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Expression of canine distemper virus receptor nectin-4 in the central nervous system of dogs

Canine distemper virus (CDV) exhibits lymphotropic, epitheliotropic, and neurotropic nature, and causes a severe systemic infection in susceptible animals. Initially, signaling lymphocyte activation molecule (SLAM) expressed on immune cells has been identified as a crucial cellular receptor for CDV....

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Autores principales: Pratakpiriya, Watanyoo, Ping Teh, Angeline Ping, Radtanakatikanon, Araya, Pirarat, Nopadon, Thi Lan, Nguyen, Takeda, Makoto, Techangamsuwan, Somporn, Yamaguchi, Ryoji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428276/
https://www.ncbi.nlm.nih.gov/pubmed/28336928
http://dx.doi.org/10.1038/s41598-017-00375-6
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author Pratakpiriya, Watanyoo
Ping Teh, Angeline Ping
Radtanakatikanon, Araya
Pirarat, Nopadon
Thi Lan, Nguyen
Takeda, Makoto
Techangamsuwan, Somporn
Yamaguchi, Ryoji
author_facet Pratakpiriya, Watanyoo
Ping Teh, Angeline Ping
Radtanakatikanon, Araya
Pirarat, Nopadon
Thi Lan, Nguyen
Takeda, Makoto
Techangamsuwan, Somporn
Yamaguchi, Ryoji
author_sort Pratakpiriya, Watanyoo
collection PubMed
description Canine distemper virus (CDV) exhibits lymphotropic, epitheliotropic, and neurotropic nature, and causes a severe systemic infection in susceptible animals. Initially, signaling lymphocyte activation molecule (SLAM) expressed on immune cells has been identified as a crucial cellular receptor for CDV. Currently, nectin-4 expressed in epithelia has been shown to be another receptor for CDV. Our previous study demonstrated that neurons express nectin-4 and are infected with CDV. In this study, we investigated the distribution pattern of nectin-4 in various cell types in the canine central nervous system and showed its relation to CDV infection to further clarify the pathology of disease. Histopathological, immunohistochemical and immunofluorescent analyses were done using formalin-fixed paraffin-embedded tissues of CDV-infected dogs. Dual staining of nectin-4 and CDV antigen or nectin-4 and brain cell markers was performed. Nectin-4 was detected in ependymal cells, epithelia of choroid plexus, meningeal cells, neurons, granular cells, and Purkinje’s cells. CDV antigens were detected in these nectin-4-positive cells, further suggesting contribution of nectin-4 for the CDV neurovirulence. On the other hand, astrocytes did not express nectin-4, although they were frequently infected with CDV. Since astrocytes are negative for SLAM expression, they must express an unidentified CDV receptor, which also contributes to CDV neurovirulence.
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spelling pubmed-54282762017-05-15 Expression of canine distemper virus receptor nectin-4 in the central nervous system of dogs Pratakpiriya, Watanyoo Ping Teh, Angeline Ping Radtanakatikanon, Araya Pirarat, Nopadon Thi Lan, Nguyen Takeda, Makoto Techangamsuwan, Somporn Yamaguchi, Ryoji Sci Rep Article Canine distemper virus (CDV) exhibits lymphotropic, epitheliotropic, and neurotropic nature, and causes a severe systemic infection in susceptible animals. Initially, signaling lymphocyte activation molecule (SLAM) expressed on immune cells has been identified as a crucial cellular receptor for CDV. Currently, nectin-4 expressed in epithelia has been shown to be another receptor for CDV. Our previous study demonstrated that neurons express nectin-4 and are infected with CDV. In this study, we investigated the distribution pattern of nectin-4 in various cell types in the canine central nervous system and showed its relation to CDV infection to further clarify the pathology of disease. Histopathological, immunohistochemical and immunofluorescent analyses were done using formalin-fixed paraffin-embedded tissues of CDV-infected dogs. Dual staining of nectin-4 and CDV antigen or nectin-4 and brain cell markers was performed. Nectin-4 was detected in ependymal cells, epithelia of choroid plexus, meningeal cells, neurons, granular cells, and Purkinje’s cells. CDV antigens were detected in these nectin-4-positive cells, further suggesting contribution of nectin-4 for the CDV neurovirulence. On the other hand, astrocytes did not express nectin-4, although they were frequently infected with CDV. Since astrocytes are negative for SLAM expression, they must express an unidentified CDV receptor, which also contributes to CDV neurovirulence. Nature Publishing Group UK 2017-03-23 /pmc/articles/PMC5428276/ /pubmed/28336928 http://dx.doi.org/10.1038/s41598-017-00375-6 Text en © The Author(s) 2017 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Pratakpiriya, Watanyoo
Ping Teh, Angeline Ping
Radtanakatikanon, Araya
Pirarat, Nopadon
Thi Lan, Nguyen
Takeda, Makoto
Techangamsuwan, Somporn
Yamaguchi, Ryoji
Expression of canine distemper virus receptor nectin-4 in the central nervous system of dogs
title Expression of canine distemper virus receptor nectin-4 in the central nervous system of dogs
title_full Expression of canine distemper virus receptor nectin-4 in the central nervous system of dogs
title_fullStr Expression of canine distemper virus receptor nectin-4 in the central nervous system of dogs
title_full_unstemmed Expression of canine distemper virus receptor nectin-4 in the central nervous system of dogs
title_short Expression of canine distemper virus receptor nectin-4 in the central nervous system of dogs
title_sort expression of canine distemper virus receptor nectin-4 in the central nervous system of dogs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428276/
https://www.ncbi.nlm.nih.gov/pubmed/28336928
http://dx.doi.org/10.1038/s41598-017-00375-6
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