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Review
. 2015 May 28:8:292.
doi: 10.1186/s13071-015-0902-6.

Diagnosis of toxoplasmosis and typing of Toxoplasma gondii

Affiliations
Review

Diagnosis of toxoplasmosis and typing of Toxoplasma gondii

Quan Liu et al. Parasit Vectors. .

Abstract

Toxoplasmosis, caused by the obligate intracellular protozoan Toxoplasma gondii, is an important zoonosis with medical and veterinary importance worldwide. The disease is mainly contracted by ingesting undercooked or raw meat containing viable tissue cysts, or by ingesting food or water contaminated with oocysts. The diagnosis and genetic characterization of T. gondii infection is crucial for the surveillance, prevention and control of toxoplasmosis. Traditional approaches for the diagnosis of toxoplasmosis include etiological, immunological and imaging techniques. Diagnosis of toxoplasmosis has been improved by the emergence of molecular technologies to amplify parasite nucleic acids. Among these, polymerase chain reaction (PCR)-based molecular techniques have been useful for the genetic characterization of T. gondii. Serotyping methods based on polymorphic polypeptides have the potential to become the choice for typing T. gondii in humans and animals. In this review, we summarize conventional non-DNA-based diagnostic methods, and the DNA-based molecular techniques for the diagnosis and genetic characterization of T. gondii. These techniques have provided foundations for further development of more effective and accurate detection of T. gondii infection. These advances will contribute to an improved understanding of the epidemiology, prevention and control of toxoplasmosis.

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Figures

Fig. 1
Fig. 1
Schematic diagram of ELISA. a Indirect ELISA system almost all used for detection of T. gondii antibodies rather than antigens involves the specific antigen coated onto the solid phase, enzyme-conjugated secondary antibody and substrate. b Sandwich ELISA system detecting T. gondii antigens involves the specific antibody coated onto the solid phase, enzyme-conjugated antibody and substrate
Fig. 2
Fig. 2
Schematic diagram of the immunochromatographic test for detection of T. gondii-specific antibody. The colloidal gold-labeled antigen or antibody is used as the tracer and the cellulose membrane is used as the solid support

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