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.

Saved in:
Bibliographic Details
Main Authors: Marín-López, A., Bermúdez, R., Calvo Pinilla, Eva María, Moreno Fernández, Sandra, Brun Torres, Alejandro, Ortego Alonso, Francisco Javier
Format: journal article biblioteca
Language:English
Published: Ivyspring International Publisher 2016
Subjects:Bluetongue virus, IFNAR(-/-), Leukocyte, Cytokine, Pathology,
Online Access:http://hdl.handle.net/20.500.12792/2628
http://hdl.handle.net/10261/293216
Tags: Add Tag
No Tags, Be the first to tag this record!
id dig-inia-es-10261-293216
record_format koha
spelling 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
institution INIA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-inia-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del INIA España
language English
topic Bluetongue virus
IFNAR(-/-)
Leukocyte
Cytokine
Pathology
Bluetongue virus
IFNAR(-/-)
Leukocyte
Cytokine
Pathology
spellingShingle 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
description 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 AT marinlopeza pathologicalcharacterizationofifnarmiceinfectedwithbluetonguevirusserotype4
AT bermudezr pathologicalcharacterizationofifnarmiceinfectedwithbluetonguevirusserotype4
AT calvopinillaevamaria pathologicalcharacterizationofifnarmiceinfectedwithbluetonguevirusserotype4
AT morenofernandezsandra pathologicalcharacterizationofifnarmiceinfectedwithbluetonguevirusserotype4
AT bruntorresalejandro pathologicalcharacterizationofifnarmiceinfectedwithbluetonguevirusserotype4
AT ortegoalonsofranciscojavier pathologicalcharacterizationofifnarmiceinfectedwithbluetonguevirusserotype4
_version_ 1767603445105164288