Evidence map›Paper›PMID 32381067›Full record

ArticleVeterinary research2020

Porcine DNAJB6 promotes PCV2 replication via enhancing the formation of autophagy in host cells.

Cong Han, Qian Du, Lei Zhu, Nannan Chen, Le Luo, Qiao Chen, Jiatong Yin, Xingchen Wu, Dewen Tong, Yong Huang

Open access · goldAbstract read
In one paragraph

Article in Veterinary research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Autophagy and porcine circovirus infection: a mini review.Frontiers in cellular and infection microbiology · 2025
    Review
  5. Review
  6. Review
  7. The Multi-Faceted Role of Autophagy During Animal Virus Infection.Frontiers in cellular and infection microbiology · 2022
    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 2 institutions in 1 country.

Cong HanCollege of Veterinary Medicine, Northwest A&F University, Yangling, China.
Qian DuCollege of Veterinary Medicine, Northwest A&F University, Yangling, China.
Lei ZhuCollege of Veterinary Medicine, Northwest A&F University, Yangling, China.
Nannan ChenCollege of Veterinary Medicine, Northwest A&F University, Yangling, China.
Le LuoCollege of Veterinary Medicine, Northwest A&F University, Yangling, China.
Qiao ChenCollege of Veterinary Medicine, Northwest A&F University, Yangling, China.
Jiatong YinCollege of Veterinary Medicine, Northwest A&F University, Yangling, China.
Xingchen WuCollege of Veterinary Medicine, Northwest A&F University, Yangling, China.
Dewen TongCollege of Veterinary Medicine, Northwest A&F University, Yangling, China. dwtong@nwsuaf.edu.cn.
Yong HuangCollege of Veterinary Medicine, Northwest A&F University, Yangling, China. yonghuang@nwsuaf.edu.cn.ORCID http://orcid.org/0000-0001-7444-5182
Northwest A&F University · CNNorth West Agriculture and Forestry University · CN

Funding

Central Project of Major Agricultural Technology Promotion funds K3360217060Fundamental Research Funds for the Central Universities 2452017023Key Research and Development Program of Shaanxi Province 2018ZDCXL-NY-02-04Key Research and Development Program of Shaanxi Province 2018ZDCXL-NY-02-07National Natural Science Foundation of China 31672535National Natural Science Foundation of China 31872447National Natural Science Foundation of China 31972686
6 · The paper itself

Abstract

Hsp40/DnaJ family proteins play important roles in the infection process of various viruses. Porcine DNAJB6 (pDNAJB6) is a major member of this family, but its role in modulating the replication of porcine circovirus type 2 (PCV2) is still unclear. In the present study, pDNAJB6 was found to be significantly upregulated by PCV2 infection, and confirmed to be interacted with PCV2 capsid (Cap) protein and co-localized at both cytoplasm and nucleus in the PCV2-infected cells. Knockout of pDNAJB6 significantly reduced the formation of autophagosomes in PCV2-infected cells or in the cells expressing Cap protein, whereas overexpression of pDNAJB6 showed an opposite effect. In addition, the domain mapping assay showed that the J domain of pDNAJB6 (amino acids (aa) 1-99) and the C terminus of Cap (162-234 aa) were required for the interaction of pDNAJB6 with Cap. Notably, the interaction of pDNAJB6 with Cap was very important to promoting the formation of autophagosomes induced by PCV2 infection or Cap expression and enhancing the replication of PCV2. Taken together, the results presented here show a novel function of pDNAJB6 in regulation of porcine circovirus replication that pDNAJB6 enhances the formation of autophagy to promote viral replication through interacting with viral capsid protein during PCV2 infection.

Indexed as

Virus ReplicationAnimalsAutophagosomesAutophagyCircoviridae InfectionsCircovirusGene Knockout TechniquesHSP40 Heat-Shock ProteinsMutationSus scrofaSwineSwine DiseasesUp-RegulationVirionHSP40 Heat-Shock Proteins

Identifiers

PMID32381067
PMCPMC7203849
OpenAlexW3021894509

What OpenQuestion 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 OpenQuestion graph.