AI Article Synopsis

  • A new hybridoma cell line (1F8) was created that produces a highly effective anti-P27 monoclonal antibody (mAb), which can detect multiple ALV strains and identifies a previously unreported minimal epitope (IIKYVLDRQK).
  • A novel sandwich ELISA method was developed for detecting ALV antigens, showing improved sensitivity compared to existing commercial kits, which aids in creating better diagnostic tools for ALV.

Article Abstract

Avian leukosis virus (ALV) is an avian oncogenic retrovirus that can impair immunological function, stunt growth and decrease egg production in avian flocks. The capsid protein (P27) is an attractive candidate for ALV diagnostics. In the present study, a new hybridoma cell (1F8) stably secreting an anti-P27 monoclonal antibody (mAb) was developed. The mAb exhibited a high affinity constant (Ka) of 8.65 × 10 L/mol, and it could be used for the detection of ALV-A/B/J/K strains. Moreover, a total of eight truncated recombinant proteins and five synthetic polypeptides were utilized for the identification of the B-cell epitopes present on P27. The results revealed that IIKYVLDRQK was the minimal epitope recognized by 1F8, which had never been reported before. Additionally, the epitopes could strongly react with different ALV subgroup's specific positive serum and had a complete homology among all the ALV subgroups strains. Finally, a new sandwich ELISA method was created for the detection of ALV antigens, demonstrating increased sensitivity compared to a commercially available ELISA kit. These results offer essential knowledge for further characterizing the antigenic composition of ALV P27 and will facilitate the development of diagnostic reagents for ALV.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11202774PMC
http://dx.doi.org/10.3390/cimb46060350DOI Listing

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