Cargando…
Porcine reproductive and respiratory syndrome virus impacts on gut microbiome in a strain virulence‐dependent fashion
Porcine reproductive and respiratory syndrome (PRRS) is a viral disease defined by reproductive problems, respiratory distress and a negative impact on growth rate and general condition. Virulent PRRS virus (PRRSV) strains have emerged in the last years with evident knowledge gaps in their impact on...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8913879/ https://www.ncbi.nlm.nih.gov/pubmed/33656781 http://dx.doi.org/10.1111/1751-7915.13757 |
_version_ | 1784667556128227328 |
---|---|
author | Argüello, Héctor Rodríguez‐Gómez, Irene Magdalena Sánchez‐Carvajal, Jose María Pallares, Francisco José Díaz, Iván Cabrera‐Rubio, Raúl Crispie, Fiona Cotter, Paul D. Mateu, Enric Martín‐Valls, Gerard Carrasco, Librado Gómez‐Laguna, Jaime |
author_facet | Argüello, Héctor Rodríguez‐Gómez, Irene Magdalena Sánchez‐Carvajal, Jose María Pallares, Francisco José Díaz, Iván Cabrera‐Rubio, Raúl Crispie, Fiona Cotter, Paul D. Mateu, Enric Martín‐Valls, Gerard Carrasco, Librado Gómez‐Laguna, Jaime |
author_sort | Argüello, Héctor |
collection | PubMed |
description | Porcine reproductive and respiratory syndrome (PRRS) is a viral disease defined by reproductive problems, respiratory distress and a negative impact on growth rate and general condition. Virulent PRRS virus (PRRSV) strains have emerged in the last years with evident knowledge gaps in their impact on the host immune response. Thus, the present study examines the impact of acute PRRS virus (PRRSV) infection, with two strains of different virulence, on selected immune parameters and on the gut microbiota composition of infected pigs using 16S rRNA compositional sequencing. Pigs were infected with a low virulent (PRRS_3249) or a virulent (Lena) PRRSV‐1 strain and euthanized at 1, 3, 6, 8 or 13 days post‐inoculation (dpi). Faeces were collected from each animal at the necropsy time‐point. Alpha and beta diversity analyses demonstrated that infection, particularly with the Lena strain, impacted the microbiome composition from 6 dpi onwards. Taxonomic differences revealed that infected pigs had higher abundance of Treponema and Methanobrevibacter (FDR < 0.05). Differences were more considerable for Lena‐ than for PRRS_3249‐infected pigs, showing the impact of strain virulence in the intestinal changes. Lena‐infected pigs had reduced abundancies of anaerobic commensals such as Roseburia, Anaerostipes, Butyricicoccus and Prevotella (P < 0.05). The depletion of these desirable commensals was significantly correlated to infection severity measured by viraemia, clinical signs, lung lesions and immune parameters (IL‐6, IFN‐γ and Hp serum levels). Altogether, the results from this study demonstrate the indirect impact of PRRSV infection on gut microbiome composition in a strain virulence‐dependent fashion and its association with selected immune markers. |
format | Online Article Text |
id | pubmed-8913879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89138792022-03-17 Porcine reproductive and respiratory syndrome virus impacts on gut microbiome in a strain virulence‐dependent fashion Argüello, Héctor Rodríguez‐Gómez, Irene Magdalena Sánchez‐Carvajal, Jose María Pallares, Francisco José Díaz, Iván Cabrera‐Rubio, Raúl Crispie, Fiona Cotter, Paul D. Mateu, Enric Martín‐Valls, Gerard Carrasco, Librado Gómez‐Laguna, Jaime Microb Biotechnol Brief Report Porcine reproductive and respiratory syndrome (PRRS) is a viral disease defined by reproductive problems, respiratory distress and a negative impact on growth rate and general condition. Virulent PRRS virus (PRRSV) strains have emerged in the last years with evident knowledge gaps in their impact on the host immune response. Thus, the present study examines the impact of acute PRRS virus (PRRSV) infection, with two strains of different virulence, on selected immune parameters and on the gut microbiota composition of infected pigs using 16S rRNA compositional sequencing. Pigs were infected with a low virulent (PRRS_3249) or a virulent (Lena) PRRSV‐1 strain and euthanized at 1, 3, 6, 8 or 13 days post‐inoculation (dpi). Faeces were collected from each animal at the necropsy time‐point. Alpha and beta diversity analyses demonstrated that infection, particularly with the Lena strain, impacted the microbiome composition from 6 dpi onwards. Taxonomic differences revealed that infected pigs had higher abundance of Treponema and Methanobrevibacter (FDR < 0.05). Differences were more considerable for Lena‐ than for PRRS_3249‐infected pigs, showing the impact of strain virulence in the intestinal changes. Lena‐infected pigs had reduced abundancies of anaerobic commensals such as Roseburia, Anaerostipes, Butyricicoccus and Prevotella (P < 0.05). The depletion of these desirable commensals was significantly correlated to infection severity measured by viraemia, clinical signs, lung lesions and immune parameters (IL‐6, IFN‐γ and Hp serum levels). Altogether, the results from this study demonstrate the indirect impact of PRRSV infection on gut microbiome composition in a strain virulence‐dependent fashion and its association with selected immune markers. John Wiley and Sons Inc. 2021-03-03 /pmc/articles/PMC8913879/ /pubmed/33656781 http://dx.doi.org/10.1111/1751-7915.13757 Text en © 2021 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. https://creativecommons.org/licenses/by-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nd/4.0/ (https://creativecommons.org/licenses/by-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited and no modifications or adaptations are made. |
spellingShingle | Brief Report Argüello, Héctor Rodríguez‐Gómez, Irene Magdalena Sánchez‐Carvajal, Jose María Pallares, Francisco José Díaz, Iván Cabrera‐Rubio, Raúl Crispie, Fiona Cotter, Paul D. Mateu, Enric Martín‐Valls, Gerard Carrasco, Librado Gómez‐Laguna, Jaime Porcine reproductive and respiratory syndrome virus impacts on gut microbiome in a strain virulence‐dependent fashion |
title | Porcine reproductive and respiratory syndrome virus impacts on gut microbiome in a strain virulence‐dependent fashion |
title_full | Porcine reproductive and respiratory syndrome virus impacts on gut microbiome in a strain virulence‐dependent fashion |
title_fullStr | Porcine reproductive and respiratory syndrome virus impacts on gut microbiome in a strain virulence‐dependent fashion |
title_full_unstemmed | Porcine reproductive and respiratory syndrome virus impacts on gut microbiome in a strain virulence‐dependent fashion |
title_short | Porcine reproductive and respiratory syndrome virus impacts on gut microbiome in a strain virulence‐dependent fashion |
title_sort | porcine reproductive and respiratory syndrome virus impacts on gut microbiome in a strain virulence‐dependent fashion |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8913879/ https://www.ncbi.nlm.nih.gov/pubmed/33656781 http://dx.doi.org/10.1111/1751-7915.13757 |
work_keys_str_mv | AT arguellohector porcinereproductiveandrespiratorysyndromevirusimpactsongutmicrobiomeinastrainvirulencedependentfashion AT rodriguezgomezirenemagdalena porcinereproductiveandrespiratorysyndromevirusimpactsongutmicrobiomeinastrainvirulencedependentfashion AT sanchezcarvajaljosemaria porcinereproductiveandrespiratorysyndromevirusimpactsongutmicrobiomeinastrainvirulencedependentfashion AT pallaresfranciscojose porcinereproductiveandrespiratorysyndromevirusimpactsongutmicrobiomeinastrainvirulencedependentfashion AT diazivan porcinereproductiveandrespiratorysyndromevirusimpactsongutmicrobiomeinastrainvirulencedependentfashion AT cabrerarubioraul porcinereproductiveandrespiratorysyndromevirusimpactsongutmicrobiomeinastrainvirulencedependentfashion AT crispiefiona porcinereproductiveandrespiratorysyndromevirusimpactsongutmicrobiomeinastrainvirulencedependentfashion AT cotterpauld porcinereproductiveandrespiratorysyndromevirusimpactsongutmicrobiomeinastrainvirulencedependentfashion AT mateuenric porcinereproductiveandrespiratorysyndromevirusimpactsongutmicrobiomeinastrainvirulencedependentfashion AT martinvallsgerard porcinereproductiveandrespiratorysyndromevirusimpactsongutmicrobiomeinastrainvirulencedependentfashion AT carrascolibrado porcinereproductiveandrespiratorysyndromevirusimpactsongutmicrobiomeinastrainvirulencedependentfashion AT gomezlagunajaime porcinereproductiveandrespiratorysyndromevirusimpactsongutmicrobiomeinastrainvirulencedependentfashion |