Malaysia has experienced four waves of H5N1 outbreak but no humandeaths were recorded which is in 2004, 2006, 2007 and latest outbreak in 2017 at Kelantan. The objective of this paper is tocollect, analyse and summarise the data of HPAI cases from the outbreak from 1 March to 22 June 2017. A total of 1,634 cases, 8,544 samples were received at the Registration Unit and Virology Section, Regional Veterinary Laboratory in Kota Bharu (RVLKB) for diagnosis and surveillance of H5N1 during this period. The samples received were pooled organs and intestines from post-mortem (41 cases) and cloaca swabs in tryptose phosphate buffer from surveillance (1,593 cases), which were sent to RVL, Kota Bharu and Veterinary Research Institute, Ipoh, Perak (VRI). They were processed and diagnosed using quantitative real-time reverse transcriptase PCR (RT qPCR) technique to detect and subtyping of the virus. Total positive cases for H5N1 were 53 out of 1,634 with 18 diagnostic cases and 35 surveillance cases. All positive cases during outbreak were detected from 43 locations from six districts of Kota Bharu, Bachok, Pasir Puteh, Pasir Mas, Tumpat and Tanah Merah, with 19 locations in Kota Bharu which is thehighest affected by H5N1, seven locations in Bachok, four in Pasir Putih, six in PasirMas, six in Tumpat and one in Tanah Merah. Many factors could have led to the acute spread of the virus between the districts like chicken smuggling, legal and illegal poultry trade, migration of infected wild birds and others. Understanding the source of outbreak and how it spread is important to control, eradicate and prevent the spread of the disease as it is zoonotic and infects human.

Ever since infectious bursal disease (IBD) was recognised in Nigeria over forty years ago, it continues to pose a threat to poultry production with limited information on the likely role of other avian species especially those raised in close proximity with chickens. For this study, blood samples were obtained from184 unvaccinated apparently healthy birds comprised of Japanese quails (63) andindigenous chickens (60) on smallholdings as well as pigeons (61) in a live-bird market in Osun and Oyo states, southwest Nigeria.Sera from these birds were analysed for IBD virus antibodies using a commercial ELISA kit. Overall, 69 (37.5%) sera were positive for IBDV with 52.8% (65/184) and 6.6% (4/184)from birds on smallholdings and live-bird market, respectively. These findings indicate that these birds were sub-clinically infected and could serve as reservoirs shedding the virus into the environment and perhaps, corroborate the suggestion that the inability to effectively control or eradicate the disease from poultry flocks in Nigeria may be due to limited information on the contributions of other avian species other than chicken in the spread of IBD virus.

Increased emergence in microbial resistance to antibiotics is a growing problem globally. A retrospective investigation was made of antimicrobial resistance in a total of 2,345 Escherichia coli isolates from clinical cases submitted to Regional Veterinary Laboratory of Bukit Tengah, Penang, Malaysia between January 2000 and December 2015. Analysis using WHONET 5.6 revealed that resistance to ampicillin, norfloxacin and aminoglycosides was detected in isolates from poultry and pigs more often than ruminants. Resistant to colistin was higher in ruminants compared to other animal groups. Nor floxacin susceptibility was very high in isolates from ruminants, pet birds (82.2%) and zoo animals (88.6%). Isolates from pet birds had higher resistant rate to all of the antimicrobials tested compared to zoo and companion animals. Multidrug-resistant (MDR) E. coli isolates (29.25%, 684/2345) were detected in this study. Further efforts, for instance, national monitoring and surveillance, are required to quantify the exposure of animals to antimicrobial agents and resistant pathogenic or commensal bacteria in the animals and also its environment. Such useful information indeed will assist the prudent use of antimicrobial agents in veterinary practice; therefore, suppress the emergence of antimicrobial resistance in animals.

This study was conducted to investigate whether dietary enzymes alter the caecal microbial profile of broilers fed sorghum-based diets. Four sorghum-based diets (918 g sorghum/kg diet) were prepared. One was the control diet and three had enzymes (xylanase, phytase andprotease) added. Broilers, 35-day-old, were reared (8 birds/cage) in an environmentally controlled shed and randomly allocated to replicated (n=4) assay diets and free access to feed and water all time. On day-42, birds were euthanized and caecal contents collected, pooled on a per/pen basis and frozen (-20 °C). The DNA was extracted from caecal samples using a bead-beating protocol and the V2V3 regionof the bacterial 16S rRNA gene amplified by PCR. Amplicons were separated on sequence difference using Denaturing Gradient Gel Electrophoresis (DGGE) and microbial profiles generated and compared.The DGGE profiles, when analysed, indicated that there was approximately 80% similarity between caecal microflora in all types of the diet treatments. This suggests that there was no overalldifference between any of the profiles and therefore the addition of different types of feed enzymes in a sorghum-based diet had no impact on the overall composition of the broiler caecal microflora.

A study was conducted on 240 scavenging chickens randomly obtained from various districts from the state of Penang, Peninsular Malaysia. The chickens were closely examined for visible ectoparasites in the laboratory. The ectoparasites were collected using a blunt forceps and stored in universal bottles containing 70% ethanol. Ten species of ectoparasites were noted which consisted of five species of lice, two species of mites, two species of ticks and one species of chigger. The lice identifi ed were Menopon gallinae, Menacanthus pallidulus, Lipeurus caponis, Goniocotes gallinae and Goniodes dissimilis. These lice occurred in the fl uff of the feathers of the body especially the neck, back, abdomen and wings. The mites were Megninia sp. and Pterolichus sp. Examinations of the ears and combs revealed Haemaphysalis sp., the hard tick. Meanwhile, Ornithonyssus sp., the soft tick was found on feathers, whereas chigger, Leptotrombidium sp. was found attached to the skins. The study also revealed that M. gallinae was the most common ectoparasite with 76.7% occurrence, followed by Pterolichus sp. (69.6%), L. caponis (63.3%), M. pallidulus (41.7%), Leptotrombidium sp. (17.5%), G. gallinae (9.5%), Haemaphysalis sp. (6.7%), Megninia sp. (3.8%) and Ornithonyssus sp. (3.8%). The least common ectoparasite was G. dissimilis occurring in 2.1% of the chickens.

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.

The Department of Veterinary Services (DVS) established a subsidy programme to build low cost swiftlet houses, under the auspices ofthe eKasih programme. This programme is aimed at aiding entrepreneurs in the swiftlet industry to produce good qualitybird’s nests. In 2013, eleven swiftlet houses under eKasih Program in Johor, Perlis and Pahang were chosen randomly to be evaluated after a year of completion. The main factors affecting its functionality, such as temperature, relative humidity and light intensity inside the swiftlet houses were recorded and analysed. The results showed that most of the eKasih swiftlet houses built under this programme did not meet the recommended in house conditions due to several reasons. The houses built in this programme failed to attract the birds into the houses to build nests. Although there were some houses that produced bird’s nests, it was found to be substandard in terms of quality. Thus, this study revealed the importance of various factors needed for the successful establishment of swiftlet houses to produce good quality bird’s nests.

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.