Evidence map›Paper›PMID 42593857›Full record

ArticleThe Journal of general virology2026

Broad permissiveness of mammalian nectin-4 orthologs for morbilliviruses: a notable exception in dolphin nectin-4.

Mizuki Tominaga, Fumio Seki, Hiroki Nagata, Ayumu Hyodo, Yukiko Akahori, Yuki Kitai, Hiroshi Katoh, Makoto Takeda

Abstract read
In one paragraph

Article in The Journal of general virology, 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
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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

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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

8 authors.

Mizuki TominagaDepartment of Microbiology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo, Bunkyo-ku 113-0033, Tokyo, Japan.
Fumio SekiDepartment of Respiratory Viruses, National Institute of Infectious Diseases, Japan Institute of Health Security, Musashimurayama 208-0011, Tokyo, Japan.
Hiroki NagataDepartment of Microbiology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo, Bunkyo-ku 113-0033, Tokyo, Japan.
Ayumu HyodoDepartment of Microbiology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo, Bunkyo-ku 113-0033, Tokyo, Japan.
Yukiko AkahoriDepartment of Microbiology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo, Bunkyo-ku 113-0033, Tokyo, Japan.
Yuki KitaiDepartment of Microbiology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo, Bunkyo-ku 113-0033, Tokyo, Japan.
Hiroshi KatohDepartment of Microbiology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo, Bunkyo-ku 113-0033, Tokyo, Japan.
Makoto TakedaDepartment of Microbiology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo, Bunkyo-ku 113-0033, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Morbilliviruses utilize signalling lymphocytic activation molecule (SLAM) and nectin-4 as their major cellular receptors and exhibit distinct host specificities despite sharing common receptor usage. While species-specific differences in SLAM have been extensively investigated, the contribution of nectin-4 to morbillivirus host range remains poorly understood because nectin-4 is highly conserved among mammals. Here, we systematically compared the receptor activities of nectin-4 orthologs from human, dolphin, bat, dog and seal for representative morbilliviruses, including measles virus (MV), cetacean morbillivirus (CeMV), canine distemper virus (CDV), phocine distemper virus (PDV) and Myotis bat morbillivirus (MBaMV). Cell-cell fusion, virus infection and plaque assays demonstrated that most nectin-4 orthologs efficiently supported infection by all tested viruses. In contrast, dolphin nectin-4 exhibited markedly reduced receptor activity for MV, PDV and MBaMV, while remaining fully functional for CeMV and CDV. This phenotype was consistently observed with multiple clinical MV isolates. Mutational analyses identified amino acid residue 63 as a key determinant of this receptor specificity. Substitution of glutamic acid at position 63 in dolphin nectin-4 with glycine restored MV receptor activity to a level comparable to that of human nectin-4. These findings demonstrate that nectin-4 is generally a broadly permissive morbillivirus receptor but that specific amino acid differences can substantially influence receptor usage. Our results indicate that receptor compatibility contributes to morbillivirus host range and cross-species transmission while being insufficient on its own to fully explain viral host specificity.

Indexed as

Cell Adhesion MoleculesMorbillivirusMorbillivirus InfectionsNectinsReceptors, VirusAnimalsCell LineChiropteraDogsDolphinsHost SpecificityHumansCell Adhesion MoleculesNECTIN4 protein, humanNectinsReceptors, Virushost rangeMorbillivirusnectin-4receptor

Identifiers

PMID42593857
PMCPMC13472537

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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.