An alternative to conventional insect marking procedures: detection of a protein mark on pink bollworm by ELISA*

Four experiments were conducted to examine the feasibility of marking pink bollworm, Pectinophora gossypiella (Saunders) with rabbit immunoglobulin G (IgG) protein for mark‐release‐recapture studies. Pink bollworm were internally marked by feeding larvae an enriched rabbit IgG diet or externally marked by submerging pupae and spraying adults. Individuals were then assayed for the presence of rabbit IgG by sandwich enzyme‐linked immunosorbent assay (ELISA) using anti‐rabbit IgG. The internal marker was retained in larvae and retained in prepupae and pupae, but not in adults. A second experiment showed that rabbit IgG was retained on adults that were externally marked as pupae. A third series of tests examined the feasibility of externally marking adults with rabbit IgG. Rabbit IgG was retained on externally marked adults for six days in the field. Protein was retained on marked moths in the laboratory after they were captured on and removed from sticky traps. Finally, laboratory tests showed that large groups of externally marked moths transferred rabbit IgG to unmarked moths, but individual males do not readily transfer the protein to unmarked females in small vials.