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.

Highly pathogenic avian influenza (HPAI) is caused by influenza virus A from the family Orthomyxoviridae. It is a severe, systemic disease with high mortality in avians. The mortality can be as high as 100% in a few days. On 28 February 2017, HPAI virus of H5N1 subtype was confirmed in village chickens at Kampung Pulau Tebu, Batu 5, Tunjong Kota Bharu, Kelantan. It wasthe second outbreak of HPAI in Kelantan after the first reported case at Tumpat Kelantan on 17 August 2004. Most of the dead poultry showed similar clinical signs of sudden death with high mortality, cyanosis and oedema of head, comb, wattle and snood as well as red discolouration of shanks and feet. Post-mortem was performed on dead poultry and there were generalised haemorrhages of all internal organs, congested mesenteric blood vessels andpinpoint haemorrhages on proventriculus. Histopathological examination revealed generalised pulmonary haemorrhages with moderate interstitial pneumonia, generalised hepatic haemorrhages and hepatitis with multifocal area of hepatic necrosis, generalised haemorrhagic myocarditis and generalised haemorrhagicnephritis. Confirmation test was performed using RT-PCR and viral isolation at Veterinary Research Institute, Ipoh. 36 foci wereaffected involving five districts (Kota Bharu, Tumpat, Bachok, Pasir Mas and Tanah Merah) causing depopulation of 56,953 poultryand 17,531 eggs. Surveillance and control measures were taken by Department of Veterinary Services to contain the disease from spreading to other areas.

Brucellosis in goats is mainly caused by the bacterium Brucellamelitensis, which is one of the most important pathogenic species in the world. In Malaysia, the annual prevalence data of brucellosis was recorded in goats and the control strategy of the disease basedon test and cull of infected animals. This strategy has caused huge economic losses to farmers and government alike. Therefore, whole genome sequencing of B. melitensis local strain is essential forimproving the current vaccine. B. melitensis strain VRI 6530/11 wasobtained from veterinary research institute biobank, Ipoh. The strain was submitted for classical identification procedures and the total genomic DNA was extracted by using DNeasy blood and tissue kit(QIAGEN). The concentration and purity of DNA were determined by using agarose gel electrophoresis and spectrophotometer (DNA/RNA) assay respectively. The genome was sequenced by using IlluminaHiSeq platform with insert size ~200 bp. A total of 1.0 Gb data was generated from the sample. More than 95% of sequencing data was retained in the sample after quality filtering, this indicatethe sequencing reads are of high quality. Final assembly had 33 scaffolds with total size ~3.28 Mb, 44 contigs, GC content is 57.25%, N50 is 293,291. A total of 3,238 protein coding genes, 48 tRNAs and 3rRNAs were predicted and over 87% of the genes were functionally annotated. Genome sequencing of a local B. melitensis strain is the first of its kind in Malaysia and work from this study can contribute towards the development of a new effective vaccine for the control ofthe disease in the country.

The animal trade is an important risk factor that affects the spread of diseases among animals and herds. The goal of the present study was to characterize the cattle movement network in Pernambuco, Brazil, based on the animal movement permits (Guias de Trânsito Animal; GTAs) from 2012 to 2013, and identify the intensity of the commercial relationship between farm premises. A total of 737,950 GTAs were issued, and the movement of 3,481,185 cattle (1,688,585 in 2012 and 1,792,600 in 2013) was analyzed. Of the moved animals analyzed, 52.57% (1,829,907/3,481,185) were involved in the movement of cattle in or out of livestock markets, indicating that livestock markets played a major role in the network. Approximately 20% of the more-connected premises were responsible for approximately 87% of the movement related to sales and 95% of the movement related to purchases. Considering the important role of livestock markets and the intense cattle trade between farm premises, surveillance, and control measures could be more efficient if targeted to livestock markets and highly connected premises to prevent the spread of infectious diseases.

Over the past two decades, many Brazilian cities have been reporting an increasing incidence and spread of feline sporotrichosis. The disease is neglected, and little is known about the causal processes underlying its epidemic occurrence. This study characterized the spatiotemporal dynamics of feline sporotrichosis in Guarulhos. Moreover, we proposed and tested a causal explanation for its occurrence and zoonotic transmission, giving a key role to social vulnerability. A direct acyclic graph represented the causal explanation, while Bayesian spatial models supported its test as well as the attribution of a risk-based priority index to the census tracts of the city. Between 2011 and 2017, the disease grew exponentially and the spatial spread increased. The model findings showed a dose-response pattern between an index of social vulnerability and the incidence of feline sporotrichosis. This pattern was not strictly monotonic, so some census tracts received a higher priority index than others with higher vulnerability. According to our causal explanation, there will not be effective prevention of feline and zoonotic sporotrichosis as long as social inequities continue imposing precarious livelihoods.