Evidence map›Paper›PMID 38870131›Full record

ArticlePloS one2024

Difference in TMPRSS2 usage by Delta and Omicron variants of SARS-CoV-2: Implication for a sudden increase among children.

Sosuke Kakee, Kyosuke Kanai, Akeno Tsuneki-Tokunaga, Keisuke Okuno, Noriyuki Namba, Katsuyuki Tomita, Hiroki Chikumi, Seiji Kageyama

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

8 authors.

Sosuke KakeeDivision of Virology, Department of Microbiology and Immunology, Faculty of Medicine, Tottori University, Yonago, Japan.
Kyosuke KanaiDivision of Virology, Department of Microbiology and Immunology, Faculty of Medicine, Tottori University, Yonago, Japan.
Akeno Tsuneki-TokunagaDivision of Virology, Department of Microbiology and Immunology, Faculty of Medicine, Tottori University, Yonago, Japan.
Keisuke OkunoDivision of Pediatrics and Perinatology, Department of Multidisciplinary Internal Medicine, Faculty of Medicine, Tottori University, Yonago, Japan.ORCID 0000-0003-1602-0527
Noriyuki NambaDivision of Pediatrics and Perinatology, Department of Multidisciplinary Internal Medicine, Faculty of Medicine, Tottori University, Yonago, Japan.
Katsuyuki TomitaDepartment of Respiratory Medicine, National Hospital Organization Yonago Medical Center, Yonago, Japan.ORCID 0000-0002-4050-775X
Hiroki ChikumiDepartment of Infectious Diseases, Yonago, Japan.
Seiji KageyamaDivision of Virology, Department of Microbiology and Immunology, Faculty of Medicine, Tottori University, Yonago, Japan.ORCID 0000-0002-5220-6137

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has been postulated from a combination of evidence that a sudden increase in COVID-19 cases among pediatric patients after onset of the Omicron wave was attributed to a reduced requirement for TMPRSS2-mediated entry in pediatric airways with lower expression levels of TMPRSS2. Epidemic strains were isolated from the indigenous population in an area, and the levels of TMPRSS2 required for Delta and Omicron variants were assessed. As a result, Delta variants proliferated fully in cultures of TMPRSS2-positive Vero cells but not in TMPRSS2-negative Vero cell culture (350-fold, Delta vs 9.6-fold, Omicron). There was no obvious age-dependent selection of Omicron strains affected by the TMPRSS2 (9.6-fold, Adults vs. 12-fold, Children). A phylogenetic tree was generated and Blast searches (up to 100 references) for the spread of strains in the study area showed that each strain had almost identical homology (>99.5%) with foreign isolates, although indigenous strains had obvious differences from each other. This suggested that the differences had been present abroad for a long period. Therefore, the lower requirement for TMPRSS2 by Omicron strains might be applicable to epidemic strains globally. In conclusion, the property of TMPRSS2-independent cleavage makes Omicron proliferate with ease and allows epidemics among children with fewer TMPRSS2 on epithelial surfaces of the respiratory organs.

Indexed as

COVID-19SARS-CoV-2Serine EndopeptidasesAdultAnimalsChildChild, PreschoolChlorocebus aethiopsFemaleHumansInfantMalePhylogenyVero CellsSerine EndopeptidasesTMPRSS2 protein, human

Identifiers

PMID38870131
PMCPMC11175390

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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.