Pathological characterization of IFNAR(-/-) mice infected with bluetongue virus serotype 4
Bluetongue virus (BTV) replicates in lymphoid tissues where infected mononuclear leukocytes secrete proinflammatory and vasoactive mediators that can contribute to bluetongue (BT) pathogenesis. Using the well-characterized IFNAR(-/-) mice animal model, we have now studied the histopathology and dynamics of leukocyte populations in different target tissues (spleen, thymus, and lung) during BTV-4 infection by histological and immunohistochemical techniques. The spleen and thymus of BTV-4 infected mice showed severe lymphoid depletion on H&E stained sections. This finding was confirmed by IHC, showing moderate decreased immunopositivity against CD3 in the thymus, and scarce immunoreactivity against CD3 and CD79 in the rest of the white pulp in the spleen, together with an increase in MAC387 immunostaining. BTV-4 infection also induced the expression of active caspase-3 in the spleen, where apoptotic debris was observed by H&E. A dramatic increase in iNOS immunoreactivity associated to necrotic areas of the white pulp was observed, being less noticeable in the thymus and the lung. The induction of pro-inflammatory cytokines in tissues where BTV replicates was evaluated by measuring transcript levels by RT-qPCR. BTV-4 infection led to enhance transcription of IFN-γ, TNF, IL-6, IL-12-p40, and IL-1β mRNA in the thymus, spleen and lung, correlating with the level of virus replication in these tissues. Disease progression and pathogenesis in IFNAR(-/-) mice closely mimics hallmarks of bluetongue disease in ruminants. IFNAR(-/-) mice are a good choice to facilitate a faster advance in the field of orbiviruses. � Ivyspring International Publisher.
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Format: | journal article biblioteca |
Language: | English |
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Ivyspring International Publisher
2016
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Subjects: | Bluetongue virus, IFNAR(-/-), Leukocyte, Cytokine, Pathology, |
Online Access: | http://hdl.handle.net/20.500.12792/2628 http://hdl.handle.net/10261/293216 |
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dig-inia-es-10261-2932162023-02-20T10:26:16Z Pathological characterization of IFNAR(-/-) mice infected with bluetongue virus serotype 4 Marín-López, A. Bermúdez, R. Calvo Pinilla, Eva María Moreno Fernández, Sandra Brun Torres, Alejandro Ortego Alonso, Francisco Javier Bluetongue virus IFNAR(-/-) Leukocyte Cytokine Pathology Bluetongue virus (BTV) replicates in lymphoid tissues where infected mononuclear leukocytes secrete proinflammatory and vasoactive mediators that can contribute to bluetongue (BT) pathogenesis. Using the well-characterized IFNAR(-/-) mice animal model, we have now studied the histopathology and dynamics of leukocyte populations in different target tissues (spleen, thymus, and lung) during BTV-4 infection by histological and immunohistochemical techniques. The spleen and thymus of BTV-4 infected mice showed severe lymphoid depletion on H&E stained sections. This finding was confirmed by IHC, showing moderate decreased immunopositivity against CD3 in the thymus, and scarce immunoreactivity against CD3 and CD79 in the rest of the white pulp in the spleen, together with an increase in MAC387 immunostaining. BTV-4 infection also induced the expression of active caspase-3 in the spleen, where apoptotic debris was observed by H&E. A dramatic increase in iNOS immunoreactivity associated to necrotic areas of the white pulp was observed, being less noticeable in the thymus and the lung. The induction of pro-inflammatory cytokines in tissues where BTV replicates was evaluated by measuring transcript levels by RT-qPCR. BTV-4 infection led to enhance transcription of IFN-γ, TNF, IL-6, IL-12-p40, and IL-1β mRNA in the thymus, spleen and lung, correlating with the level of virus replication in these tissues. Disease progression and pathogenesis in IFNAR(-/-) mice closely mimics hallmarks of bluetongue disease in ruminants. IFNAR(-/-) mice are a good choice to facilitate a faster advance in the field of orbiviruses. � Ivyspring International Publisher. 2023-02-20T10:26:16Z 2023-02-20T10:26:16Z 2016 journal article International Journal of Biological Sciences 12(12): 1448-1460 (2016) http://hdl.handle.net/20.500.12792/2628 http://hdl.handle.net/10261/293216 10.7150/ijbs.14967 1449-2288 en open Ivyspring International Publisher |
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Bluetongue virus IFNAR(-/-) Leukocyte Cytokine Pathology Bluetongue virus IFNAR(-/-) Leukocyte Cytokine Pathology |
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Bluetongue virus IFNAR(-/-) Leukocyte Cytokine Pathology Bluetongue virus IFNAR(-/-) Leukocyte Cytokine Pathology Marín-López, A. Bermúdez, R. Calvo Pinilla, Eva María Moreno Fernández, Sandra Brun Torres, Alejandro Ortego Alonso, Francisco Javier Pathological characterization of IFNAR(-/-) mice infected with bluetongue virus serotype 4 |
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Bluetongue virus (BTV) replicates in lymphoid tissues where infected mononuclear leukocytes secrete proinflammatory and vasoactive mediators that can contribute to bluetongue (BT) pathogenesis. Using the well-characterized IFNAR(-/-) mice animal model, we have now studied the histopathology and dynamics of leukocyte populations in different target tissues (spleen, thymus, and lung) during BTV-4 infection by histological and immunohistochemical techniques. The spleen and thymus of BTV-4 infected mice showed severe lymphoid depletion on H&E stained sections. This finding was confirmed by IHC, showing moderate decreased immunopositivity against CD3 in the thymus, and scarce immunoreactivity against CD3 and CD79 in the rest of the white pulp in the spleen, together with an increase in MAC387 immunostaining. BTV-4 infection also induced the expression of active caspase-3 in the spleen, where apoptotic debris was observed by H&E. A dramatic increase in iNOS immunoreactivity associated to necrotic areas of the white pulp was observed, being less noticeable in the thymus and the lung. The induction of pro-inflammatory cytokines in tissues where BTV replicates was evaluated by measuring transcript levels by RT-qPCR. BTV-4 infection led to enhance transcription of IFN-γ, TNF, IL-6, IL-12-p40, and IL-1β mRNA in the thymus, spleen and lung, correlating with the level of virus replication in these tissues. Disease progression and pathogenesis in IFNAR(-/-) mice closely mimics hallmarks of bluetongue disease in ruminants. IFNAR(-/-) mice are a good choice to facilitate a faster advance in the field of orbiviruses. � Ivyspring International Publisher. |
format |
journal article |
topic_facet |
Bluetongue virus IFNAR(-/-) Leukocyte Cytokine Pathology |
author |
Marín-López, A. Bermúdez, R. Calvo Pinilla, Eva María Moreno Fernández, Sandra Brun Torres, Alejandro Ortego Alonso, Francisco Javier |
author_facet |
Marín-López, A. Bermúdez, R. Calvo Pinilla, Eva María Moreno Fernández, Sandra Brun Torres, Alejandro Ortego Alonso, Francisco Javier |
author_sort |
Marín-López, A. |
title |
Pathological characterization of IFNAR(-/-) mice infected with bluetongue virus serotype 4 |
title_short |
Pathological characterization of IFNAR(-/-) mice infected with bluetongue virus serotype 4 |
title_full |
Pathological characterization of IFNAR(-/-) mice infected with bluetongue virus serotype 4 |
title_fullStr |
Pathological characterization of IFNAR(-/-) mice infected with bluetongue virus serotype 4 |
title_full_unstemmed |
Pathological characterization of IFNAR(-/-) mice infected with bluetongue virus serotype 4 |
title_sort |
pathological characterization of ifnar(-/-) mice infected with bluetongue virus serotype 4 |
publisher |
Ivyspring International Publisher |
publishDate |
2016 |
url |
http://hdl.handle.net/20.500.12792/2628 http://hdl.handle.net/10261/293216 |
work_keys_str_mv |
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1767603445105164288 |