Evidence map›Paper›PMID 27681626›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Functional receptor molecules CD300lf and CD300ld within the CD300 family enable murine noroviruses to infect cells.

Kei Haga, Akira Fujimoto, Reiko Takai-Todaka, Motohiro Miki, Yen Hai Doan, Kosuke Murakami, Masaru Yokoyama, Kazuyoshi Murata, Akira Nakanishi, Kazuhiko Katayama

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed, 1 pooled it
17.4field-weighted citation impact, top 1% 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

123 citing papers in PubMed, 1 synthesis or guideline pooled it, 177 citations in OpenAlex.

  1. Pooled it
  2. Plscr1 inhibits murine norovirus entry.bioRxiv : the preprint server for biology · 2026
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  8. Review
  9. Article
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  12. Article
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  15. Impaired K48-polyubiquitination downmodulates mouse norovirus propagation.Frontiers in cellular and infection microbiology · 2025
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Neonatal Fc receptor is a functional receptor for classical human astrovirus.Genes to cells : devoted to molecular & cellular mechanisms · 2024
    Article

63 more citing papers are in PubMed but not listed here.

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 at 3 institutions in 1 country.

Kei HagaDepartment of Virology II, National Institute of Infectious Diseases, Tokyo 208-0011, Japan.
Akira FujimotoDepartment of Virology II, National Institute of Infectious Diseases, Tokyo 208-0011, Japan.
Reiko Takai-TodakaDepartment of Virology II, National Institute of Infectious Diseases, Tokyo 208-0011, Japan.
Motohiro MikiDepartment of Virology II, National Institute of Infectious Diseases, Tokyo 208-0011, Japan; New Business Planning Division, Innovative Diagnostics Research Center, Denka Innovation Center, Denka Company Limited, Tokyo 194-8560, Japan.
Yen Hai DoanDepartment of Virology II, National Institute of Infectious Diseases, Tokyo 208-0011, Japan.
Kosuke MurakamiDepartment of Virology II, National Institute of Infectious Diseases, Tokyo 208-0011, Japan.
Masaru YokoyamaPathogen Genomics Center, National Institute of Infectious Diseases, Tokyo 208-0011, Japan.
Kazuyoshi MurataNational Institute for Physiological Sciences, Aichi 444-8585, Japan.
Akira NakanishiSection of Gene Therapy, Department of Aging Intervention, National Center for Geriatrics and Gerontology, Aichi 474-8511, Japan nakanish@ncgg.go.jp katayama@nih.go.jp.
Kazuhiko KatayamaDepartment of Virology II, National Institute of Infectious Diseases, Tokyo 208-0011, Japan; nakanish@ncgg.go.jp katayama@nih.go.jp.
National Institute of Infectious Diseases · JPNational Center for Geriatrics and Gerontology · JPNational Institute for Physiological Sciences · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Norovirus is the leading cause of acute gastroenteritis worldwide. Since the discovery of human norovirus (HuNoV), an efficient and reproducible norovirus replication system has not been established in cultured cells. Although limited amounts of virus particles can be produced when the HuNoV genome is directly transfected into cells, the HuNoV cycle of infection has not been successfully reproduced in any currently available cell-culture system. Those results imply that the identification of a functional cell-surface receptor for norovirus might be the key to establishing a norovirus culture system. Using a genome-wide CRISPR/Cas9 guide RNA library, we identified murine CD300lf and CD300ld as functional receptors for murine norovirus (MNV). The treatment of susceptible cells with polyclonal antibody against CD300lf significantly reduced the production of viral progeny. Additionally, ectopic CD300lf expression in nonsusceptible cell lines derived from other animal species enabled MNV infection and progeny production, suggesting that CD300lf has potential for dictating MNV host tropism. Furthermore, CD300ld, which has an amino acid sequence in the N-terminal region of its extracellular domain that is highly homologous to that of CD300lf, also functions as a receptor for MNV. Our results indicate that direct interaction of MNV with two cell-surface molecules, CD300lf and CD300ld, dictates permissive noroviral infection.

Indexed as

Amino Acid SequenceAnimalsCaliciviridae InfectionsCapsid ProteinsCell LineCells, CulturedDisease SusceptibilityGene ExpressionHost-Pathogen InteractionsHumansMacrophagesMiceModels, MolecularMutationNorovirusProtein BindingCapsid ProteinsCLM-1 protein, mouseReceptors, ImmunologicReceptors, VirusCD300ldCD300lfCD300 moleculesmurine norovirusnorovirus proteinaceous receptors

Identifiers

PMID27681626
PMCPMC5068309
OpenAlexW2526399218

What OpenQuestion holds

Textmetadata
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.