Effects of Spike Mutations in SARS-CoV-2 Variants of Concern on Human or Animal ACE2-Mediated Virus Entry and Neutralization.

Yunjeong Kim1 Natasha N Gaudreault1 David A Meekins1 Krishani D Perera1 Dashzeveg Bold1 Jessie D Trujillo1 Igor Morozov1 Chester D McDowell1 Kyeong-Ok Chang1 Juergen A Richt1
Affiliations 1 institutions
  1. Department of Diagnostic Medicine/Pathobiology, College of Veterinary Medicine, Kansas State Universitygrid.36567.31, Manhattan, Kansas, USA.

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a zoonotic agent capable of infecting humans and a wide range of animal species. Over the duration of the pandemic, mutations in the SARS-CoV-2 spike (S) protein have arisen, culminating in the spread of several variants of concern (VOCs) with various degrees of altered virulence, transmissibility, and neutralizing antibody escape. In this study, we used pseudoviruses that express specific SARS-CoV-2 S protein substitutions and cell lines that express angiotensin-converting enzyme 2 (ACE2) from nine different animal species to gain insights into the effects of VOC mutations on viral entry and antibody neutralization capability. All animal ACE2 receptors tested, except mink, support viral cell entry for pseudoviruses expressing the ancestral prototype S at levels comparable to human ACE2. Most single S substitutions did not significantly change virus entry, although 614G and 484K resulted in a decreased efficiency. Conversely, combinatorial VOC substitutions in the S protein were associated with increased entry of pseudoviruses. Neutralizing titers in sera from various animal species were significantly reduced against pseudoviruses expressing the S proteins of Beta, Delta, or Omicron VOCs compared to the parental S protein. Especially, substitutions in the S protein of the Omicron variant significantly reduced the neutralizing titers of the sera. This study reveals important insights into the host range of SARS-CoV-2 and the effect of recently emergent S protein substitutions on viral entry, virus replication, and antibody-mediated viral neutralization. IMPORTANCE The ongoing coronavirus disease 2019 (COVID-19) pandemic, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), continues to have devastating impacts on global health and socioeconomics. The recent emergence of SARS-CoV-2 variants of concern, which contain mutations that can affect the virulence, transmission, and effectiveness of licensed vaccines and therapeutic antibodies, are currently becoming the common strains circulating in humans worldwide. In addition, SARS-CoV-2 has been shown to infect a wide variety of animal species, which could result in additional mutations of the SARS-CoV-2 virus. In this study, we investigate the effect of mutations present in SARS-CoV-2 variants of concern and determine the effects of these mutations on cell entry, virulence, and antibody neutralization activity in humans and a variety of animals that might be susceptible to SARS-CoV-2 infection. This information is essential to understand the effects of important SARS-CoV-2 mutations and to inform public policy to create better strategies to control the COVID-19 pandemic.

Supporting text Virus Host Location
neutralization 9 SARS-CoV-2 550 spike mutations 2 variants of concern 5 virus entry 10 virus replication 192 COVID-19 425 SARS-CoV-2 453 Angiotensin-Converting Enzyme 2 177 Animals 1948 Antibodies, Neutralizing 80 Antibodies, Viral 212 Humans 1440 Mutation 209 Pandemics 108 Spike Glycoprotein, Coronavirus 274 Virus Internalization 100 SARS-CoV-2 variants 86 spike protein, SARS-CoV-2 157

Evidence records

4 total
Zoonotic Surveillance
1 records · 1 evidence types
Evidence type
1 records
OVE6017
Key finding

Sera from various animal species showed significantly reduced neutralizing antibody titers against SARS-CoV-2 Beta, Delta, and Omicron variant pseudoviruses compared with the parental spike.

Virus
Host
Not specified
Location
Not specified
Supporting text

Neutralizing titers in sera from various animal species were significantly reduced against pseudoviruses expressing the S proteins of Beta, Delta, or Omicron VOCs compared to the parental S protein.

Method
neutralization assay
Sample type
sera
Experimental Infection
1 records · 1 evidence types
Evidence type
1 records
OVE6014
Key finding

Pseudoviruses expressing the ancestral prototype SARS-CoV-2 spike entered cells expressing ACE2 from nine animal species at levels comparable to human ACE2, except for mink ACE2 which supported little or no entry.

Virus
Host
Location
Not specified
Supporting text

All animal ACE2 receptors tested, except mink, support viral cell entry for pseudoviruses expressing the ancestral prototype S at levels comparable to human ACE2.

Method
pseudovirus infection assay | cell entry assay | ACE2 receptor expression system
Experimental system
pseudovirus entry assay using cells expressing animal ACE2 receptors
Functional Mechanism
2 records · 1 evidence types
Evidence type
2 records
OVE6015
Key finding

SARS-CoV-2 spike mutations 614G and 484K individually reduced viral entry efficiency, whereas combinatorial variant-of-concern spike substitutions enhanced pseudovirus entry.

Virus
Host
Not specified
Location
Not specified
Supporting text

Most single S substitutions did not significantly change virus entry, although 614G and 484K resulted in a decreased efficiency. Conversely, combinatorial VOC substitutions in the S protein were associated with increased entry of pseudoviruses.

Genes or proteins
Spike (S) protein
Receptors
ACE2
Mutations
614G | 484K
Mechanism types
host entry | receptor usage | transmission fitness
OVE6016
Key finding

Substitutions in the SARS-CoV-2 Omicron spike protein significantly reduced serum neutralizing titers, consistent with immune escape adaptations.

Virus
Host
Not specified
Location
Not specified
Supporting text

Especially, substitutions in the S protein of the Omicron variant significantly reduced the neutralizing titers of the sera.

Genes or proteins
Spike (S) protein
Mechanism types
immune escape | virulence adaptation