Effect of rSAG-1(P30) immunisation on the circulating and tissue parasites in guinea pigs as determined by quantitative PCR
Autor: | Laetitia Tardy, Bahrie Bellete, P. Flori, Alain Jacquet, Roger Tran Manh Sung, J. Hafid, H. Raberin |
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Rok vydání: | 2006 |
Předmět: |
Protozoan Vaccines
Telencephalon medicine.medical_specialty Guinea Pigs Protozoan Proteins Antibodies Protozoan Antigens Protozoan Caviidae Animal Inoculation Parasitemia Polymerase Chain Reaction Parasite load Guinea pig Medical microbiology Adjuvants Immunologic medicine Animals Parasite hosting Lung Vaccines Synthetic General Veterinary biology Toxoplasma gondii General Medicine DNA Protozoan biology.organism_classification Virology Disease Models Animal Toxoplasmosis Animal Infectious Diseases Real-time polymerase chain reaction Immunoglobulin G Insect Science Vaccines Subunit Female Parasitology Toxoplasma |
Zdroj: | Parasitology Research. 98:511-518 |
ISSN: | 1432-1955 0932-0113 |
DOI: | 10.1007/s00436-005-0074-y |
Popis: | The efficacy of immunisation with Toxoplasma gondii recombinant protein (rSAG-1) was evaluated in the guinea pig model. For the infectious challenge, two strains, namely, strain C56 (10,000 tachyzoites) and strain 76K (100 cysts), were used to infect a group of 32 guinea pigs each. The circulating, cerebral and pulmonary parasite loads were determined with the real-time polymerase chain reaction (PCR) after immunisation. With the C56 strain, immunisation showed high activity with a reduction of greater than 1 log of the circulating and tissue parasite loads. Thus, there was a significantly lower circulating parasite load in the rSAG-1 + adjuvant group (0.5+/-1.5 Eq parasites/ml) as compared to that in the control group (67+/-110 Eq parasites/ml; p0.05). In the same manner, the cerebral parasite load was much lower in the rSAG-1 + adjuvant group (10+/-20 Eq parasites/g) than that in the control group (339+/-291 Eq parasites/g; p0.01). On the other hand, with the 76K strain, the effect of immunisation was much less and that only on the pulmonary parasite load [p(lung)0.05]. This could be due to the use of different strains and stages of the parasite and/or the difference in the route of administration for challenge. The quantitative PCR technique used has shown a good correlation with animal inoculation, and when associated with the guinea pig model, it seems to be a useful and reproducible technique for future vaccine studies. |
Databáze: | OpenAIRE |
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