AI Article Synopsis

  • There has been a significant increase in inclusion body hepatitis (IBH) cases since 2012, leading to major economic losses in the poultry industry.
  • The study focused on the highly pathogenic fowl adenovirus (FAdV) strain HN1472, isolated from a laying flock affected by IBH, examining its genetic mutations, pathogenicity, and phylogenetic information.
  • Findings indicated that HN1472 is a recombinant strain with notable genetic divergence, causing high mortality in chickens and suggesting a widespread presence in various tissues following infection.

Article Abstract

Since 2012, there has been a noticeable upward trend in the global incidence of inclusion body hepatitis (IBH) cases, leading to substantial economic losses in the poultry industry. In response to this trend, the current study aimed to investigate the phylogenetic information, genetic mutations, and pathogenicity of the highly pathogenic fowl adenovirus (FAdV) strain HN1472, which was isolated from liver samples obtained from a laying flock affected by IBH. This investigation was carried out using 1-day-old specific pathogen-free (SPF) chickens. Recombination and phylogenetic analyses confirmed that HN1472 is a recombinant strain derived from FAdV-8a and FAdV-8b, and exhibited significant genetic divergence in the hexon, fiber, and ORF19 genes. Notably, the phylogenetic analysis identified recombination events in these regions. Furthermore, animal experiments revealed that HN1472 is a highly pathogenic isolate, causing 80% mortality and manifesting clinical signs of IBH in SPF chickens. Furthermore, the recombinant FAdV serotype 8b (FAdV-8b) was found to be widely distributed in various tissues, with a higher concentration in the livers and gizzard tissue at 3 d postchallenge (dpc). Collectively, these findings contribute to our current understanding of the factors influencing the pathogenicity and genetic diversity of FAdV serotype 8b (FAdV-8b) in China.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11017358PMC
http://dx.doi.org/10.1016/j.psj.2024.103725DOI Listing

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