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Inhibition of Ebola Virus by a Molecularly Engineered Banana Lectin

Ebolaviruses cause an often rapidly fatal syndrome known as Ebola virus disease (EVD), with average case fatality rates of ~50%. There is no licensed vaccine or treatment for EVD, underscoring the urgent need to develop new anti-ebolavirus agents, especially in the face of an ongoing outbreak in the...

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Autores principales: Covés-Datson, Evelyn M., Dyall, Julie, DeWald, Lisa Evans, King, Steven R., Dube, Derek, Legendre, Maureen, Nelson, Elizabeth, Drews, Kelly C., Gross, Robin, Gerhardt, Dawn M., Torzewski, Lisa, Postnikova, Elena, Liang, Janie Y., Ban, Bhupal, Shetty, Jagathpala, Hensley, Lisa E., Jahrling, Peter B., Olinger, Gene G., White, Judith M., Markovitz, David M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687191/
https://www.ncbi.nlm.nih.gov/pubmed/31356611
http://dx.doi.org/10.1371/journal.pntd.0007595
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author Covés-Datson, Evelyn M.
Dyall, Julie
DeWald, Lisa Evans
King, Steven R.
Dube, Derek
Legendre, Maureen
Nelson, Elizabeth
Drews, Kelly C.
Gross, Robin
Gerhardt, Dawn M.
Torzewski, Lisa
Postnikova, Elena
Liang, Janie Y.
Ban, Bhupal
Shetty, Jagathpala
Hensley, Lisa E.
Jahrling, Peter B.
Olinger, Gene G.
White, Judith M.
Markovitz, David M.
author_facet Covés-Datson, Evelyn M.
Dyall, Julie
DeWald, Lisa Evans
King, Steven R.
Dube, Derek
Legendre, Maureen
Nelson, Elizabeth
Drews, Kelly C.
Gross, Robin
Gerhardt, Dawn M.
Torzewski, Lisa
Postnikova, Elena
Liang, Janie Y.
Ban, Bhupal
Shetty, Jagathpala
Hensley, Lisa E.
Jahrling, Peter B.
Olinger, Gene G.
White, Judith M.
Markovitz, David M.
author_sort Covés-Datson, Evelyn M.
collection PubMed
description Ebolaviruses cause an often rapidly fatal syndrome known as Ebola virus disease (EVD), with average case fatality rates of ~50%. There is no licensed vaccine or treatment for EVD, underscoring the urgent need to develop new anti-ebolavirus agents, especially in the face of an ongoing outbreak in the Democratic Republic of the Congo and the largest ever outbreak in Western Africa in 2013–2016. Lectins have been investigated as potential antiviral agents as they bind glycans present on viral surface glycoproteins, but clinical use of them has been slowed by concerns regarding their mitogenicity, i.e. ability to cause immune cell proliferation. We previously engineered a banana lectin (BanLec), a carbohydrate-binding protein, such that it retained antiviral activity but lost mitogenicity by mutating a single amino acid, yielding H84T BanLec (H84T). H84T shows activity against viruses containing high-mannose N-glycans, including influenza A and B, HIV-1 and -2, and hepatitis C virus. Since ebolavirus surface glycoproteins also contain many high-mannose N-glycans, we assessed whether H84T could inhibit ebolavirus replication. H84T inhibited Ebola virus (EBOV) replication in cell cultures. In cells, H84T inhibited both virus-like particle (VLP) entry and transcription/replication of the EBOV mini-genome at high micromolar concentrations, while inhibiting infection by transcription- and replication-competent VLPs, which measures the full viral life cycle, in the low micromolar range. H84T did not inhibit assembly, budding, or release of VLPs. These findings suggest that H84T may exert its anti-ebolavirus effect(s) by blocking both entry and transcription/replication. In a mouse model, H84T partially (maximally, ~50–80%) protected mice from an otherwise lethal mouse-adapted EBOV infection. Interestingly, a single dose of H84T pre-exposure to EBOV protected ~80% of mice. Thus, H84T shows promise as a new anti-ebolavirus agent with potential to be used in combination with vaccination or other agents in a prophylactic or therapeutic regimen.
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spelling pubmed-66871912019-08-15 Inhibition of Ebola Virus by a Molecularly Engineered Banana Lectin Covés-Datson, Evelyn M. Dyall, Julie DeWald, Lisa Evans King, Steven R. Dube, Derek Legendre, Maureen Nelson, Elizabeth Drews, Kelly C. Gross, Robin Gerhardt, Dawn M. Torzewski, Lisa Postnikova, Elena Liang, Janie Y. Ban, Bhupal Shetty, Jagathpala Hensley, Lisa E. Jahrling, Peter B. Olinger, Gene G. White, Judith M. Markovitz, David M. PLoS Negl Trop Dis Research Article Ebolaviruses cause an often rapidly fatal syndrome known as Ebola virus disease (EVD), with average case fatality rates of ~50%. There is no licensed vaccine or treatment for EVD, underscoring the urgent need to develop new anti-ebolavirus agents, especially in the face of an ongoing outbreak in the Democratic Republic of the Congo and the largest ever outbreak in Western Africa in 2013–2016. Lectins have been investigated as potential antiviral agents as they bind glycans present on viral surface glycoproteins, but clinical use of them has been slowed by concerns regarding their mitogenicity, i.e. ability to cause immune cell proliferation. We previously engineered a banana lectin (BanLec), a carbohydrate-binding protein, such that it retained antiviral activity but lost mitogenicity by mutating a single amino acid, yielding H84T BanLec (H84T). H84T shows activity against viruses containing high-mannose N-glycans, including influenza A and B, HIV-1 and -2, and hepatitis C virus. Since ebolavirus surface glycoproteins also contain many high-mannose N-glycans, we assessed whether H84T could inhibit ebolavirus replication. H84T inhibited Ebola virus (EBOV) replication in cell cultures. In cells, H84T inhibited both virus-like particle (VLP) entry and transcription/replication of the EBOV mini-genome at high micromolar concentrations, while inhibiting infection by transcription- and replication-competent VLPs, which measures the full viral life cycle, in the low micromolar range. H84T did not inhibit assembly, budding, or release of VLPs. These findings suggest that H84T may exert its anti-ebolavirus effect(s) by blocking both entry and transcription/replication. In a mouse model, H84T partially (maximally, ~50–80%) protected mice from an otherwise lethal mouse-adapted EBOV infection. Interestingly, a single dose of H84T pre-exposure to EBOV protected ~80% of mice. Thus, H84T shows promise as a new anti-ebolavirus agent with potential to be used in combination with vaccination or other agents in a prophylactic or therapeutic regimen. Public Library of Science 2019-07-29 /pmc/articles/PMC6687191/ /pubmed/31356611 http://dx.doi.org/10.1371/journal.pntd.0007595 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Covés-Datson, Evelyn M.
Dyall, Julie
DeWald, Lisa Evans
King, Steven R.
Dube, Derek
Legendre, Maureen
Nelson, Elizabeth
Drews, Kelly C.
Gross, Robin
Gerhardt, Dawn M.
Torzewski, Lisa
Postnikova, Elena
Liang, Janie Y.
Ban, Bhupal
Shetty, Jagathpala
Hensley, Lisa E.
Jahrling, Peter B.
Olinger, Gene G.
White, Judith M.
Markovitz, David M.
Inhibition of Ebola Virus by a Molecularly Engineered Banana Lectin
title Inhibition of Ebola Virus by a Molecularly Engineered Banana Lectin
title_full Inhibition of Ebola Virus by a Molecularly Engineered Banana Lectin
title_fullStr Inhibition of Ebola Virus by a Molecularly Engineered Banana Lectin
title_full_unstemmed Inhibition of Ebola Virus by a Molecularly Engineered Banana Lectin
title_short Inhibition of Ebola Virus by a Molecularly Engineered Banana Lectin
title_sort inhibition of ebola virus by a molecularly engineered banana lectin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687191/
https://www.ncbi.nlm.nih.gov/pubmed/31356611
http://dx.doi.org/10.1371/journal.pntd.0007595
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