Transmembrane Protein 39A Promotes the Replication of Encephalomyocarditis Virus

ATG7 autophagy encephalomyocarditis virus replication transmembrane protein 39A

Journal

Frontiers in microbiology
ISSN: 1664-302X
Titre abrégé: Front Microbiol
Pays: Switzerland
ID NLM: 101548977

Informations de publication

Date de publication:
2019
Historique:
received: 25 08 2019
accepted: 05 11 2019
entrez: 19 12 2019
pubmed: 19 12 2019
medline: 19 12 2019
Statut: epublish

Résumé

Encephalomyocarditis virus (EMCV) causes encephalitis, myocarditis, neuropathy, reproductive disorders, and diabetes in animals. EMCV is known to induce cell autophagy; however, the molecular mechanisms underlying this remain unclear. Here, we show that the type III-transmembrane protein, transmembrane protein 39A (TMEM39A), plays a critical role in EMCV replication. We showed that EMCV GS01 strain infection upregulated TMEM39A expression. Importantly, EMCV induced autophagy in a range of host cells. The autophagy chemical inhibitor, 3-MA, inhibited EMCV replication and reduced TMEM39A expression. This is the first study demonstrating TMEM39A promoting the replication of EMCV

Identifiants

pubmed: 31849860
doi: 10.3389/fmicb.2019.02680
pmc: PMC6901969
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2680

Informations de copyright

Copyright © 2019 Li, Ma, Li, Li, Zhang, Xie, Bai, Idris and Feng.

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Auteurs

Xiangrong Li (X)

Key Laboratory of Biotechnology and Bioengineering of State Ethnic Affairs Commission, Biomedical Research Center, Northwest Minzu University, Lanzhou, China.
Gansu Tech Innovation Center of Animal Cell, Biomedical Research Center, Lanzhou, China.

Ruixian Ma (R)

Key Laboratory of Biotechnology and Bioengineering of State Ethnic Affairs Commission, Biomedical Research Center, Northwest Minzu University, Lanzhou, China.
Life Science and Engineering College, Northwest Minzu University, Lanzhou, China.

Qian Li (Q)

Key Laboratory of Biotechnology and Bioengineering of State Ethnic Affairs Commission, Biomedical Research Center, Northwest Minzu University, Lanzhou, China.
Life Science and Engineering College, Northwest Minzu University, Lanzhou, China.

Shengjun Li (S)

Key Laboratory of Biotechnology and Bioengineering of State Ethnic Affairs Commission, Biomedical Research Center, Northwest Minzu University, Lanzhou, China.
Life Science and Engineering College, Northwest Minzu University, Lanzhou, China.

Haixia Zhang (H)

Key Laboratory of Biotechnology and Bioengineering of State Ethnic Affairs Commission, Biomedical Research Center, Northwest Minzu University, Lanzhou, China.
Gansu Tech Innovation Center of Animal Cell, Biomedical Research Center, Lanzhou, China.

Jingying Xie (J)

College of Veterinary Medicine, Gansu Agricultural University, Lanzhou, China.

Jialin Bai (J)

Key Laboratory of Biotechnology and Bioengineering of State Ethnic Affairs Commission, Biomedical Research Center, Northwest Minzu University, Lanzhou, China.
Gansu Tech Innovation Center of Animal Cell, Biomedical Research Center, Lanzhou, China.

Adi Idris (A)

School of Medical Science, Menzies Health Institute Queensland, Griffith University, Gold Coast, QLD, Australia.

Ruofei Feng (R)

Key Laboratory of Biotechnology and Bioengineering of State Ethnic Affairs Commission, Biomedical Research Center, Northwest Minzu University, Lanzhou, China.
Gansu Tech Innovation Center of Animal Cell, Biomedical Research Center, Lanzhou, China.

Classifications MeSH