4.7 Article

Identification of Beclin-1 from orange-spotted grouper (Epinephelus coioides) involved in viral infection

期刊

FISH & SHELLFISH IMMUNOLOGY
卷 94, 期 -, 页码 336-345

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fsi.2019.09.029

关键词

Beclin-1; Orange-spotted grouper; RGNNV; Interferon; Inflammatory; Autophagy

资金

  1. National Natural Science Foundation of China [31302226, 31572651]
  2. Technology Planning Project of Guangdong Province of China [2015A020209181]
  3. National Key R&D Program of China [2018YFD0900501]
  4. Special foundation for achieving the first class of Guangdong Province [231419013]
  5. Guangdong South China Sea Key Laboratory of Aquaculture for Aquatic Economic Animals, Guangdong Ocean University [KFKT2019YB11]
  6. College Student Innovation and Entrepreneurship Training Program of Guangdong Ocean University

向作者/读者索取更多资源

Beclin-1 is an essential autophagic regulator that plays diverse roles in physiology and disease. However, reports about the function of fish Beclin-1 during pathogen infection are still very limited. In this study, a Beclin-1 homolog (EcBeclin-1) from orange-spotted grouper (Epinephelus coioides) was identified and its roles in viral infection were investigated. EcBeclin-1 encoded 447amino acids protein with a BH3 domain, a CCD domain and an ECD domain, which shared high identities (97%-82%) with reported Beclin-1 proteins from mammal to fish. Quantitative real-time PCR (qRT-PCR) analysis revealed that EcBeclin-1 was predominantly expressed in brain and muscle of healthy grouper. Using fluorescence microscopy, we found that EcBeclin-1 was co-localized with endoplasmic reticulum (ER) in grouper spleen cells (EAGS). After red-spotted grouper nervous necrosis virus (RGNNV) infection in vitro, EcBeclin-1 transcript was significantly up-regulated, implying that EcBeclin-1 might be involved in viral infection. Furthermore, the in vitro studies of EcBeclin-1 overexpression promoted RGNNV induced autophagy, as well as the expression of coat protein (CP) and RNA-dependent RNA polymerase (RdRp). The overexpression of EcBeclin-1 suppressed the expressions of interferon pathway-related factors, inflammatory-related factors and activities of NF-kappa B and ISRE. Additionally, EcBeclin-1 could interact with EcBcl-xL in vitro. These data suggest that EcBeclin-1 affect viral replication through modulating IFN and inflammatory responses, as well as virus-induced cell death, which will help us to further explore the immune response of fish during viral infection.

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