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Mixed viral infections in village chickens
2015
Leow, B. L. | Norazura B. | Mohd Jihan R. | Mohd Khairil A. | Basirah M. A. | Ong, G. H. | Faizul Fikri M. Y. | Ramlan M. | Maizatul Z. | Muhammad Redzwan S.
A mixed viral infection of Newcastle Disease (ND), Marek’s Disease (MD) and Avian Leukosis (AL) was reported in village chickens. Analysis of the deduced amino acid sequences of the F protein cleavage site of ND virus showed that the isolate was virulent with sequence KRRKR for the C-terminus of the F2 protein and phenylanine (F) at residue 117, the N-terminus of the F1 protein. Basic Local Alignment Search Tool (BLAST) analysis showed the isolate was ND which was 96% similar identity with Indonesia Sukorejo genotype VII, MD 99% similar identity with China very virulent strain and ALV 100% similar identity with Taiwan ALV strain. Due to the free ranging type of management, causes of the diseases in the poultry were uncertain as many factors can contribute to the disease occurrence. However, good hygiene practices can help to improve the farm’s sanitary. Basic biosecurity system can be applied although the success may be limited. Vaccination is another alternative that can be considered to prevent the diseases with the help from certain parties.
Mostrar más [+] Menos [-]Histomoniasis and incidental finding of Schistosoma mansoni in turkey birds
2015
Nurul Ana A. B. | Jamal-Nasir M. H. | Maswati M. A. | Salmeah A. R. | Jamaiyah I. | Jin, Seng O. | Shahaza O. | Norina L. | Suhaimi A.
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.
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