Evidence map›Paper›PMID 40799542›Full record

ArticlebioRxiv : the preprint server for biology2025

Selective knockout of key CMV receptors in fetal cells blocks direct and endocytic pathways of entry in the guinea pig.

Yushu Qin, K Yeon Choi, Nadia El-Hamdi, Alistair McGregor

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Yushu QinDepartment of Microbial Pathogenesis & Immunology, Texas A&M University, Health Science Center, College of Medicine, Bryan, Texas, United States of America.
K Yeon ChoiDepartment of Microbial Pathogenesis & Immunology, Texas A&M University, Health Science Center, College of Medicine, Bryan, Texas, United States of America.
Nadia El-HamdiDepartment of Microbial Pathogenesis & Immunology, Texas A&M University, Health Science Center, College of Medicine, Bryan, Texas, United States of America.
Alistair McGregorDepartment of Microbial Pathogenesis & Immunology, Texas A&M University, Health Science Center, College of Medicine, Bryan, Texas, United States of America.

Funding

Development of a universal DISC vaccine strategy against congenital cytomegalovirusR01AI155561 · NIAID · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI MCGREGOR, ALISTAIR · 2021 to 2025
$3.3M
CMV pentameric complex based vaccine strategies for prevention of congenital CMVR01HD090065 · NICHD · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI MCGREGOR, ALISTAIR · 2017 to 2021
$1.5M
Placental trophoblast infection and TLR mediated response to congenital CMVR01AI100933 · NIAID · UNIVERSITY OF MINNESOTA · PI MCGREGOR, ALISTAIR · 2012 to 2015
$1.5M
Development of an effective DISC vaccine strategy against congenital CMVR01AI098984 · NIAID · UNIVERSITY OF MINNESOTA · PI MCGREGOR, ALISTAIR · 2012 to 2015
$1.4M
NIAID NIH HHS R01 AI098984NIAID NIH HHS R01 AI100933NIAID NIH HHS R01 AI155561NICHD NIH HHS R01 HD090065
6 · The paper itself

Abstract

Cytomegalovirus is a leading cause of congenital disease and a vaccine is a high priority. Guinea pig with guinea pig cytomegalovirus (GPCMV) is the only small animal model for congenital CMV (cCMV). GPCMV encodes functionally essential viral entry glycoprotein complexes similar to HCMV, which are neutralizing antibody targets. As with HCMV, GPCMV has two pathways of cell entry (direct and endocytic). Common to both pathways and essential for infection is the fusogenic viral glycoprotein gB. Additional gH/gL-based complexes are necessary for receptor interaction and cell entry: gH/gL/gO trimer (direct); pentamer complex, PC (endocytic). Direct cell entry requires host PDGFRA receptor and viral trimer. An endocytic PC receptor has not been identified for GPCMV or any animal CMV. GPCMV endocytic entry was blocked by acidic flux inhibition but not direct cell entry, requiring knockout of PDGFRA. We hypothesized that cellular knockout of GPCMV direct and endocytic receptors would completely block infection. Two PC receptor candidates, guinea pig NRP2 and CD147, present on all established guinea pig cell lines were evaluated. Results demonstrated that NRP2 interacted with PC unlike CD147 in immunoprecipitation assays. Double knockout of PDGFRA and NRP2 completely blocked GPCMV but had no impact on control HSV-1 infection. In contrast, CD147/PDGFRA double knockout had limited inhibition of GPCMV and no impact on HSV-1. Ectopic expression of cell receptors restored infection to normal levels on knockout cell lines. Overall, results demonstrate GPCMV conservation with HCMV for key receptors and cell entry pathways enhancing the translational importance of this model.

Identifiers

PMID40799542
PMCPMC12340832

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Registered trials

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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.