Evidence map›Paper›PMID 41328592›Full record

ArticleVirulence2025

Genome-scale CRISPR screen identifies host factors associated with bovine parainfluenza virus 3 infection.

Yuanchen Geng, Chuanwen Jiang, Huaiyi Zhang, Hao Yang, Yongchong Peng, Yingyu Chen, Changmin Hu, Hailong Liu, Sheng Li, Huanchun Chen and 2 more

Abstract read
In one paragraph

Article in Virulence, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

12 authors.

Yuanchen GengThe National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
Chuanwen JiangThe National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
Huaiyi ZhangThe National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
Hao YangThe National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
Yongchong PengThe National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
Yingyu ChenThe National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.ORCID 0000-0002-1200-5314
Changmin HuCollege of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China.
Hailong LiuKey Laboratory of Agricultural Animal Genetics, Breeding and Reproduction of Ministry of Education & Key Lab of Swine Genetics and Breeding of Ministry of Agriculture and Rural Affairs, College of Animal Science and Technology, Huazhong Agricultural University, Wuhan, China.
Sheng LiHubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.
Huanchun ChenThe National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
Shengsong XieHubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, China.ORCID 0000-0001-5124-2673
Aizhen GuoThe National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.ORCID 0000-0002-7460-8356

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bovine parainfluenza virus type 3 (BPIV-3) is a major pathogen associated with the bovine respiratory disease complex. However, the limited understanding of host factors crucial for BPIV-3 replication has hindered the development of effective preventive and therapeutic strategies. To tackle this critical issue, we constructed a bovine genome-wide CRISPR/Cas9 knockout library in Madin-Darby bovine kidney cells, which was then used to systematically identify and characterize the host genes essential for BPIV-3a replication. Subsequently, 10 genes were validated using both RT-qPCR and viral titration assays. Furthermore, through gene knockout or knockdown and rescue experiments, we identified three key genes required for BPIV-3a replication: Wnt family member 5A (WNT5A), solute carrier family 16 member 13 (SLC16A13), and selenoprotein N (SELENON). However, their effects on viral adhesion and internalization varied. WNT5A was involved in both processes, SLC16A13 participated solely in internalization, while SELENON had no significant impact on either. Beyond BPIV-3a, these three genes were also found to be essential for the infection of BPIV-3c and Bovine enterovirus. In conclusion, this study offers novel insights into the molecular mechanisms governing the replication and pathogenesis of BPIV-3a, BPIV-3c, and bovine enterovirus within host cells, thereby providing a foundation for identifying potential targets in the development of novel antiviral strategies.

Indexed as

Cattle DiseasesHost-Pathogen InteractionsParainfluenza Virus 3, BovineRespirovirus InfectionsAnimalsCattleCell LineCRISPR-Cas SystemsGene Knockout TechniquesVirus InternalizationVirus ReplicationWnt-5a ProteinWnt-5a ProteinBPIV-3CRISPR screenhost factorsSELENONSLC16A13WNT5A

Identifiers

PMID41328592
PMCPMC12674325

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.