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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279859/ https://www.ncbi.nlm.nih.gov/pubmed/22347271 |
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author | Jafar pour Azami, S Keshavarz, H Rezaian, M Mohebali, M Shojaee, S |
author_facet | Jafar pour Azami, S Keshavarz, H Rezaian, M Mohebali, M Shojaee, S |
author_sort | Jafar pour Azami, S |
collection | PubMed |
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 5×10(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. |
format | Online Article Text |
id | pubmed-3279859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-32798592012-02-16 Rapid Detection of Toxoplasma gondii Antigen in Experimentally Infected Mice by Dot- ELISA Jafar pour Azami, S Keshavarz, H Rezaian, M Mohebali, M Shojaee, S Iran J Parasitol Original Article 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. Tehran University of Medical Sciences 2011-03 /pmc/articles/PMC3279859/ /pubmed/22347271 Text en © 2011 Iranian Society of Parasitology & Tehran University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly. |
spellingShingle | Original Article Jafar pour Azami, S Keshavarz, H Rezaian, M Mohebali, M Shojaee, S Rapid Detection of Toxoplasma gondii Antigen in Experimentally Infected Mice by Dot- ELISA |
title | 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_short | 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 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279859/ https://www.ncbi.nlm.nih.gov/pubmed/22347271 |
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