Prostaglandin A inhibits the replication of vesicular stomatitis virus: effect on virus glycoprotein

Prostaglandins of the A series were found to strongly suppress the replication of vesicular stomatitis virus (VSV) in mouse L fibroblasts. The highest non-toxic dose of PGA1,4 gg/ml, decreased VSV production by 93-6~. At this dose, PGAx did not alter DNA, RNA or protein synthesis in uninfected L cells for periods up to 24 h, whereas it further suppressed protein synthesis and slightly increased RNA synthesis in VSV-infected cells. The presence of PGAx during virus adsorption, with no treatment after infection, reduced VSV yields by 63.69/oo. However, the presence of PGAa during an early step of VSV replication was not essential for the antiviral action tooccur (PGA1 treatment could be started 1 to 2 h post-infection). Apart from a slight overall inhibition of virus protein synthesis, PGAt strongly suppressed the synthesis of the VSV glycoprotein G; moreover, itproduced an alteration in the mobility of this protein in SDS-polyacrylamide g ls. We propose that this slight decrease in molecular weight (about 4000) of the G protein in the presence of PGA 1 could be due to an alteration in the glycosylation process. Prostaglandins (PGs) are a group of cyclic 20-carbon fatty acids that are synthesized by mos