Avian haemoparasites are known to exert negative pressures on theirhosts causing considerable pathology and mortalities. The present study reports on the prevalence of haemoprotozoa and microfilaria in various species of wild birds and domestic poultry in Selangor, Malaysia, and contributes to the database on the occurrence of thesepathogens among avifauna in the country. Giemsa-stained thin blood smears were screened from 728 birds representing five avian orders, namely Galliformes, Anseriformes, Phoenicopteriformes, Pelecaniformes and Gruiformes. The most common haemoparasite was Plasmodium, with a prevalence of 8.0%. The aquatic/wetland species of birds (Anseriformes and Gruiformes) were the most common hosts for this pathogen with high infection rates (31.8% – 50.0%). The prevalence of Plasmodium in domestic poultry was moderate (2.7%). Leucocytozoon sabrazesi and L. caulleryi were confined to the Galliformes with relatively low average infection rates of 0.7% and 0.5%, respectively. Haemoproteus was detected for the first time in domestic poultry and Red Jungle fowls in the country, with anaverage prevalence of 0.8%. Trypanosomes and microfilaria were only present in the village chickens and Red Jungle fowls, with high microfilaraemia rates (19.0%) in the latter. The current compilation will contribute to our understanding on avianhaemoparasite transmission in the country.

This report describes the parasitological and pathological information retrieved from the samples submitted to Regional Veterinary Laboratory, Bukit Tengah, Penang (MVKBT) followingan episode of histomoniasis in a small scale poultry farm. Liver and ceca from two dead turkey birds, water (n=5) and freshwater snails (Pomacea sp, n=7) were stored between 4°C to 10°C until analyzed. Soil samples (n=7) were preserved in 5% formalin and kept at room temperature prior to further testing. The soil samples were filtered through laboratory test sieves before the filtrates at each level were examined using direct microscopy. Portions of the liver were processed using routine paraffin technique for histopathological examination and found positive for Histomoniasis. Results from direct microscopy of the liver samples revealed Schistosoma mansoni ova, Sarcocystis sporocysts and Fasciola sp. Heterakis sp ova were detected from cecal content. Four out of seven soil samples were positive for Sarcocystis sporocysts, Coccidia oocyst, Strongyles ova and nematod larva. Water and freshwater snail samples were negative for cercaria of Schistosoma mansoni. This case was concluded as Histomoniasis, Sarcocystosis and helminthiasis with incidental finding of Schistosoma mansoni.