Intranasal vaccination with a Newcastle disease virus-vectored vaccine protects hamsters from SARS-CoV-2 infection and disease
Summary: The pandemic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the cause of coronavirus disease 2019 (COVID-19). Worldwide efforts are being made to develop vaccines to mitigate this pandemic. We engineered two recombinant Newcastle disease virus (NDV) vectors expressing eithe...
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Elsevier
2021
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oai:doaj.org-article:a9d6cd355eb7470ba0489696155667f52021-11-20T05:08:24ZIntranasal vaccination with a Newcastle disease virus-vectored vaccine protects hamsters from SARS-CoV-2 infection and disease2589-004210.1016/j.isci.2021.103219https://doaj.org/article/a9d6cd355eb7470ba0489696155667f52021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2589004221011871https://doaj.org/toc/2589-0042Summary: The pandemic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the cause of coronavirus disease 2019 (COVID-19). Worldwide efforts are being made to develop vaccines to mitigate this pandemic. We engineered two recombinant Newcastle disease virus (NDV) vectors expressing either the full-length SARS-CoV-2 spike protein (NDV-FLS) or a version with a 19 amino acid deletion at the carboxy terminus (NDV-Δ19S). Hamsters receiving two doses (prime-boost) of NDV-FLS developed a robust SARS-CoV-2-neutralizing antibody response, with elimination of infectious virus in the lungs and minimal lung pathology at five days post-challenge. Single-dose vaccination with NDV-FLS significantly reduced SARS-CoV-2 replication in the lungs but only mildly decreased lung inflammation. NDV-Δ19S-treated hamsters had a moderate decrease in SARS-CoV-2 titers in lungs and presented with severe microscopic lesions, suggesting that truncation of the spike protein was a less effective strategy. In summary, NDV-vectored vaccines represent a viable option for protection against COVID-19.Bryce M. WarnerLisa A. SantryAlexander LeacyMable ChanPhuc H. PhamRobert VendramelliYanlong PeiNikesh TailorEmelissa ValcourtAnders LeungShihua HeBryan D. GriffinJonathan AudetMarnie WillmanKevin TierneyAlixandra AlbietzKathy L. FrostJacob G.E. YatesRobert C. MouldLily ChanYeganeh MehraniJason P. KnappJessica A. MinottLogan BanadygaDavid SafronetzHeidi WoodStephanie BoothPierre P. MajorByram W. BridleLeonardo SustaDarwyn KobasaSarah K. WoottonElsevierarticleImmune responsVirologyScienceQENiScience, Vol 24, Iss 11, Pp 103219- (2021) |
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Immune respons Virology Science Q Bryce M. Warner Lisa A. Santry Alexander Leacy Mable Chan Phuc H. Pham Robert Vendramelli Yanlong Pei Nikesh Tailor Emelissa Valcourt Anders Leung Shihua He Bryan D. Griffin Jonathan Audet Marnie Willman Kevin Tierney Alixandra Albietz Kathy L. Frost Jacob G.E. Yates Robert C. Mould Lily Chan Yeganeh Mehrani Jason P. Knapp Jessica A. Minott Logan Banadyga David Safronetz Heidi Wood Stephanie Booth Pierre P. Major Byram W. Bridle Leonardo Susta Darwyn Kobasa Sarah K. Wootton Intranasal vaccination with a Newcastle disease virus-vectored vaccine protects hamsters from SARS-CoV-2 infection and disease |
description |
Summary: The pandemic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the cause of coronavirus disease 2019 (COVID-19). Worldwide efforts are being made to develop vaccines to mitigate this pandemic. We engineered two recombinant Newcastle disease virus (NDV) vectors expressing either the full-length SARS-CoV-2 spike protein (NDV-FLS) or a version with a 19 amino acid deletion at the carboxy terminus (NDV-Δ19S). Hamsters receiving two doses (prime-boost) of NDV-FLS developed a robust SARS-CoV-2-neutralizing antibody response, with elimination of infectious virus in the lungs and minimal lung pathology at five days post-challenge. Single-dose vaccination with NDV-FLS significantly reduced SARS-CoV-2 replication in the lungs but only mildly decreased lung inflammation. NDV-Δ19S-treated hamsters had a moderate decrease in SARS-CoV-2 titers in lungs and presented with severe microscopic lesions, suggesting that truncation of the spike protein was a less effective strategy. In summary, NDV-vectored vaccines represent a viable option for protection against COVID-19. |
format |
article |
author |
Bryce M. Warner Lisa A. Santry Alexander Leacy Mable Chan Phuc H. Pham Robert Vendramelli Yanlong Pei Nikesh Tailor Emelissa Valcourt Anders Leung Shihua He Bryan D. Griffin Jonathan Audet Marnie Willman Kevin Tierney Alixandra Albietz Kathy L. Frost Jacob G.E. Yates Robert C. Mould Lily Chan Yeganeh Mehrani Jason P. Knapp Jessica A. Minott Logan Banadyga David Safronetz Heidi Wood Stephanie Booth Pierre P. Major Byram W. Bridle Leonardo Susta Darwyn Kobasa Sarah K. Wootton |
author_facet |
Bryce M. Warner Lisa A. Santry Alexander Leacy Mable Chan Phuc H. Pham Robert Vendramelli Yanlong Pei Nikesh Tailor Emelissa Valcourt Anders Leung Shihua He Bryan D. Griffin Jonathan Audet Marnie Willman Kevin Tierney Alixandra Albietz Kathy L. Frost Jacob G.E. Yates Robert C. Mould Lily Chan Yeganeh Mehrani Jason P. Knapp Jessica A. Minott Logan Banadyga David Safronetz Heidi Wood Stephanie Booth Pierre P. Major Byram W. Bridle Leonardo Susta Darwyn Kobasa Sarah K. Wootton |
author_sort |
Bryce M. Warner |
title |
Intranasal vaccination with a Newcastle disease virus-vectored vaccine protects hamsters from SARS-CoV-2 infection and disease |
title_short |
Intranasal vaccination with a Newcastle disease virus-vectored vaccine protects hamsters from SARS-CoV-2 infection and disease |
title_full |
Intranasal vaccination with a Newcastle disease virus-vectored vaccine protects hamsters from SARS-CoV-2 infection and disease |
title_fullStr |
Intranasal vaccination with a Newcastle disease virus-vectored vaccine protects hamsters from SARS-CoV-2 infection and disease |
title_full_unstemmed |
Intranasal vaccination with a Newcastle disease virus-vectored vaccine protects hamsters from SARS-CoV-2 infection and disease |
title_sort |
intranasal vaccination with a newcastle disease virus-vectored vaccine protects hamsters from sars-cov-2 infection and disease |
publisher |
Elsevier |
publishDate |
2021 |
url |
https://doaj.org/article/a9d6cd355eb7470ba0489696155667f5 |
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