WAVLD Symposium Handbook_V4.indd - csiro
WAVLD Symposium Handbook_V4.indd - csiro
WAVLD Symposium Handbook_V4.indd - csiro
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World Association of Veterinary Laboratory Diagnosticians – 13 th International <strong>Symposium</strong>, Melbourne, Australia, 11-14 November 2007<br />
HOW MANY PESTIVIRUSES CIRCULATE IN NATURE? PESTIRUSES IN FREE-LIVING ANIMALS:<br />
PRESENT STATUS AND PROBLEMS<br />
S.Vilcek 1* , P.F. Nettleton 2<br />
1 University of Veterinary Medicine, Kosice, Slovakia; 2 Moredun Research Institute, Pentlands Science Park, Penicuik, Midlothian EH26<br />
0PZ, UK<br />
Four pestivirus species infect domestic animals. BVDV-1 and BVDV-2 mostly infect cattle, CSFV – swine,<br />
BDV – sheep. Pestiviruses are not strictly host specific because they can infect many other animals. Genetic<br />
analysis of pestiviruses by rapid sequencing of PCR products coupled with phylogenetic analysis revealed<br />
new viral genotypes, some of them in free-living animals.<br />
Mainly BVDV specific antibodies have been reported in captive and free-living animals. Pestivirus specific<br />
antibodies were detected in over 40 animal species but the isolation of viruses from wild animals is relatively<br />
rare. It is generally known that CSFV infects not only domestic pigs but also wild boars which are significant<br />
reservoirs of this virus. The BVDV-1 isolates were already detected for example in deer, roe deer, mouse<br />
deer, lama, yak, eland, buffalo, bison. Recently, a pestivirus isolated from reindeer has been typed as BDV-2<br />
genotype (Becher et al., 2003). Pestivirus identified in chamois has been typed as BDV-4 genotype causing<br />
significant problems in chamois population in Pyrenees (Arnal et al., 2004). The first giraffe pestivirus strain<br />
was identified in 60-ties, the second giraffe strain just several years ago. Both strains belong to the<br />
unclassified pestivirus species and in the phylogenetic analysis form a giraffe pestivirus genotype (Avalos-<br />
Raminez et al., 2001). Pestivirus isolated from a pronghorn antelope found dead in Wyoming (Vilcek et al.,<br />
2005) as well as recently identified Bungowannah pestivirus in pig (Kirkland et al., 2007) are representants of<br />
two most distinct pestivirus genotypes so far.<br />
All together six pestivirus genotypes (CSFV, BVDV-1, BDV-2, BDV-4, giraffe and pronghorn antelope) have<br />
been identified in wild animal population. Viruses of BVDV-2, BDV-1 or BDV-3 genotype infecting mostly<br />
cattle and sheep have not been found in wild animals yet.<br />
Most data presented in scientific literature suggest that pestivruses are more likely transmitted from domestic<br />
animals to wildlife population. The transmission in opposite way is not exactly proved but theoretically it can<br />
not be excluded that transmission of highly virulent pestivirus strain from domestic to wild animals or vice<br />
versa could have a devastating effect on the eradication programmes as well as on wildlife population.<br />
There are potential problems with the identification of new pestiviruses:<br />
i/ selection of the correct virus for use in serological studies<br />
ii/ use of the correct cells for the isolation of new pestiviruses<br />
iii/ proper selection of RT-PCR primers for the detection of new pestivirus genomes<br />
All data suggest that pestiviruses are highly efficient viruses infecting domestic and many free-living animal<br />
species and they evolved well-adapted strategy to survive in nature. Taking into account present status with<br />
the identification of new pestiviruses we can conclude that wild animals may be infected with more<br />
pestiviruses than we have identified at present. No doubt that there is a need for more systematic research<br />
focused on the occurrence of pestiviruses in free-living animals.<br />
References<br />
Arnal, M., et al.: J. Gen. Virol., 85, 3653, 2004.<br />
Avalos-Raminez, R., et al.: Virology 286, 456, 2001.<br />
Becher, P., et al.: Virology 311, 96, 2003.<br />
Kirkland, P.D. et al. : Virus Res., 129, 26, 2007.<br />
Vilcek S., et al.: Virus Res., 108, 187, 2005.<br />
Mon 12 November<br />
Mon 12 November<br />
World Association of Veterinary Laboratory Diagnosticians – 13 th International <strong>Symposium</strong>, Melbourne, Australia, 11-14 November 2007<br />
CHARACTERIZATION AND DETECTION OF BVDV RELATED<br />
REPRODUCTIVE DISEASE IN WHITE-TAILED DEER<br />
J.F. Ridpath 1* , E.A. Driskell 2 , C.C. Chase 3 , J.D. Neill 1<br />
1 NADC/ARS/USDA, Ames, IA, 2 University of Georgia, Athens, GA, 3 South Dakota State University, Brookings, SD<br />
Introduction<br />
Bovine viral diarrhea viruses (BVDV) are the causative agent of reproductive and respiratory disease in<br />
cattle resulting in significant economic loss to the beef and dairy industries. The primary consequences of<br />
reproductive infection are due to the direct infection of the fetus and the outcome depends on the stage of<br />
gestation in which the fetal infection occurs 1 . Although abortions and weak calves have been attributed to<br />
BVDV infection in late gestation 6 , infections occurring earlier in gestation generally have greater impact.<br />
Fetal infections in cattle, occurring during the first trimester, result in fetal reabsorption, mummification,<br />
abortion or the establishment of persistently infected (PI) animals. PI cattle are considered the main vector<br />
for introduction of the virus to naïve herds.<br />
BVDV also replicates in white-tailed deer (Odocoileus virginianus) 2-5 . Free ranging white-tailed deer<br />
populations are frequently in contact with domestic cattle in the U.S., therefore, possible transfer of BVDV<br />
between cattle and deer has significant implications for proposed BVDV control programs. The goal of this<br />
study was to examine the effects of BVDV infection in pregnant white-tailed deer<br />
Material & methods<br />
Eleven white-tailed does were purchased from a commercial breeder and housed in BSL2 containment.<br />
Pregnancy status was confirmed and the calculated stage of pregnancy was based on date of contact with<br />
buck. Does were inoculated with one of two BVDV previously recovered from wild white-tailed deer. Levels<br />
of BVDV neutralizing serum antibodies were determined prior to inoculation and 21 or 35 days post<br />
inoculation. Virus isolation was performed on tissues from aborted fetuses, tissues from does that died and<br />
from blood samples from live fawns. Additionally, ear notches of live fawns were tested for BVDV antigen by<br />
antigen capture ELISA (ACE).<br />
Results<br />
Two of the does had serum antibody titers against BVDV (>512) prior to inoculation; the remaining 9 does<br />
were seronegative. Both seropositive animals gave birth to normal fawns. Of the remaining 9 seronegative<br />
animals, one was not pregnant at the start of the study, four died (death between 8 to 79 days post<br />
inoculation), one apparently readsorbed its fetus, two aborted and one gave birth to two probable PI fawns.<br />
BVDV was isolated from fetuses, maternal tissues and PI fawns. Ear notches of PI fawns were positive by<br />
ACE.<br />
Discussions & conclusions<br />
Following BVDV infection of deer we confirmed infection of fetal tissues within the first 7 – 8 days of<br />
infection. We observed abortion and mummification following infection and the birth of apparently<br />
persistently infected fawns. The fawns of does that had serum neutralizing antibodies against BVDV at the<br />
time of inoculation were protected. These observations are consistent with the clinical presentation of BVDV<br />
associated reproductive disease in cattle following exposure before 125 days gestation. Further research<br />
needs to be done to determine if the similarities between BVDV associated reproductive disease in whitetailed<br />
deer and cattle hold at later stages of gestation and to determine, more exactly, the window of fetal<br />
vulnerability for development of persistent BVDV infection in white-tailed deer.<br />
References<br />
1 Brock KV, Grooms DL, Givens MD: 2005, Reproductive disease and persistent infections. In: Bovine viral<br />
diarrhea virus: diagnossis, management and control, eds. Goyal SMRidpath JF, pp. 145-156.<br />
Blackwell Publishing, Ames, IA.<br />
2 Chase CCL, Braun LJ, Leslie-Steen P, et al.: 2007, Evidence of bovine viral diarrhea virus persistent<br />
infection in two white-tailed deer in southeastern South Dakota. Journal of Wildlife Diseases In<br />
press.<br />
3 Passler T, Walz PH, Ditchkoff SS, et al.: 2007, Experimental persistent infection with bovine viral diarrhea<br />
virus in white-tailed deer. Vet Microbiol 122:350-356.<br />
4 Ridpath JF, Mark CS, Chase CCL, et al.: 2007, Febrile response and decrease in circulating lymphocytes<br />
following acute infection of white tail deer fawns with either a BVDV1 or a BVDV2 strain Journal of<br />
Wildlife Diseases 43:In press.<br />
5 Van Campen H, Williams ES, Edwards J, et al.: 1997, Experimental infection of deer with bovine viral<br />
diarrhea virus. J Wildl Dis 33:567-573.<br />
6 Ward GM, Roberts SJ, McEntee K, Gillespie JH: 1969, A study of experimentally induced bovine viral<br />
diarrhea-mucosal disease in pregnant cows and their progeny. Cornell Vet 59:525-538.