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Plasmalemmal vesicle associated protein (PV1) modulates SV40 virus infectivity in CV-1 cells.


ABSTRACT: Plasmalemmal vesicle associated protein (Plvap/PV1) is a structural protein required for the formation of the stomatal diaphragms of caveolae. Caveolae are plasma membrane invaginations that were implicated in SV40 virus entry in primate cells. Here we show that de novo Plvap/PV1 expression in CV-1 green monkey epithelial cells significantly reduces the ability of SV40 virus to establish productive infection, when cells are incubated with low concentrations of the virus. However, in presence of high viral titers PV1 has no effect on SV40 virus infectivity. Mechanistically, PV1 expression does not reduce the cell surface expression of known SV40 receptors such as GM1 ganglioside and MHC class I proteins. Furthermore, PV1 does not reduce the binding of virus-like particles made by SV40 VP1 protein to the CV-1 cell surface and does not impact their internalization when cells are incubated with either high or low VLP concentrations. These results suggest that PV1 protein is able to block SV40 infectivity at low but not at high viral concentration either by interfering with the infective internalization pathway at the cell surface or at a post internalization step.

SUBMITTER: Tse D 

PROVIDER: S-EPMC3171970 | biostudies-literature | 2011 Aug

REPOSITORIES: biostudies-literature

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Plasmalemmal vesicle associated protein (PV1) modulates SV40 virus infectivity in CV-1 cells.

Tse Dan D   Armstrong David A DA   Oppenheim Ariella A   Kuksin Dmitry D   Norkin Leonard L   Stan Radu V RV  

Biochemical and biophysical research communications 20110730 2


Plasmalemmal vesicle associated protein (Plvap/PV1) is a structural protein required for the formation of the stomatal diaphragms of caveolae. Caveolae are plasma membrane invaginations that were implicated in SV40 virus entry in primate cells. Here we show that de novo Plvap/PV1 expression in CV-1 green monkey epithelial cells significantly reduces the ability of SV40 virus to establish productive infection, when cells are incubated with low concentrations of the virus. However, in presence of  ...[more]

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