A study was conducted to identify the current status of Fasciolaand Paramphistomum infections in small ruminants in Terengganu. A total of 267 faecal samples from small ruminants were collected and subjected to sedimentation technique. Serum samples were diagnosed for detection of IgG antibody for Fasciola infection using sELISA method. Results showed that there were 4% of the goats positive with Paramphistomum eggs whereas Fasciola egg was not observed in any of the faecal samples. However, it was found that 89% of the serum samples from goats were positive with IgG antibody for Fasciola infection. Small ruminants in Terengganu were not infected with severe Fasciola and Paramphistomum infections yet the results obtained from this study will update the current status of the infections. This information will help the farmers and the Department of Veterinary Services to plan on management to maintain the animals’ health.

Brucellosis, caused by Brucella melitensis, is a significantproblem for both public and animal health worldwide. The Rose Bengal plate test (RBPT) antigen from Brucella melitensis local isolates were developed in this study. The performance of the assay wasinvestigated using serum samples collected from goats. A total of 1063 serum samples obtained from goats were examined for thepresence of antibodies against Brucella by in-house RBPT (LRBPT), commercial RBPT (Veterinary Laboratory Agency – VLA, UK) and Compliment Fixation test (CFT). The sensitivity and specificity wascalculated using CFT as the gold standard. Out of 1063 goats sera analyzed 364 (34.24%), 335 (31.51%), and 373 (35.08%) were found to be positive by LRBPT, commercial RBPT and CFT, respectively. The sensitivity calculated for the LRBPT, was 90.1% compared to commercial RBPT 85.0%. However, the specificity of the LRBPT was lower (95.9%), than the commercial RBPT (97.4%). Furthermorethe LRBPT has better value of NPV (94.7%) than commercial RBPT NPV(92.3%). While the PPV, of the commercial RBPT is higher (94.6%) than LRBPT (92.3%) respectively. High sensitive and low cost LRBPT compared to cRBPT B. melitensis RBPT test was successfully developed in this present study. Therefore it was concluded that this diagnostic test kit can complement and replace the availablecommercial RBPT which is relatively more expensive and less sensitive in detection of brucellosis in goats. It could also be used for epidemiological surveillance of caprine brucellosis in Malaysia.

Ever since infectious bursal disease (IBD) was recognised in Nigeria over forty years ago, it continues to pose a threat to poultry production with limited information on the likely role of other avian species especially those raised in close proximity with chickens. For this study, blood samples were obtained from184 unvaccinated apparently healthy birds comprised of Japanese quails (63) andindigenous chickens (60) on smallholdings as well as pigeons (61) in a live-bird market in Osun and Oyo states, southwest Nigeria.Sera from these birds were analysed for IBD virus antibodies using a commercial ELISA kit. Overall, 69 (37.5%) sera were positive for IBDV with 52.8% (65/184) and 6.6% (4/184)from birds on smallholdings and live-bird market, respectively. These findings indicate that these birds were sub-clinically infected and could serve as reservoirs shedding the virus into the environment and perhaps, corroborate the suggestion that the inability to effectively control or eradicate the disease from poultry flocks in Nigeria may be due to limited information on the contributions of other avian species other than chicken in the spread of IBD virus.

The aim of this study was to test the potential diagnostic usefulness of recombinant Toxoplasma gondii SAG1 antigen and
excretory-secretory antigen (ESA), with respect to toxoplasmosis detection and infection phase distinction in laboratory mouse by determining specifi c serum IgM and IgG antibodies with the use of indirect ELISA technique. The highest titre at the beginning of infection was demonstrated by immunoglobulin M while the highest titre at the end of the infection was displayed by immunoglobulin G. In contrast, sera of chronically infected mice, positive IgG titre was detected on day 14 p.i. for ESA or day seven p.i. with rSAG1 and increased thereafter until day 70 p.i. after which the titre stabilized. IgA antibody also showed similar kinetics as IgG. Potentially rSAG1 may be a suitable diagnostic antigen than ESA in the diagnosis of acute and chronic toxoplasmosis.

Conventional methods of detecting Corynebacterium pseudotuberculosis, a bacterium that causes caseous lymphadenitis (CLA) in sheeps and goats focused on several serodiagnostic tests such as ELISA, Western blotting and various inhibition and precipitation techniques. This paper described a Surface Plasmon Resonance (SPR) protocol for the direct detection of polyclonal
antibodies against Corynebacterium pseudotuberculosis with immobilisation of the antigen on unmodified transducer surface. The lower limit of detection was determined to be 2 μg mL-1 of immobilised antigen (Ag). Sufficient binding interaction was monitored on unmodified transducer; and saturation of the binding interaction was observed at 80 μg mL-1 of interacted antibody.

A total of 3430 serum samples from various animal species and humans were tested using microscopic agglutination test (MAT) to determine
the frequency of the important leptospiral serovars involved in animals and humans. The sera were screened against 14 serovars of pathogenic Leptospira interogans and 1 serovar of non-pathogenic Leptospira biflexa. Altogether, 441 (12.86%) of the tested serum samples were found to be positive serologically. Tested sera reacted to all 15 serovars used in this study. The most predominant serovar in cattle and sheep is hardjo (39.60% and 66.67%). However, in goat, buffalo and horse, the most frequent serovar detected is hebdomadis (30.00%, 32.58% and 57.14%). In dog, the most predominant serovar is bataviae (19.23%). In humans, the most predominant serovar is cynopteri (3.26%). Among all the samples tested, there were no positive samples from pig and cat. Domestic animals, rodents and
pets can infect the environment or transmit the disease to human or other animals. This study showed that domestic animals could play a role in the epidemiology of leptospirosis and represents a threat to
public health.