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Extracellular vesicles derived from PPRV-infected cells enhance signaling lymphocyte activation molecular (SLAM) receptor expression and facilitate virus infection

Peste des petits ruminants virus (PPRV) is an important pathogen that seriously influences the productivity of small ruminants worldwide. PPRV is lymphotropic in nature and SLAM was identified as the primary receptor for PPRV and other Morbilliviruses. Many viruses have been demonstrated to engage e...

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Autores principales: Chen, Yan, Wang, Ting, Yang, Yang, Fang, Yuan, Zhao, Bao, Zeng, Wei, Lv, Daiyue, Zhang, Leyan, Zhang, Yanming, Xue, Qinghong, Chen, Xiwen, Wang, Jingyu, Qi, Xuefeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491601/
https://www.ncbi.nlm.nih.gov/pubmed/36084159
http://dx.doi.org/10.1371/journal.ppat.1010759
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author Chen, Yan
Wang, Ting
Yang, Yang
Fang, Yuan
Zhao, Bao
Zeng, Wei
Lv, Daiyue
Zhang, Leyan
Zhang, Yanming
Xue, Qinghong
Chen, Xiwen
Wang, Jingyu
Qi, Xuefeng
author_facet Chen, Yan
Wang, Ting
Yang, Yang
Fang, Yuan
Zhao, Bao
Zeng, Wei
Lv, Daiyue
Zhang, Leyan
Zhang, Yanming
Xue, Qinghong
Chen, Xiwen
Wang, Jingyu
Qi, Xuefeng
author_sort Chen, Yan
collection PubMed
description Peste des petits ruminants virus (PPRV) is an important pathogen that seriously influences the productivity of small ruminants worldwide. PPRV is lymphotropic in nature and SLAM was identified as the primary receptor for PPRV and other Morbilliviruses. Many viruses have been demonstrated to engage extracellular vesicles (EVs) to facilitate their replication and pathogenesis. Here, we provide evidence that PPRV infection significantly induced the secretion levels of EVs from goat PBMC, and that PPRV-H protein carried in EVs can enhance SLAM receptor expression in the recipient cells via suppressing miR-218, a negative miRNA directly targeting SLAM gene. Importantly, EVs-mediated increased SLAM expression enhances PPRV infectivity as well as the expression of various cytokines related to SLAM signaling pathway in the recipient cells. Moreover, our data reveal that PPRV associate EVs rapidly entry into the recipient cells mainly through macropinocytosis pathway and cooperated with caveolin- and clathrin-mediated endocytosis. Taken together, our findings identify a new strategy by PPRV to enhance virus infection and escape innate immunity by engaging EVs pathway.
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spelling pubmed-94916012022-09-22 Extracellular vesicles derived from PPRV-infected cells enhance signaling lymphocyte activation molecular (SLAM) receptor expression and facilitate virus infection Chen, Yan Wang, Ting Yang, Yang Fang, Yuan Zhao, Bao Zeng, Wei Lv, Daiyue Zhang, Leyan Zhang, Yanming Xue, Qinghong Chen, Xiwen Wang, Jingyu Qi, Xuefeng PLoS Pathog Research Article Peste des petits ruminants virus (PPRV) is an important pathogen that seriously influences the productivity of small ruminants worldwide. PPRV is lymphotropic in nature and SLAM was identified as the primary receptor for PPRV and other Morbilliviruses. Many viruses have been demonstrated to engage extracellular vesicles (EVs) to facilitate their replication and pathogenesis. Here, we provide evidence that PPRV infection significantly induced the secretion levels of EVs from goat PBMC, and that PPRV-H protein carried in EVs can enhance SLAM receptor expression in the recipient cells via suppressing miR-218, a negative miRNA directly targeting SLAM gene. Importantly, EVs-mediated increased SLAM expression enhances PPRV infectivity as well as the expression of various cytokines related to SLAM signaling pathway in the recipient cells. Moreover, our data reveal that PPRV associate EVs rapidly entry into the recipient cells mainly through macropinocytosis pathway and cooperated with caveolin- and clathrin-mediated endocytosis. Taken together, our findings identify a new strategy by PPRV to enhance virus infection and escape innate immunity by engaging EVs pathway. Public Library of Science 2022-09-09 /pmc/articles/PMC9491601/ /pubmed/36084159 http://dx.doi.org/10.1371/journal.ppat.1010759 Text en © 2022 Chen et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Chen, Yan
Wang, Ting
Yang, Yang
Fang, Yuan
Zhao, Bao
Zeng, Wei
Lv, Daiyue
Zhang, Leyan
Zhang, Yanming
Xue, Qinghong
Chen, Xiwen
Wang, Jingyu
Qi, Xuefeng
Extracellular vesicles derived from PPRV-infected cells enhance signaling lymphocyte activation molecular (SLAM) receptor expression and facilitate virus infection
title Extracellular vesicles derived from PPRV-infected cells enhance signaling lymphocyte activation molecular (SLAM) receptor expression and facilitate virus infection
title_full Extracellular vesicles derived from PPRV-infected cells enhance signaling lymphocyte activation molecular (SLAM) receptor expression and facilitate virus infection
title_fullStr Extracellular vesicles derived from PPRV-infected cells enhance signaling lymphocyte activation molecular (SLAM) receptor expression and facilitate virus infection
title_full_unstemmed Extracellular vesicles derived from PPRV-infected cells enhance signaling lymphocyte activation molecular (SLAM) receptor expression and facilitate virus infection
title_short Extracellular vesicles derived from PPRV-infected cells enhance signaling lymphocyte activation molecular (SLAM) receptor expression and facilitate virus infection
title_sort extracellular vesicles derived from pprv-infected cells enhance signaling lymphocyte activation molecular (slam) receptor expression and facilitate virus infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491601/
https://www.ncbi.nlm.nih.gov/pubmed/36084159
http://dx.doi.org/10.1371/journal.ppat.1010759
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