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Differential interactions of virulent and non-virulent H. parasuis strains with naïve or swine influenza virus pre-infected dendritic cells

Pigs possess a microbiota in the upper respiratory tract that includes Haemophilus parasuis. Pigs are also considered the reservoir of influenza viruses and infection with this virus commonly results in increased impact of bacterial infections, including those by H. parasuis. However, the mechanisms...

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Autores principales: Mussá, Tufária, Rodríguez-Cariño, Carolina, Sánchez-Chardi, Alejandro, Baratelli, Massimiliano, Costa-Hurtado, Mar, Fraile, Lorenzo, Domínguez, Javier, Aragon, Virginia, Montoya, María
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585918/
https://www.ncbi.nlm.nih.gov/pubmed/23157617
http://dx.doi.org/10.1186/1297-9716-43-80
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author Mussá, Tufária
Rodríguez-Cariño, Carolina
Sánchez-Chardi, Alejandro
Baratelli, Massimiliano
Costa-Hurtado, Mar
Fraile, Lorenzo
Domínguez, Javier
Aragon, Virginia
Montoya, María
author_facet Mussá, Tufária
Rodríguez-Cariño, Carolina
Sánchez-Chardi, Alejandro
Baratelli, Massimiliano
Costa-Hurtado, Mar
Fraile, Lorenzo
Domínguez, Javier
Aragon, Virginia
Montoya, María
author_sort Mussá, Tufária
collection PubMed
description Pigs possess a microbiota in the upper respiratory tract that includes Haemophilus parasuis. Pigs are also considered the reservoir of influenza viruses and infection with this virus commonly results in increased impact of bacterial infections, including those by H. parasuis. However, the mechanisms involved in host innate responses towards H. parasuis and their implications in a co-infection with influenza virus are unknown. Therefore, the ability of a non-virulent H. parasuis serovar 3 (SW114) and a virulent serovar 5 (Nagasaki) strains to interact with porcine bone marrow dendritic cells (poBMDC) and their modulation in a co-infection with swine influenza virus (SwIV) H3N2 was examined. At 1 hour post infection (hpi), SW114 interaction with poBMDC was higher than that of Nagasaki, while at 8 hpi both strains showed similar levels of interaction. The co-infection with H3N2 SwIV and either SW114 or Nagasaki induced higher levels of IL-1β, TNF-α, IL-6, IL-12 and IL-10 compared to mock or H3N2 SwIV infection alone. Moreover, IL-12 and IFN-α secretion differentially increased in cells co-infected with H3N2 SwIV and Nagasaki. These results pave the way for understanding the differences in the interaction of non-virulent and virulent strains of H. parasuis with the swine immune system and their modulation in a viral co-infection.
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spelling pubmed-35859182013-03-03 Differential interactions of virulent and non-virulent H. parasuis strains with naïve or swine influenza virus pre-infected dendritic cells Mussá, Tufária Rodríguez-Cariño, Carolina Sánchez-Chardi, Alejandro Baratelli, Massimiliano Costa-Hurtado, Mar Fraile, Lorenzo Domínguez, Javier Aragon, Virginia Montoya, María Vet Res Research Pigs possess a microbiota in the upper respiratory tract that includes Haemophilus parasuis. Pigs are also considered the reservoir of influenza viruses and infection with this virus commonly results in increased impact of bacterial infections, including those by H. parasuis. However, the mechanisms involved in host innate responses towards H. parasuis and their implications in a co-infection with influenza virus are unknown. Therefore, the ability of a non-virulent H. parasuis serovar 3 (SW114) and a virulent serovar 5 (Nagasaki) strains to interact with porcine bone marrow dendritic cells (poBMDC) and their modulation in a co-infection with swine influenza virus (SwIV) H3N2 was examined. At 1 hour post infection (hpi), SW114 interaction with poBMDC was higher than that of Nagasaki, while at 8 hpi both strains showed similar levels of interaction. The co-infection with H3N2 SwIV and either SW114 or Nagasaki induced higher levels of IL-1β, TNF-α, IL-6, IL-12 and IL-10 compared to mock or H3N2 SwIV infection alone. Moreover, IL-12 and IFN-α secretion differentially increased in cells co-infected with H3N2 SwIV and Nagasaki. These results pave the way for understanding the differences in the interaction of non-virulent and virulent strains of H. parasuis with the swine immune system and their modulation in a viral co-infection. BioMed Central 2012 2012-11-16 /pmc/articles/PMC3585918/ /pubmed/23157617 http://dx.doi.org/10.1186/1297-9716-43-80 Text en Copyright ©2012 Mussá et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Mussá, Tufária
Rodríguez-Cariño, Carolina
Sánchez-Chardi, Alejandro
Baratelli, Massimiliano
Costa-Hurtado, Mar
Fraile, Lorenzo
Domínguez, Javier
Aragon, Virginia
Montoya, María
Differential interactions of virulent and non-virulent H. parasuis strains with naïve or swine influenza virus pre-infected dendritic cells
title Differential interactions of virulent and non-virulent H. parasuis strains with naïve or swine influenza virus pre-infected dendritic cells
title_full Differential interactions of virulent and non-virulent H. parasuis strains with naïve or swine influenza virus pre-infected dendritic cells
title_fullStr Differential interactions of virulent and non-virulent H. parasuis strains with naïve or swine influenza virus pre-infected dendritic cells
title_full_unstemmed Differential interactions of virulent and non-virulent H. parasuis strains with naïve or swine influenza virus pre-infected dendritic cells
title_short Differential interactions of virulent and non-virulent H. parasuis strains with naïve or swine influenza virus pre-infected dendritic cells
title_sort differential interactions of virulent and non-virulent h. parasuis strains with naïve or swine influenza virus pre-infected dendritic cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585918/
https://www.ncbi.nlm.nih.gov/pubmed/23157617
http://dx.doi.org/10.1186/1297-9716-43-80
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