TY - JOUR
T1 - Identification and characterization of a novel secreted antigen 1 of Babesia microti and evaluation of its potential use in enzyme-linked immunosorbent assay and immunochromatographic test
AU - Luo, Yuzi
AU - Jia, Honglin
AU - Terkawi, M. Alaa
AU - Goo, Youn Kyoung
AU - Kawano, Suguru
AU - Ooka, Hideo
AU - Li, Yan
AU - Yu, Longzheng
AU - Cao, Shinuo
AU - Yamagishi, Junya
AU - Fujisaki, Kozo
AU - Nishikawa, Yoshifumi
AU - Saito-Ito, Atsuko
AU - Igarashi, Ikuo
AU - Xuan, Xuenan
PY - 2011/6
Y1 - 2011/6
N2 - Here, we identified a novel secreted antigen designated as Babesia microti secreted antigen 1 (BmSA1) by immunoscreening a B. microti cDNA expression library using the sera from hamsters immunized with plasma, putatively containing secreted antigens, from B. microti-infected hamsters. Antibodies raised in mice immunized with recombinant BmSA1 (r. BmSA1) recognized a native 33-kDa parasite protein. An enzyme-linked immunosorbent assay (ELISA) of r. BmSA1 detected specific antibodies as early as 6 and 4. days post-infection in sera from a hamster experimentally infected with B. microti Gray strain (US type) and a mouse experimentally infected with B. microti Munich strain (rodent isolate), respectively. Moreover, a rapid immunochromatographic test (ICT) using r. BmSA1 detected specific antibodies in a hamster experimentally infected with B. microti from day 6 to at least day 270 post-infection, which was quite consistent with the results of the ELISA. In addition, analysis of the sera involved in the first case of human babesiosis in Japan (Kobe type) showed that specific antibodies were detectable in the patient and the positive donor by ELISA using r. BmSA1, and the ICT result was identical to the ELISA data. Taken together, these results indicated that BmSA1 could be a promising and universal target for developing both ELISA and ICT for the serodiagnosis of human babesiosis and for an epidemiological survey of its rodent reservoir.
AB - Here, we identified a novel secreted antigen designated as Babesia microti secreted antigen 1 (BmSA1) by immunoscreening a B. microti cDNA expression library using the sera from hamsters immunized with plasma, putatively containing secreted antigens, from B. microti-infected hamsters. Antibodies raised in mice immunized with recombinant BmSA1 (r. BmSA1) recognized a native 33-kDa parasite protein. An enzyme-linked immunosorbent assay (ELISA) of r. BmSA1 detected specific antibodies as early as 6 and 4. days post-infection in sera from a hamster experimentally infected with B. microti Gray strain (US type) and a mouse experimentally infected with B. microti Munich strain (rodent isolate), respectively. Moreover, a rapid immunochromatographic test (ICT) using r. BmSA1 detected specific antibodies in a hamster experimentally infected with B. microti from day 6 to at least day 270 post-infection, which was quite consistent with the results of the ELISA. In addition, analysis of the sera involved in the first case of human babesiosis in Japan (Kobe type) showed that specific antibodies were detectable in the patient and the positive donor by ELISA using r. BmSA1, and the ICT result was identical to the ELISA data. Taken together, these results indicated that BmSA1 could be a promising and universal target for developing both ELISA and ICT for the serodiagnosis of human babesiosis and for an epidemiological survey of its rodent reservoir.
KW - Babesia microti
KW - ELISA
KW - Immunochromatographic test
KW - Secreted antigen 1
UR - http://www.scopus.com/inward/record.url?scp=79953779610&partnerID=8YFLogxK
U2 - 10.1016/j.parint.2010.11.001
DO - 10.1016/j.parint.2010.11.001
M3 - Article
C2 - 21070864
AN - SCOPUS:79953779610
SN - 1383-5769
VL - 60
SP - 119
EP - 125
JO - Parasitology International
JF - Parasitology International
IS - 2
ER -