Histopathological changes were studied in Swiss albino mice (N:36)which were challenged with the South Indian local strain of Trypanosoma evansi. Each animal was infected with 5×105 trypanosomes intraperitoneally. The animals were examined daily for development of clinical signs and infection status by wet blood-films made from the tail veins. The infected mice were dull and depressed from two days post-infection (DPI) onwards. Systematic post-mortem examination of the infected mice was performed and pathological changes were recorded. The different tissue samples were collected in 10% formalin and were used to study the histopathological changes. Postmortem examination from 3-4 DPI (the maximum period of observation) revealed splenomegaly, hepatomegaly, marked congestion of lungs, presence of fl uid in peritoneal cavity. Histopathologically, heart muscles showed hyaline degenerative changes and haemorrhages. Liver parenchyma revealed congestion of central vein and sinusoids, binucleated hepatocytes and fatty change of hepatic cells. Thickening of interstitial space with mononuclear infiltration, areas of collapse, areas of emphysema, edema and dilated and congested blood vessels were the histopathological changes noticed in the lungs of the infected mice. In the spleen, giant cells aggregation, hyperplasia, thickening of capsule and trabecule were the changes indicating irreversible degeneration. The affected kidney showed inter-tubular hemorrhages in the cortex, medullary hemorrhages, congested glomerulus, atrophied glomerulus, desquamated tubular epithelium and disruption of renal tubules at some places.

Many parasitology laboratories practiced the McMaster technique as a method in obtaining the quantitative diagnosis of Strongyle eggs burden in farm animals especially ruminants. The McMaster technique also play a crucial role in faecal egg count reduction test (FECRT) for anthelmintic resistance identification. Some laboratoriesrecommend two-chamber counting method while some recommend single chamber counting method. This study focuses on the comparison between single and double counting in McMaster technique fordetection of Strongyle egg count. In this study, it is shown that there is no significant difference between both methods basedon the p-value obtained which is p>0.05 from 127 fresh goat faecal samples. The techniques practised during the study follow the standard established technique. Single chamber counting is suitable for a large number of faecal samples from big herds because it is faster, less laborious and produces sensitive and reliable results in Strongyle egg count. As more commercial farms are set up, there is a need to conduct a fast and efficient test to help farmers evaluate their livestock worm burden.

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.

A study was conducted on 16 commercial free range chickens (8 malesand 8 females) sourced from Alor Setar, Kedah in order to determine the prevalence of ecto and endoparasites. Results showed that there were 12 different species of ectoand endoparasites from these chickens. Four (4) species of ectoparasites which consist of three lice and a tick have been discovered. The highest prevalence of ectoparasite was Menopon gallinae (93.8%). The other ectoparasites were Menacanthus pallidulus (81.3%), Haemaphysalis sp. (37.5%) and Lipeurus caponis (18.8%). On the other hand, eight species of endoparasites which consist of four nematodes and four cestodes were discovered. Rallietina echinobothrida showed the highest prevalence of endoparasite (100%) followed by Heterakis gallinarum (93.8%), Acuaria spiralis (87.5%), Ascaria galli (81.3%), Rallietina tetragona(43.8%), Gongylonema ingluvicola (37.5%), Hymenolepis carioca (12.5%)and Hymenolepis cantiana (12.5%). Endoparasites infestation was recorded highest on male chicken (52.6%) compared to female (47.4%). However, there was no statistically significant difference betweenthe number of endoparasites and both sexes; t (14) = 0.817, p>0.05.

Quail closed-house system is a house that support quails’ optimumrequirements as far as temperature, relative humidity, ventilation and light are concerned. One of the four units of quail closed-house systems at the Institute of Poultry Technology, Malacca was used in this study. The objective of this project was to evaluate the performance of the quail closed-house system by comparing the condition of the house under current management condition and after the Standard Operating Procedure determined by DVS was adhered. Thehouse performance was evaluated by observing its ability to achieve an optimum temperature range of 20°C to 27°C with a relative humidity between 60% to 80% as perfect surroundings for quails. At the end of the experiments, the results showed a decline in internal temperature at almost 3°C and increasing in a relative humidity of 10% after all the specifications and procedures were followed.

A primary fibroblast cells from embryos of brown quail Coturnixypsilophora has been established and partially characterized. The cells were maintained in Modified Eagle’s medium (MEM) supplemented with 10% fetal bovine serum. The cells were able to grow at temperatures between 35°C and 38°C with optimum temperature of 37°C. The growth rate of primary quail fibroblast cells increased as the FBS proportion increased from 5% to 20% at 37°C with optimum growth at the concentrations of 10% or 15% FBS. The cells showed no microbial contamination throughout the period of experiment and the total chromosome number of a diploid cell was 78, according to karyotyping and chromosome analysis. The susceptibility of quail primary cells for avian viruses was investigated in this study after inoculation with ND and IB viruses. Both viruses showed a satisfactory CPE development and the infectivity were assayed by virus titration (TCID50). This suggests that the quail primary cells can be used for isolation of various avian viruses with further steps of infectivity confirmation in the future.