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Establishment of an Alphavirus-Specific Neutralization Assay to Distinguish Infections with Different Members of the Semliki Forest Complex

Background: Alphaviruses are transmitted by arthropod vectors and can be found worldwide. Alphaviruses of the Semliki Forest complex such as chikungunya virus (CHIKV), Mayaro virus (MAYV) or Ross River virus (RRV) cause acute febrile illness and long-lasting arthralgia in humans, which cannot be cli...

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Autores principales: Henss, Lisa, Yue, Constanze, Kandler, Joshua, Faddy, Helen M., Simmons, Graham, Panning, Marcus, Lewis-Ximenez, Lia Laura, Baylis, Sally A., Schnierle, Barbara S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356848/
https://www.ncbi.nlm.nih.gov/pubmed/30669393
http://dx.doi.org/10.3390/v11010082
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author Henss, Lisa
Yue, Constanze
Kandler, Joshua
Faddy, Helen M.
Simmons, Graham
Panning, Marcus
Lewis-Ximenez, Lia Laura
Baylis, Sally A.
Schnierle, Barbara S.
author_facet Henss, Lisa
Yue, Constanze
Kandler, Joshua
Faddy, Helen M.
Simmons, Graham
Panning, Marcus
Lewis-Ximenez, Lia Laura
Baylis, Sally A.
Schnierle, Barbara S.
author_sort Henss, Lisa
collection PubMed
description Background: Alphaviruses are transmitted by arthropod vectors and can be found worldwide. Alphaviruses of the Semliki Forest complex such as chikungunya virus (CHIKV), Mayaro virus (MAYV) or Ross River virus (RRV) cause acute febrile illness and long-lasting arthralgia in humans, which cannot be clinically discriminated from a dengue virus or Zika virus infection. Alphaviruses utilize a diverse array of mosquito vectors for transmission and spread. For instance, adaptation of CHIKV to transmission by Aedes albopictus has increased its spread and resulted in large outbreaks in the Indian Ocean islands. For many alphaviruses commercial diagnostic tests are not available or show cross-reactivity among alphaviruses. Climate change and globalization will increase the spread of alphaviruses and monitoring of infections is necessary and requires virus-specific methods. Method: We established an alphavirus neutralization assay in a 384-well format by using pseudotyped lentiviral vectors. Results: MAYV-specific reactivity could be discriminated from CHIKV reactivity. Human plasma from blood donors infected with RRV could be clearly identified and did not cross-react with other alphaviruses. Conclusion: This safe and easy to use multiplex assay allows the discrimination of alphavirus-specific reactivity within a single assay and has potential for epidemiological surveillance. It might also be useful for the development of a pan-alphavirus vaccine.
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spelling pubmed-63568482019-02-05 Establishment of an Alphavirus-Specific Neutralization Assay to Distinguish Infections with Different Members of the Semliki Forest Complex Henss, Lisa Yue, Constanze Kandler, Joshua Faddy, Helen M. Simmons, Graham Panning, Marcus Lewis-Ximenez, Lia Laura Baylis, Sally A. Schnierle, Barbara S. Viruses Article Background: Alphaviruses are transmitted by arthropod vectors and can be found worldwide. Alphaviruses of the Semliki Forest complex such as chikungunya virus (CHIKV), Mayaro virus (MAYV) or Ross River virus (RRV) cause acute febrile illness and long-lasting arthralgia in humans, which cannot be clinically discriminated from a dengue virus or Zika virus infection. Alphaviruses utilize a diverse array of mosquito vectors for transmission and spread. For instance, adaptation of CHIKV to transmission by Aedes albopictus has increased its spread and resulted in large outbreaks in the Indian Ocean islands. For many alphaviruses commercial diagnostic tests are not available or show cross-reactivity among alphaviruses. Climate change and globalization will increase the spread of alphaviruses and monitoring of infections is necessary and requires virus-specific methods. Method: We established an alphavirus neutralization assay in a 384-well format by using pseudotyped lentiviral vectors. Results: MAYV-specific reactivity could be discriminated from CHIKV reactivity. Human plasma from blood donors infected with RRV could be clearly identified and did not cross-react with other alphaviruses. Conclusion: This safe and easy to use multiplex assay allows the discrimination of alphavirus-specific reactivity within a single assay and has potential for epidemiological surveillance. It might also be useful for the development of a pan-alphavirus vaccine. MDPI 2019-01-18 /pmc/articles/PMC6356848/ /pubmed/30669393 http://dx.doi.org/10.3390/v11010082 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
Henss, Lisa
Yue, Constanze
Kandler, Joshua
Faddy, Helen M.
Simmons, Graham
Panning, Marcus
Lewis-Ximenez, Lia Laura
Baylis, Sally A.
Schnierle, Barbara S.
Establishment of an Alphavirus-Specific Neutralization Assay to Distinguish Infections with Different Members of the Semliki Forest Complex
title Establishment of an Alphavirus-Specific Neutralization Assay to Distinguish Infections with Different Members of the Semliki Forest Complex
title_full Establishment of an Alphavirus-Specific Neutralization Assay to Distinguish Infections with Different Members of the Semliki Forest Complex
title_fullStr Establishment of an Alphavirus-Specific Neutralization Assay to Distinguish Infections with Different Members of the Semliki Forest Complex
title_full_unstemmed Establishment of an Alphavirus-Specific Neutralization Assay to Distinguish Infections with Different Members of the Semliki Forest Complex
title_short Establishment of an Alphavirus-Specific Neutralization Assay to Distinguish Infections with Different Members of the Semliki Forest Complex
title_sort establishment of an alphavirus-specific neutralization assay to distinguish infections with different members of the semliki forest complex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356848/
https://www.ncbi.nlm.nih.gov/pubmed/30669393
http://dx.doi.org/10.3390/v11010082
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