Rapid Detection of Toxoplasma Gondii Antigen in Experimentally Infected Mice by Dot- ELISA
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 detectio...
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Tehran University of Medical Sciences
2011-03-01
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Series: | Iranian Journal of Parasitology |
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doaj-637aa816ec2d4e1e8dbe3dc2a3d967602021-03-02T01:04:25ZengTehran University of Medical SciencesIranian Journal of Parasitology1735-70202008-238X2011-03-01612833Rapid Detection of Toxoplasma Gondii Antigen in Experimentally Infected Mice by Dot- ELISAM MohebaliM RezaianH KeshavarzS Jafar pour AzamiS ShojaeeBackground: 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 5×103 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.http://journals.tums.ac.ir/upload_files/pdf/17733.pdf |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
M Mohebali M Rezaian H Keshavarz S Jafar pour Azami S Shojaee |
spellingShingle |
M Mohebali M Rezaian H Keshavarz S Jafar pour Azami S Shojaee Rapid Detection of Toxoplasma Gondii Antigen in Experimentally Infected Mice by Dot- ELISA Iranian Journal of Parasitology |
author_facet |
M Mohebali M Rezaian H Keshavarz S Jafar pour Azami S Shojaee |
author_sort |
M Mohebali |
title |
Rapid Detection of Toxoplasma Gondii Antigen in Experimentally Infected Mice by Dot- ELISA |
title_short |
Rapid Detection of Toxoplasma Gondii Antigen in Experimentally Infected Mice by Dot- ELISA |
title_full |
Rapid Detection of Toxoplasma Gondii Antigen in Experimentally Infected Mice by Dot- ELISA |
title_fullStr |
Rapid Detection of Toxoplasma Gondii Antigen in Experimentally Infected Mice by Dot- ELISA |
title_full_unstemmed |
Rapid Detection of Toxoplasma Gondii Antigen in Experimentally Infected Mice by Dot- ELISA |
title_sort |
rapid detection of toxoplasma gondii antigen in experimentally infected mice by dot- elisa |
publisher |
Tehran University of Medical Sciences |
series |
Iranian Journal of Parasitology |
issn |
1735-7020 2008-238X |
publishDate |
2011-03-01 |
description |
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 5×103 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. |
url |
http://journals.tums.ac.ir/upload_files/pdf/17733.pdf |
work_keys_str_mv |
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