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Recombinant antigens for immunodiagnosis of cystic echinococcosis
Three cDNAs, termed EpC1, TPxEg and EgG5, were isolated by immunoscreening from an Echinococcus granulosus cDNA library. The recombinant phages exhibited strong reactivity with sera from humans with confirmed cystic echinococcosis (CE) and with sera from mice infected with E. granulosus oncospheres....
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Biological Procedures Online
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC411165/ https://www.ncbi.nlm.nih.gov/pubmed/15188015 http://dx.doi.org/10.1251/bpo74 |
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author | Li, Jun Zhang, Wen-Bao McManus, Donald P. |
author_facet | Li, Jun Zhang, Wen-Bao McManus, Donald P. |
author_sort | Li, Jun |
collection | PubMed |
description | Three cDNAs, termed EpC1, TPxEg and EgG5, were isolated by immunoscreening from an Echinococcus granulosus cDNA library. The recombinant phages exhibited strong reactivity with sera from humans with confirmed cystic echinococcosis (CE) and with sera from mice infected with E. granulosus oncospheres. The cDNAs were subcloned into a pET vector, expressed as fusion proteins tagged with GST and affinity purified against the GST tag. Of the three recombinant proteins, EpC1 achieved the highest performance for serodiagnosis of CE in Western blot analysis using a panel of clinically defined human sera to initially address the sensitivity and specificity of the molecules. The protein yielded an overall sensitivity of 92.2% and specificity of 95.6%, levels unprecedented taking into account the large panel of 896 human sera that were tested. The strategy used may also prove suitable for improved immunodiagnosis of other parasitic infections. |
format | Text |
id | pubmed-411165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Biological Procedures Online |
record_format | MEDLINE/PubMed |
spelling | pubmed-4111652004-05-18 Recombinant antigens for immunodiagnosis of cystic echinococcosis Li, Jun Zhang, Wen-Bao McManus, Donald P. Biol Proced Online Research Article Three cDNAs, termed EpC1, TPxEg and EgG5, were isolated by immunoscreening from an Echinococcus granulosus cDNA library. The recombinant phages exhibited strong reactivity with sera from humans with confirmed cystic echinococcosis (CE) and with sera from mice infected with E. granulosus oncospheres. The cDNAs were subcloned into a pET vector, expressed as fusion proteins tagged with GST and affinity purified against the GST tag. Of the three recombinant proteins, EpC1 achieved the highest performance for serodiagnosis of CE in Western blot analysis using a panel of clinically defined human sera to initially address the sensitivity and specificity of the molecules. The protein yielded an overall sensitivity of 92.2% and specificity of 95.6%, levels unprecedented taking into account the large panel of 896 human sera that were tested. The strategy used may also prove suitable for improved immunodiagnosis of other parasitic infections. Biological Procedures Online 2004-05-10 /pmc/articles/PMC411165/ /pubmed/15188015 http://dx.doi.org/10.1251/bpo74 Text en Copyright © May 05, 2004, J Li et al. Published in Biological Procedures Online under license from the authors. Copying, printing, redistribution and storage permitted. |
spellingShingle | Research Article Li, Jun Zhang, Wen-Bao McManus, Donald P. Recombinant antigens for immunodiagnosis of cystic echinococcosis |
title | Recombinant antigens for immunodiagnosis of cystic echinococcosis |
title_full | Recombinant antigens for immunodiagnosis of cystic echinococcosis |
title_fullStr | Recombinant antigens for immunodiagnosis of cystic echinococcosis |
title_full_unstemmed | Recombinant antigens for immunodiagnosis of cystic echinococcosis |
title_short | Recombinant antigens for immunodiagnosis of cystic echinococcosis |
title_sort | recombinant antigens for immunodiagnosis of cystic echinococcosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC411165/ https://www.ncbi.nlm.nih.gov/pubmed/15188015 http://dx.doi.org/10.1251/bpo74 |
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