121 Feline Viruses in Wildcats From Scotland

download 121 Feline Viruses in Wildcats From Scotland

of 4

Transcript of 121 Feline Viruses in Wildcats From Scotland

  • 7/28/2019 121 Feline Viruses in Wildcats From Scotland

    1/4

    121

    Journal of Wildlife Diseases, 35(1), 1999, pp. 121124 Wildlife Disease Association 1999

    Feline Viruses in Wildcats from Scotland

    M. J. Daniels,1,3 M. C. Golder,2 O. Jarrett,2 D. W. MacDonald1 1 Wildlife Conservation Research Unit, Depart-ment of Zoology, University of Oxford, South Parks Road, OXFORD OX1 3PS, UK; 2 Department of VeterinaryPathology, University of Glasgow, Bearsden, GLASGOW G61 1QH, UK; 3 Corresponding author.

    ABSTRACT: Few data are available on theprevalence of feline viruses in European wild-cats (Felis silvestris). Previous surveys have in-dicated that wildcats may be infected with thecommon viruses of domestic cats, apart fromfeline immunodeficiency virus (FIV). In thepresent study, 50 wildcats trapped throughoutScotland (UK) between August 1992 and Jan-uary 1997 were tested for evidence of viral in-fection. All were negative for FIV by severalserological or virological methods. By contrast,10% of the cats were positive for feline leuke-mia virus (FeLV) antigen and infectious virus

    was isolated from 13% of a smaller subset. Ofthe wildcats tested for respiratory viruses, 25%

    yielded feline calicivirus (FCV) and althoughno feline herpesvirus was isolated, 16% of thesamples had neutralizing antibodies to this vi-rus. Antibodies to feline coronavirus (FCoV)

    were found in 6% of samples. Feline foamy vi-rus (FFV) was an incidental finding in 33% ofsamples tested. This study confirms that wild-cats in Scotland are commonly infected withthe major viruses of the domestic cat, exceptfor FIV.

    Key words: Feline calicivirus, feline coronavirus, feline foamy virus, feline herpesvirus, fe-line immunodeficiency virus, feline leukemia

    virus, Felis silvestris, survey, wildcats.

    Domestic cats (Felis silvestris catus) andEuropean wildcats (Felis silvestris silves-tris) are considered subspecies and thereare currently no exclusive morphologicalor genetic criteria for distinguishing be-tween the two (reviewed in Daniels et al.,1998). However, there is evidence for clin-al variation in morphology, genetics andecology, such that cats living wild in north-ern Scotland (UK) may be consideredwildcats (Daniels, 1997). A small number

    of wildcats was sampled in Scotland forcommon feline viruses (McOrist et al.,1991). Although there was evidence of in-fection with some viruses, none tested pos-itive for feline immunodeficiency virus(FIV), in contrast to prevalence of up to57% reported in feral domestic cats inEngland (Yamaguchi et al., 1996).

    More recently an opportunity arose toextend these findings. A sample of 50 wild-cats (27 females and 23 males) wastrapped throughout northern Scotland be-tween August 1992 and January 1997 andtested for FIV and five other feline virusesincluding feline leukemia virus (FeLV), fe-line coronavirus (FCoV), feline calicivirus(FCV), feline herpesvirus (FHV) and fe-line foamy virus (FFV). After samplingwildcats were released. Details of trappingtechniques, anesthesia, sampling tech-niques, and the locations of wildcatstrapped are described in Daniels (1997)and Daniels et al. (1998).

    Blood was obtained from anesthetizedcats into lithium heparin and oropharyngealswabs were collected into transport medi-um (Leibovitz-15 medium (Life Technolo-gies Ltd, Paisley, UK) with 10% fetal bo-vine serum and antibiotics). The sampleswere posted and arrived in the laboratorywithin 48 hr of collection. Plasma was sep-

    arated from the blood and tested for FeLVp27 antigen (Indochem C Lutz, Ruedlin-gen, Switzerland) by enzyme immunoassayand virus isolation at (Feline Virus Unit,University of Glascow, Glascow, UK; Jarrettand Ganiere, 1996). Antibodies to FCoVwere assayed by indirect immunofluores-cence (IF; Addie and Jarrett, 1992) at Fe-line Virus Unit (M. C. Golder, unpubl.data). A similar IF test was used to detectanti-FIV antibodies, using CrFK cells (fromR. A. Crandell) infected with FIVGL-8 astarget cells. Antibodies to FIV were alsodetected by western blotting (M. C. Gold-er, unpubl. data); (supplied by Feline VirusUnit) (Hosie and Jarrett, 1990). Isolation ofFIV was attempted by the growth of virusfrom concanavalin A activated peripheralblood mononuclear cells (PBMC) (Hosieand Jarrett, 1990). Growth of FIV was de-

  • 7/28/2019 121 Feline Viruses in Wildcats From Scotland

    2/4

  • 7/28/2019 121 Feline Viruses in Wildcats From Scotland

    3/4

    SHORT COMMUNICATION 123

    or Florida panthers (Roelke et al., 1993).Given that it has been suggested that theseriousness of FIV infection in domesticcats is a result of a relatively recent infec-

    tion rather than the proposed historical ge-netic host-parasite symbiosis found in pu-mas (Carpenter et al., 1996; Vande Woudeet al., 1997), then potentially lack of ex-posure could pose a threat.

    The prevalence of FeLV is similar tothat reported for domestic cats (Yamagu-chi et al., 1996). One possibility for thesurvival of this virus in wildcats is that thevir us may be transmitted conge nitallywithin a few families since transmission ofFeLV is mainly by the oronasal route oracross the placenta (Jarrett, 1994). Alter-

    natively, transmission could be a result ofcontact with domestic or feral domesticcats.

    The isolation rate of FCV was relativelyhigh and may indicate that this virus wasacquired by direct contact with other car-riers. It is also possible that the virus wastransmitted from carrier dams to theiryoung kittens. The failure to isolate FHVis not surprising since in domestic cats thisvirus is carried as a latent infection and isshed only intermittently from the orophar-ynx (Gaskell and Dawson, 1994). However,the population had been exposed to FHVsince 16% of the wildcats tested had highlevels of FHV neutralizing antibodies.

    Comparable prevalence of FCV andFCoV has been reported in populations ofwild felids with no evidence of associatedmortality (e.g., Roelke et al., 1993; Paul-Murphy et al., 1994). The low prevalenceof antibodies to FCoV (3/49) was consis-tent with the fact that this virus is muchmore common in domestic cats in multicathouseholds than in free-ranging pet cats

    kept singly or in feral or stray cats. Directcontact is not necessary for the transmis-sion of FCoV which may be spread indi-rectly through the contamination of theenvironment with infected feces (Stoddartand Bennett, 1994).

    The incidental finding of FFV in cul-tures from PBMC is the first demonstra-

    tion of this virus in free-living wildcats inScotland. The rates for the isolation ofFFV were similar to those for domesticcats in the UK (Jarrett et al., 1974). While

    FFV is common in domestic cats, it is asyet not associated with any disease condi-tion (Gaskell and Bennett, 1994) and un-likely to be a significant pathogen in thewild population.

    Trapping was carried out under licencefrom Scottish Natural Heritage (SRA:02:96/(R)SRA:02:96) and anesthesia andblood sampling under Home Office Li-cence (PIL 60/4400). The study was fund-ed by Scottish Natural Heritage, TuskForce, J&B Care For The Rare and vehi-cles kindly supplied by Asia and Kia Mo-

    tors. We gratefully acknowledge the land-owners throughout Scotland who gave per-mission to work on their land. We thankM. McDonald and J. Simpson of the Fe-line Virus Unit for their valuable assistancein analyses of samples.

    LITERATURE CITED

    ADDIE, D. D., AND O. JARRETT. 1992. A study ofnaturally occuring feline coronavirus infectionsin kittens. Veterinary Record 130: 133137.

    ARTOIS, M., AND M. REDMOND. 1994. Viral diseasesas a threat to free-living wild cats (Felis silvestris)

    in continental Europe. Veterinary Record 134:651652.

    BROWN, E. W., N. YUHKI, C . PACKER, AND S. J.OBRIEN. 1994. A lion lentivirus related to felineimmunodeficiency virus: Epidemiologic and phy-logenetic aspects. Journal of Virology 68: 59535968.

    CALLANAN, J. J. 1995. Feline immunodeficiency virusinfection: A clinical and pathological perspective.In Feline immunology and immunodeficiency, B.J. Willet, and O. Jarrett (eds.). Oxford UniversityPress, Oxford, UK, pp. 111129.

    CARPENTER, M. A., E. W. BROWN, M. CULVER, W.E. JOHNSON, J. PECON. 1996. Genetic and phy-logenetic divergence of feline immunodeficiency

    virus in the Puma (Puma concolor). Journal ofVirology 70: 66826693.

    DANIELS, M. J. 1997. The biology and conservationof the wildcat in Scotland. Ph.D. Dissertation,Oxford University, Oxford, UK, 207 pp.

    DANIELS, M . J . , D . BALHARRY, D . HIRST, A . C.KITCHENER, AND R. J. ASPINALL. 1998. Morpho-logical and pelage characteristics of wild livingcats in Scotland: Implications for defining the

  • 7/28/2019 121 Feline Viruses in Wildcats From Scotland

    4/4

    124 JOURNAL OF WILDLIFE DISEASES, VOL. 35, NO. 1, JANUARY 1999

    wildcat. Journal of Zoology, London 244: 231247.

    EVERMANN, J. F., W. J. FOREYT, B. HALL, AND A. J.MCKEIRNAN. 1997. Occurrence of Puma lenti-virus infection in cougars from Washington. Jour-

    nal of Wildlife Diseases 33: 316320.GASKELL, R. M. AND M. BENNETT. 1994. Other fe-

    line virus infections. In Feline medicine andtherapeutics, 2nd Edition. E. A. Chandler, C. J.Gaskell, and R. M. Gaskell (eds.). Blackwell Sci-entific Publications, Oxford, UK, pp. 535543.

    , AND S. DAWSON. 1994. Viral induced upperrespiratory tract disease. In Feline medicine andtherapuetics, 2nd Edition. E. A. Chandler, C. J.Gaskell, and R. M. Gaskell (eds.). Blackwell Sci-entific Publications, Oxford, UK, pp. 453472.

    HORIMOTO, T., J. A. LIMCUMPAO, Y. TOHYA, E. TAK-AHASHI, AND E. MIKAMI. 1989. Enhancement ofneutralizing activity of antifeline herpesvirus type1 sera by complement supplementation. Japa-

    nese Journal of Veterinary Science 51: 10251027.

    HOSIE, M. J., AND O. JARRETT. 1990. Serological re-sponses of cats to feline immunodeficiency virus.AIDS 4: 215220.

    , C. ROBERTSON, AND O. JARRETT. 1989. Prev-alence of feline leukemia virus and antibodies tofeline immunodeficiency virus in cats in theUnited Kingdom. Veterinary Record 128: 293297.

    JARRETT, O. 1994. Feline leukemia virus. In Felinemedicine and therapuetics, 2nd Edition. E. A.Chandler, C. J. Gaskell, and R. M. Gaskell (eds.).Blackwell Scientific Publications, Oxford, UK,pp. 473487.

    , H. M. LAIRD AND D. HAY. 1973. Determi-nants of the host range of feline leukaemia vi-ruses. Journal of General Virology 20: 169175.

    , D. HAY, AND H. M. LAIRD. 1974. Infection

    by feline syncytium-forming virus in Britain. Vet-erinary Record 69: 201.

    , AND J. P. GANIERE, J. P. 1996. Comparativeefficacy studies with a recombinant feline leu-kemia virus. Veterinary Record 138: 711.

    MCORIST, S., R. BOID, T. W. JONES, N. EASTERBEE,A. L. HUBBARD, AND O. JARRETT. 1991. Someviral and protozool diseases in the EuropeanWildcat (Felis silvestris). Journal of Wildlife Dis-ease 27: 693696.

    ORMEROD, E., AND O. JARRETT. 1978. A classificationof feline calicivirus isolates based on plaque mor-phology. Journal of General Virology 39: 537540.

    PAUL-MURPHY, J., T. WORK, D. HUNTER, E. MCFIE,AND D. FJELINE. 1994. Serological survey andserum biochemical reference ranges of the freeranging mountain lion (Felis concolor) in Cali-fornia. Journal of Wildlife Diseases 30: 205215.

    ROELKE, M. E. D. J. FORRESTER, E. R. JACOBSON,G. V. KOLLIAS, F. W. SCOTT, M. C. BARR, J. F.

    EVERMANN, AND E. C. PIRTLE. 1993. Seroprev-elance of infectious disease agents in free-rang-ing Florida panthers (Felis concolor corgi). Jour-nal of Wildlife Diseases 29: 3649.

    STODDART, M. E., AND M. BENNETT. 1994. Felinecoronavirus infection. In Feline medicine andtherapuetics, 2nd Edition. E. A. Chandler, C. J.Gaskell, and R. M. Gaskell (eds.). Blackwell Sci-entific Publications, Oxford, UK, pp. 506514.

    VANDEWOUDE, S., S. J. OBRIEN, AND E. A. HOO-VER. 1997. Infectivity of lion and puma lentivi-ruses for domestic cats. Journal of General Vi-rology 78: 795800.

    YAMAGUCHI, N., D. W. MACDONALD, W. C. PASSAN-ISI, D. A. HARBOUR, AND C. D. HOPPER. 1996.Parasite prevalence in free-ranging farm cats,Felis silvestris catus. Epidemiology and Infection116: 217223.

    Received for publication 5 December 1997.