Evidence map›Paper›PMID 37450601›Full record

ArticleScience advances2023

Lrp1 is essential for lethal Rift Valley fever hepatic disease in mice.

Madeline M Schwarz, Safder S Ganaie, Annie Feng, Griffin Brown, Tenzin Yangdon, J Michael White, Ryan M Hoehl, Cynthia M McMillen, Rachael E Rush, Kaleigh A Connors and 5 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

18 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  15. Laboratory Animal Models for Rift Valley Fever Virus Disease.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  16. Making Rift Valley Fever Viral Particles Fluorescent.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  17. An Introduction to Rift Valley Fever Virus.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  18. Article
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

15 authors at 2 institutions in 1 country.

Madeline M SchwarzCenter for Vaccine Research, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0002-9038-4655
Safder S GanaieDepartment of Pathology & Immunology, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.ORCID 0000-0002-9014-6577
Annie FengDepartment of Pathology & Immunology, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.ORCID 0000-0003-4973-5350
Griffin BrownDepartment of Pathology & Immunology, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.ORCID 0000-0002-5369-7134
Tenzin YangdonDepartment of Pathology & Immunology, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.ORCID 0000-0002-2335-2354
J Michael WhiteTransgenic, Knockout and Micro-Injection Core, Department of Pathology & Immunology, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.ORCID 0000-0001-5110-6567
Ryan M HoehlCenter for Vaccine Research, University of Pittsburgh, Pittsburgh, PA, USA.
Cynthia M McMillenCenter for Vaccine Research, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0001-9211-7908
Rachael E RushCenter for Vaccine Research, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0001-7481-7134
Kaleigh A ConnorsCenter for Vaccine Research, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0002-7278-0590
Xiaoxia CuiGenome Engineering & Stem Cell Center, Department of Genetics, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.ORCID 0000-0002-3073-7332
Daisy W LeungDepartment of Pathology & Immunology, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.ORCID 0000-0002-7189-9557
Takeshi EgawaDepartment of Pathology & Immunology, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.ORCID 0000-0001-7489-1051
Gaya K AmarasingheDepartment of Pathology & Immunology, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.ORCID 0000-0002-0418-9707
Amy L HartmanCenter for Vaccine Research, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0002-0857-2973
Washington University in St. Louis · USUniversity of Pittsburgh · US

Funding

The transcription factor c-MYC in lymphocyte expansion and restriction of stemnessR01AI130152 · NIAID · WASHINGTON UNIVERSITY · PI Takeshi Egawa · 2017 to 2026
$4.6M
Identification and Characterization of Entry Factors Critical for Rift Valley Fever Virus Infection and PathogenesisR01AI161765 · NIAID · WASHINGTON UNIVERSITY · PI AMARASINGHE, GAYA K., HARTMAN, AMY L · 2021 to 2025
$3.7M
Live-attenuated Rift Valley fever vaccines: comparative mechanisms of trans-placental transmission and vaccine efficacy for developing fetusesR01AI150792 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HARTMAN, AMY L · 2020 to 2025
$3.7M
Characterizing the role of LDL related receptor 1 (Lrp1) as host entry factor for multiple bunyavirusesR01AI169850 · NIAID · WASHINGTON UNIVERSITY · PI Gaya K. Amarasinghe, Amy L Hartman · 2023 to 2026
$3.1M
Comparative Analysis of Bunyavirus NeuropathogenesisR56AI171920 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HARTMAN, AMY L · 2022 to 2022
$1.1M
Role of the novel entry factor Lrp1 in in vivo tropism and pathogenesis of Rift Valley fever virusR21AI163603 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HARTMAN, AMY L · 2021 to 2022
$442k
NIAID NIH HHS R01 AI130152NIAID NIH HHS R01 AI150792NIAID NIH HHS R01 AI161765NIAID NIH HHS R01 AI169850NIAID NIH HHS R21 AI163603NIAID NIH HHS R56 AI171920
6 · The paper itself

Abstract

Rift Valley fever virus (RVFV) is an emerging arbovirus found in Africa. While RVFV is pantropic and infects many cells and tissues, viral replication and necrosis within the liver play a critical role in mediating severe disease. The low-density lipoprotein receptor-related protein 1 (Lrp1) is a recently identified host factor for cellular entry and infection by RVFV. The biological significance of Lrp1, including its role in hepatic disease in vivo, however, remains to be determined. Because Lrp1 has a high expression level in hepatocytes, we developed a mouse model in which Lrp1 is specifically deleted in hepatocytes to test how the absence of liver Lrp1 expression affects RVF pathogenesis. Mice lacking Lrp1 expression in hepatocytes showed minimal RVFV replication in the liver, longer time to death, and altered clinical signs toward neurological disease. In contrast, RVFV infection levels in other tissues showed no difference between the two genotypes. Therefore, Lrp1 is essential for RVF hepatic disease in mice.

Indexed as

Rift Valley FeverRift Valley fever virusAfricaAnimalsHepatocytesLow Density Lipoprotein Receptor-Related Protein-1MiceLow Density Lipoprotein Receptor-Related Protein-1Lrp1 protein, mouse

Identifiers

PMID37450601
PMCPMC10348670
OpenAlexW4384296889

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.