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Structure of infective Getah virus at 2.8 Å resolution determined by cryo-electron microscopy
Getah virus (GETV), a member of the genus alphavirus, is a mosquito-borne pathogen that can cause pyrexia and reproductive losses in animals. Although antibodies to GETV have been found in over 10% of healthy people, there are no reports of clinical symptoms associated with GETV. The biological and...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832435/ https://www.ncbi.nlm.nih.gov/pubmed/35149682 http://dx.doi.org/10.1038/s41421-022-00374-6 |
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author | Wang, Aojie Zhou, Feng Liu, Congcong Gao, Dongsheng Qi, Ruxi Yin, Yiheng Liu, Sheng Gao, Yuanzhu Fu, Lutang Xia, Yinhe Xu, Yawei Wang, Chuanqing Liu, Zheng |
author_facet | Wang, Aojie Zhou, Feng Liu, Congcong Gao, Dongsheng Qi, Ruxi Yin, Yiheng Liu, Sheng Gao, Yuanzhu Fu, Lutang Xia, Yinhe Xu, Yawei Wang, Chuanqing Liu, Zheng |
author_sort | Wang, Aojie |
collection | PubMed |
description | Getah virus (GETV), a member of the genus alphavirus, is a mosquito-borne pathogen that can cause pyrexia and reproductive losses in animals. Although antibodies to GETV have been found in over 10% of healthy people, there are no reports of clinical symptoms associated with GETV. The biological and pathological properties of GETV are largely unknown and antiviral or vaccine treatments against GETV are still unavailable due to a lack of knowledge of the structure of the GETV virion. Here, we present the structure of infective GETV at a resolution of 2.8 Å with the atomic models of the capsid protein and the envelope glycoproteins E1 and E2. We have identified numerous glycosylation and S-acylation sites in E1 and E2. The surface-exposed glycans indicate a possible impact on viral immune evasion and host cell invasion. The S-acylation sites might be involved in stabilizing the transmembrane assembly of E1 and E2. In addition, a cholesterol and a phospholipid molecule are observed in a transmembrane hydrophobic pocket, together with two more cholesterols surrounding the pocket. The cholesterol and phospholipid stabilize the hydrophobic pocket in the viral envelope membrane. The structural information will assist structure-based antiviral and vaccine screening, design, and optimization. |
format | Online Article Text |
id | pubmed-8832435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-88324352022-02-18 Structure of infective Getah virus at 2.8 Å resolution determined by cryo-electron microscopy Wang, Aojie Zhou, Feng Liu, Congcong Gao, Dongsheng Qi, Ruxi Yin, Yiheng Liu, Sheng Gao, Yuanzhu Fu, Lutang Xia, Yinhe Xu, Yawei Wang, Chuanqing Liu, Zheng Cell Discov Article Getah virus (GETV), a member of the genus alphavirus, is a mosquito-borne pathogen that can cause pyrexia and reproductive losses in animals. Although antibodies to GETV have been found in over 10% of healthy people, there are no reports of clinical symptoms associated with GETV. The biological and pathological properties of GETV are largely unknown and antiviral or vaccine treatments against GETV are still unavailable due to a lack of knowledge of the structure of the GETV virion. Here, we present the structure of infective GETV at a resolution of 2.8 Å with the atomic models of the capsid protein and the envelope glycoproteins E1 and E2. We have identified numerous glycosylation and S-acylation sites in E1 and E2. The surface-exposed glycans indicate a possible impact on viral immune evasion and host cell invasion. The S-acylation sites might be involved in stabilizing the transmembrane assembly of E1 and E2. In addition, a cholesterol and a phospholipid molecule are observed in a transmembrane hydrophobic pocket, together with two more cholesterols surrounding the pocket. The cholesterol and phospholipid stabilize the hydrophobic pocket in the viral envelope membrane. The structural information will assist structure-based antiviral and vaccine screening, design, and optimization. Springer Singapore 2022-02-11 /pmc/articles/PMC8832435/ /pubmed/35149682 http://dx.doi.org/10.1038/s41421-022-00374-6 Text en © The Author(s) 2022 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 Wang, Aojie Zhou, Feng Liu, Congcong Gao, Dongsheng Qi, Ruxi Yin, Yiheng Liu, Sheng Gao, Yuanzhu Fu, Lutang Xia, Yinhe Xu, Yawei Wang, Chuanqing Liu, Zheng Structure of infective Getah virus at 2.8 Å resolution determined by cryo-electron microscopy |
title | Structure of infective Getah virus at 2.8 Å resolution determined by cryo-electron microscopy |
title_full | Structure of infective Getah virus at 2.8 Å resolution determined by cryo-electron microscopy |
title_fullStr | Structure of infective Getah virus at 2.8 Å resolution determined by cryo-electron microscopy |
title_full_unstemmed | Structure of infective Getah virus at 2.8 Å resolution determined by cryo-electron microscopy |
title_short | Structure of infective Getah virus at 2.8 Å resolution determined by cryo-electron microscopy |
title_sort | structure of infective getah virus at 2.8 å resolution determined by cryo-electron microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832435/ https://www.ncbi.nlm.nih.gov/pubmed/35149682 http://dx.doi.org/10.1038/s41421-022-00374-6 |
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