Alonso Molina, JL.; Amoros, I.; Cañigral Cárcel, I. (2011). Development and evaluation of a real-time PCR assay for quantification of Giardia and Cryptosporidium in sewage samples. Applied Microbiology and Biotechnology. 89(4):1203-1211. https://doi.org/10.1007/s00253-010-2984-6
Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/139922
Título:
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Development and evaluation of a real-time PCR assay for quantification of Giardia and Cryptosporidium in sewage samples
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Autor:
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Alonso Molina, José Luís
Amoros, Inmaculada
Cañigral Cárcel, Irene
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Entidad UPV:
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Universitat Politècnica de València. Instituto Universitario de Ingeniería del Agua y del Medio Ambiente - Institut Universitari d'Enginyeria de l'Aigua i Medi Ambient
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Fecha difusión:
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Resumen:
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[EN] Cryptosporidium and Giardia are major causes of diarrheal disease in humans worldwide and are major causes of protozoan waterborne diseases. Two DNA TaqMan PCR-based Giardia and Cryptosporidium methods targeting a ...[+]
[EN] Cryptosporidium and Giardia are major causes of diarrheal disease in humans worldwide and are major causes of protozoan waterborne diseases. Two DNA TaqMan PCR-based Giardia and Cryptosporidium methods targeting a 74-bp sequence of the ß-giardin Giardia gene and a 151-bp sequence of the COWP Cryptosporidium gene, respectively, were used as models to compare two different LNA/DNA TaqMan probes to improve the detection limit in a real-time PCR assay. The LNA probes were the most sensitive resulting in 0.96 to 1.57 lower C t values than a DNA Giardia TaqMan probe and 0.56 to 2.21 lower than a DNA Cryptosporidium TaqMan probe. Evaluation of TaqMan Giardia and Cryptosporidium probes with LNA substitutions resulted in real-time PCR curves with an earlier C t values than conventional DNA TaqMan probes. In conclusion, the LNA probes could be useful for more sensitive detection limits. © 2011 Springer-Verlag.
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Palabras clave:
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Cryptosporidium
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Giardia
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LightCycler
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LNA probe
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QPCR
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Sewage
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TaqMan
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DNA
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Genes
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Nucleic acids
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Probes
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Polymerase chain reaction
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Assay
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Diarrheal disease
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Gene expression
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Genetic analysis
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Protozoan
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Sensitivity analysis
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Species diversity
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Waterborne disease
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Article
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DNA extraction
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Gene sequence
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Nonhuman
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Nucleic acid probe
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Quantitative analysis
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Real time polymerase chain reaction
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Sampling
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Cytoskeletal Proteins
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Humans
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Oligonucleotide Probes
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Parasitology
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Protozoan Proteins
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Sensitivity and Specificity
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Protozoa
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Derechos de uso:
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Reserva de todos los derechos
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Fuente:
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Applied Microbiology and Biotechnology. (issn:
0175-7598
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DOI:
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10.1007/s00253-010-2984-6
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Editorial:
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SPRINGER
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Versión del editor:
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https://doi.org/10.1007/s00253-010-2984-6
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Código del Proyecto:
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info:eu-repo/grantAgreement/MEC//AGL2005-07776-C03-03/ES/DETECCION DE PROTOZOOS EN AGUAS Y ALIMENTOS CON METODOS MOLECULARES EN TIEMPO REAL/
info:eu-repo/grantAgreement/MICINN//AGL2008-05275-C03-03/ES/ANALISIS INTEGRADO DE PROTOZOOS PATOGENOS EN ALIMENTOS,/
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Agradecimientos:
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This work was supported by the Spanish Ministerio de Ciencia e Innovacion grants AGL2005-07776-C03-03 and AGL2008-05275-C03-03/ALI). Part of this work was also funded by the Fondo Europeo de Desarrollo Regional (Feder) ...[+]
This work was supported by the Spanish Ministerio de Ciencia e Innovacion grants AGL2005-07776-C03-03 and AGL2008-05275-C03-03/ALI). Part of this work was also funded by the Fondo Europeo de Desarrollo Regional (Feder) grant POICV 2000-2006. We thank staff at the wastewater treatment plants and the Entidad de Saneamiento de Aguas for assistance in sample collection.
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Tipo:
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Artículo
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