The world widely distributed infection by Rhodococcus equi usually leads to pneumonia and associated respiratory signs. This study is aimed at detecting the occurrence of this pathogen in selected horse farms. A total of 12 R. equi isolates from few samples (13.89%) were successfully obtained from soil and faeces collected from two selected farms. However, based on the vapA gene classification, only one virulent R. equi isolate was identified.

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.

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.

A study was conducted to determine the prevalence of Newcastle disease (ND) and Avian Influenza (AI) from backyard chickens and ducks in Sabah. A total of 2,117 samples consisting of 1,498 swabs and 619 serum samples were taken from all districts in the state.
All samples tested were negative to Avian Influenza virus. 23.59% of the 619 serum samples collected were sero-positive for Newcastle Disease with the highest HI titre being 1/256. Only one pool of 4
trachael swabs or 0.27% of the total 1,498 swabs was positive on virus isolation for Newcastle Disease. No Avian influenza virus was isolated from all the samples collected.

Blastocystis is considered to be a zoonoses and it is believed that animals such as chicken constitute large reservoirs for human infection via the faecal-oral route. Therefore, Blastocystis infection was surveyed in free-range chicken and cage reared chicken comprising broiler birds for consumption as well as jungle fowls andsilkie chicken kept for recreation. Fresh faecal samples collected were examined by wet smear preparation and were cultured in Jones medium supplemented with 10% horse serum. Out of 107 chickens, it was found that most of the free-range chicken was positive for Blastocystis sp. with a high prevalence rate of 80%–100% in village chicken, jungle fowl and white silkie chicken. However, the cage-reared chicken, consisting of broiler chicken had no infection. The vacuolar form was the most common Blastocystis cell form found in cultures, similar to B. hominis.These cells were usually spherical and vary greatly in size, ranging from 10 μm to 30 μm in diameter. Owing to the free ranging and scavenging habits, the likelihood of acquiring the infection fromthe environment contaminated with the faecal material of animals with Blastocystis is high in free-range chicken as compared to caged chicken.

The emergence of Highly Pathogenic Avian Influenza (H5N1) in 2004 draws attention to the safety of rearing edible bird nest swiftlets within the vicinity of human dwellings in urban areas. There is also concern on the safety of the product itself. Convenient sampling of edible bird nest swiftlets (A. fuciphagus and A. maximus) was conducted by the Department of Veterinary Services and Animal Industry from September 2004 until June 2011. A total of 137 samples
were collected from four premises and two natural caves in four locations, namely Tawau, Kunak, Sandakan and Penampang. The samples were collected for Egg Innoculation Tests for H5N1 and Newcastle Disease (ND). All samples yielded negative results for both diseases.