# A Newcastle Disease Virus (NDV) Expressing a Membrane-Anchored Spike as a Cost-Effective Inactivated SARS-CoV-2 Vaccine

**Authors:** Weina Sun, Stephen McCroskery, Wen-Chun Liu, Sarah R. Leist, Yonghong Liu, Randy A. Albrecht, Stefan Slamanig, Justine Oliva, Fatima Amanat, Alexandra Schäfer, Kenneth H. Dinnon, Bruce L. Innis, Adolfo García-Sastre, Florian Krammer, Ralph S. Baric, Peter Palese

PMC · DOI: 10.3390/vaccines8040771 · 2020-12-17

## TL;DR

Researchers developed a low-cost, inactivated SARS-CoV-2 vaccine using a modified Newcastle disease virus that protects against infection in animal models.

## Contribution

A novel, cost-effective inactivated SARS-CoV-2 vaccine using a Newcastle disease virus expressing a membrane-anchored spike is proposed.

## Key findings

- The inactivated NDV-S vaccine induced strong binding and neutralizing antibodies in mice and hamsters.
- The vaccine protected animals from SARS-CoV-2 infections.
- Antigen-sparing with an adjuvant maintained protective efficacy while reducing costs.

## Abstract

A successful severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine must not only be safe and protective, but must also meet the demand on a global scale at a low cost. Using the current influenza virus vaccine production capacity to manufacture an egg-based inactivated Newcastle disease virus (NDV)/SARS-CoV-2 vaccine would meet that challenge. Here, we report pre-clinical evaluations of an inactivated NDV chimera stably expressing the membrane-anchored form of the spike (NDV-S) as a potent coronavirus disease 2019 (COVID-19) vaccine in mice and hamsters. The inactivated NDV-S vaccine was immunogenic, inducing strong binding and/or neutralizing antibodies in both animal models. More importantly, the inactivated NDV-S vaccine protected animals from SARS-CoV-2 infections. In the presence of an adjuvant, antigen-sparing could be achieved, which would further reduce the cost while maintaining the protective efficacy of the vaccine.

## Linked entities

- **Diseases:** SARS-CoV-2 (MONDO:0100096), coronavirus disease 2019 (MONDO:0100096), Newcastle disease (MONDO:0005875)
- **Species:** Mus musculus (taxon 10090), Cricetinae (taxon 10026)

## Full-text entities

- **Genes:** Vtn (vitronectin) [NCBI Gene 22370] {aka Vn}, NEU1 (neuraminidase 1) [NCBI Gene 4758] {aka NANH, NEU, SIAL1}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}, HN [NCBI Gene 37627205], Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}
- **Diseases:** Infection (MESH:D007239), Weight loss (MESH:D015431), SARS-CoV-2 (MESH:D000086382), SPIKE PROTEIN (MESH:D031261), Influenza (MESH:D007251), RECOMBINANT NEWCASTLE DISEASE (MESH:D009521)
- **Chemicals:** S-F (MESH:D005461), Allantoic Fluid (-), formaldehyde (MESH:D005557), PBS (MESH:D007854), NaCl (MESH:D012965), water (MESH:D014867), penicillin (MESH:D010406), sucrose (MESH:D013395), beta-propiolactone (MESH:D011420), oil (MESH:D009821), P/S (MESH:D010758), HCl (MESH:D006851), streptomycin (MESH:D013307), CO2 (MESH:D002245), bicinchoninic acid (MESH:C047117), HEPES (MESH:D006531), disodium phosphate (MESH:C018279), D-glucose (MESH:D005947), PVDF (MESH:C024865), o-phenylenediamine dihydrochloride (MESH:C034193), SDS (MESH:D012967), EDTA (MESH:D004492), L-glutamine (MESH:D005973), S (MESH:D013455), DOTAP (MESH:C070046), Tween 20 (MESH:D011136), AddaVax (MESH:C000590912), MF-59 (MESH:C089950), ice (MESH:D007053)
- **Species:** Cricetinae (hamsters, subfamily) [taxon 10026], Mus musculus (house mouse, species) [taxon 10090], Cricetus cricetus (black-bellied hamster, species) [taxon 10034], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606], Escherichia coli (E. coli, species) [taxon 562], Mesocricetus auratus (golden hamster, species) [taxon 10036], Gallus gallus (bantam, species) [taxon 9031], NDV [taxon 11176]
- **Mutations:** L289A
- **Cell lines:** BALB/cJ — Mus musculus (Mouse), Embryonic stem cell (CVCL_2H82), Vero — Chlorocebus sabaeus (Green monkey), Spontaneously immortalized cell line (CVCL_0059), L289A_S-F — Homo sapiens (Human), Melanoma, Cancer cell line (CVCL_8760), Vero E6 — Chlorocebus sabaeus (Green monkey), Spontaneously immortalized cell line (CVCL_0574), pCI — Homo sapiens (Human), Induced pluripotent stem cell (CVCL_UI80), -2 — Homo sapiens (Human), Colon carcinoma, Cancer cell line (CVCL_A628), BSRT7 — Cricetulus griseus (Chinese hamster), Spontaneously immortalized cell line (CVCL_H340), BALB/c — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0184)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC7766959/full.md

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Source: https://tomesphere.com/paper/PMC7766959