The study was conducted toknow the anatomy of the brachial plexus ofWhite New Zealand Rabbit (Oryctolaguscuniculus). Ten healthy male and femaleWhite New Zealand rabbits were dissectedin this study. It was found that the brachialplexus of the White New Zealand Rabbitwas formed by ventral branches of C5,C6, C7, C8, T1 and T2 spinal nerves.The cranial trunk was formed by thecaudal branch of C5, C6 and caudal trunkformed by rami ventralis of C7, C8, T1and the cranial branch of ventral ramusof T2. Cranial pectoral nerve originatedfrom the caudal trunk spreading into thepectoral muscles. The musculocutaneousnerve innervates into the brachial muscleand the axillary nerve into the subscapularmuscle. The radial nerve was dividedinto two branches as ramus profundusand ramus superficial then divided intothe digital dorsal common III and IV.The thoracodorsal nerve innervates thelatissimusdorsi muscle. The median nervewas divided into digital dorsal commonI, II, III and IV nerves. The ulnar nerveformed the caudal cutaneous antebrachialthen digital dorsal common IV and Vnerves. Lateral thoracic and caudal pectoralnerves originated from the caudal trunk.The origin and distribution of brachialplexus resemble that of porcupines butdiffer from other mammals.

This is a case report ofa captive female green peafowl (Pavomuticus) that was presented with severescaly legs with raised encrusted scaleson both legs. Diagnosis of scaly leg mitewas made based on history, clinical signs,and results of parasitological examinationfrom deep skin scrapping from the areaof lesions and response to treatment.Treatment consisted of Ivermectinsolution, administered orally at a doserate of 0.2 mg/kg. The gross lesionswere completely resolved 28 days posttreatment. It was concluded that based onthe treatment given, knemidocoptiasis orscaly leg can be successfully controlledwith good prognosis in captive birds. Careshould be taken as the mite is transmittedfrom bird to bird through prolonged closeor direct contact.

Trypanosomiasis positive cases were reported in Sahom Farm Retreatin Gopeng, Perak; with multispecies livestock animals. Nzi and Vavoua traps were applied to survey the population of biting flies; stable flies (Muscidae: Stomoxyinae) and horse flies (Tabanidae)as the vector for surra. Results indicated the presence of Trypanosomiasis infection diagnosed by buffy coat examination, thinblood stained smears and serological test (Surra Sero K-Set test) and identification of its insect vectors. The presence of bothbiting flies provides the missing link between the occurrence of the disease and host or environmental factors precipitatingthe disease. Besides trypanosomiasis in cattle, other parasitic infections were also recorded with heavy infections for liver fluke (Fasciola gigantica ova) and coccidia oocysts. Therefore, some control measures are recommended to eradicate the vectors and to treat infected animals in order to prevent the dissemination ofthe trypanosmiasis.

A 2-year-old (63 days) pregnant female dachshund dog was presented to the Teaching Veterinary Clinical Complex (TVCC) with complaint of a progressively growing swelling in the caudal ventral abdominal area. History, physical examination, radiography and ultrasonography confirmed an inguinal hystrocoele. A ventral midline incisionon the mass was made to relieve the foetuses and reduction of contents, and herniorrhaphy was performed. Sutures were removed on 7th post-operative day and the animal had an uneventful recovery.

Splenic abscess is an uncommon condition in dogs. A 10-year oldGerman Shepherd dog was presented to the small animal medical unit of the University Veterinary Hospital, Mannuthy, with the history of anorexia. Abdominal palpation revealed splenomegaly and onultrasonography a circumscribed mixed echogenic mass was noticed within splenic parenchyma. Post-mortem examination of the spleen and histopathology of the splenic lesion was consistent with splenicabscess.

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.

There is increasing alarm and awareness about the health dangerposed by the arthropod vector causing Onchocerciasis. This study was carried out with the aim to throw more light on the prevalence of the arthropod vector, Simulun damnosum. This research enabled us toproffer preventive advice to government and citizens. In carrying out this study, villages around flowing waters were used as sample sites. The method applied was direct observation, coupled with efficientrecording. Atmospheric temperature readings were periodically taken along with the density of the insect population observed under such temperature. The same was done for relative humidity (%), solar radiation (gm-ca/cm2, lum) and luminescence (cd/m2) in relation to the insect population of available FMH at every given period (fly per man hour). Our findings showed that climate conditions influence the reproductive level and numbers of the vector. The wet season is most conducive for the arthropod vector to reproduce and multiply. The humidity is high and temperature seems to be at the average. It is during this period that greater preventive measures need to beintentionally heightened to subdue the dangerous activities of the vector.

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.

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.

This is a study conducted to test the effectiveness of Azadirachta indica (Neem), Clinacanthus nutans (Sabah Snake Grass) water extracts and neem decoction against natural gastrointestinal helminthsin 4 groups of goats for a period of 4 weeks. This study was done on 24 experimental goats which were randomly chosen from a private farm at Gopeng, Perak. They were divided into four groups; control (n=6) and three treatment groups (n=6). Faecal egg counts and faecal culture to identify the L3 larvae were done and recorded weeklyfrom January until February 2015. Blood parameters such as FAMACHA and PCV were observed and recorded twice at the beginning and end of the study. The FEC results indicated that none of the threetreatments were significantly different to control group (P > 0.05).