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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...

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Autores principales: Kramer, Marianne F, Vesey, Graham, Look, Natasha L, Herbert, Ben R, Simpson-Stroot, Joyce M, Lim, Daniel V
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
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.
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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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