Y. Inoshima et al., Use of protein AG in an enzyme-linked immunosorbent assay for screening for antibodies against parapoxvirus in wild animals in Japan, CL DIAG LAB, 6(3), 1999, pp. 388-391
Using protein AC in an enzyme-linked immunosorbent assay (ELISA), we tried
to detect antibodies against parapoxvirus in 9 species of wild animals in J
apan: the Japanese badger (Meles meles anakuma), Japanese black bear (Ursus
thibetanus japonicus), Japanese deer (Cervus nippon centralis), Japanese m
onkey (Macaca fuscata), Japanese raccoon dog (Nyctereutes procyonoides vive
rrinus), Japanese serow (Capricornis crispus), Japanese wild boar (Sus scro
fa leucomystax), masked palm civet (Paguma larvata), and nutria (Myocastor
coypus). A total of 272 serum samples were collected over the period from 1
984 to 1995 and were tested by the protein AG-ELISA, the agar gel immunodif
fusion test, and an indirect Immunofluorescence assay. The protein AG-ELISA
was effective in a serological survey for parapoxvirus in wild animals, an
d antibodies were detected only in Japanese serows, A total of 24 of 66 (36
.4%) Japanese serows reacted positively, and they were found in almost all
prefectures in all years tested. These results suggest that epizootic cycle
s of parapoxvirus exist widely in Japanese serows and that they could be re
servoirs for the virus in the field in Japan. Moreover, it is probable that
they might carry the virus to domestic animals such as cattle, sheep, and
goats.