A serological survey for antibodies to foot-and-mouth disease virus in indigenous Tswana goats and sheep in Kasane, Maun and Shakawe districts in northwestern Botswana.

A serological survey was conducted in apparently healthy, unvaccinated indigenous Tswana goats and sheep in Kasane, Maun and Shakawe districts in northwestern Botswana in order to determine in these animals, the levels of exposure to the South African Territories (SAT) serotypes: SAT 1, SAT 2 and SAT 3 of foot-and-mouth disease virus (FMDV). A total of 250, 142 and 134 goat sera originating respectively from Kasane, Maun and Shakawe districts were tested for FMDV antibodies against the three SAT serotypes by the liquid phase blocking enzyme-linked immunosorbent assay and 26 of 250 (10.4%), 5 of 142 (3.5%) and 18 of 134 (13.4%) were positive either to SAT 1 or SAT 3, or to both serotypes. None of the goats' sera was positive to SAT 2 serotype. All sheep sera (n = 9) tested negative against all three serotypes of the virus. The findings are discussed in relation to results of other serological surveys carried out elsewhere.

Molecular epidemiology of rabies in Botswana: a comparison between antibody typing and nucleotide sequence phylogeny.

A panel of rabies virus isolates (RABV) endemic within Botswana between 1988 and 1992 have been typed by anti-nucleocapsid monoclonal antibodies (MAb) into two dominant groups. The first associated with the domestic dog (Canis familiaris) and the second associated with a range of wildlife species. Using nucleoprotein coding sequence data, we have applied molecular phylogenetic techniques to the same panel of 35 well-characterised rabies virus isolates from throughout Botswana in an attempt to compare both techniques and to further investigate the virus/host species relationships within this African country. The results confirm that there are indeed two major groups and that these are related primarily to biotype. The wildlife-associated biotype appeared more phylogenetically diverse and was more commonly isolated in the southeast of the country, with the canine-associated group dominating the north of the country. In addition, molecular phylogeny identified further groupings within both biotypes and a small number of isolates, which were not classified by MAb typing, could be assigned to a group. During the study period (4 years) there appeared to be little sequence variation within groups suggesting that distinct lineages persisted throughout the study and that there appears to be little evolutionary pressure on the nucleoprotein coding region of the viral genome.

Incidence of abortion and association with putative causes in dairy herds in New Zealand.

AIM: To estimate the distribution and causes of abortion in dairy herds across New Zealand during the 2001/2002 breeding season. METHODS: A questionnaire survey was sent to all veterinary practices that employed members of the New Zealand Veterinary Association. Veterinarians were requested to record the numbers of dairy herds serviced by their practice in which the rate of aborting cows was zero (0%), low (1-5%) and high (6-10% and >10%), and all laboratory submissions, specimens, tests and results related to their investigation of abortions in these herds, for each category. RESULTS: Forty-two large animal practices serving 1,431 dairy clients from all except one region in New Zealand responded. The within-herd incidence of abortion was zero in 497 herds (34.7%), low in 876 herds (61.2%), and high in 58 herds (4.1%) in the season 2001/2002. Within the high category, 0.6% herds reported abortions at a frequency as high as may be expected in epidemic abortions (>10%). Compared to other regions, the abortion incidences tended to be relatively high in Northland, Auckland and the Bay of Plenty, and low in Hawke Bay, Waikato and Nelson (p<0.001). Cases were submitted for laboratory investigation from 51/934 (5.5%) herds. Even though submission rates increased with the level of abortion, most submissions originated from herds with a low abortion rate. The main agents identified among submissions as the cause of abortion were Neospora caninum (Nc) (35%) and bovine viral diarrhoea virus (BVDV) (16%). Among 39 submissions from low abortion herds, 33% were suspected due to Nc and 15% to BVDV, and this was not statistically different (p>0.10) from the distribution in 13 submissions from high abortion herds (46% Nc, 23% BVDV). While cases associated with Nc were submitted in April, May and June, submissions for suspected BVDV spread evenly over the months of March to July. CONCLUSION: In the 2001/2002 season, approximately 4% of dairy herds in New Zealand recorded a relatively high incidence of abortion (>5%) and 0.6% herds experienced an incidence of >10%. BVDV and Nc were the most frequently diagnosed agents associated with abortion, regardless of whether the seasonal incidence of abortion within a herd was low or high.

Validation of a bulk tank milk antibody ELISA to detect dairy herds likely infected with bovine viral diarrhoea virus in New Zealand.

AIMS: To assess the sensitivity and specificity of a bulk tank milk (BTM) antibody enzyme-linked immunosorbent assay (ELISA) to detect likely infection of a dairy herd with bovine viral diarrhoea virus (BVDV). The ELISA was subsequently used to estimate the prevalence of likely infected herds in parts of the North Island of New Zealand. METHODS: BTM samples from 724 randomly selected dairy herds in the Waikato, Bay of Plenty and Northland regions of New Zealand were tested for BVDV antibodies. From this group, 20 herds were again randomly selected from each of the quartiles of the ELISA percentage inhibition (%INH) result. From each participant herd, serum from 15 randomly selected calves aged 6-18 months and 15 cows was collected and tested using an indirect blocking ELISA for BVDV antibodies. RESULTS: Among serum results from calves from 50 herds available for analysis, 34 (68%) herds were classified as likely non-infected (0-3 seropositive among 15 calves) and 16 (32%) as likely infected (5-15 seropositive among 15 calves). Receiver-operator characteristic (ROC) analysis identified an optimal cut-off for BTM of 80%INH associated with 81% sensitivity and 91% specificity for likely herd infection. The prevalence of BVDV antibodies in cows within herds and %INH for BVDV in bulk milk were positively correlated (p<0.01). The association between bulk milk %INH and the prevalence of BVDV antibodies in calves was stronger than the same association in cows. Based on the threshold of 80%INH, the 95% confidence interval (CI) for prevalence of likely infection in the 724 herds in the Waikato, Bay of Plenty and Northland regions of New Zealand was 12-17%. Vaccination against BVDV was not significantly associated with the likely infection status of the herd based on prevalence of BVDV antibodies among calves. CONCLUSION: An ELISA test result for BVDV antibodies in BTM >/=80%INH can be used as a threshold to indicate the presence of likely infection with BVDV in dairy herds in New Zealand, with 81% sensitivity and 91% specificity.