Pathogenesis of highly pathogenic avian influenza a virus (H7N1) infection in chickens inoculated with three different doses

Aida J. Chaves, Núria Busquets, Naiana Campos, Antonio Ramis, Roser Dolz, Raquel Rivas, Rosa Valle, F. Xavier Abad, Ayub Darji, Natália Majó

Research output: Contribution to journalArticleResearchpeer-review

13 Citations (Scopus)

Abstract

To study the pathogenesis of a H7N1 highly pathogenic avian influenza virus strain, specific pathogen free chickens were inoculated with decreasing concentrations of virus: 105.5 median embryo lethal dose (ELD50) (G1), 103.5 ELD50 (G2) and 101.5 ELD50 (G3). Disease progression was monitored over a period of 16 days and sequential necropsies and tissue samples were collected for histological and immunohistochemical examination. Viral RNA loads were also quantified in different tissues, blood, oropharyngeal swabs, and cloacal swabs using quantitative real-time reverse transcriptase-polymerase chain reaction (RT-qPCR). Clinical signs of depression, apathy, listlessness, huddling and ruffled feathers were recorded in G1 and a few G2 birds, whilst neurological signs were only observed in chickens inoculated with the highest dose. Gross lesions of haemorrhages were observed in the unfeathered skin of the comb and legs, and skeletal muscle, lung, pancreas and kidneys of birds inoculated with 105.5 ELD50 and 103.5 ELD50 doses. Microscopic lesions and viral antigen were demonstrated in cells of the nasal cavity, lung, heart, skeletal muscle, brain, spinal cord, gastrointestinal tract, pancreas, liver, bone marrow, thymus, bursa of Fabricius, spleen, kidney, adrenal gland and skin. Viral RNA was detected by RT-qPCR in kidney, lung, intestine, and brain samples of G1 and G2 birds. However, in birds infected with the lowest dose, viral RNAwas detected only in brain and lung samples in low amounts at 5 and 7 days post infection. Interestingly, viral shedding was observed in oropharyngeal and cloacal swabs with proportionate decrease with the inoculation dose. We conclude that although an adequate infectious dose is critical in reproducing the clinical infection, chickens exposed to lower doses can be infected and shed virus representing a risk for the dissemination of the viral agent. © 2011 Houghton Trust Ltd.
Original languageEnglish
Pages (from-to)163-172
JournalAvian Pathology
Volume40
DOIs
Publication statusPublished - 1 Apr 2011

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