Evidence map›Paper›PMID 42685021›Full record

ArticlePloS one2026

Lactobacillus delbrueckii ssp. bulgaricus OLL1073R-1-derived exopolysaccharide suppresses murine norovirus replication by modulating innate immune response.

Shuyi Tang, Shoko Ishii, Reiko Takai-Todaka, Miho Ogawa, Reiko Watanabe, Hiroshi Kano, Toshihiro Sashihara, Kenichi Hojo, Kazuhiko Katayama, Kei Haga

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Shuyi TangFood Microbiology and Function Research Laboratories, R&D Division, Meiji Co., Ltd., Nanakuni, Hachioji, Tokyo, Japan.ORCID https://orcid.org/0009-0004-1403-9392
Shoko IshiiFood Microbiology and Function Research Laboratories, R&D Division, Meiji Co., Ltd., Nanakuni, Hachioji, Tokyo, Japan.
Reiko Takai-TodakaLaboratory of Viral Infection Control, Ōmura Satoshi Memorial Institute, Graduate School of Infection Control Sciences, Kitasato University, Shirokane, Minato-ku, Tokyo, Japan.
Miho OgawaFood Microbiology and Function Research Laboratories, R&D Division, Meiji Co., Ltd., Nanakuni, Hachioji, Tokyo, Japan.
Reiko WatanabeFood Microbiology and Function Research Laboratories, R&D Division, Meiji Co., Ltd., Nanakuni, Hachioji, Tokyo, Japan.
Hiroshi KanoFood Microbiology and Function Research Laboratories, R&D Division, Meiji Co., Ltd., Nanakuni, Hachioji, Tokyo, Japan.
Toshihiro SashiharaFood Microbiology and Function Research Laboratories, R&D Division, Meiji Co., Ltd., Nanakuni, Hachioji, Tokyo, Japan.
Kenichi HojoFood Microbiology and Function Research Laboratories, R&D Division, Meiji Co., Ltd., Nanakuni, Hachioji, Tokyo, Japan.
Kazuhiko KatayamaLaboratory of Viral Infection Control, Ōmura Satoshi Memorial Institute, Graduate School of Infection Control Sciences, Kitasato University, Shirokane, Minato-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0002-7692-1151
Kei HagaLaboratory of Viral Infection Control, Ōmura Satoshi Memorial Institute, Graduate School of Infection Control Sciences, Kitasato University, Shirokane, Minato-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0002-8524-1078

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Norovirus is a major cause of foodborne acute gastroenteritis, yet effective strategies to prevent norovirus infection have not been established. Given that an exopolysaccharide (EPS) can be orally consumed as a dietary component, we evaluated its potential to suppress norovirus replication in vitro. Here, we tested the antiviral effect of EPS derived from Lactobacillus delbrueckii ssp. bulgaricus OLL1073R-1 (R-1 EPS) against murine norovirus (MNV) in vitro using the mouse macrophage-like cell line, RAW264.7. Post-infection treatment significantly reduced the viral load of MNV in culture supernatants. Microarray-based transcriptome analysis showed that R-1 EPS treatment modulated MNV-induced host transcriptional responses, promoting preferential engagement of interferon (IFN)-mediated antiviral and inflammatory pathways. Consistent with the microarray-based transcriptome analysis, expression analysis using ELISA and RT-qPCR indicated increased expression of IFN, IFN-stimulated genes, and proinflammatory cytokines in infected cells treated with R-1 EPS. The results suggest that R-1 EPS modulated host innate immune responses, such as type I IFN and proinflammatory cytokine responses, during MNV infection, which may contribute to antiviral activity. Our results provide mechanistic insights into the host-directed antiviral effect of microbial EPS.

Indexed as

Antiviral AgentsImmunity, InnateLactobacillus delbrueckiiNorovirusPolysaccharides, BacterialVirus ReplicationAnimalsCell LineCytokinesGene Expression ProfilingMiceAntiviral AgentsCytokinesPolysaccharides, Bacterial

Identifiers

PMID42685021
PMCPMC13537558

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.