The ultrastructural aspects of the replication cycle of the turbot aqu
areovirus (TRV) were studied using CHSE-214 cells. Although this virus
in general followed the typical pattern of reovirus replication and m
orphogenesis, it presented some important differences. Internalisation
of virions into the host cell occurred by direct penetration through
the plasma membrane (even at temperatures below 4 degrees C), and this
step was independent of trypsin treatment. Two size classes of viral
particles were detected in the cytoplasm of infected cells: (i) partic
les of 30 nm diameter, probably corresponding to cores, located inside
cytoplasmic viroplasms, and (ii) 45 nm diameter particles, located in
Vesicles of the endoplasmic reticulum, probably corresponding to sing
le-shelled virions. Double-shelled complete viral particles (75-80 nm
diameter) were only detected at the exterior of the cell. Cores formed
inside the viroplasms were transformed into 45 nm immature virions by
budding from viroplasms to cytoplasmic vesicles. The vesicles carried
those subviral particles towards the periphery of the cell. Final mat
uration occurred by budding of the immature virions through the plasma
membrane. During this process, incomplete virions acquired an externa
l protein layer, to form the 75 nm double-shelled complete virions rel
eased to the exterior. Thus, release of TRV viral progeny was not nece
ssarily associated with cell lysis. Replication of TRV was cytoplasmic
, and some of the ultrastructural changes caused by the viral replicat
ion included development of many dense fibrillar bodies, and cell cyto
skeleton alterations. (C) 1998 Published by Elsevier Science B.V.