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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2022
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.
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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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