A Plant-Produced Porcine Parvovirus 1-82 VP2 Subunit Vaccine Protects Pregnant Sows against Challenge with a Genetically Heterologous PPV1 Strain
Porcine parvovirus (PPV) causes reproductive failure in sows, and vaccination remains the most effective means of preventing infection. The NADL-2 strain has been used as a vaccine for ~50 years; however, it does not protect animals against genetically heterologous PPV strains. Thus, new effective a...
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Published in | Vaccines (Basel) Vol. 11; no. 1; p. 54 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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26.12.2022
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ISSN | 2076-393X 2076-393X |
DOI | 10.3390/vaccines11010054 |
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Abstract | Porcine parvovirus (PPV) causes reproductive failure in sows, and vaccination remains the most effective means of preventing infection. The NADL-2 strain has been used as a vaccine for ~50 years; however, it does not protect animals against genetically heterologous PPV strains. Thus, new effective and safe vaccines are needed. In this study, we aimed to identify novel PPV1 strains, and to develop PPV1 subunit vaccines. We isolated and sequenced PPV1 VP2 genes from 926 pigs and identified ten PPV1 strains (belonging to Groups C, D and E). We selected the Group D PPV1-82 strain as a vaccine candidate because it was close to the highly pathogenic 27a strain. The PPV1-82 VP2 protein was produced in Nicotiana benthamiana. It formed virus-like particles and exhibited a 211 agglutination value. The PPV1-190313 strain (Group E), isolated from an aborted fetus, was used as the challenging strain because it was pathogenic. The unvaccinated sow miscarried at 8 days postchallenge, and mummified fetuses were all PPV1-positive. By contrast, pregnant sows vaccinated with PPV1-82 VP2 had 9–11 Log2 antibody titers and produced normal fetuses after PPV1-190313 challenge. These results suggest the PPV1-82 VP2 subunit vaccine protects pregnant sows against a genetically heterologous PPV1 strain by inducing neutralizing antibodies. |
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AbstractList | Porcine parvovirus (PPV) causes reproductive failure in sows, and vaccination remains the most effective means of preventing infection. The NADL-2 strain has been used as a vaccine for ~50 years; however, it does not protect animals against genetically heterologous PPV strains. Thus, new effective and safe vaccines are needed. In this study, we aimed to identify novel PPV1 strains, and to develop PPV1 subunit vaccines. We isolated and sequenced PPV1 VP2 genes from 926 pigs and identified ten PPV1 strains (belonging to Groups C, D and E). We selected the Group D PPV1-82 strain as a vaccine candidate because it was close to the highly pathogenic 27a strain. The PPV1-82 VP2 protein was produced in Nicotiana benthamiana. It formed virus-like particles and exhibited a 211 agglutination value. The PPV1-190313 strain (Group E), isolated from an aborted fetus, was used as the challenging strain because it was pathogenic. The unvaccinated sow miscarried at 8 days postchallenge, and mummified fetuses were all PPV1-positive. By contrast, pregnant sows vaccinated with PPV1-82 VP2 had 9–11 Log2 antibody titers and produced normal fetuses after PPV1-190313 challenge. These results suggest the PPV1-82 VP2 subunit vaccine protects pregnant sows against a genetically heterologous PPV1 strain by inducing neutralizing antibodies. Porcine parvovirus (PPV) causes reproductive failure in sows, and vaccination remains the most effective means of preventing infection. The NADL-2 strain has been used as a vaccine for ~50 years; however, it does not protect animals against genetically heterologous PPV strains. Thus, new effective and safe vaccines are needed. In this study, we aimed to identify novel PPV1 strains, and to develop PPV1 subunit vaccines. We isolated and sequenced PPV1 genes from 926 pigs and identified ten PPV1 strains (belonging to Groups C, D and E). We selected the Group D PPV1-82 strain as a vaccine candidate because it was close to the highly pathogenic 27a strain. The PPV1-82 VP2 protein was produced in It formed virus-like particles and exhibited a 2 agglutination value. The PPV1-190313 strain (Group E), isolated from an aborted fetus, was used as the challenging strain because it was pathogenic. The unvaccinated sow miscarried at 8 days postchallenge, and mummified fetuses were all -positive. By contrast, pregnant sows vaccinated with PPV1-82 VP2 had 9-11 Log antibody titers and produced normal fetuses after PPV1-190313 challenge. These results suggest the PPV1-82 VP2 subunit vaccine protects pregnant sows against a genetically heterologous PPV1 strain by inducing neutralizing antibodies. Porcine parvovirus (PPV) causes reproductive failure in sows, and vaccination remains the most effective means of preventing infection. The NADL-2 strain has been used as a vaccine for ~50 years; however, it does not protect animals against genetically heterologous PPV strains. Thus, new effective and safe vaccines are needed. In this study, we aimed to identify novel PPV1 strains, and to develop PPV1 subunit vaccines. We isolated and sequenced PPV1 VP2 genes from 926 pigs and identified ten PPV1 strains (belonging to Groups C, D and E). We selected the Group D PPV1-82 strain as a vaccine candidate because it was close to the highly pathogenic 27a strain. The PPV1-82 VP2 protein was produced in Nicotiana benthamiana. It formed virus-like particles and exhibited a 211 agglutination value. The PPV1-190313 strain (Group E), isolated from an aborted fetus, was used as the challenging strain because it was pathogenic. The unvaccinated sow miscarried at 8 days postchallenge, and mummified fetuses were all PPV1-positive. By contrast, pregnant sows vaccinated with PPV1-82 VP2 had 9-11 Log2 antibody titers and produced normal fetuses after PPV1-190313 challenge. These results suggest the PPV1-82 VP2 subunit vaccine protects pregnant sows against a genetically heterologous PPV1 strain by inducing neutralizing antibodies.Porcine parvovirus (PPV) causes reproductive failure in sows, and vaccination remains the most effective means of preventing infection. The NADL-2 strain has been used as a vaccine for ~50 years; however, it does not protect animals against genetically heterologous PPV strains. Thus, new effective and safe vaccines are needed. In this study, we aimed to identify novel PPV1 strains, and to develop PPV1 subunit vaccines. We isolated and sequenced PPV1 VP2 genes from 926 pigs and identified ten PPV1 strains (belonging to Groups C, D and E). We selected the Group D PPV1-82 strain as a vaccine candidate because it was close to the highly pathogenic 27a strain. The PPV1-82 VP2 protein was produced in Nicotiana benthamiana. It formed virus-like particles and exhibited a 211 agglutination value. The PPV1-190313 strain (Group E), isolated from an aborted fetus, was used as the challenging strain because it was pathogenic. The unvaccinated sow miscarried at 8 days postchallenge, and mummified fetuses were all PPV1-positive. By contrast, pregnant sows vaccinated with PPV1-82 VP2 had 9-11 Log2 antibody titers and produced normal fetuses after PPV1-190313 challenge. These results suggest the PPV1-82 VP2 subunit vaccine protects pregnant sows against a genetically heterologous PPV1 strain by inducing neutralizing antibodies. Porcine parvovirus (PPV) causes reproductive failure in sows, and vaccination remains the most effective means of preventing infection. The NADL-2 strain has been used as a vaccine for ~50 years; however, it does not protect animals against genetically heterologous PPV strains. Thus, new effective and safe vaccines are needed. In this study, we aimed to identify novel PPV1 strains, and to develop PPV1 subunit vaccines. We isolated and sequenced PPV1 VP2 genes from 926 pigs and identified ten PPV1 strains (belonging to Groups C, D and E). We selected the Group D PPV1-82 strain as a vaccine candidate because it was close to the highly pathogenic 27a strain. The PPV1-82 VP2 protein was produced in Nicotiana benthamiana. It formed virus-like particles and exhibited a 2 11 agglutination value. The PPV1-190313 strain (Group E), isolated from an aborted fetus, was used as the challenging strain because it was pathogenic. The unvaccinated sow miscarried at 8 days postchallenge, and mummified fetuses were all PPV1 -positive. By contrast, pregnant sows vaccinated with PPV1-82 VP2 had 9–11 Log 2 antibody titers and produced normal fetuses after PPV1-190313 challenge. These results suggest the PPV1-82 VP2 subunit vaccine protects pregnant sows against a genetically heterologous PPV1 strain by inducing neutralizing antibodies. |
Author | Min, Kyung-Min Ouh, In-Ohk Kang, Hyang-Ju Park, Young-Min Song, Jae-Young Park, Choi-Kyu Cho, Kyou-Nam Choi, Bo-Hwa Park, Min-Hee Hyun, Bang-Hun Yun, Su-Yeong Lee, Yoon-Hee |
AuthorAffiliation | 3 BioPOA, Hwaseong-si 18469, Gyeonggi-do, Republic of Korea 1 BioApplications Inc., Pohang-si 37668, Gyeongsangbuk-do, Republic of Korea 2 Viral Disease Division, Animal and Plant Quarantine Agency, Gimcheon-si 39660, Gyeongsangbuk-do, Republic of Korea 4 College of Veterinary Medicine, Kyungpook National University, Daegu-si 41566, Gyeongsang-do, Republic of Korea |
AuthorAffiliation_xml | – name: 1 BioApplications Inc., Pohang-si 37668, Gyeongsangbuk-do, Republic of Korea – name: 4 College of Veterinary Medicine, Kyungpook National University, Daegu-si 41566, Gyeongsang-do, Republic of Korea – name: 2 Viral Disease Division, Animal and Plant Quarantine Agency, Gimcheon-si 39660, Gyeongsangbuk-do, Republic of Korea – name: 3 BioPOA, Hwaseong-si 18469, Gyeonggi-do, Republic of Korea |
Author_xml | – sequence: 1 givenname: Kyou-Nam orcidid: 0000-0003-1773-3633 surname: Cho fullname: Cho, Kyou-Nam – sequence: 2 givenname: In-Ohk surname: Ouh fullname: Ouh, In-Ohk – sequence: 3 givenname: Young-Min orcidid: 0000-0003-1174-3793 surname: Park fullname: Park, Young-Min – sequence: 4 givenname: Min-Hee surname: Park fullname: Park, Min-Hee – sequence: 5 givenname: Kyung-Min surname: Min fullname: Min, Kyung-Min – sequence: 6 givenname: Hyang-Ju surname: Kang fullname: Kang, Hyang-Ju – sequence: 7 givenname: Su-Yeong orcidid: 0000-0003-1874-2769 surname: Yun fullname: Yun, Su-Yeong – sequence: 8 givenname: Jae-Young surname: Song fullname: Song, Jae-Young – sequence: 9 givenname: Bang-Hun surname: Hyun fullname: Hyun, Bang-Hun – sequence: 10 givenname: Choi-Kyu surname: Park fullname: Park, Choi-Kyu – sequence: 11 givenname: Bo-Hwa surname: Choi fullname: Choi, Bo-Hwa – sequence: 12 givenname: Yoon-Hee orcidid: 0000-0003-4827-0686 surname: Lee fullname: Lee, Yoon-Hee |
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Cites_doi | 10.1016/j.meegid.2012.04.020 10.1186/s12917-022-03236-1 10.3390/v9080196 10.1080/19420862.2016.1227901 10.1126/science.aaf6638 10.1007/s00705-021-05106-x 10.1186/1743-422X-7-366 10.1006/viro.1993.1288 10.1007/s00253-020-10483-5 10.1099/vir.0.82302-0 10.4142/jvs.2001.2.3.201 10.1111/pbi.13040 10.1111/tpj.13847 10.1016/j.vetmic.2012.12.019 10.1007/BF01317841 10.1016/j.vetmic.2020.108795 10.1186/s12917-020-02329-z 10.1016/0264-410X(92)90090-7 10.1186/s12917-018-1487-z 10.1007/978-1-4939-3008-1_3 10.1080/21645515.2017.1356497 10.1007/s11262-016-1322-1 10.1099/vir.0.012054-0 10.1099/jgv.0.000446 10.1016/0021-9975(69)90053-X 10.1099/vir.0.033662-0 10.1016/j.jplph.2020.153359 10.1186/s12917-015-0396-7 10.1016/j.virol.2012.06.029 10.1146/annurev-virology-100114-055150 10.1016/S0264-410X(00)00512-0 10.3389/fvets.2021.726884 10.1016/j.meegid.2015.10.007 |
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Keywords | porcine parvovirus 1 cross reactivation plant-produced subunit vaccine viral protein 2 virus-like particle |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 These authors contributed equally to this work. Current address: Korea Disease Control and Prevention Agency, Osong-eup, Cheongju-si 28160, Chungcheongbuk-do, Republic of Korea. |
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SubjectTerms | Agglutination Antibodies cross reactivation Disease prevention Fetuses Genes Hogs Infections Manufacturers Parvoviruses Phylogenetics plant-produced subunit vaccine porcine parvovirus 1 Pregnancy Proteins Reproductive failure Sodium Strains (organisms) Swine Vaccines viral protein 2 virus-like particle Virus-like particles VP2 protein |
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Title | A Plant-Produced Porcine Parvovirus 1-82 VP2 Subunit Vaccine Protects Pregnant Sows against Challenge with a Genetically Heterologous PPV1 Strain |
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