Epidemiological studies of bovine spumavirus.

Bovine spumavirus (BSV) infection is shown to be endemic in some herds in north Queensland. The virus was readily isolated from leucocytes of the majority of mature cattle which were BSV antibody positive (BSV reactors) in the agar gel precipitin test (AGPT). Calves born to dams which were BSV reactors showed no BSV antibody or circulatory leucocyte-associated BSV (CLAB) at birth, but became BSV reactors following ingestion of colostrum, and maintained such evidence of passive immunity until 3-5 months of age. Experimental infection of dams with BSV at 5-7 months of gestation did not cause foetal infection. In groups of young animals at pasture, segregated by age and sex, no evidence of BSV infection occurred, following loss of passive immunity, until 18-24 months of age. At this time, occasional members of some groups (both male and female) became BSV reactors and showed CLAB. At approximately 24 months old, following mixing in groups with older cows, and single-sire mating, 34% of heifers became BSV reactors within 10 weeks. A herd survey indicated 85% of 2-3-year-old cows to be BSV reactors; thereafter, the percentage of reactors declined gradually with increasing age. Using BSV grown in cell culture, transmission of infection by throat spray was the most successful route, 7 of 7 (100%) of susceptible cattle becoming BSV reactors within 8 weeks of spraying. Using the intravenous route, only 2 of 5 (40%) susceptible cattle became BSV reactors, and swabbing of cell culture virus into the prepuce or vagina did not result in infection of 4 BSV-susceptible animals.(ABSTRACT TRUNCATED AT 250 WORDS)

Detection of immunological tolerance to bovine spumavirus (BSV) with evidence for salivary excretion and spread of BSV from the tolerant animal.

A group of 17 Friesian-Holstein steers held in individual pens was examined for evidence of infection with bovine spumavirus (BSV). Serum was examined for specific antibody by 2 serological procedures, and circulatory leucocytes and throat swabs were examined for the presence of circulatory leucocyte-associated BSV (CLAB) and saliva-associated BSV (SAB). Initial tests showed that 7 of the 17 steers had specific antibody to BSV by both serological procedures, and a further steer developed such antibody during the first 3 months of holding the animals in single contiguous pens. All 8 of these specific antibody-positive steers were CLAB positive and SAB negative. Nine steers showed no specific antibody to BSV by either of the 2 serological procedures; 8 of these 9 steers showed no evidence of CLAB or SAB. The exception was one steer which was CLAB- and SAB-positive at each of 30 samplings taken over a period of 9 months observation, whilst remaining specific-antibody free. This steer was classed as immunologically tolerant of BSV, and epidemiological data suggested that lateral spread of infection had originated from this animal through the agency of saliva.