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Journal of Clinical Microbiology, June 2006, p. 2133-2140, Vol. 44, No. 6
0095-1137/06/$08.00+0     doi:10.1128/JCM.00237-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Chimeric Antigens of Toxoplasma gondii: Toward Standardization of Toxoplasmosis Serodiagnosis Using Recombinant Products

Elisa Beghetto,1 Andrea Spadoni,1 Luca Bruno,1 Wilma Buffolano,2 and Nicola Gargano1*

Kenton Laboratories, Rome, Italy,1 Department of Pediatrics, Federico II University, Naples, Italy2

Received 2 February 2006/ Returned for modification 21 March 2006/ Accepted 29 March 2006

We have evaluated the diagnostic utility of six antigenic regions of the Toxoplasma gondii MIC2, MIC3, M2AP, GRA3, GRA7, and SAG1 gene products, assembled in recombinant chimeric antigens by genetic engineering, in order to replace the soluble, whole-cell tachyzoite extract in serological assays. Serum samples from 100 adults with acquired T. gondii infection and from 30 infants born to mothers with primary toxoplasmosis contracted during pregnancy, of whom 20 were congenitally infected, were included. Immunoglobulin G (IgG) and IgM antibodies against epitopes carried by chimeric antigens were measured by performing parallel enzyme immunoassays (recombinant enzyme-linked immunosorbent assays [Rec-ELISAs]), and the results obtained by standard commercial assays with the whole-cell Toxoplasma antigen and assays with the chimeric antigens were compared. Our results demonstrate that IgG and IgM Rec-ELISAs with individual chimeric antigens have performance characteristics comparable to those of the corresponding commercial assays. Furthermore, we show that IgM-capture assays based on chimeric antigens improve the ability to diagnose congenital toxoplasmosis postnatally compared with the ability to diagnose congenital toxoplasmosis by the use of standard assays. The use of recombinant chimeric antigens is effective in distinguishing T. gondii-infected individuals from T. gondii-uninfected individuals and shows that immunoassays based on recombinant products could provide the basis for standardized commercial tests for the serodiagnosis of toxoplasmosis.


* Corresponding author. Mailing address: Kenton Laboratories, Via Pontina km 30.400, 00040 Rome, Italy. Phone: 39-06-91611494. Fax: 39-06-91629012. E-mail: gargano{at}kenton.it.


Journal of Clinical Microbiology, June 2006, p. 2133-2140, Vol. 44, No. 6
0095-1137/06/$08.00+0     doi:10.1128/JCM.00237-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.







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