Paratuberculosis, one of the chronic granulomatous enteritis that
predominantly affects ruminants worldwide, is caused by Mycobacterium avium
subsp. paratuberculosis (MAP). It is most efficiently diagnosed by MAP from
faeces by Polymerase Chain Reaction (PCR). Serological tests like Enzyme
Linked Immuno Sorbent Assay (ELISA) also provides a rapid and cost-effective
alternative diagnostic tool. Present study was carried out to directly
evaluate the sensitivity and specificity of ELISA (ID vet innovative
diagnostics; France) using IS900 PCR as a gold standard. Serum and faecal
samples were collected from 180 adult goats of either sex, from Malappuram
and Thrissur districts of Kerala with unknown paratuberculosis status. Faecal
samples were processed for direct IS900 PCR and serum samples were tested for
MAP antibodies using Indirect ELISA kit. IS900 PCR detected 38 out of 180
confirmed to be shedding MAP. ELISA detected 22 out of 180 animals as
positive. Overall, ELISA was 50 % sensitive and 97.9 % specific in comparison
to IS900 PCR. The IS900 PCR outperformed ELISA in detecting animals
potentially infected with MAP and is more sensitive than ELISA at detecting
animals suspected of paratuberculosis. But, for early diagnosis of
paratuberculosis in goats, ELISA can be done as easy and rapid farm level
identification and IS900 PCR as individual confirmatory test.