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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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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. |
format | Online Article Text |
id | pubmed-9491601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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