rapid detection of toxoplasma gondii antigen in experimentally infected mice by dot- elisa

نویسندگان

s jafar pour azami dept of medical parasitology and mycology, school of public health, tehran university of medical sciences, tehran, iran

h keshavarz dept of medical parasitology and mycology, school of public health, tehran university of medical sciences, tehran, iran

m rezaian dept of medical parasitology and mycology, school of public health, tehran university of medical sciences, tehran, iran

m mohebali dept of medical parasitology and mycology, school of public health, tehran university of medical sciences, tehran, iran

چکیده

background : toxoplasmosis is a worldwide endemic disease. in congenitally infected infants and aids patients, toxoplasmosis causes high rates of morbidity and mortality. in these cases antibody detection is difficult; so detection of parasite or its components could be useful tool for early detection and following treatment of the infection. methods : sixty-three balb/c mice were injected intra-peritoneal with 5×10 3 tachyzoites of toxoplasma gondii rh strain, nine mice were sacrificed daily for 7 days. fourteen mice were in­jected with phosphate buffer saline as control group. dot-elisa was performed for detection of t.gondii antigen in mice sera and capture - elisa was done as golden standard assay too. results : toxoplasma gondii antigen was detected from day 2 in mice sera ; 22% of mice sera on day 2, 33% on day 3,77% on day 4 and 100% on day 5 till their death on day 7 had shown antigene­mia by dot - elisa, no positive result was detected in control mice by dot- elisa. conclusion: dot-elisa is a sensitive method for diagnosis of t. gondii infection in the animal model; also, this technique is more rapid and easy to perform method in comparison with cap­ture-elisa.

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عنوان ژورنال:
iranian journal of parasitology

جلد ۶، شماره ۱، صفحات ۲۸-۳۳

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