Simian type-D retrovirus (SRV) infection is a health problem in captiv
e and wild-caught macaques; it interferes with acquired immune deficie
ncy syndrome-related research. Because the enzyme-linked immunosorbent
assay (ELISA) with gradient-purified SRV-2 virus yields a high percen
tage of false-positive results, the assay was modified with membrane a
ntigens from SRV-2-infected and uninfected A549 cells. The SRV-2 membr
ane antigen contains the major proteins detected in positive sera by W
estern blotting: enu proteins gp70 and gp20 and gag proteins p27, p14,
p12, and p10. The original purified virus ELISA had a specificity of
74% compared with Western immunoblot. The modified ELISA using the dif
ference in optical density between infected and control cell membrane
antigens resulted in a specificity of 100% when the same samples were
tested.