Early endocytosis pathways in SSN-1 cells infected by dragon grouper nervous necrosis virus
Author(s) -
Wangta Liu,
ChiHsin Hsu,
YiRen Hong,
ShuChuan Wu,
Chun-Hsiung Wang,
Yi-Min Wu,
Chia-Ben Chao,
Chan-Shing Lin
Publication year - 2005
Publication title -
journal of general virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.55
H-Index - 167
eISSN - 1465-2099
pISSN - 0022-1317
DOI - 10.1099/vir.0.81021-0
Subject(s) - biology , pinocytosis , endocytosis , membrane ruffling , virus , virology , internalization , multiplicity of infection , syncytium , virus like particle , grouper , microbiology and biotechnology , cell , biochemistry , cytoskeleton , gene , recombinant dna , fishery , fish <actinopterygii>
Many fish undergo betanodavirus infection. To study the infection process of dragon grouper nervous necrosis virus (DGNNV), native virus and virus-like particles (VLPs) were used to analyse the binding and internalization in SSN-1 cells. The binding of DGNNV and VLPs to SSN-1 cells was demonstrated using Western blotting and immunofluorescence microscopy. As estimated by indirect ELISA, the DGNNV particles bound SSN-1 cells in a dose-dependent manner up to 8 x 10(4) particles per cell. The binding of VLPs was sensitive to neuraminidase and tunicamycin, suggesting that cell-surface sialic acid is involved in binding. The penetration of DGNNV into cells, which was monitored by electron microscopy, appeared to occur mainly via the spherical pit and membrane ruffling pathways. Occasionally, a spherical pit was engulfed by membrane ruffling so as to form a large figure-of-eight-shaped vesicle with an open connection. Our observations suggest that DGNNV utilizes both micro- and macropinocytosis pathways to enter SSN-1 cells.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom