Immunological response to porcine reproductive and respiratory syndrome virus in young pigs obtained from a PRRSV-positive exposure status herd in a PRRSV endemic area

© 2019 Elsevier B.V. Porcine reproductive and respiratory syndrome (PRRS), caused by the PRRS virus (PRRSV), remains a major economic threat to swine production throughout the world. The aim of this study was to investigate the humoral and cell-mediated immune responses to PRRSV in 10 PRRSV vaccinat...

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Main Authors: Nattinee Kittiwan, Panuwat Yamsakul, Pakpoom Tadee, Phacharaporn Tadee, Aniroot Nuangmek, Phongsakorn Chuammitri, Prapas Patchanee
Format: Journal
Published: 2020
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/67862
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-678622020-04-02T15:20:41Z Immunological response to porcine reproductive and respiratory syndrome virus in young pigs obtained from a PRRSV-positive exposure status herd in a PRRSV endemic area Nattinee Kittiwan Panuwat Yamsakul Pakpoom Tadee Phacharaporn Tadee Aniroot Nuangmek Phongsakorn Chuammitri Prapas Patchanee Immunology and Microbiology Veterinary © 2019 Elsevier B.V. Porcine reproductive and respiratory syndrome (PRRS), caused by the PRRS virus (PRRSV), remains a major economic threat to swine production throughout the world. The aim of this study was to investigate the humoral and cell-mediated immune responses to PRRSV in 10 PRRSV vaccinated and 10 non-vaccinated young pigs obtained from a PRRSV-seropositive herd under field conditions. On day 35 days of post-vaccination (dpv), two PRRSV seropositive mixed-litter pigs were added to each group to co-mingle the animals. Serum and whole blood samples were collected from all pigs on the first day of vaccination, as well as on the 21, 35, 49, and 63 dpv. The PRRSV-specific humoral and cell-mediated immune response was determined by ELISA and flow cytometry analysis. The PRRSV ELISA sample to positive (S/P) ratio was found to be positive at the threshold level until the age of 84 days in both non-vaccinated and vaccinated groups, whereas the IFN-γ positive staining cytotoxic (CD8+) cells were rapidly expressed in the early periods of vaccination and co-mingling, but were not found to be specific to PRRSV. This result might have been due to an unspecific response to stress antigens. Further studies should be conducted to obtain more immune response data over long-term observation periods and to study the effect of PRRSV endemic strain vaccinations in endemically-infected herds. 2020-04-02T15:08:00Z 2020-04-02T15:08:00Z 2019-12-01 Journal 18732534 01652427 2-s2.0-85072532350 10.1016/j.vetimm.2019.109935 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85072532350&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/67862
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Immunology and Microbiology
Veterinary
spellingShingle Immunology and Microbiology
Veterinary
Nattinee Kittiwan
Panuwat Yamsakul
Pakpoom Tadee
Phacharaporn Tadee
Aniroot Nuangmek
Phongsakorn Chuammitri
Prapas Patchanee
Immunological response to porcine reproductive and respiratory syndrome virus in young pigs obtained from a PRRSV-positive exposure status herd in a PRRSV endemic area
description © 2019 Elsevier B.V. Porcine reproductive and respiratory syndrome (PRRS), caused by the PRRS virus (PRRSV), remains a major economic threat to swine production throughout the world. The aim of this study was to investigate the humoral and cell-mediated immune responses to PRRSV in 10 PRRSV vaccinated and 10 non-vaccinated young pigs obtained from a PRRSV-seropositive herd under field conditions. On day 35 days of post-vaccination (dpv), two PRRSV seropositive mixed-litter pigs were added to each group to co-mingle the animals. Serum and whole blood samples were collected from all pigs on the first day of vaccination, as well as on the 21, 35, 49, and 63 dpv. The PRRSV-specific humoral and cell-mediated immune response was determined by ELISA and flow cytometry analysis. The PRRSV ELISA sample to positive (S/P) ratio was found to be positive at the threshold level until the age of 84 days in both non-vaccinated and vaccinated groups, whereas the IFN-γ positive staining cytotoxic (CD8+) cells were rapidly expressed in the early periods of vaccination and co-mingling, but were not found to be specific to PRRSV. This result might have been due to an unspecific response to stress antigens. Further studies should be conducted to obtain more immune response data over long-term observation periods and to study the effect of PRRSV endemic strain vaccinations in endemically-infected herds.
format Journal
author Nattinee Kittiwan
Panuwat Yamsakul
Pakpoom Tadee
Phacharaporn Tadee
Aniroot Nuangmek
Phongsakorn Chuammitri
Prapas Patchanee
author_facet Nattinee Kittiwan
Panuwat Yamsakul
Pakpoom Tadee
Phacharaporn Tadee
Aniroot Nuangmek
Phongsakorn Chuammitri
Prapas Patchanee
author_sort Nattinee Kittiwan
title Immunological response to porcine reproductive and respiratory syndrome virus in young pigs obtained from a PRRSV-positive exposure status herd in a PRRSV endemic area
title_short Immunological response to porcine reproductive and respiratory syndrome virus in young pigs obtained from a PRRSV-positive exposure status herd in a PRRSV endemic area
title_full Immunological response to porcine reproductive and respiratory syndrome virus in young pigs obtained from a PRRSV-positive exposure status herd in a PRRSV endemic area
title_fullStr Immunological response to porcine reproductive and respiratory syndrome virus in young pigs obtained from a PRRSV-positive exposure status herd in a PRRSV endemic area
title_full_unstemmed Immunological response to porcine reproductive and respiratory syndrome virus in young pigs obtained from a PRRSV-positive exposure status herd in a PRRSV endemic area
title_sort immunological response to porcine reproductive and respiratory syndrome virus in young pigs obtained from a prrsv-positive exposure status herd in a prrsv endemic area
publishDate 2020
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85072532350&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/67862
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