Evidence map›Paper›PMID 35543509›Full record

ArticleJournal of virology2022

SARS-CoV-2 Variants of Concern Hijack IFITM2 for Efficient Replication in Human Lung Cells.

Rayhane Nchioua, Annika Schundner, Dorota Kmiec, Caterina Prelli Bozzo, Fabian Zech, Lennart Koepke, Alexander Graf, Stefan Krebs, Helmut Blum, Manfred Frick and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of virology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 5% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

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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

12 authors at 2 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.
Dorota KmiecInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Caterina Prelli BozzoInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Fabian ZechInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Lennart KoepkeInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Alexander GrafLaboratory for Functional Genome Analysis, Gene Center, LMU München, Munich, Germany.
Stefan KrebsLaboratory for Functional Genome Analysis, Gene Center, LMU München, Munich, Germany.
Helmut BlumLaboratory for Functional Genome Analysis, Gene Center, LMU München, Munich, Germany.
Manfred FrickInstitute of General Physiology, Ulm University Medical Center, Ulm, Germany.
Konstantin M J SparrerInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.
Frank KirchhoffInstitute of Molecular Virology, Ulm University Medical Center, Ulm, Germany.ORCID 0000-0002-7052-2360
Universität Ulm · DELudwig-Maximilians-Universität München · 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

It has recently been shown that an early SARS-CoV-2 isolate (NL-02-2020) hijacks interferon-induced transmembrane proteins (IFITMs) for efficient replication in human lung cells, cardiomyocytes, and gut organoids. To date, several "variants of concern" (VOCs) showing increased infectivity and resistance to neutralization have emerged and globally replaced the early viral strains. Here, we determined whether the five current SARS-CoV-2 VOCs (Alpha, Beta, Gamma, Delta, and Omicron) maintained the dependency on IFITM proteins for efficient replication. We found that depletion of IFITM2 strongly reduces viral RNA production by all VOCs in the human epithelial lung cancer cell line Calu-3. Silencing of IFITM1 had modest effects, while knockdown of IFITM3 resulted in an intermediate phenotype. Strikingly, depletion of IFITM2 generally reduced infectious virus production by more than 4 orders of magnitude. In addition, an antibody directed against the N terminus of IFITM2 inhibited SARS-CoV-2 VOC replication in induced pluripotent stem cell (iPSC)-derived alveolar epithelial type II cells, thought to represent major viral target cells in the lung. In conclusion, endogenously expressed IFITM proteins (especially IFITM2) are critical cofactors for efficient replication of genuine SARS-CoV-2 VOCs, including the currently dominant Omicron variant.

Indexed as

LungMembrane ProteinsSARS-CoV-2Virus ReplicationCell Line, TumorCOVID-19HumansRNA-Binding ProteinsVirus InternalizationIFITM2 protein, humanIFITM3 protein, humanMembrane ProteinsRNA-Binding Proteinsinterferon-induced transmembrane proteinsiPSC-derived alveolar epithelial type II cellsOmicronSARS-CoV-2variants of concern

Identifiers

PMID35543509
PMCPMC9175628
OpenAlexW4280595612

What OpenQuestion holds

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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 OpenQuestion graph.