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Development of a Cryptosporidium oocyst assay using an automated fiber optic-based biosensor
An intestinal protozoan parasite, Cryptosporidium parvum, is a major cause of waterborne gastrointestinal disease worldwide. Detection of Cryptosporidium oocysts in potable water is a high priority for the water treatment industry to reduce potential outbreaks among the consumer populace. Anti-Crypt...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2241826/ https://www.ncbi.nlm.nih.gov/pubmed/18271980 http://dx.doi.org/10.1186/1754-1611-1-3 |
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author | Kramer, Marianne F Vesey, Graham Look, Natasha L Herbert, Ben R Simpson-Stroot, Joyce M Lim, Daniel V |
author_facet | Kramer, Marianne F Vesey, Graham Look, Natasha L Herbert, Ben R Simpson-Stroot, Joyce M Lim, Daniel V |
author_sort | Kramer, Marianne F |
collection | PubMed |
description | An intestinal protozoan parasite, Cryptosporidium parvum, is a major cause of waterborne gastrointestinal disease worldwide. Detection of Cryptosporidium oocysts in potable water is a high priority for the water treatment industry to reduce potential outbreaks among the consumer populace. Anti-Cryptosporidium oocyst polyclonal and monoclonal antibodies were tested as capture and detection reagents for use in a fiber optic biosensor assay for the detection of Cryptosporidium oocysts. Antibodies were validated using enzyme-linked immunosorbent assays, flow cytometry, Western blotting and fluorescent microscopy. Oocysts could be detected at a concentration of 10(5 )oocysts/ml when the polyclonal antibodies were used as the capture and detection reagents. When oocysts were boiled prior to detection, a ten-fold increase in sensitivity was achieved using the polyclonal antibody. Western blotting and immunofluorescence revealed that both the monoclonal and polyclonal antibodies recognize a large (>300 kDa) molecular weight mucin-like antigen present on the surface of the oocyst wall. The polyclonal antibody also reacted with a small (105 kDa) molecular weight antigen that was present in boiled samples of oocysts. Preliminary steps to design an in-line biosensor assay system have shown that oocysts would have to be concentrated from water samples and heat treated to allow detection by a biosensor assay. |
format | Text |
id | pubmed-2241826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22418262008-02-14 Development of a Cryptosporidium oocyst assay using an automated fiber optic-based biosensor Kramer, Marianne F Vesey, Graham Look, Natasha L Herbert, Ben R Simpson-Stroot, Joyce M Lim, Daniel V J Biol Eng Research An intestinal protozoan parasite, Cryptosporidium parvum, is a major cause of waterborne gastrointestinal disease worldwide. Detection of Cryptosporidium oocysts in potable water is a high priority for the water treatment industry to reduce potential outbreaks among the consumer populace. Anti-Cryptosporidium oocyst polyclonal and monoclonal antibodies were tested as capture and detection reagents for use in a fiber optic biosensor assay for the detection of Cryptosporidium oocysts. Antibodies were validated using enzyme-linked immunosorbent assays, flow cytometry, Western blotting and fluorescent microscopy. Oocysts could be detected at a concentration of 10(5 )oocysts/ml when the polyclonal antibodies were used as the capture and detection reagents. When oocysts were boiled prior to detection, a ten-fold increase in sensitivity was achieved using the polyclonal antibody. Western blotting and immunofluorescence revealed that both the monoclonal and polyclonal antibodies recognize a large (>300 kDa) molecular weight mucin-like antigen present on the surface of the oocyst wall. The polyclonal antibody also reacted with a small (105 kDa) molecular weight antigen that was present in boiled samples of oocysts. Preliminary steps to design an in-line biosensor assay system have shown that oocysts would have to be concentrated from water samples and heat treated to allow detection by a biosensor assay. BioMed Central 2007-10-10 /pmc/articles/PMC2241826/ /pubmed/18271980 http://dx.doi.org/10.1186/1754-1611-1-3 Text en Copyright © 2007 Kramer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Kramer, Marianne F Vesey, Graham Look, Natasha L Herbert, Ben R Simpson-Stroot, Joyce M Lim, Daniel V Development of a Cryptosporidium oocyst assay using an automated fiber optic-based biosensor |
title | Development of a Cryptosporidium oocyst assay using an automated fiber optic-based biosensor |
title_full | Development of a Cryptosporidium oocyst assay using an automated fiber optic-based biosensor |
title_fullStr | Development of a Cryptosporidium oocyst assay using an automated fiber optic-based biosensor |
title_full_unstemmed | Development of a Cryptosporidium oocyst assay using an automated fiber optic-based biosensor |
title_short | Development of a Cryptosporidium oocyst assay using an automated fiber optic-based biosensor |
title_sort | development of a cryptosporidium oocyst assay using an automated fiber optic-based biosensor |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2241826/ https://www.ncbi.nlm.nih.gov/pubmed/18271980 http://dx.doi.org/10.1186/1754-1611-1-3 |
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