Editorial
Copyright ©2013 Baishideng. All rights reserved.
World J Virol. Feb 12, 2013; 2(1): 1-5
Published online Feb 12, 2013. doi: 10.5501/wjv.v2.i1.1
Betanodavirus: Mitochondrial disruption and necrotic cell death
Jiann-Ruey Hong
Jiann-Ruey Hong, Laboratory of Molecular Virology and Biotechnology, Institute of Biotechnology, National Cheng Kung University, Tainan 701, Taiwan
Author contributions: Hong JR solely contributed to this paper.
Supported by A grant awarded Dr. Jiann-Ruey Hong from the National Science Council, Taiwan, No. NSC 97-2313-B-006-004-MY3
Correspondence to: Dr. Jiann-Ruey Hong, Laboratory of Molecular Virology and Biotechnology, Institute of Biotechnology, National Cheng Kung University, No.1, University Road, Tainan 701, Taiwan. jrhong@mail.ncku.edu.tw
Telephone: +886-6-2003082 Fax: +886-6-2766505
Received: March 8, 2012
Revised: February 3, 2013
Accepted: February 8, 2013
Published online: February 12, 2013
Processing time: 34 Days and 22.4 Hours
Abstract

Betanodaviruses cause viral nervous necrosis, an infectious neuropathological condition in fish that is characterized by necrosis of the central nervous system, including the brain and retina. This disease can cause mass mortality in larval and juvenile populations of several teleost species and is of global economic importance. The mechanism of brain and retina damage during betanodavirus infection is poorly understood. In this review, we will focus recent results that highlight betanodavirus infection-induced molecular death mechanisms in vitro. Betanodavirus can induce host cellular death and post-apoptotic necrosis in fish cells. Betanodavirus-induced necrotic cell death is also correlated with loss of mitochondrial membrane potential in fish cells, as this necrotic cell death is blocked by the mitochondrial membrane permeability transition pore inhibitor bongkrekic acid and the expression of the anti-apoptotic Bcl-2 family member zfBcl-xL. Moreover, this mitochondria-mediated necrotic cell death may require a caspase-independent pathway. A possible cellular death pathway involving mitochondrial function and the modulator zfBcl-xs is discussed which may provide new insights into the necrotic pathogenesis of betanodavirus.

Keywords: Nervous necrosis virus; Mitochondrial membrane potential; Bongkrekic acid; zfBcl-xL; Caspase-independent; Brain damage