Evidence map›Paper›PMID 32747526›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Necroptosis-based CRISPR knockout screen reveals Neuropilin-1 as a critical host factor for early stages of murine cytomegalovirus infection.

Rebecca K Lane, Hongyan Guo, Amanda D Fisher, Jonathan Diep, Zhao Lai, Yidong Chen, Jason W Upton, Jan Carette, Edward S Mocarski, William J Kaiser

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Immune surveillance of cytomegalovirus in tissues.Cellular & molecular immunology · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Neuropilin (NRPs) Related Pathological Conditions and Their Modulators.International journal of molecular sciences · 2022
    Review
  15. Review
  16. Review
  17. Neuropilin-1, a myeloid cell-specific protein, is an inhibitor of HIV-1 infectivity.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  18. Review
  19. Article
  20. A widespread viral entry mechanism: The C-end Rule motif-neuropilin receptor interaction.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Review
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 5 institutions in 1 country.

Rebecca K LaneDepartment of Microbiology, Immunology, and Molecular Genetics, University of Texas Health at San Antonio, San Antonio, TX 78229.ORCID 0000-0002-5233-5422
Hongyan GuoDepartment of Biology, Viral Immunology Center, Georgia State University, Atlanta, GA 30303; hguo@gsu.edu wkaiser@inzentx.com.
Amanda D FisherDepartment of Microbiology, Immunology, and Molecular Genetics, University of Texas Health at San Antonio, San Antonio, TX 78229.
Jonathan DiepDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305.
Zhao LaiDepartment of Molecular Medicine, University of Texas Health at San Antonio, San Antonio, TX 78229.
Yidong ChenGreehey Children's Cancer Research Institute, University of Texas Health at San Antonio, San Antonio, TX 78229.
Jason W UptonDepartment of Biological Sciences, Auburn University, Auburn, AL 36849.
Jan CaretteDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305.ORCID 0000-0002-5187-8070
Edward S MocarskiDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322.
William J KaiserDepartment of Microbiology, Immunology, and Molecular Genetics, University of Texas Health at San Antonio, San Antonio, TX 78229; hguo@gsu.edu wkaiser@inzentx.com.
The University of Texas Health Science Center at San Antonio · USStanford University · USAuburn University · USEmory University · USGeorgia State University · US

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Robin Jean Leach · 1991 to 2026
$59.1M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR001120 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, HARGREAVES, KENNETH M · 2013 to 2017
$16.5M
Institutional Research Training GrantT32DE014318 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Kenneth M Hargreaves · 2002 to 2026
$12.1M
CYTOMEGALOVIRUS DNA REPLICATION AND RECOMBINATIONR01AI020211 · NIAID · STANFORD UNIVERSITY · PI EDWARD S MOCARSKI, EDWARD S. · 1985 to 2021
$5.9M
Host Genes Critical for Flavivirus InfectionR01AI141970 · NIAID · STANFORD UNIVERSITY · PI CARETTE, JAN E · 2019 to 2023
$2.0M
RIP1 and RIP3 regulation of apoptosis, necrosis, and inflammationDP5OD012198 · OD · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI KAISER, WILLIAM JOSEPH · 2012 to 2016
$1.9M
Neuropilin-1 is a putative entry receptor for murine cytomegalovirusF31DE029395 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LANE, REBECCA · 2020 to 2020
$27k
NCATS NIH HHS UL1 TR001120NCI NIH HHS P30 CA054174NIAID NIH HHS R01 AI020211NIAID NIH HHS R01 AI141970NIDCR NIH HHS F31 DE029395NIDCR NIH HHS T32 DE014318NIH HHS DP5 OD012198
6 · The paper itself

Abstract

Herpesviruses are ubiquitous human pathogens that cause a wide range of health complications. Currently, there is an incomplete understanding of cellular factors that contribute to herpesvirus infection. Here, we report an antiviral necroptosis-based genetic screen to identify novel host cell factors required for infection with the β-herpesvirus murine cytomegalovirus (MCMV). Our genome-wide CRISPR-based screen harnessed the capacity of herpesvirus mutants that trigger antiviral necroptotic cell death upon early viral gene expression. Vascular endothelial growth factor (VEGF) and semaphorin-binding receptor Neuropilin-1 (Nrp-1) emerge as crucial determinants of MCMV infection. We find that elimination of Nrp-1 impairs early viral gene expression and reduces infection rates in endothelial cells, fibroblasts, and macrophages. Furthermore, preincubation of virus with soluble Nrp-1 dramatically inhibits infection by reducing virus attachment. Thus, Nrp-1 is a key determinant of the initial phase of MCMV infection.

Indexed as

AnimalsCell LineClustered Regularly Interspaced Short Palindromic RepeatsCytomegalovirus InfectionsGene DeletionGene Expression Regulation, ViralMiceMuromegalovirusNecroptosisNeuropilin-1Neuropilin-1CRISPRcytomegolovirusnecroptosisneuropilin

Identifiers

PMID32747526
PMCPMC7443917
OpenAlexW3047048437

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.