This case report describes paramphistomosis from the rumen ofan infected 3-year-old Bos indicus or also known as Zebu cattle that was sent to the Veterinary Research Institute (VRI), Ipoh,Perak for post-mortem examination with a history of a sudden death. On post-mortem, it was found that the rumen contents hada large number of pink, pear shaped flukes, which measured about 1 cm in length attached to the rumen wall. On performing the sedimentation technique on the rumen contents, operculated eggs with germ cells were observed microscopically under compound microscope with a magnification of 100×. Regular screening of cattle for flukes is an important part of parasite controlprogrammes especially in endemic areas as it can cause anaemia and deterioration in body condition.

In the Malaysian environment horses are primarily used in sports activities such as racing, endurance, dressage and show jumping as well as in recreational pursuits and police work. Recently, the Perak Turf Club witnessed the death of a four-yearold thoroughbred mare which was given enrofloxacin injection as treatment and was regularly dewormed and vaccinated againstequine influenza, Japanese encephalitis and tetanus. Post-mortem examination of intestinal contents revealed presence of worms. The sample was then sent to the Veterinary Research Institute (VRI), Perak for morphological identification of the worm. The worm was identified as Parascaris equorum. Thus, awareness ongastrointestinal parasites should be raised especially by recommending improved management practices such as proper manure disposal and deworming procedures to control parasite infestations as well as good management and nutrition.

A monitoring program for melamine in milk and feed was conducted in response to global melamine alertness in the year 2008. Two screening methods were adopted i.e., a liquid chromatography triple quadrupole tandem mass spectrometry (LC-MS/MS) and enzyme-linked
immunosorbent assay (ELISA). The liquid chromatography method developed by several international research centers was adapted. This method consisted of an initial extraction with 10%trichloroacetic acid (TCA) for milk samples or 60% methanol/water for feed samples, followed by a series of centrifugation, dilution and filtration steps. Melamine was analysed in the chromatographic program using a zwitterionic HILIC LC column. Electrospray ionisation in positive ion mode was used. The quantity of melamine
present was determined with a calibration curve consisting of sample extracts from milk or feed fortified from 25 to 50 ppb that were taken through the extraction procedure. The ranges of recovery from
fortified raw milk samples (n=20) and feed samples (n=21) was 70–80% and 68%, respectively. The limit of detection was estimated at 10 ppb for both matrixes. Milk samples were found negative for melamine,
however 4.5% of feed samples were found to contain the compound at concentrations between 1 to 5 ppm.

The purpose of this study is to evaluate the use of Breeding Soundness Examination (BSE) and sperm quality for bull fertility screening by using Brahman bulls. A total of 17 Brahman bulls were sampled from the Department of Veterinary Services’ farm at Pusat Ternakan Haiwan (PTH) Ulu Lepar, Kuantan, Pahang, with age ranging between 2 to 7 years old. All candidates had undergone BSE and sperm quality test. All the data collected were analysed using SPSS software. The average age of the Brahman in this study was 55.06±14.37 months with 36.53±3.21 cm of scrotal diameter. The average libido score recorded for Brahman bulls in this study was 5.35±1.90. The minimum libido score was two (2) while the maximum score was seven (7). For sperm quality traits, the average parameter recorded for Brahman bulls were as follows: 54.41±20.15 % (sperm motility), 62.94±26.94 % (live sperm) and 49.40±8.53 % (normal sperm). The minimum and maximum score for sperm motility was 10 % and 80 %, respectively. For live sperm, the minimum score was 10 % and maximum score was 80 %. Meanwhile, normal sperm had a minimum score of 30 % and a maximum score of 65 %. The bull that fulfilled the requirements of the screening can be assigned as a superior bull for breeding program, thus making fertility screening a useful tool in monitoring potential breeder of the farm.

The rapid method for predicting palm kernel cake quality with near infrared reflectance spectroscopy was investigated. Chemical tests for moisture, ash, crude protein, crude fat, crude fibre, total digestible nutrients (TDN), nitrogen free extract (NFE), metabolisable energy (ME), calcium and phosphorous were time
consuming and involve high cost. This technology can save considerable time by testing all the parameters simultaneously;
however accurate calibration of the equipment is essential. Near infrared (NIR) partial least square (PLS) regression models for determination of several palm kernel cake quality parameters were
developed from NIRFlex Model N-500 (Buchi). In general, reliable prediction results were obtained for the TDN (SEP = 0.85 r2 = 0.99), NFE (SEP = 0.42 r2 = 0.97) and crude protein (SEP = 0.57 r2 = 0.98)
PLS regression models.

Strangles is an extremely contagious bacterial infection specific to
equine species( horses, mules and zebras). A nationwide screening of S. equi was conducted among horses following an isolation of Streptococcus equi subsp. equi (S. equi) from a horse. All horses were monitored for the presence of respiratory signs, nasal discharge and submandibular swelling. This paper reports the isolation of S. equi from horses during a nationwide survey from August 2010 to December 2010. From August 2010 to December 2010 our laboratory received 2,825 nasal swabs, 9 guttural pouch flushes, 1 submandibular swab and 1 submandibular abscess. The samples were subjected to conventional bacterial isolation and identification.
Streptococcus equi-positive samples were also confirmed by detecting the M-gene (SeM) of the bacteria by using PCR. Two nasal swabs from two horses and one submandibular abscess from a horse were positive for S. equi by culture and subsequently by PCR. Surveillance for S. equi should be continued for the control of the strangles. PCR can be carried out in parallel to bacterial culture to increase the
detection rate of carriers and shedders.