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Phenotypic Characterization of a Virulent PRRSV-1 Isolate in a Reproductive Model With and Without Prior Heterologous Modified Live PRRSV-1 Vaccination

Reproductive disorders induced by porcine reproductive and respiratory syndrome virus (PRRSV) cause high economic losses in the pig industry worldwide. In this study, we aimed to phenotypically characterize a virulent PRRSV-1 subtype 1 isolate (AUT15-33) in a reproductive model. Furthermore, the pro...

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Autores principales: Kreutzmann, Heinrich, Stadler, Julia, Knecht, Christian, Sassu, Elena L., Ruczizka, Ursula, Zablotski, Yury, Vatzia, Eleni, Balka, Gyula, Zaruba, Marianne, Chen, Hann-Wei, Riedel, Christiane, Rümenapf, Till, Ladinig, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022457/
https://www.ncbi.nlm.nih.gov/pubmed/35464363
http://dx.doi.org/10.3389/fvets.2022.820233
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author Kreutzmann, Heinrich
Stadler, Julia
Knecht, Christian
Sassu, Elena L.
Ruczizka, Ursula
Zablotski, Yury
Vatzia, Eleni
Balka, Gyula
Zaruba, Marianne
Chen, Hann-Wei
Riedel, Christiane
Rümenapf, Till
Ladinig, Andrea
author_facet Kreutzmann, Heinrich
Stadler, Julia
Knecht, Christian
Sassu, Elena L.
Ruczizka, Ursula
Zablotski, Yury
Vatzia, Eleni
Balka, Gyula
Zaruba, Marianne
Chen, Hann-Wei
Riedel, Christiane
Rümenapf, Till
Ladinig, Andrea
author_sort Kreutzmann, Heinrich
collection PubMed
description Reproductive disorders induced by porcine reproductive and respiratory syndrome virus (PRRSV) cause high economic losses in the pig industry worldwide. In this study, we aimed to phenotypically characterize a virulent PRRSV-1 subtype 1 isolate (AUT15-33) in a reproductive model. Furthermore, the protective effect of a heterologous modified live virus vaccine (ReproCyc® PRRS EU) was evaluated. In addition, PRRSV AUT15-33 was genotypically compared to other well-characterized isolates. Sixteen gilts were equally divided into four groups: a vaccinated and infected group (V–I), a vaccinated and non-infected group (V–NI), a non-vaccinated and infected group (NV–I), and a non-vaccinated and non-infected (NV–NI) group. After PRRSV infection on gestation day 84, all gilts were clinically examined on a daily basis, and blood samples were taken at five timepoints. Necropsy was performed 3 weeks after infection. The fetal preservation status was assessed, and PRRSV RNA concentrations were measured in the blood and tissue samples from all gilts and fetuses. After infection, all four gilts in the NV–I group were viremic throughout 17 days post-infection (dpi), whereas two gilts in the V–I group were viremic at only one timepoint at 6 dpi. The viral load was significantly higher in gilt serum, tracheobronchial lymph nodes, uterine lymph nodes, maternal endometrium, and fetal placenta of NV–I gilts compared to the V–I ones (p < 0.05). Moreover, the preservation status of the fetuses derived from NV–I gilts was significantly impaired (55.9% of viable fetuses) compared to the other groups (p < 0.001). Upon comparison with other known isolates, the phylogenetic analyses revealed the closest relation to a well-characterized PRRSV-1 subtype 1 field isolate from Belgium. In conclusion, the high virulence of AUT15-33 was phenotypically confirmed in an experimental reproductive model. The vaccination of the gilts showed promising results in reducing viremia, fetal damage, and transplacental transmission of the PRRSV-1 strain characterized in this study.
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spelling pubmed-90224572022-04-22 Phenotypic Characterization of a Virulent PRRSV-1 Isolate in a Reproductive Model With and Without Prior Heterologous Modified Live PRRSV-1 Vaccination Kreutzmann, Heinrich Stadler, Julia Knecht, Christian Sassu, Elena L. Ruczizka, Ursula Zablotski, Yury Vatzia, Eleni Balka, Gyula Zaruba, Marianne Chen, Hann-Wei Riedel, Christiane Rümenapf, Till Ladinig, Andrea Front Vet Sci Veterinary Science Reproductive disorders induced by porcine reproductive and respiratory syndrome virus (PRRSV) cause high economic losses in the pig industry worldwide. In this study, we aimed to phenotypically characterize a virulent PRRSV-1 subtype 1 isolate (AUT15-33) in a reproductive model. Furthermore, the protective effect of a heterologous modified live virus vaccine (ReproCyc® PRRS EU) was evaluated. In addition, PRRSV AUT15-33 was genotypically compared to other well-characterized isolates. Sixteen gilts were equally divided into four groups: a vaccinated and infected group (V–I), a vaccinated and non-infected group (V–NI), a non-vaccinated and infected group (NV–I), and a non-vaccinated and non-infected (NV–NI) group. After PRRSV infection on gestation day 84, all gilts were clinically examined on a daily basis, and blood samples were taken at five timepoints. Necropsy was performed 3 weeks after infection. The fetal preservation status was assessed, and PRRSV RNA concentrations were measured in the blood and tissue samples from all gilts and fetuses. After infection, all four gilts in the NV–I group were viremic throughout 17 days post-infection (dpi), whereas two gilts in the V–I group were viremic at only one timepoint at 6 dpi. The viral load was significantly higher in gilt serum, tracheobronchial lymph nodes, uterine lymph nodes, maternal endometrium, and fetal placenta of NV–I gilts compared to the V–I ones (p < 0.05). Moreover, the preservation status of the fetuses derived from NV–I gilts was significantly impaired (55.9% of viable fetuses) compared to the other groups (p < 0.001). Upon comparison with other known isolates, the phylogenetic analyses revealed the closest relation to a well-characterized PRRSV-1 subtype 1 field isolate from Belgium. In conclusion, the high virulence of AUT15-33 was phenotypically confirmed in an experimental reproductive model. The vaccination of the gilts showed promising results in reducing viremia, fetal damage, and transplacental transmission of the PRRSV-1 strain characterized in this study. Frontiers Media S.A. 2022-04-07 /pmc/articles/PMC9022457/ /pubmed/35464363 http://dx.doi.org/10.3389/fvets.2022.820233 Text en Copyright © 2022 Kreutzmann, Stadler, Knecht, Sassu, Ruczizka, Zablotski, Vatzia, Balka, Zaruba, Chen, Riedel, Rümenapf and Ladinig. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Veterinary Science
Kreutzmann, Heinrich
Stadler, Julia
Knecht, Christian
Sassu, Elena L.
Ruczizka, Ursula
Zablotski, Yury
Vatzia, Eleni
Balka, Gyula
Zaruba, Marianne
Chen, Hann-Wei
Riedel, Christiane
Rümenapf, Till
Ladinig, Andrea
Phenotypic Characterization of a Virulent PRRSV-1 Isolate in a Reproductive Model With and Without Prior Heterologous Modified Live PRRSV-1 Vaccination
title Phenotypic Characterization of a Virulent PRRSV-1 Isolate in a Reproductive Model With and Without Prior Heterologous Modified Live PRRSV-1 Vaccination
title_full Phenotypic Characterization of a Virulent PRRSV-1 Isolate in a Reproductive Model With and Without Prior Heterologous Modified Live PRRSV-1 Vaccination
title_fullStr Phenotypic Characterization of a Virulent PRRSV-1 Isolate in a Reproductive Model With and Without Prior Heterologous Modified Live PRRSV-1 Vaccination
title_full_unstemmed Phenotypic Characterization of a Virulent PRRSV-1 Isolate in a Reproductive Model With and Without Prior Heterologous Modified Live PRRSV-1 Vaccination
title_short Phenotypic Characterization of a Virulent PRRSV-1 Isolate in a Reproductive Model With and Without Prior Heterologous Modified Live PRRSV-1 Vaccination
title_sort phenotypic characterization of a virulent prrsv-1 isolate in a reproductive model with and without prior heterologous modified live prrsv-1 vaccination
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022457/
https://www.ncbi.nlm.nih.gov/pubmed/35464363
http://dx.doi.org/10.3389/fvets.2022.820233
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