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Systematic analysis of protein identity between Zika virus and other arthropod-borne viruses
OBJECTIVE: To analyse the proportions of protein identity between Zika virus and dengue, Japanese encephalitis, yellow fever, West Nile and chikungunya viruses as well as polymorphism between different Zika virus strains. METHODS: We used published protein sequences for the Zika virus and obtained p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
World Health Organization
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487971/ https://www.ncbi.nlm.nih.gov/pubmed/28670016 http://dx.doi.org/10.2471/BLT.16.182105 |
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author | Chang, Hsiao-Han Huber, Roland G Bond, Peter J Grad, Yonatan H Camerini, David Maurer-Stroh, Sebastian Lipsitch, Marc |
author_facet | Chang, Hsiao-Han Huber, Roland G Bond, Peter J Grad, Yonatan H Camerini, David Maurer-Stroh, Sebastian Lipsitch, Marc |
author_sort | Chang, Hsiao-Han |
collection | PubMed |
description | OBJECTIVE: To analyse the proportions of protein identity between Zika virus and dengue, Japanese encephalitis, yellow fever, West Nile and chikungunya viruses as well as polymorphism between different Zika virus strains. METHODS: We used published protein sequences for the Zika virus and obtained protein sequences for the other viruses from the National Center for Biotechnology Information (NCBI) protein database or the NCBI virus variation resource. We used BLASTP to find regions of identity between viruses. We quantified the identity between the Zika virus and each of the other viruses, as well as within-Zika virus polymorphism for all amino acid k-mers across the proteome, with k ranging from 6 to 100. We assessed accessibility of protein fragments by calculating the solvent accessible surface area for the envelope and nonstructural-1 (NS1) proteins. FINDINGS: In total, we identified 294 Zika virus protein fragments with both low proportion of identity with other viruses and low levels of polymorphisms among Zika virus strains. The list includes protein fragments from all Zika virus proteins, except NS3. NS4A has the highest number (190 k-mers) of protein fragments on the list. CONCLUSION: We provide a candidate list of protein fragments that could be used when developing a sensitive and specific serological test to detect previous Zika virus infections. |
format | Online Article Text |
id | pubmed-5487971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | World Health Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-54879712017-07-01 Systematic analysis of protein identity between Zika virus and other arthropod-borne viruses Chang, Hsiao-Han Huber, Roland G Bond, Peter J Grad, Yonatan H Camerini, David Maurer-Stroh, Sebastian Lipsitch, Marc Bull World Health Organ Research OBJECTIVE: To analyse the proportions of protein identity between Zika virus and dengue, Japanese encephalitis, yellow fever, West Nile and chikungunya viruses as well as polymorphism between different Zika virus strains. METHODS: We used published protein sequences for the Zika virus and obtained protein sequences for the other viruses from the National Center for Biotechnology Information (NCBI) protein database or the NCBI virus variation resource. We used BLASTP to find regions of identity between viruses. We quantified the identity between the Zika virus and each of the other viruses, as well as within-Zika virus polymorphism for all amino acid k-mers across the proteome, with k ranging from 6 to 100. We assessed accessibility of protein fragments by calculating the solvent accessible surface area for the envelope and nonstructural-1 (NS1) proteins. FINDINGS: In total, we identified 294 Zika virus protein fragments with both low proportion of identity with other viruses and low levels of polymorphisms among Zika virus strains. The list includes protein fragments from all Zika virus proteins, except NS3. NS4A has the highest number (190 k-mers) of protein fragments on the list. CONCLUSION: We provide a candidate list of protein fragments that could be used when developing a sensitive and specific serological test to detect previous Zika virus infections. World Health Organization 2017-07-01 2016-07-18 /pmc/articles/PMC5487971/ /pubmed/28670016 http://dx.doi.org/10.2471/BLT.16.182105 Text en (c) 2017 The authors; licensee World Health Organization. This is an open access article distributed under the terms of the Creative Commons Attribution IGO License (http://creativecommons.org/licenses/by/3.0/igo/legalcode), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. In any reproduction of this article there should not be any suggestion that WHO or this article endorse any specific organization or products. The use of the WHO logo is not permitted. This notice should be preserved along with the article's original URL. |
spellingShingle | Research Chang, Hsiao-Han Huber, Roland G Bond, Peter J Grad, Yonatan H Camerini, David Maurer-Stroh, Sebastian Lipsitch, Marc Systematic analysis of protein identity between Zika virus and other arthropod-borne viruses |
title | Systematic analysis of protein identity between Zika virus and other arthropod-borne viruses |
title_full | Systematic analysis of protein identity between Zika virus and other arthropod-borne viruses |
title_fullStr | Systematic analysis of protein identity between Zika virus and other arthropod-borne viruses |
title_full_unstemmed | Systematic analysis of protein identity between Zika virus and other arthropod-borne viruses |
title_short | Systematic analysis of protein identity between Zika virus and other arthropod-borne viruses |
title_sort | systematic analysis of protein identity between zika virus and other arthropod-borne viruses |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487971/ https://www.ncbi.nlm.nih.gov/pubmed/28670016 http://dx.doi.org/10.2471/BLT.16.182105 |
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