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A cross-sectional study was made in a major cattle-breeding area of Switzerland to investigate the prevalence and local distribution of animals antibody positive to bovine viral diarrhoea (BVD) virus and of persistently infected animals. The sample size and statistical analysis took into account the possible clustering of persistently infected animals on individual farms. Of 3440 animals tested on 121 farms, 1982 were found to have antibodies to BVD virus (95 per cent confidence interval for the population prevalence: 57.6+/-4.5 per cent) and 22 were persistently infected (estimate for the population prevalence: 0.64+/-0.34 per cent). The detection of persistent infection in animals less than seven months old was improved either by retesting one year later, by using an antigen-capture ELISA or, in selected cases, by the analysis of original serum samples by reverse-transcription PCR. The results showed that the prevalence of persistent infection may be underestimated by as much as one-third when antigen detection alone is used. None of the 121 farms investigated was free of antibody-positive animals and one in eight herds had at least one animal that was persistently infected. The prevalence of antibodies was lowest in seven- to 12-month-old animals (22.9 per cent) and highest in animals aged five years or over (84.9 per cent).

In this study, six immunocompetent calves were experimentally infected with a noncytopathic strain of bovine viral diarrhea virus (BVDV), and the effects of the viral infection on parameters of the innate immune response of the host were analyzed. Clinical and virological data were compared with the temporal activation of the alpha/beta interferon-regulated Mx gene in white blood cells (WBC) and skin as well as the upregulation of the acute-phase serum proteins haptoglobin (Hp) and serum amyloid A (SAA). The viral strain used did provoke transient health impairment, namely, fever and leukopenia that were associated with viremia, viral shedding with nasal secretions, and antiviral seroconversion. Complete recovery was observed within 3 weeks. Elevated levels of SAA and Hp were apparent from days 4 to 13 and 8 to 11, respectively. In WBC, the levels of Mx mRNA and Mx protein were elevated from days 2 to 15. In the context of this study with BVDV, the level of Mx protein expression in WBC provided the most telling diagnostic window to monitor the host's ongoing innate immune response.

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