A total of thirty-eight Mafriwal cattle were selected from a localcattle herd of a government cattle farm; of which 36 animals were sub-fertile Mafriwal female dams and two bulls which were considered as control animals (one male Mafriwal and one male Jersey). Two markers were used in the detection of Y chromosome in the sub-fertile female animal which are testis specific proteins Y-encoded (TSPY) and amelogenin (AMLX/AMLY) genes. The genes were amplified using PCR. The DNA bands from a normal male for TSPY gene size was approximately 260 bp while AMLX/ AMLY gene were approximately 341 and 467 bp. The examination of all samples showed that the sub-fertile cow revealedonly 467 bp while three fragments were detected in the control group; 260 bp (testis specific protein, Y-encoded gene), 341 and 467 bp (Amelogenin gene). The results showed that the sex chromosomeanomalies associated with Y chromosome did not occur in this group. These two sex markers can be used for the diagnosis of Y chromosome abnormality in a sub-fertile cow through polymerase chain reactionwhich is a rapid and reliable method for use in breeding herds.

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.

A total of 145,347 samples (4,322 cases) were received for the passive surveillance of melioidosis in the Serology Laboratory of Veterinary Research Institute (VRI) from the year 2012 to 2016. From the samples received, 0.63% were positive and 99.37% were negative. The objective of this study is to determine the seropositive rate and distribution of melioidosis in livestockbased on cases received which comprise of sheep (37.24%, n=54,130), goat (54.01%, n=78,500), cattle (8.12%, n=11,804) andbuffalo (0.63%, n=913) within the period of 5 years. A geographical mapping of seropositive cases was designed using thedata from the passive surveillance and the results were visualized in a geographical mapping which provides a clear visual description on the distribution of the diseases. By 2016, positive cases were found to be concentrated in the states on the east coast of Peninsular Malaysia and Sabah. To sum up, the percentage of seropositive cases of melioidosis in 5 years has increased from 1.79% in 2012 to 12.17% in 2015 and decreased to 1.04% in 2016. From the findings, this study can provide the dataneeded as the indicator for the evaluation of surveillance and vaccination programmes, disease eradication planning and to monitor the distribution of seropositive cases of melioidosis in Malaysia.

Zoonotic parasitic gastroenteritis has been well-known as a serious limitation to humans as well as livestock productivityin terms of man-power, pathology and fiscal losses, as human infection with these helminths from cattle can resultfrom consumption of meat containing the infective stage of the worm. This study therefore investigates the presence ofzoonotic helminth infections among cattle in Minna metropolis, and scientific basis for their potential transmission to humanpopulation. A total of 184 diarrhoeic faecal samples from cattle were collected from September 2014 to June 2015 in Minna,Niger state and processed using the direct faecal microscopic examination techniques. The obtained results showed that a total of 81 (44%) samples were positive including Ascaris sp, Fasciola gigantica, Trichuris sp. and Taenia sp. with infection rates of 22.3%, 12%, 2.2% and 0.5% respectively, and mixed infections of Fasciola gigantic with Ascaris sp. (4.3%) , and Ascaris sp. with Trichuris sp. (2.7%). Poor human hygiene, inadequate livestock husbandry managements and restriction of animals to residential areas are the major factors responsible for the high prevalence of zoonotic helminths and geo-helminths in the study area. Therefore veterinarians, animal handlers and livestock owners should practice personal hygienic and safe management practices for animal rearing and treatments.

Bovine haemoparasites are cosmopolitan in distribution and are known to cause substantial losses to the cattle industry. In spite of their economic importance, there remains a dearth of information on their molecular epidemiology in many parts of the world including Malaysia. To ascertain the molecular prevalence and species co-infection of bovine haemoparasites in the country, blood samples were collected from 1,045 heads of beef and dairy cattle on 43 farms from six geographical zones throughout Peninsular Malaysia. Samples subjected to PCR amplification of parasite species-specific genetic fragments revealed that Anaplasma marginale was the most prevalent haemoparasite (72.6%),followed by Theileria orientalis(49.8%),Candidatus Mycoplasma haemobos ( 47. 0 % ),Babesia bovis(32. 5%), Babesia bigemina (30.5%) and Trypanosomaevansi(17.9%). A high percentage (92.1%) of cattle was infected with either one or more haemoparasites. Triple haemoparasite species co-infection was the most prevalent (25.6%), followed closely by double species co-infection (25.1%). The most common (8.8%) and significantly correlated(rs= 0.250; p<0.01) combination was A. marginale+ T.orientalis. The present study constitutes the first attempt in the country to document the molecular prevalence and species co-infection of bovine haemoparasites over a wide spatial distribution. The data obtained will facilitate treatment, control and prevention measures to improve the local cattle industry.

A total of 65 Pasteurella multocida were isolated and identified from various animal’s samples received by Veterinary Research Institute (VRI) during the period of 2014 to 2016. These animals comprises of cattle, goat, pig, chicken, duck and rabbit. The serogroup of Pasteurella multocida were carried out using designation system of Carter’s capsular typing and molecular serogrouping method. Based on cases submitted to VRI, the prevalence of pasteurellosis in Malaysia ranging from 1.0% to 3.2% (2014 to 2016). It is low compared to previous reports and the pattern of predominant serogroups and animal hosts were found to be changing every year. In 2014, 80% (12/15) of the isolates were Pasteurella multocida Carter’s type D where all were isolated from goats. In 2015, the predominant serogroup changed to Pasteurella multocida Carter’s type A with a prevalence rate of 40.6% (13/32) which were mostly isolated from duck and cattle. While for Pasteurella multocida Carter’s type D, the prevalence in 2015 reduced to 21.9% (7/32) compared to the previous year and it was isolated from various animal species. Interestingly, in 2015 there was one isolate of Pasteurella multocida Carter’s type B isolated from goat with no reported history of outbreak. In 2016, the prevalence of Pasteurella multocida Carter’s type A increased to 72.2% (13/18), with a high percentage (92.3%) infection in young calves showing clinical signs with high mortality and morbidity in infected farms. Furthermore, during these 3 years of study, 3 isolates of Pasteurella multocida serogroup F were also identified each from pig, goat and chicken, respectively. In conclusion, this study revealed that pasteurellosis had become sporadic in Malaysia and the distribution of serogroups were diverse in all species of animal with no definitive host.

Monitoring of veterinary drug residues in chicken, swine and cattle was conducted in Peninsular Malaysia from 2010 to 2016. Tissue samples were collected from slaughterhouses and processing plants. A total of six groups of veterinary drugs were analysed in 8,708 samples using bioassay or immunoassay and LCMS method. The average violation rate was 3.4%, 2.5%, 1.9%, 0.8%, 1.6% and 2.7% for year 2010, 2011 and 2012, 2013, 2014, 2015 and 2016, respectively

Traceability system for livestock is an important infrastructurenecessary to monitor animal health, animal disease emergencies and quality assurance. The aim of this study was to evaluate farmer and trader willingness to use and pay for an animal identification and traceability system in Peninsular Malaysia. Data was obtained from aquestionnaire that was completed by 543 farmers and traders from the 10 states in the peninsula. Our results show that up to 54% respondents were willing to use and pay for an animal identification and traceability system. Gender and the length of experience of farmers and traders were factors significantly associated with theoutcome of this study. Female farmers and traders were less willing to use and pay for an animal identification and traceability system while farmers and traders with more experience in the cattle industrywere significantly more likely to provide a favourable response.

The Kedah-Kelantan cattle (KK) is an indigenous cattle breed and is mainly kept for meat production in Malaysia. Due to lack of information about polymorphism of growth traits in these cattle, Insulin-like Growth Factor 1 (IGF-1) was chosen to be the candidate gene in this preliminary study. The aim of this study is to investigate the polymorphism of IGF-1 gene in KK and to show that the PCR-RFLP technique can be used as a basis for use as molecular markers in cattle. A total of 46 KK blood samples were collected for DNA extraction performed using a commercial kit. The exon 1 of IGF-1 gene was amplified to produce a 249 bp fragment. The amplified fragments were digested with Eco105I restriction endonuclease and then subjected to electrophoretic separation in Fluorosafe stained 2.5 % agarose gel. The result revealed two alleles, A and B. Threegenotypes were observed: AA, AB and BB. Frequencies were 0.07, 0.13 and 0.80 for AA, AB and BB, respectively. This gives frequencies of 0.13 and 0.87 for A and B alleles. It is concluded that the population is in Hardy-Weinberg disequilibrium (p<0.05). It is possible that this gene has been exposed to selection.