An ELISA based on whole virus for the detection of antibodies to small-ruminant lentiviruses.

A new ELISA kit was developed, based on highly purified whole-virus antigen derived from the Swiss maedi-visna virus strain OLV. The sensitivity, specificity and accuracy of this assay were compared with that of an established ELISA based on recombinant GAG (group-specific antigens)-GST (glutathione S-transferase) fusion protein expressed in E. coli (GAG-GST ELISA).

Diagnosis of bovine virus diarrhoea by two enzyme-linked immunosorbent assays.

Two enzyme-linked immunosorbent assays (ELISAs) for the diagnosis of bovine virus diarrhoea (BVD) are described: CHEKIT-BVD-VIRUS and CHEKIT-BVD-SERO. The first test detects virus antigen in leucocytes, resulting in identification of persistently-infected animals, while the second detects antibodies to BVD virus (BVDV). It is well known that even persistently-infected animals may have antibodies to heterologous BVDV strains.

Enzyme-linked immunosorbent assay (ELISA) for the detection of antibodies against Salmonella enteritidis in chicken blood or egg yolk.

Tracing of flock infection remains one of the most serious unsolved problems of controlling salmonellosis in poultry. In order to overcome this problem, a serological test kit for the detection of antibody to Salmonella enteritidis (1, 9, 12:[f], g, m, [p]:[1, 7]) in chicken flocks was developed. In this study, samples of antisera and the yolk of eggs from different chicken flocks were tested with the ELISA kit, and the resulting flock profiles were compared.

[Progression of the rabies virus in the visual system of the rat].

The CVS rabies virus, inoculated in the anterior chamber of the eye, is transported from the retina to the central nervous system only along the accessory optic tract and invades transsynaptically its terminal nuclei. On the other hand the retino-geniculo-cortical system is affected much later. Thus the virus shows a special affinity for a well defined neuronal system and behaves as a precise tracer of its intracerebral connections.

Potency testing of inactivated rabies vaccines in mice, dogs and cats.

The high variability that exists in the NIH potency test for inactivated rabies vaccines is well known. To control this variability, the use of a reference preparation of rabies vaccine in parallel with the test vaccines is recommended. However, our data indicate, that the NIH test is more variable when calculating antigenic values using the reference vaccine CRV1 than when calculating only PD50 values.