Evidence map›Paper›PMID 35715782›Full record

ArticleBMC veterinary research2022

Characterization of B cell receptor H-CDR3 repertoire of spleen in PRV-infected mice.

Lishuang Deng, Fan Yang, Zhiwen Xu, Fengqin Li, Jun Zhao, Huidan Deng, Zhijie Jian, Siyuan Lai, Xiangang Sun, Ling Zhu

Open access · goldAbstract read
In one paragraph

Article in BMC veterinary research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

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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 2 institutions in 1 country.

Lishuang Deng *College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.
Fan Yang *College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.
Zhiwen XuCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.
Fengqin LiCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.
Jun ZhaoCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.
Huidan DengCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.
Zhijie JianCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.
Siyuan LaiCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.
Xiangang SunCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.
Ling ZhuCollege of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China. abtczl72@126.com.
Sichuan Agricultural University · CNXichang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pseudorabies virus (PRV), also known as suid Alphaherpesvirus 1 (SuHV-1), which is one of the most devastating infectious pathogen of swine industry worldwide. Vaccination is the safest and most effective PRV prevention and control strategy. B cell receptor (BCR) is membrane-bound immunoglobulin located on the surface of B cells capable of specifically binding foreign antigens, which is one of the most important molecules regulating the proliferation and function of B cells. Here, to assess the molecular diversity of BCR H-CDR3 repertoire after different PRV strains infection, we detected the IGHV, IGHD, IGHJ genes usage and CDR3 sequence changes of mice spleen with PRV vaccine strain (Bartha-K61), variant strain (XJ) and mock infection by high-throughput sequencing. We found that PRV-infected groups shared partial BCR sequences, which are most likely to be PRV-specific BCR candidates. However, there were still differences in the IGHV genes usage as well as the combined usage of IGHV and IGHJ genes between the Bartha-K61 strain and XJ strain infection groups. In addition, the CDR3 sequences exhibited large differences in the types and lengths in PRV infection groups. Our study contributes to a better understanding of the host adaptive immune response to PRV infection and provides a theoretical basis for further research on novel and efficient PRV vaccines in the future.

Indexed as

Herpesvirus 1, SuidPseudorabiesSwine DiseasesAnimalsMicePseudorabies VaccinesReceptors, Antigen, B-CellSpleenSwinePseudorabies VaccinesReceptors, Antigen, B-CellCDR3High-throughput sequencingIGHMicePRVVaccine

Identifiers

PMID35715782
PMCPMC9204683
OpenAlexW4283025508

What OpenQuestion holds

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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 OpenQuestion graph.