Highly pathogenic porcine reproductive and respiratory syndrome virus GP5 B antigenic region is not a neutralizing antigenic region

In 2006, highly pathogenic porcine reproductive and respiratory syndrome virus (HP-PRRSV) caused great economic losses emerged in China and continues to be a threat for the pig industry. B antigenic region (AR) (37SHL/FQLIYNL45) of GP5 was considered to be a major linear neutralizing AR in PRRSV cla...

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Veröffentlicht in:Veterinary microbiology 2012-10, Vol.159 (3-4), p.273-281
Hauptverfasser: Leng, Chao-Liang, An, Tong-Qing, Chen, Jia-Zeng, Gong, Da-Qing, Peng, Jin-Mei, Yang, Yong-Qian, Wu, Jiang, Guo, Juan-Juan, Li, Deng-Yun, Zhang, Yi, Meng, Zhen-Xiang, Wu, Yu-Quan, Tian, Zhi-Jun, Tong, Guang-Zhi
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container_end_page 281
container_issue 3-4
container_start_page 273
container_title Veterinary microbiology
container_volume 159
creator Leng, Chao-Liang
An, Tong-Qing
Chen, Jia-Zeng
Gong, Da-Qing
Peng, Jin-Mei
Yang, Yong-Qian
Wu, Jiang
Guo, Juan-Juan
Li, Deng-Yun
Zhang, Yi
Meng, Zhen-Xiang
Wu, Yu-Quan
Tian, Zhi-Jun
Tong, Guang-Zhi
description In 2006, highly pathogenic porcine reproductive and respiratory syndrome virus (HP-PRRSV) caused great economic losses emerged in China and continues to be a threat for the pig industry. B antigenic region (AR) (37SHL/FQLIYNL45) of GP5 was considered to be a major linear neutralizing AR in PRRSV classical strains. However, peptide-purified antibodies against this AR did not neutralize PRRSV in a recent report. Compared with classical PRRSV, one amino acid mutation (L/F39→I39) was found in B AR of HP-PRRSV. To study the ability of B AR of HP-PRRSV to induce neutralizing antibody (NA) in vitro and in vivo, rabbit antisera against B AR with and without the mutation and pig hyperimmune sera with high titer of NAs against HP-PRRSV were prepared. Immunofluorescence assays (IFA) showed that the two rabbit antisera both had reactivity to classical PRRSV CH-1a and HP-PRRSV HuN4 with no observable difference in IFA titer. However, antisera did not have neutralizing activity against classical PRRSV CH-1a and HP-PRRSV HuN4. No correlation was observed between the levels of anti-B AR peptide antibodies and NAs in pig hyperimmune sera that were detected by indirect ELISA and virus neutralization, respectively. B AR peptide-specific serum antibodies had no neutralizing activity and, GST-B fusion protein could not inhibit neutralization of NAs in pig hyperimmune sera. Based on these findings, we conclude that B AR of HP-PRRSV is not a neutralizing AR of HP-PRRSV GP5.
doi_str_mv 10.1016/j.vetmic.2012.06.018
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B antigenic region (AR) (37SHL/FQLIYNL45) of GP5 was considered to be a major linear neutralizing AR in PRRSV classical strains. However, peptide-purified antibodies against this AR did not neutralize PRRSV in a recent report. Compared with classical PRRSV, one amino acid mutation (L/F39→I39) was found in B AR of HP-PRRSV. To study the ability of B AR of HP-PRRSV to induce neutralizing antibody (NA) in vitro and in vivo, rabbit antisera against B AR with and without the mutation and pig hyperimmune sera with high titer of NAs against HP-PRRSV were prepared. Immunofluorescence assays (IFA) showed that the two rabbit antisera both had reactivity to classical PRRSV CH-1a and HP-PRRSV HuN4 with no observable difference in IFA titer. However, antisera did not have neutralizing activity against classical PRRSV CH-1a and HP-PRRSV HuN4. 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B antigenic region (AR) (37SHL/FQLIYNL45) of GP5 was considered to be a major linear neutralizing AR in PRRSV classical strains. However, peptide-purified antibodies against this AR did not neutralize PRRSV in a recent report. Compared with classical PRRSV, one amino acid mutation (L/F39→I39) was found in B AR of HP-PRRSV. To study the ability of B AR of HP-PRRSV to induce neutralizing antibody (NA) in vitro and in vivo, rabbit antisera against B AR with and without the mutation and pig hyperimmune sera with high titer of NAs against HP-PRRSV were prepared. Immunofluorescence assays (IFA) showed that the two rabbit antisera both had reactivity to classical PRRSV CH-1a and HP-PRRSV HuN4 with no observable difference in IFA titer. However, antisera did not have neutralizing activity against classical PRRSV CH-1a and HP-PRRSV HuN4. No correlation was observed between the levels of anti-B AR peptide antibodies and NAs in pig hyperimmune sera that were detected by indirect ELISA and virus neutralization, respectively. B AR peptide-specific serum antibodies had no neutralizing activity and, GST-B fusion protein could not inhibit neutralization of NAs in pig hyperimmune sera. Based on these findings, we conclude that B AR of HP-PRRSV is not a neutralizing AR of HP-PRRSV GP5.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>22771210</pmid><doi>10.1016/j.vetmic.2012.06.018</doi><tpages>9</tpages></addata></record>
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subjects Animals
Antibodies, Neutralizing
Applied microbiology
B antigenic region
Biological and medical sciences
China
Enzyme-Linked Immunosorbent Assay
Fundamental and applied biological sciences. Psychology
GP5
Highly pathogenic porcine reproductive and respiratory syndrome virus
Microbiology
Miscellaneous
Neutralizing antibody
Peptides - chemistry
Peptides - immunology
Porcine Reproductive and Respiratory Syndrome - immunology
Porcine respiratory and reproductive syndrome virus
Porcine respiratory and reproductive syndrome virus - chemistry
Rabbits
Recombinant Fusion Proteins - chemistry
Recombinant Fusion Proteins - immunology
Swine
Vaccine
Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)
Viral Proteins - chemistry
Viral Proteins - immunology
Viral Vaccines - immunology
Virology
title Highly pathogenic porcine reproductive and respiratory syndrome virus GP5 B antigenic region is not a neutralizing antigenic region
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