusz, K. Serologic survey for bovine pathogens in free- ranging European bison from Poland. Journal of Wildlife Diseases. 1991;27:16-20.

14. Frolich, K., Hamblin, C., Parida, S., Tuppurainen, E. & Schettler, E. Serological survey for potential disease agents of free- ranging cervids in six selected national parks from Germany. Journal ofWildlife Diseases. 2006;42:836-43.

15. Gentile, L., Mari, F., Cardeti, G. & Macri, G. Serologic survey in a chamois population of Abruzzo. Hystrix. 2000;11:115-9.

16. Guiguen, F., Mselli-Lakhal, L., Durand, J. et al. Experimental infection of Mouflon-domestic sheep hybrids with caprine arthritis-encephalitis virus. American Journal of Veterinary Research. 2000;61:456-61.

17. Erhouma, E., Guiguen, F., Chebloune, Y. et al. Small ruminant lenti- virus proviral sequences from wild ibexes in contact with domestic goats. Journal of General Virology. 2008;89:1478-84.

18. Starick, E., Dedek, J., Enke, K.H. & Loeppelmann, H.

Serologic investigations on the occurrence of Maedi-Visna antibodies in game ruminants (in German). Deutsche Tierarztliche Wochenschrift. 1995;102: 202-3.

19. Lopez-Olvera, J., Vidal, D., Vicente, J., Perez, M., Lujan, L. & Gor- tazar, C. Serological survey of selected infectious diseases in mouflon (Ovis aries musimon) from south-central Spain. European Journal of Wildlife Research. 2009;55:75-9.

20. Movassagui, A.R. & Davazdah Emami, M.R. Ethmoturbinate adeno- carninoma in a Persian fallow deer (Dama dama mesopotamicot). Veteri­nary Record. 2001;149:493-4.

21. Borg, K. & Nilsson, P.O. Ethmoid tumors in moose and roe deer. Nordisk veterinaermedicin. 1985;37:145-60.

22. Hecht, S.J., Stedman, K.E., Carlson, J.O. & DeMartini, J.C. Distribu­tion of endogenous type B and type D sheep retrovirus sequences in ungulates and other mammals. Proceedings of the National Academy of Sciences of the United States of America. 1996;93:3297-302.

23. DeMartini, J.C., Carlson, J.O., Leroux, C., Spencer, T & Palmarini, M. Endogenous retroviruses related to jaagsiekte sheep retrovirus. Current Topics in Microbiology and Immunology. 2003;275:117-37.

<< | >>
Source: Gavier-Widen D., Meredith A., Duff Paul J. (eds.). Infectious Diseases of Wild Mammals and Birds in Europe. London: Wiley-Blackwell,2012. — 568 p.. 2012
More medical literature on Medic.Studio

More on the topic OTHER RETROVIRUS INFECTIONS:

  1. OTHER RETROVIRUS INFECTIONS
  2. Retroelements and retrovirus INFECTIONS
  3. AVIAN RETROVIRUS INFECTIONS
  4. 6 DISEASES BY CLINICAL PRESENTATIONS, MAMMALS
  5. 5 Appendices
  6. Mammary Neoplasia
  7. HIV Type 1
  8. Other Gram-Negative Bacterial Infections Bordetella hinzii Infection
  9. CONTENTS
  10. Content