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Myeloid-associated differentiation marker is an essential host factor for human parechovirus PeV-A3 entry
Human parechovirus (PeV-A) is an RNA virus that belongs to the family Picornaviridae and it is currently classified into 19 genotypes. PeV-As usually cause mild illness in children and adults. Among the genotypes, PeV-A3 can cause severe diseases in neonates and young infants, resulting in neurologi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10066301/ https://www.ncbi.nlm.nih.gov/pubmed/37002207 http://dx.doi.org/10.1038/s41467-023-37399-8 |
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author | Watanabe, Kanako Oka, Tomoichiro Takagi, Hirotaka Anisimov, Sergei Yamashita, Shun-ichi Katsuragi, Yoshinori Takahashi, Masahiko Higuchi, Masaya Kanki, Tomotake Saitoh, Akihiko Fujii, Masahiro |
author_facet | Watanabe, Kanako Oka, Tomoichiro Takagi, Hirotaka Anisimov, Sergei Yamashita, Shun-ichi Katsuragi, Yoshinori Takahashi, Masahiko Higuchi, Masaya Kanki, Tomotake Saitoh, Akihiko Fujii, Masahiro |
author_sort | Watanabe, Kanako |
collection | PubMed |
description | Human parechovirus (PeV-A) is an RNA virus that belongs to the family Picornaviridae and it is currently classified into 19 genotypes. PeV-As usually cause mild illness in children and adults. Among the genotypes, PeV-A3 can cause severe diseases in neonates and young infants, resulting in neurological sequelae and death. In this study, we identify the human myeloid-associated differentiation marker (MYADM) as an essential host factor for the entry of six PeV-As (PeV-A1 to PeV-A6), including PeV-A3. The infection of six PeV-As (PeV-A1 to PeV-A6) to human cells is abolished by knocking out the expression of MYADM. Hamster BHK-21 cells are resistant to PeV-A infection, but the expression of human MYADM in BHK-21 confers PeV-A infection and viral production. Furthermore, VP0 capsid protein of PeV-A3 interacts with one extracellular domain of human MYADM on the cell membrane of BHK-21. The identification of MYADM as an essential entry factor for PeV-As infection is expected to advance our understanding of the pathogenesis of PeV-As. |
format | Online Article Text |
id | pubmed-10066301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100663012023-04-02 Myeloid-associated differentiation marker is an essential host factor for human parechovirus PeV-A3 entry Watanabe, Kanako Oka, Tomoichiro Takagi, Hirotaka Anisimov, Sergei Yamashita, Shun-ichi Katsuragi, Yoshinori Takahashi, Masahiko Higuchi, Masaya Kanki, Tomotake Saitoh, Akihiko Fujii, Masahiro Nat Commun Article Human parechovirus (PeV-A) is an RNA virus that belongs to the family Picornaviridae and it is currently classified into 19 genotypes. PeV-As usually cause mild illness in children and adults. Among the genotypes, PeV-A3 can cause severe diseases in neonates and young infants, resulting in neurological sequelae and death. In this study, we identify the human myeloid-associated differentiation marker (MYADM) as an essential host factor for the entry of six PeV-As (PeV-A1 to PeV-A6), including PeV-A3. The infection of six PeV-As (PeV-A1 to PeV-A6) to human cells is abolished by knocking out the expression of MYADM. Hamster BHK-21 cells are resistant to PeV-A infection, but the expression of human MYADM in BHK-21 confers PeV-A infection and viral production. Furthermore, VP0 capsid protein of PeV-A3 interacts with one extracellular domain of human MYADM on the cell membrane of BHK-21. The identification of MYADM as an essential entry factor for PeV-As infection is expected to advance our understanding of the pathogenesis of PeV-As. Nature Publishing Group UK 2023-03-31 /pmc/articles/PMC10066301/ /pubmed/37002207 http://dx.doi.org/10.1038/s41467-023-37399-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Watanabe, Kanako Oka, Tomoichiro Takagi, Hirotaka Anisimov, Sergei Yamashita, Shun-ichi Katsuragi, Yoshinori Takahashi, Masahiko Higuchi, Masaya Kanki, Tomotake Saitoh, Akihiko Fujii, Masahiro Myeloid-associated differentiation marker is an essential host factor for human parechovirus PeV-A3 entry |
title | Myeloid-associated differentiation marker is an essential host factor for human parechovirus PeV-A3 entry |
title_full | Myeloid-associated differentiation marker is an essential host factor for human parechovirus PeV-A3 entry |
title_fullStr | Myeloid-associated differentiation marker is an essential host factor for human parechovirus PeV-A3 entry |
title_full_unstemmed | Myeloid-associated differentiation marker is an essential host factor for human parechovirus PeV-A3 entry |
title_short | Myeloid-associated differentiation marker is an essential host factor for human parechovirus PeV-A3 entry |
title_sort | myeloid-associated differentiation marker is an essential host factor for human parechovirus pev-a3 entry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10066301/ https://www.ncbi.nlm.nih.gov/pubmed/37002207 http://dx.doi.org/10.1038/s41467-023-37399-8 |
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