Evidence map›Paper›PMID 42716929›Full record

ArticleNature communications2026

Loss-of-function mutation in Omicron variants reduces spike protein expression and attenuates SARS-CoV-2 infection.

Michelle N Vu, R Elias Alvarado, Dorothea R Morris, Kumari G Lokugamage, Yiyang Zhou, Angelica L Morgan, Yani P Ahearn, Nicholas C Hazell, Leah K Estes, Alyssa M McLeland and 13 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors.

Michelle N VuDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
R Elias AlvaradoDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Dorothea R MorrisDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Kumari G LokugamageDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Yiyang ZhouDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.ORCID http://orcid.org/0000-0001-8956-3229
Angelica L MorganDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Yani P AhearnDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Nicholas C HazellDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Leah K EstesDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Alyssa M McLelandDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Craig SchindewolfDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Jessica A PlanteDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.ORCID http://orcid.org/0000-0002-4768-7458
William M MeyersDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, USA.
Jordan T MurrayDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Patricia A Crocquet-ValdesDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, USA.ORCID http://orcid.org/0000-0002-2079-0076
Scott C WeaverDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.ORCID http://orcid.org/0000-0001-8016-8556
Mehul S SutharDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.ORCID http://orcid.org/0000-0002-2686-8380
David H WalkerDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, USA.
William K RussellDepartment of Biochemistry and Microbiology, University of Texas Medical Branch, Galveston, TX, USA.ORCID http://orcid.org/0000-0003-1931-4555
Andrew L RouthDepartment of Microbiology and Immunology, Scripps Research, La Jolla, CA, USA.ORCID http://orcid.org/0000-0002-2874-5990
Haitao HuDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Kenneth S PlanteDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.ORCID http://orcid.org/0000-0002-7485-3167
Vineet D MenacheryDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA. vineet.d.menachery@emory.edu.ORCID http://orcid.org/0000-0001-8803-7606

Funding

Biodefense Training ProgramT32AI060549 · NIAID · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI ASHOK K CHOPRA, Janice J Endsley · 2004 to 2026
$3.0M
The Host Genetics of Age-Dependent SusceptibilityR21AI145400 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI MENACHERY, VINEET D · 2020 to 2021
$451k
NIAID NIH HHS R21 AI145400NIAID NIH HHS T32 AI060549U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI060549U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI145400
6 · The paper itself

Abstract

SARS-CoV-2 Omicron variants emerged in 2022 with >30 novel mutations in the spike alone. While most studies focus on receptor binding domain changes, mutations in the C-terminus of S1 (CTS1), adjacent to the furin cleavage site, have largely been ignored. Here, we examine three Omicron mutations in CTS1: H655Y, N679K, and P681H. Generating a SARS-CoV-2 triple mutant (YKH), we find that the mutant increases spike processing, consistent with prior reports for H655Y/P681H. In addition, the YKH mutant induces attenuated disease, but augments viral loads in male golden Syrian hamsters. Next, we generate a single N679K mutant, finding it reduces viral replication in Calu3 human respiratory cells and induces less disease in male golden Syrian hamsters. Mechanistically, the N679K mutant has increased spike processing but also reduces spike in purified virions; spike decreases are further exacerbated in infected Calu3 cell lysates. Importantly, exogenous spike expression reveals that N679K reduces overall spike protein in the context of the epidemic strain. Although a loss-of-function mutation, transmission competition demonstrates that N679K confers a replication advantage in the upper airway, potentially impacting transmissibility. Together, the data show that N679K reduces overall spike protein during Omicron infection, which has implications for infection, immunity, and transmission.

Indexed as

COVID-19SARS-CoV-2Spike Glycoprotein, CoronavirusAnimalsCell LineCricetinaeHumansMaleMesocricetusMutationViral LoadVirus ReplicationSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID42716929
PMCPMC13558758

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.