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The Optimal Concentration of Formaldehyde is Key to Stabilizing the Pre-Fusion Conformation of Respiratory Syncytial Virus Fusion Protein

Background: To date, there is no licensed vaccine available to prevent respiratory syncytial virus (RSV) infection. The valuable pre-fusion conformation of the fusion protein (pre-F) is prone to lose high neutralizing antigenic sites. The goals of this study were to stabilize pre-F protein by fixati...

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Autores principales: Zhang, Wei, Zhang, Lu-Jing, Zhan, Lu-Ting, Zhao, Min, Wu, Guang-Hua, Si, Jun-Yu, Chen, Li, Lin, Xue, Sun, Yong-Peng, Lin, Min, Yu, Chao, Fang, Mu-Jin, Wang, Ying-Bin, Zheng, Zi-Zheng, Xia, Ning-Shao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669674/
https://www.ncbi.nlm.nih.gov/pubmed/31288455
http://dx.doi.org/10.3390/v11070628
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author Zhang, Wei
Zhang, Lu-Jing
Zhan, Lu-Ting
Zhao, Min
Wu, Guang-Hua
Si, Jun-Yu
Chen, Li
Lin, Xue
Sun, Yong-Peng
Lin, Min
Yu, Chao
Fang, Mu-Jin
Wang, Ying-Bin
Zheng, Zi-Zheng
Xia, Ning-Shao
author_facet Zhang, Wei
Zhang, Lu-Jing
Zhan, Lu-Ting
Zhao, Min
Wu, Guang-Hua
Si, Jun-Yu
Chen, Li
Lin, Xue
Sun, Yong-Peng
Lin, Min
Yu, Chao
Fang, Mu-Jin
Wang, Ying-Bin
Zheng, Zi-Zheng
Xia, Ning-Shao
author_sort Zhang, Wei
collection PubMed
description Background: To date, there is no licensed vaccine available to prevent respiratory syncytial virus (RSV) infection. The valuable pre-fusion conformation of the fusion protein (pre-F) is prone to lose high neutralizing antigenic sites. The goals of this study were to stabilize pre-F protein by fixatives and try to find the possibility of developing an inactivated RSV vaccine. Methods: The screen of the optimal fixative condition was performed with flow cytometry. BALB/c mice were immunized intramuscularly with different immunogens. The serum neutralizing antibody titers of immunized mice were determined by neutralization assay. The protection and safety of these immunogens were assessed. Results: Fixation in an optimal concentration of formaldehyde (0.0244%–0.0977%) or paraformaldehyde (0.0625%–1%) was able to stabilize pre-F. Additionally, BALB/c mice inoculated with optimally stabilized pre-F protein (opti-fixed) induced a higher anti-RSV neutralization (9.7 log(2), mean value of dilution rate) than those inoculated with unstable (unfixed, 8.91 log(2), p < 0.01) or excessively fixed (exce-fixed, 7.28 log(2), p < 0.01) pre-F protein. Furthermore, the opti-fixed immunogen did not induce enhanced RSV disease. Conclusions: Only the proper concentration of fixatives could stabilize pre-F and the optimal formaldehyde condition provides a potential reference for development of an inactivated RSV vaccine.
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spelling pubmed-66696742019-08-08 The Optimal Concentration of Formaldehyde is Key to Stabilizing the Pre-Fusion Conformation of Respiratory Syncytial Virus Fusion Protein Zhang, Wei Zhang, Lu-Jing Zhan, Lu-Ting Zhao, Min Wu, Guang-Hua Si, Jun-Yu Chen, Li Lin, Xue Sun, Yong-Peng Lin, Min Yu, Chao Fang, Mu-Jin Wang, Ying-Bin Zheng, Zi-Zheng Xia, Ning-Shao Viruses Article Background: To date, there is no licensed vaccine available to prevent respiratory syncytial virus (RSV) infection. The valuable pre-fusion conformation of the fusion protein (pre-F) is prone to lose high neutralizing antigenic sites. The goals of this study were to stabilize pre-F protein by fixatives and try to find the possibility of developing an inactivated RSV vaccine. Methods: The screen of the optimal fixative condition was performed with flow cytometry. BALB/c mice were immunized intramuscularly with different immunogens. The serum neutralizing antibody titers of immunized mice were determined by neutralization assay. The protection and safety of these immunogens were assessed. Results: Fixation in an optimal concentration of formaldehyde (0.0244%–0.0977%) or paraformaldehyde (0.0625%–1%) was able to stabilize pre-F. Additionally, BALB/c mice inoculated with optimally stabilized pre-F protein (opti-fixed) induced a higher anti-RSV neutralization (9.7 log(2), mean value of dilution rate) than those inoculated with unstable (unfixed, 8.91 log(2), p < 0.01) or excessively fixed (exce-fixed, 7.28 log(2), p < 0.01) pre-F protein. Furthermore, the opti-fixed immunogen did not induce enhanced RSV disease. Conclusions: Only the proper concentration of fixatives could stabilize pre-F and the optimal formaldehyde condition provides a potential reference for development of an inactivated RSV vaccine. MDPI 2019-07-08 /pmc/articles/PMC6669674/ /pubmed/31288455 http://dx.doi.org/10.3390/v11070628 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhang, Wei
Zhang, Lu-Jing
Zhan, Lu-Ting
Zhao, Min
Wu, Guang-Hua
Si, Jun-Yu
Chen, Li
Lin, Xue
Sun, Yong-Peng
Lin, Min
Yu, Chao
Fang, Mu-Jin
Wang, Ying-Bin
Zheng, Zi-Zheng
Xia, Ning-Shao
The Optimal Concentration of Formaldehyde is Key to Stabilizing the Pre-Fusion Conformation of Respiratory Syncytial Virus Fusion Protein
title The Optimal Concentration of Formaldehyde is Key to Stabilizing the Pre-Fusion Conformation of Respiratory Syncytial Virus Fusion Protein
title_full The Optimal Concentration of Formaldehyde is Key to Stabilizing the Pre-Fusion Conformation of Respiratory Syncytial Virus Fusion Protein
title_fullStr The Optimal Concentration of Formaldehyde is Key to Stabilizing the Pre-Fusion Conformation of Respiratory Syncytial Virus Fusion Protein
title_full_unstemmed The Optimal Concentration of Formaldehyde is Key to Stabilizing the Pre-Fusion Conformation of Respiratory Syncytial Virus Fusion Protein
title_short The Optimal Concentration of Formaldehyde is Key to Stabilizing the Pre-Fusion Conformation of Respiratory Syncytial Virus Fusion Protein
title_sort optimal concentration of formaldehyde is key to stabilizing the pre-fusion conformation of respiratory syncytial virus fusion protein
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669674/
https://www.ncbi.nlm.nih.gov/pubmed/31288455
http://dx.doi.org/10.3390/v11070628
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