SOJ Veterinary Sciences
Open Access Research Articleinfection has been demonstrated for cattle [2] and is assumed to be the case for all ruminants. Cross species transmission is possible, including in wildlife. MAP is highly resistant in the environment [3].There are four phases of the disease. First, silent infection, which can be detected only by necropsy and tissue culture. Second, subclinical disease, in which only a small percentage of animals have detectable antibodies and most animals are fecalculture-negative with intermittent shedding of low numbers of MAP in feces in only a few animals. Third, clinical disease, often seen several years after infection. In cattle, clinical signs are of gradual weight loss, rough hair coat, and diarrhea and drop in
AbstractControl of Johne's Disease (JD) is a high priority, it causes significant economic losses in the livestock industry. An efficacious vaccine for JD is not currently available and no satisfactory treatment exists, so control programs depend on diagnostic tests based on detection of the immune response generated after infection with Mycobacterium avium subsp. paratuberculosis (MAP)-the causative agent of JD-to identify and remove infected animals and management practices to interrupt transmission.
Objectives:The objective of this study was to evaluate a new, commercially-available, Enzyme-Linked, Immunosorbent Assay (ELISA) that was developed for cattle, for use with goat serum. For comparison, a United States Department of Agriculture (USDA)-approved ELISA kit for goats, an Agar Gel Immunodiffusion (AGID) test and a Polymerase Chain Reaction (PCR) test to detect MAP in fecal samples were also evaluated.Methods: Infection status at necropsy was taken as the reference standard, determined by gross, histological and microbiological examination of tissue specimens. The serum and fecal samples were taken from goat kids that had participated in a previous vaccine efficacy study. Eighty goat kids were vaccinated either once subcutaneously at eight weeks with a commercial vaccine, or orally at eight and 10 weeks with one of five experimental oral vaccines or a sham-control oral vaccine. Kids were challenged orally with a bovine isolate of MAP, three weeks after the last vaccination.Results: None of the vaccines prevented infection. Samples taken from 10 to 13 months post-challenge were used to compare the assays. The specificity of all tests was 100%. At 13 months, the new ELISA, approved ELISA, AGID test and fecal PCR test had sensitivities of 55.7%, 52.9%, 24.3% and 87.1% respectively. At 11 months the sensitivities were 48.6%, 38.6%, 10.0% and 78.6% respectively and the sensitivity of the new ELISA was significantly better than the approved ELISA (p = 0.0196).
Conclusion:The new ELISA effectively detected circulating MAP antibody in the serum of infected goats and the preliminary results in this study indicate the kit has potential for use in goat JD control programs. The results for the new ELISA in goat serum are comparable with those reported when the ELIS...