Noguera Murray, PS.; Posthuma-Trumpie, GA.; Van Tuil, M.; Van Der Wal, FJ.; De Boer, A.; Moers, APHA.; Van Amerongen, A. (2011). Carbon nanoparticles as detection labels in antibody microarrays.Detection of genes encoding virulence factors in Shiga toxin-producing Escherichia coli. Analytical Chemistry. 83:8531-8536. https://doi.org/10.1021/ac201823v
Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/30120
Título:
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Carbon nanoparticles as detection labels in antibody microarrays.Detection of genes encoding virulence factors in Shiga toxin-producing Escherichia coli
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Autor:
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Noguera Murray, Patricia Silvestre
Posthuma-Trumpie, Geertruida A
van Tuil, Marc
van der Wal, Fimme J.
de Boer, Albert
Moers, Antoine P. H. A.
van Amerongen, Aart
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Entidad UPV:
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Universitat Politècnica de València. Departamento de Química - Departament de Química
Universitat Politècnica de València. Instituto de Reconocimiento Molecular y Desarrollo Tecnológico - Institut de Reconeixement Molecular i Desenvolupament Tecnològic
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Fecha difusión:
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Resumen:
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The present study demonstrates that carbon nanoparticles (CNPs) can be used as labels in microarrays. CNPs were
used in nucleic acid microarray immunoassays (NAMIAs) for
the detection of di¿erent Shiga toxin-producing ...[+]
The present study demonstrates that carbon nanoparticles (CNPs) can be used as labels in microarrays. CNPs were
used in nucleic acid microarray immunoassays (NAMIAs) for
the detection of di¿erent Shiga toxin-producing Escherichia coli
(STEC) virulence factors: four genes speci¿c for STEC (vt1,vt2,
eae, andehxA) and the gene forE. coli16S (hui). Optimization was
performed using a Box Behnken design, andthe limit of detection
for each virulence factor was established. Finally,this NAMIA using
CNPs was tested with DNA from 48 ¿eld strains originating from
cattle feces, and its performance was evaluated by comparing
results with those achieved by the reference method q-PCR. All factors tested gave sensitivity and speci¿city values higher than 0.80 and
e¿ciency values higher than 0.92. Kappa coe¿cients showed an almost perfect agreement (k > 0.8) between NAMIA and the reference
method used forvt1, eae, and ehxA, and a perfect agreement (k = 1) forvt2 and hui. The excellent agreement between the developed
NAMIA and q-PCR demonstrates that the proposed analytical procedure is indeed ¿t for purpose, i.e., it is valuable for fast screening of
ampli¿ed genetic material such as E. coli virulence factors. This also proves the applicability of CNPs in microarrays.
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Palabras clave:
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Pathogen detection
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DNA microarray
,
Bacteria
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Assay
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Inmunoassay
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Derechos de uso:
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Cerrado |
Fuente:
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Analytical Chemistry. (issn:
0003-2700
)
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DOI:
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10.1021/ac201823v
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Editorial:
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American Chemical Society
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Versión del editor:
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http://pubs.acs.org/doi/ipdf/10.1021/ac201823v
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Código del Proyecto:
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info:eu-repo/grantAgreement/Generalitat Valenciana//BEST%2F2009%2F026/ES/BEST%2F2009%2F026/
info:eu-repo/grantAgreement/UPV//PAID-00-09-2837/
info:eu-repo/grantAgreement/LNV//KB-06-005/
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Agradecimientos:
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This work was partially supported by the Generalitat Valenciana (BEST/2009/026), the Universidad Politecnica de Valencia (PAID-00-09-2837), and the Dutch Ministry of Agriculture, Nature and Food Quality (Strategic research ...[+]
This work was partially supported by the Generalitat Valenciana (BEST/2009/026), the Universidad Politecnica de Valencia (PAID-00-09-2837), and the Dutch Ministry of Agriculture, Nature and Food Quality (Strategic research program Food Safety, Monitoring and Detection KB-06-005). The authors thank Dr. Eva Moller Nielsen at the Danish Veterinary Institute (Copenhagen, Denmark) for providing E. coli control strains and Dr. Lutz Geue (Friedrich-Loeffler-Institut, Wusterhausen, Germany) and Dr. Dorte Dopfer (School of Veterinary Medicine, University of Wisconsin, Madison, WI) for field isolates.
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Tipo:
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Artículo
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