Abstract

Toxoplasma gondii causes congenital toxoplasmosis in newborns resulting with fetal anomalies. Determining the initiation time of infection is very important for pregnant women and current serological assays have drawbacks in distinguishing the recently acute toxoplasmosis. Diagnosis of recently acute infection may be improved by using stage specific antigens in serological assays. In the present study, the diagnostic value of sporozoite specific SporoSAG, bradyzoite specific BAG1 proteins and GRA1 protein expressed by all forms of the parasite have been evaluated ELISA using sera systematically collected from mice administered orally with tissue cyst and oocysts. The anti-SporoSAG IgM antibodies in sera obtained from mice infected with oocysts peaked significantly at days 1, 10, and 15 (P<0.01). The anti-BAG1 IgM antibodies in sera obtained from mice infected with tissue cysts peaked significantly at days 15, 40, and 120 (P<0.05). The anti-GRA1 IgM antibodies in sera obtained from mice infected with oocysts peaked significantly at days 2, 10, and 40 (P<0.01). The anti-GRA1 IgM antibodies in sera obtained from mice infected with tissue cysts peaked significantly only at day 40 (P<0.05). The anti-SporoSAG, anti-BAG1, and anti-GRA1 IgG titers of mice showed significant increases at day 40 (P<0.05) and decrement started for only anti-GRA1 IgG at day 120. The presence of anti-SporoSAG IgM and IgG antibodies can be interpreted as recently acute infection between days 10–40 because IgM decreases at day 40. Similarly, presence of anti-BAG1 IgM and absence of IgG can be evaluated as a recently acute infection that occurred 40 days before because IgG peaks at day 40. A peak in anti-GRA1 antibody level at first testing and reduction in consecutive sample can be considered as an infection approximately around day 40 or prior. Overall, recombinant SporoSAG, BAG1 and GRA1 proteins can be accepted as valuable diagnostic markers of recently acute toxoplasmosis.

Highlights

  • Toxoplasma gondii is a medically important parasite that causes congenital toxoplasmosis which manifests as birth defects in unborn children when a seronegative mother is infected during pregnancy [1,2]

  • Recombinant SporoSAG, BAG1 and GRA1 proteins can be accepted as valuable diagnostic markers of recently acute toxoplasmosis

  • The expression of rSporoSAG, rBAG1, and rGRA1 were induced by 0.5 mM IPTG when the cells grow to an optical density of 0.4 at 600 nm

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Summary

Introduction

Toxoplasma gondii is a medically important parasite that causes congenital toxoplasmosis which manifests as birth defects in unborn children when a seronegative mother is infected during pregnancy [1,2]. Definitive diagnosis of toxoplasmosis has utmost importance for pregnant women. The common approach for diagnosing toxoplasmosis is by serological assays mainly using T. gondii tachyzoite lysate antigen. Determining the initiation time of infection that may have occurred in previous 3–4 months (i.e. recently acute infection) is very important for pregnant women who have not been screened for toxoplasmosis before pregnancy. The results of several serological assays are being evaluated together to resolve this issue. Current commercial or in house serological kits still present drawbacks in determining the initiation time of infection

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