Since there is no registered anthelmintic drug available for use in goats, extra-label use of drugs is a common practice in most countries. The aim of the present study was to compare the pharmacokinetic disposition of levamisole (LVM)-oxyclozanide (OXZ) combination in sheep and goats following per os administration. Goats (n = 8) and sheep (n = 8) 12- to 16-months-old were used for this study. The animals received tablet formulation of LVM and OXZ combination orally at a dose of 7.5 mg/kg and 15 mg/kg body weight, respectively. Blood samples were collected by jugular vein at different times between 5 min and 120 h after drug administrations. The plasma concentrations of LVM and OXZ were analyzed by HPLC following liquid-liquid phase extraction procedures. The plasma concentrations and systemic availabilities of both LVM and OXZ in goats were lower and the plasma persistence of LVM was shorter compared with those observed in sheep. Terminal half-lives (t1/2λz) of both molecules are shorter in goats compared with those in sheep. Goats treated with LVM-OXZ combination at the recommended dose for sheep may result in a reduced efficacy, because of under-dosing, which may increase the risk of drug resistance in parasites. Increased or repeated dose could be a strategy to provide higher plasma concentration and thus to improve the efficacy against the target parasites in goats compared with sheep. However, some adverse reactions may occur since LVM has relatively very narrow therapeutic index due to its nicotine-like structure and effect.

The aim of this study was to test the potential diagnostic usefulness of recombinant Toxoplasma gondii SAG1 antigen and
excretory-secretory antigen (ESA), with respect to toxoplasmosis detection and infection phase distinction in laboratory mouse by determining specifi c serum IgM and IgG antibodies with the use of indirect ELISA technique. The highest titre at the beginning of infection was demonstrated by immunoglobulin M while the highest titre at the end of the infection was displayed by immunoglobulin G. In contrast, sera of chronically infected mice, positive IgG titre was detected on day 14 p.i. for ESA or day seven p.i. with rSAG1 and increased thereafter until day 70 p.i. after which the titre stabilized. IgA antibody also showed similar kinetics as IgG. Potentially rSAG1 may be a suitable diagnostic antigen than ESA in the diagnosis of acute and chronic toxoplasmosis.

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.

The Malaysian Pangolin (Manis javanica) is an endangered species,
but is widely hunted for its medicinal value in body parts. A total of sixteen pangolins were screened for blood protozoa and six
pangolins were confi rmed to be positive for eperythrozoonosis infection based on morphology from blood smears stained with 8% Giemsa. The causative organism, Eperythrozoon sp., with a size of 0.3 μm were observed under a compound microscope at 100× magnification on the surface of red blood cells as blue coloured dots. This is the fi rst report of Eperythrozoon infection from pangolins in Malaysia. Further identifi cation using polymerase chain reaction (PCR) is necessary to confi rm E. ovis or wenyonii,
which is uncultivatable in artifi cial media.

A case of a cestode parasite (Choanotaenia infundibulum) egg wasfound in the intestine of chicken which was sent to the Veterinary Research Institute, Ipoh in February 2014 for post-mortem. Other parasites found in the intestine were adult tapeworm and oocyst ofcoccidia. The examination of the chicken intestine for helminth ova was undertaken using direct examination of a simple wet smear of the intestinal content which was observed under compound microscope.The cestode parasite was identified based on helminthological keys by Soulsby, 1982.