Literature DB >> 21331892

Indirect ELISA with recombinant GP5 for detecting antibodies to porcine reproductive and respiratory syndrome virus.

Yan Chen1, Hong Tian, Jian-hui He, Jin-yin Wu, You-jun Shang, Xiang-tao Liu.   

Abstract

Porcine reproductive and respiratory syndrome is caused by the PRRS virus (PRRSV), which has six structural proteins (GP2, GP3, GP4, GP5, M and N). GP5 and N protein are important targets for serological detection by enzyme-linked immunosorbent assay (ELISA) and other methods. Toward this goal, we developed an indirect ELISA with recombinant GP5 antigens and this method was validated by comparison to the LSI PRRSV-Ab ELISA kit. The results indicated that the optimal concentration of coated recombinant antigen was 0.2 μg/well for a serum dilution of 1:40. The rate of agreement with the LSI PRRSV-Ab kit was 88.7% (266/300). These results support the potential use of recombinant GP5 as an antigen for indirect ELISA to detect PRRSV antibodies in pigs.

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Year:  2011        PMID: 21331892      PMCID: PMC8222475          DOI: 10.1007/s12250-011-3154-9

Source DB:  PubMed          Journal:  Virol Sin        ISSN: 1995-820X            Impact factor:   4.327


  8 in total

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4.  Genetic variation of Chinese PRRSV strains based on ORF5 sequence.

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5.  Influence of N-linked glycosylation of porcine reproductive and respiratory syndrome virus GP5 on virus infectivity, antigenicity, and ability to induce neutralizing antibodies.

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7.  Genomic characterization of two Chinese isolates of porcine respiratory and reproductive syndrome virus.

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8.  Comparison of the structural protein coding sequences of the VR-2332 and Lelystad virus strains of the PRRS virus.

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  8 in total
  1 in total

1.  Application of GP5 protein to develop monoclonal antibody against porcine reproductive and respiratory syndrome virus.

Authors:  Hong Tian; Yan Cheng; Jin-yang Wu; Jian-hui He; You-jun Shang; Xiang-tao Liu
Journal:  Virol Sin       Date:  2011-08-17       Impact factor: 4.327

  1 in total

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