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The disease caused by porcine reproductive and respiratory syndrome virus (PRRSV) emerged independently and almost simultaneously in Europe (1990) and North America (1987). The original reservoir of the virus and the date it entered the pig populations is not known. In this study, we demonstrate an accurate molecular clock for the European PRRSV ORF 3 gene, place the root in the genealogy, estimate the rate of nucleotide substitution, and date the most recent common viral ancestor of the data set to 1979; more than 10 years before the onset of the European epidemic. Based on these findings, we conclude that PRRSV virus most likely entered the pig population some time before the epidemic emergence of the virus, and hence, that emergence of European-type PRRSV is not the result of a recent species transmission event. Together, our results show that ORF3 sequencing is a valuable epidemiologic tool for examining the emergence and spread of PRRSV in Europe. As such, the panel of well-characterized and highly divergent ORF3 sequences described in this study provides a reference point for future molecular epidemiologic studies.

An indirect ELISA test was developed as a novel tool aimed at monitoring the herd infection status of swine herds. Meat juice samples from pig carcasses were analysed for the presence of antibodies against porcine reproductive and respiratory syndrome virus (PRRSV). A study of samples from herds with known PRRS status was undertaken. The PRRS status of the herds was evaluated based on the analysis of blood samples by another serological test (blocking ELISA) capable of differentiating between infection with PRRSV of the American type and European type. The specificity of the indirect ELISA test on meat juice samples was 0.98. The sensitivity of the test depended on the type of the PRRSV strain involved. The apparent prevalence in herds infected with the American type of PRRSV was 0.44. The apparent prevalence in herds infected with the European type of PRRSV was 0.64. Herd level sampling and herd level criteria for assessing the PRRS status of herds by the new test were developed. Herds were classified as PRRS negative or PRRS seropositive based on 10 meat juice samples collected randomly at slaughter throughout a 3-month-period. Herd PRRS status classification by the indirect ELISA was validated in 47 herds by collection of blood samples from the herds. Eighteen herds were classified as PRRS negative by both test systems. Twenty-nine herds were classified as PRRS seropositive by both test systems. Acceptable herd classification was achieved using this test.

Data collected from an outbreak of excessive mortality of mink kits in 4 Danish mink farms in 1982 were analysed. The mortality of the mink kits was found to be highest for the kits from Aleutian Disease (AD)-positive females, and the Scanblack mink was found to be the most frequently affected mink type. Furthermore the mortality was found to depend on the farm of origin and to be highest for the lastest born kits. The age of the females and their location in sheds were found not to influence the mortality of the kits. However, the mortality for the Pastel mink decreased with increasing distance from the Scanblack mink. The possibility that the excess mortality of the kits might be due to an AD-virus infection is discussed.

An outbreak of increased mortality among mink kits in 4 Danish mink farms in 1982 is described. A comparison with data from 4 non-affected farms revealed obvious differences in neonatal mortality in the period from parturition until May 15th (early neonatal mortality) and in the period from May 15th to June 30th (late neonatal mortality) between the 2 groups of farms. The populations are described in terms of age, origin, types of mink and the extent of transfer of breeding females among the farms. Postmortal examination showed consistent pathological changes, but the etiology and pathogenesis of the diseases is uncertain until now. The increased mortality of kits, however, was accompanied by increasing numbers of Aleutian Disease (AD) positive reactors in the 4 populations.