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Characterization of Two Immunodominant Antigenic Peptides in NSP2 of PRRSV-2 and Generation of a Marker PRRSV Strain Based on the Peptides. | LitMetric

AI Article Synopsis

  • PRRS (Porcine reproductive and respiratory syndrome) is a significant disease in pigs, causing major economic losses, and distinguishing between infected and vaccinated pigs is difficult despite over 20 years of vaccine use.
  • This study analyzed all known NSP2 sequences of PRRSV-2 and identified two specific peptides (m1B and m2B) that reacted with antibodies from PRRSV-positive pigs in immunoassays.
  • The researchers created deletion mutants of the virus to assess the impact of these peptides, finding that removing m1B and m2B did not affect virus replication, suggesting they could serve as useful molecular markers for improving PRRSV vaccines.

Article Abstract

Porcine reproductive and respiratory syndrome (PRRS) is a widespread disease with great economic importance in the pig industry. Although vaccines against the PRRS virus (PRRSV) have been employed for more than 20 years, differentiating infected from vaccinated animals remains challenging. In this study, all 907 non-structural protein 2 (NSP2) full-length sequences of PRRSV-2 available from GenBank were aligned. Two peptides, at positions 562-627 (m1B) and 749-813 (m2B) of NSP2, were selected, and their potential for use in differential diagnosis was assessed. Both m1B and m2B were recognized by PRRSV-positive pig serum in peptide-coated enzyme-linked immunosorbent assays. Further epitope identification yielded five overlapping short peptides for the immunodominant regions of m1B and m2B. Using the infectious clone of PRRSV HuN4-F112 as a template, the deletion mutants, rHuN4-F112-m1B, rHuN4-F112-m2B, and rHuN4-F112-C5-m1B-m2B, were generated and successfully rescued in Marc-145 cells. Growth kinetics revealed that the deletion of m1B and m2B did not significantly affect virus replication. Hence, m1B and m2B show potential as molecular markers for developing a PRRSV vaccine.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189411PMC
http://dx.doi.org/10.3389/fvets.2022.902822DOI Listing

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