Evidence map›Paper›PMID 33113352›Full record

ArticleCell host & microbe2020

RTP4 Is a Potent IFN-Inducible Anti-flavivirus Effector Engaged in a Host-Virus Arms Race in Bats and Other Mammals.

Ian N Boys, Elaine Xu, Katrina B Mar, Pamela C De La Cruz-Rivera, Jennifer L Eitson, Benjamin Moon, John W Schoggins

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Tearing down the house of mosquito-transmitted viruses.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  15. MITD1 is a brain-specific interferon-inducible factor that inhibits flavivirus replication.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. RTP4 Enhances Corneal HSV-1 Infection in Mice With Type 2 Diabetes Mellitus.Investigative ophthalmology & visual science · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Ian N BoysDepartment of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Elaine XuDepartment of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Katrina B MarDepartment of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Pamela C De La Cruz-RiveraDepartment of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Jennifer L EitsonDepartment of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Benjamin MoonDepartment of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
John W SchogginsDepartment of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. Electronic address: john.schoggins@utsouthwestern.edu.
The University of Texas Southwestern Medical Center · US

Funding

INTEGRATIVE IMMUNOLOGY TRAINING PROGRAMT32AI005284 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI Nan Yan · 2003 to 2026
$7.4M
Discovery of antiviral mechanisms in batsDP2AI117922 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI SCHOGGINS, JOHN W. · 2014 to 2016
$2.6M
NIAID NIH HHS DP2 AI117922NIAID NIH HHS T32 AI005284
6 · The paper itself

Abstract

Among mammals, bats are particularly rich in zoonotic viruses, including flaviviruses. Certain bat species can be productively yet asymptomatically infected with viruses that cause overt disease in other species. However, little is known about the antiviral effector repertoire in bats relative to other mammals. Here, we report the black flying fox receptor transporter protein 4 (RTP4) as a potent interferon (IFN)-inducible inhibitor of human pathogens in the Flaviviridae family, including Zika, West Nile, and hepatitis C viruses. Mechanistically, RTP4 associates with the flavivirus replicase, binds viral RNA, and suppresses viral genome amplification. Comparative approaches revealed that RTP4 undergoes positive selection, that a flavivirus can mutate to escape RTP4-imposed restriction, and that diverse mammalian RTP4 orthologs exhibit striking patterns of specificity against distinct Flaviviridae members. Our findings reveal an antiviral mechanism that has likely adapted over 100 million years of mammalian evolution to accommodate unique host-virus genetic conflicts.

Indexed as

Host-Pathogen InteractionsAnimalsCell LineChiropteraFemaleFlavivirusGenome, ViralHumansInterferonsMaleMammalsMolecular ChaperonesSpecies SpecificityVirusesVirus ReplicationInterferonsMolecular Chaperonesantiviral immunitybatsevolutionflavivirusgenetic arms raceinterferonrestriction factorvirus-host interactions

Identifiers

PMID33113352
PMCPMC7666060
OpenAlexW3097199291

What OpenQuestion holds

Textmetadata
LicenceTDM
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.