Evidence map›Paper›PMID 36977594›Full record

ArticleLife science alliance2023

Reduced replication but increased interferon resistance of SARS-CoV-2 Omicron BA.1.

Rayhane Nchioua, Annika Schundner, Susanne Klute, Lennart Koepke, Maximilian Hirschenberger, Sabrina Noettger, Giorgio Fois, Fabian Zech, Alexander Graf, Stefan Krebs and 7 more

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.6field-weighted citation impact, top 3% of its field
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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  5. Frontiers in immunology · 2026
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  15. SARS-CoV-2 nsp15 endoribonuclease antagonizes dsRNA-induced antiviral signaling.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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  17. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 1 country.

Rayhane NchiouaInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Annika SchundnerInstitute of General Physiology, Ulm University Medical Center, Ulm, Germany.
Susanne KluteInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Lennart KoepkeInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.ORCID https://orcid.org/0000-0001-9788-1972
Maximilian HirschenbergerInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Sabrina NoettgerInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.ORCID https://orcid.org/0000-0003-0059-5289
Giorgio FoisInstitute of General Physiology, Ulm University Medical Center, Ulm, Germany.ORCID https://orcid.org/0000-0001-5414-1149
Fabian ZechInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Alexander GrafLaboratory for Functional Genome Analysis, Gene Center, LMU Munich, Munich, Germany.
Stefan KrebsLaboratory for Functional Genome Analysis, Gene Center, LMU Munich, Munich, Germany.
Peter BraubachHannover Medical School, Institute for Pathology, Hannover, Germany.
Helmut BlumLaboratory for Functional Genome Analysis, Gene Center, LMU Munich, Munich, Germany.ORCID https://orcid.org/0000-0002-3994-2332
Steffen StengerInstitute for Medical Microbiology and Hygiene, Ulm University Medical Center, Ulm, Germany.
Dorota KmiecInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Manfred FrickInstitute of General Physiology, Ulm University Medical Center, Ulm, Germany.ORCID https://orcid.org/0000-0002-4763-1104
Frank KirchhoffInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany Frank.Kirchhoff@uni-ulm.de.ORCID https://orcid.org/0000-0002-7052-2360
Konstantin Mj SparrerInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany Konstantin.Sparrer@uni-ulm.de.ORCID https://orcid.org/0000-0002-8682-1779
Universität Ulm · DELudwig-Maximilians-Universität München · DEInstitute of Medical Microbiology and Hygiene · DEMedizinische Hochschule Hannover · DE

Funding

A National iPS Cell Network with Deep Phenotyping for Translational ResearchU01TR001810 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GILAD, YOAV, KOTTON, DARRELL N. · 2016 to 2020
$4.4M
NCATS NIH HHS U01 TR001810
6 · The paper itself

Abstract

The IFN system constitutes a powerful antiviral defense machinery. Consequently, effective IFN responses protect against severe COVID-19 and exogenous IFNs inhibit SARS-CoV-2 in vitro. However, emerging SARS-CoV-2 variants of concern (VOCs) may have evolved reduced IFN sensitivity. Here, we determined differences in replication and IFN susceptibility of an early SARS-CoV-2 isolate (NL-02-2020) and the Alpha, Beta, Gamma, Delta, and Omicron VOCs in Calu-3 cells, iPSC-derived alveolar type-II cells (iAT2) and air-liquid interface (ALI) cultures of primary human airway epithelial cells. Our data show that Alpha, Beta, and Gamma replicated to similar levels as NL-02-2020. In comparison, Delta consistently yielded higher viral RNA levels, whereas Omicron was attenuated. All viruses were inhibited by type-I, -II, and -III IFNs, albeit to varying extend. Overall, Alpha was slightly less sensitive to IFNs than NL-02-2020, whereas Beta, Gamma, and Delta remained fully sensitive. Strikingly, Omicron BA.1 was least restricted by exogenous IFNs in all cell models. Our results suggest that enhanced innate immune evasion rather than higher replication capacity contributed to the effective spread of Omicron BA.1.

Indexed as

COVID-19InterferonsAntiviral AgentsHumansSARS-CoV-2Antiviral AgentsInterferons

Identifiers

PMID36977594
PMCPMC10053418
OpenAlexW4361029841

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.