AI Article Synopsis

  • Subgroup J avian leukosis virus (ALV-J) significantly impacts the poultry industry, causing economic losses.
  • The study aimed to improve ELISA's ability to differentiate between ALV-J-infected flocks and uninfected flocks containing the endogenous ALV-E.
  • Findings showed that GSA levels and anti-ALV-J antibodies were effective in distinguishing these flocks, especially at the ages of 1 and 6 weeks.

Article Abstract

Subgroup J avian leukosis virus (ALV-J) causes serious economic losses in the commercial poultry industry. Measuring group-specific antigen (GSA) by enzyme-linked immunosorbent assay (ELISA) has been used to identify chickens infected with this virus. However, the inability of ELISA to discriminate the GSA from endogenous ALV (subgroup E ALV [ALV-E]) or ALV-J infection has limited its usage. The purpose of the present study was to develop a method to discriminate between uninfected flocks having ALV-E and ALV-J-infected flocks by ELISA. The GSA and anti-ALV-J antibody in the plasma samples from chickens at different ages in three grandparent farms were measured by ELISA. Infected flocks were confirmed by reverse transcription-polymerase chain reaction with different subgroup-specific primers and sequence analysis. The results indicated that the GSA of ALV-J-infected flocks increased, but that of the uninfected flocks decreased during young ages. The anti-ALV-J antibody of infected flocks was higher and increased earlier than that of uninfected flocks. Thus, measuring GSA in blood at the ages of 1 and 6 wk by ELISA is suitable to discriminate between ALV-J-infected flocks and uninfected flocks having ALV-E.

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http://dx.doi.org/10.1637/0005-2086(2002)046[0598:SPOCIW]2.0.CO;2DOI Listing

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