Enhanced infectivity of bovine viral diarrhoea virus (BVDV) in arginase-producing bovine monocyte-derived macrophages

Macrophages are important cells of the innate immunity that play a major role in Bovine Viral Diarrhoea Virus (BVDV) pathogenesis. Macrophages are not a homogenous population; they exist in different phenotypes, typically divided into two main categories: classically (pro-inflammatory) and alternati...

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Main Authors: Barone, Lucas Jose, Cardoso, Nancy, Mansilla, Florencia Celeste, Castillo, Mariangeles, Capozzo, Alejandra
Format: info:ar-repo/semantics/artículo
Language:Inglés
Published: Taylor & Francis 2025
Subjects:
Online Access:http://hdl.handle.net/20.500.12123/22064
https://www.tandfonline.com/doi/full/10.1080/21505594.2023.2283899
https://doi.org/10.1080/21505594.2023.2283899
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author Barone, Lucas Jose
Cardoso, Nancy
Mansilla, Florencia Celeste
Castillo, Mariangeles
Capozzo, Alejandra
author_browse Barone, Lucas Jose
Capozzo, Alejandra
Cardoso, Nancy
Castillo, Mariangeles
Mansilla, Florencia Celeste
author_facet Barone, Lucas Jose
Cardoso, Nancy
Mansilla, Florencia Celeste
Castillo, Mariangeles
Capozzo, Alejandra
author_sort Barone, Lucas Jose
collection INTA Digital
description Macrophages are important cells of the innate immunity that play a major role in Bovine Viral Diarrhoea Virus (BVDV) pathogenesis. Macrophages are not a homogenous population; they exist in different phenotypes, typically divided into two main categories: classically (pro-inflammatory) and alternatively activated (anti-inflammatory) or M1 and M2, respectively. The role of bovine macrophage phenotypes on BVDV infection is still unclear. This study characterized the interaction between BVDV and monocyte-derived macrophages (Mo-Mφ) collected from healthy cattle and polarized to an M1 or M2 state by using LPS, INF-γ, IL-4, or azithromycin. Arginase activity quantitation was utilized as a marker of the M2 Mo-Mφ spectrum. There was a significant association between arginase activity and the replication rate of BVDV strains of different genotypes and biotypes. Inhibition of arginase activity also reduced BVDV infectivity. Calves treated with azithromycin-induced Mo-Mφ of the M2 state produced high levels of arginase. Interestingly, azithromycin administered in vivo increased the susceptibility of macrophages to BVDV infection ex vivo. Mo-Mφ from pregnant dams and calves produced higher arginase levels than those from non-pregnant adult animals. The increased infection of arginase-producing alternatively activated bovine macrophages with BVDV supports the need to delve into a possible leading role of M2 macrophages in establishing the immune-suppressive state during BVDV convalescence.
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institution Instituto Nacional de Tecnología Agropecuaria (INTA -Argentina)
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spelling INTA220642025-04-28T10:10:28Z Enhanced infectivity of bovine viral diarrhoea virus (BVDV) in arginase-producing bovine monocyte-derived macrophages Barone, Lucas Jose Cardoso, Nancy Mansilla, Florencia Celeste Castillo, Mariangeles Capozzo, Alejandra Macrophages Pestivirus Immunosuppression Replication Bovine Viral Diarrhoea Monocytes Macrófago Inmunodepresión Replicación Diarrea Viral Bovina Monocito Azithromycin Azitromicina Macrophages are important cells of the innate immunity that play a major role in Bovine Viral Diarrhoea Virus (BVDV) pathogenesis. Macrophages are not a homogenous population; they exist in different phenotypes, typically divided into two main categories: classically (pro-inflammatory) and alternatively activated (anti-inflammatory) or M1 and M2, respectively. The role of bovine macrophage phenotypes on BVDV infection is still unclear. This study characterized the interaction between BVDV and monocyte-derived macrophages (Mo-Mφ) collected from healthy cattle and polarized to an M1 or M2 state by using LPS, INF-γ, IL-4, or azithromycin. Arginase activity quantitation was utilized as a marker of the M2 Mo-Mφ spectrum. There was a significant association between arginase activity and the replication rate of BVDV strains of different genotypes and biotypes. Inhibition of arginase activity also reduced BVDV infectivity. Calves treated with azithromycin-induced Mo-Mφ of the M2 state produced high levels of arginase. Interestingly, azithromycin administered in vivo increased the susceptibility of macrophages to BVDV infection ex vivo. Mo-Mφ from pregnant dams and calves produced higher arginase levels than those from non-pregnant adult animals. The increased infection of arginase-producing alternatively activated bovine macrophages with BVDV supports the need to delve into a possible leading role of M2 macrophages in establishing the immune-suppressive state during BVDV convalescence. Instituto de Virología Fil: Barone, Lucas Jose. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología e Innovaciones Tecnológicas; Argentina Fil: Barone, Lucas Jose. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Cardoso, Nancy Patricia. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología e Innovaciones Tecnológicas; Argentina Fil: Cardoso, Nancy Patricia. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Mansilla, Florencia Celeste. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología e Innovaciones Tecnológicas; Argentina Fil: Mansilla, Florencia Celeste. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Castillo, Mariangeles. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología e Innovaciones Tecnológicas; Argentina Fil: Castillo, Mariangeles. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Capozzo, Alejandra. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología e Innovaciones Tecnológicas; Argentina Fil: Capozzo, Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina 2025-04-28T10:04:35Z 2025-04-28T10:04:35Z 2024 info:ar-repo/semantics/artículo info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://hdl.handle.net/20.500.12123/22064 https://www.tandfonline.com/doi/full/10.1080/21505594.2023.2283899 2150-5608 https://doi.org/10.1080/21505594.2023.2283899 eng info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) application/pdf Taylor & Francis Virulence 15 (1) : 2283899 (2024)
spellingShingle Macrophages
Pestivirus
Immunosuppression
Replication
Bovine Viral Diarrhoea
Monocytes
Macrófago
Inmunodepresión
Replicación
Diarrea Viral Bovina
Monocito
Azithromycin
Azitromicina
Barone, Lucas Jose
Cardoso, Nancy
Mansilla, Florencia Celeste
Castillo, Mariangeles
Capozzo, Alejandra
Enhanced infectivity of bovine viral diarrhoea virus (BVDV) in arginase-producing bovine monocyte-derived macrophages
title Enhanced infectivity of bovine viral diarrhoea virus (BVDV) in arginase-producing bovine monocyte-derived macrophages
title_full Enhanced infectivity of bovine viral diarrhoea virus (BVDV) in arginase-producing bovine monocyte-derived macrophages
title_fullStr Enhanced infectivity of bovine viral diarrhoea virus (BVDV) in arginase-producing bovine monocyte-derived macrophages
title_full_unstemmed Enhanced infectivity of bovine viral diarrhoea virus (BVDV) in arginase-producing bovine monocyte-derived macrophages
title_short Enhanced infectivity of bovine viral diarrhoea virus (BVDV) in arginase-producing bovine monocyte-derived macrophages
title_sort enhanced infectivity of bovine viral diarrhoea virus bvdv in arginase producing bovine monocyte derived macrophages
topic Macrophages
Pestivirus
Immunosuppression
Replication
Bovine Viral Diarrhoea
Monocytes
Macrófago
Inmunodepresión
Replicación
Diarrea Viral Bovina
Monocito
Azithromycin
Azitromicina
url http://hdl.handle.net/20.500.12123/22064
https://www.tandfonline.com/doi/full/10.1080/21505594.2023.2283899
https://doi.org/10.1080/21505594.2023.2283899
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