Evidence map›Paper›PMID 37789046›Full record

ArticleScientific reports2023

Effects of tea, catechins and catechin derivatives on Omicron subvariants of SARS-CoV-2.

Masaharu Shin-Ya, Maiko Nakashio, Eriko Ohgitani, Akiko Suganami, Masaya Kawamoto, Masaki Ichitani, Makoto Kobayashi, Takanobu Takihara, Tohru Inaba, Yoko Nukui and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Natural products as a source of Coronavirus entry inhibitors.Frontiers in cellular and infection microbiology · 2024
    Review
  8. Article
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

14 authors at 3 institutions in 1 country.

Masaharu Shin-YaDepartment of Immunology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Maiko NakashioDepartment of Immunology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Eriko OhgitaniDepartment of Immunology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Akiko SuganamiDepartment of Bioinformatics, Graduate School of Medicine, Chiba University, Chiba, Japan.
Masaya KawamotoDepartment of Immunology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Masaki IchitaniDepartment of Molecular Anti-Virus Immunology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Makoto KobayashiCentral Research Institute, ITO EN, Ltd, Shizuoka, Japan.
Takanobu TakiharaCentral Research Institute, ITO EN, Ltd, Shizuoka, Japan.
Tohru InabaDepartment of Infection Control and Laboratory Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Yoko NukuiDepartment of Infection Control and Laboratory Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Hitoshi KinugasaCentral Research Institute, ITO EN, Ltd, Shizuoka, Japan.
Hiroyasu IshikuraDepartment of Emergency and Critical Care Medicine, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Yutaka TamuraDepartment of Bioinformatics, Graduate School of Medicine, Chiba University, Chiba, Japan.
Osam MazdaDepartment of Immunology, Kyoto Prefectural University of Medicine, Kyoto, Japan. mazda@koto.kpu-m.ac.jp.
Kyoto Prefectural University of Medicine · JPChiba University · JPFukuoka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Omicron subvariants of SARS-CoV-2 have multiple mutations in the S-proteins and show high transmissibility. We previously reported that tea catechin (-)-epigallocatechin gallate (EGCG) and its derivatives including theaflavin-3,3'-di-O-digallate (TFDG) strongly inactivated the conventional SARS-CoV-2 by binding to the receptor binding domain (RBD) of the S-protein. Here we show that Omicron subvariants were effectively inactivated by green tea, Matcha, and black tea. EGCG and TFDG strongly suppressed infectivity of BA.1 and XE subvariants, while effect on BA.2.75 was weaker. Neutralization assay showed that EGCG and TFDG inhibited interaction between BA.1 RBD and ACE2. In silico analyses suggested that N460K, G446S and F490S mutations in RBDs crucially influenced the binding of EGCG/TFDG to the RBDs. Healthy volunteers consumed a candy containing green tea or black tea, and saliva collected from them immediately after the candy consumption significantly decreased BA.1 virus infectivity in vitro. These results indicate specific amino acid substitutions in RBDs that crucially influence the binding of EGCG/TFDG to the RBDs and different susceptibility of each Omicron subvariant to EGCG/TFDG. The study may suggest molecular basis for potential usefulness of these compounds in suppression of mutant viruses that could emerge in the future and cause next pandemic.

Indexed as

Camellia sinensisCatechinCOVID-19HumansSARS-CoV-2TeaCatechinTea

Identifiers

PMID37789046
PMCPMC10547759
OpenAlexW4387309630

What OpenQuestion 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 OpenQuestion graph.