Abstract
The sequential pathology of a genotype XIII Bangladeshi strain of Newcastle disease virus (NDV) was studied in 5-weeks old chickens. Layer chickens of ISA Brown breed were inoculated through the intranasal and intraocular routes with the BD-C161/2010 strain of NDV and examined at different times post-infection (pi). NDV-infected chickens showed depression at 3 days pi (dpi) followed by dropped wings, paralysis and death starting at 4 dpi. Lungs of infected chickens showed hemorrhagic lesions starting at 24 hours pi (hpi) that was followed by pallor and slight contraction by 2 to 3 dpi and subsequently developed into severe hemorrhagic pneumonia with mononuclear cell infiltration. Hemorrhagic and necrotizing lesions were found in different visceral organs including proventriculus, intestine, gut-associated lymphoid tissues, liver and kidneys starting at 3 dpi that progressed rapidly. Severe lymphoid depletion was observed in the thymus, spleen and bursa of Fabricius starting at 1–3 dpi followed by hemorrhages, necrosis, inflammation and atrophy at 4–5 dpi. In the brain, mild neuronal lesions such as focal to diffuse encephalitis with encephalomalacia was observed at 2–3 dpi and moderate and diffuse meningoencephalitis with encephalomalacia at advanced stages. In conclusion, the BD-C161/2010 strain of NDV produced lesions typical of velogenic viscerotropic pathotype of NDV.
Highlights
Newcastle disease virus (NDV) is classified as virulent strains of avian paramyxovirus type 1(APMV-1) serotype under the genus Avian orthoavulavirus 1, family Paramyxoviridae [1]
NDV infected chickens showed signs of depression at 3 days post-infection which gradually became severe with ruffled feathers, dropped wings, paralysis and death starting at 4 dpi
The Bangladeshi NDV strain BD-C161/2010 belonging to genotype XIII caused rapid mortality in chickens with signs of depression and paralysis
Summary
Newcastle disease virus (NDV) is classified as virulent strains of avian paramyxovirus type 1. There are cases in which an NDV strain is considered as virulent by ICPI but does not produce much severe clinical disease [6,14]. NDV strains with a velogenic FPCS motif and a relatively higher ICPI (>1.5) show variable clinicopathological features and virus replication in tissues upon experimental infection in specific pathogen-free (SPF) chickens [6]. XIII is a recently evolving genotype of NDV and an in-depth pathological study considering at close time points under experimental condition has not been performed yet.
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