Original Research

Inclusion body hepatitis associated with an outbreak of fowl adenovirus type 2 and type 8b in broiler flocks in South Africa

Louis H. Maartens, Hilda W. Joubert, Henry Aitchison, Estelle H. Venter
Journal of the South African Veterinary Association | Vol 85, No 1 | a1146 | DOI: https://doi.org/10.4102/jsava.v85i1.1146 | © 2014 Louis H. Maartens, Hilda W. Joubert, Henry Aitchison, Estelle H. Venter | This work is licensed under CC Attribution 4.0
Submitted: 05 December 2013 | Published: 02 December 2014

About the author(s)

Louis H. Maartens, Department of Research and Development, Deltamune (Pty) Ltd, South Africa
Hilda W. Joubert, Department of Research and Development, Deltamune (Pty) Ltd, South Africa
Henry Aitchison, Avimune (Pty) Ltd, Lyttelton, South Africa
Estelle H. Venter, Department of Veterinary Tropical Diseases, University of Pretoria, South Africa

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Inclusion body hepatitis is an acute disease of chickens ascribed to viruses of the genus Aviadenovirus and referred to as fowl adenovirus (FAdV). There are 12 FAdV types (FAdV1to FAdV8a and FAdV8b to FAdV11), classified into five species based on their genotype (designated FAdVA to FAdVE). A total of 218 000 chickens, 2–29 days of age, were affected over a 1-year period, all testing positive by microscopy, virus isolation and confirmation with polymerase chain reaction (PCR). Affected birds were depressed, lost body weight,were weak and had watery droppings. Pathological changes observed during necropsy indicated consistent changes in the liver, characterised by hepatomegaly, cholestasis and hepatitis. Lesions were also discernible in the spleen, kidney and gizzard wall and were characterised by splenomegaly, pinpoint haemorrhages, nephritis with haemorrhage,visceral gout and serosal ecchymosis of the gizzard wall. Histopathological lesions were most consistently observed in the liver but could also be seen in renal and splenic tissue. Virus isolation was achieved in embryonated eggs and most embryos revealed multifocalto diffuse hepatic necrosis, with a mixed cellular infiltrate of macrophages and heterophils(necro-granulomas), even in the absence of macroscopic pathology. Virus isolation results were verified by histopathology and PCR on embryonic material and further characterised by nucleotide sequence analysis. Two infectious bursal disease virus isolates were also made from the Klerksdorp flock. Nucleotide sequence analysis of the L1 hexon loop of all the FAdV isolates indicated homology (99%) with prototype strains P7-A for FAdV-2, as well as for FAdV-8b.


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