Serodiagnosis of recently acquired Toxoplasma gondii infection with a recombinant antigen

Citation
Sl. Li et al., Serodiagnosis of recently acquired Toxoplasma gondii infection with a recombinant antigen, J CLIN MICR, 38(1), 2000, pp. 179-184
Citations number
20
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Microbiology
Journal title
JOURNAL OF CLINICAL MICROBIOLOGY
ISSN journal
00951137 → ACNP
Volume
38
Issue
1
Year of publication
2000
Pages
179 - 184
Database
ISI
SICI code
0095-1137(200001)38:1<179:SORATG>2.0.ZU;2-T
Abstract
A portion of a cDNA encoding a 35-kDa antigen from Toxoplasma gondii was cl oned into the CKS expression vector and expressed in Escherichia coli. By u sing the enzyme-linked immunosorbent assay (ELISA), the recombinant protein (rP35 antigen) was examined for reactivity with immunoglobulin G (IgG) ant ibodies in the sera of pregnant women. Of these women, 41 had a toxoplasma serologic profile suggestive of recently acquired T. gondii infection (Sabi n-Feldman dye test [DT] titers from 1:256 to 1:32,000, positive IgM ELISA t iters from 2.3 to 9.7, positive IgA ELISA from 1 to >28, and acute patterns in the differential agglutination [AC/HS] test) (group I), and 50 women ha d a toxoplasma serologic profile suggestive of infection acquired in the di stant past (low DT titers from 1:16 to 1:512, negative IgM ELISA titers fro m 0 to 0.8, and chronic patterns in the AC/HS test) (group II). The classif ication of acute or chronic profile was based on the individual's clinical history as well as the combination of the results of the toxoplasma serolog ical profile. An additional group (group III) was composed of sera from 50 women who were seronegative for T. gondii antibodies in the DT, The results revealed that whereas 85.3% of women in group I had IgG antibodies that re acted with the rP35 antigen, only 8% of women in group II had IgG antibodie s that reacted with the same antigen. In immunoblots, the rP35 antigen was recognized by IgG antibodies in a pool of sera from individuals with a toxo plasma serologic profile compatible with acute infection but not in a pool of sera from individuals with a serologic profile characteristic of a chron ic infection. These results reveal that IgG antibodies against the P35 anti gen are produced during the acute stage of the infection but are uncommon i n the latent or chronic phase of the infection. Thus, the rP35 antigen may be a useful serologic marker to differentiate between recently acquired inf ection and that acquired in the more distant past.