O-antigen and virulence profiling of Shiga toxin-producing Escherichia coli by a rapid and cost-effective DNA microarray colorimetric method

Shiga toxin-producing Escherichia coli (STEC) is a leading cause of foodborne illness worldwide. The present study developed the use of DNA microarrays with the ampliPHOX colorimetric method to rapidly detect and genotype STEC strains. A low-density 30-mer oligonucleotide DNA microarray was design...

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Main Authors: Beatriz eQuiñones, Michelle S. Swimley, Koh-Eun eNarm, Ronak N. Patel, Michael B. Cooley, Robert E. Mandrell
Format: Article
Language:English
Published: Frontiers Media S.A. 2012-05-01
Series:Frontiers in Cellular and Infection Microbiology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fcimb.2012.00061/full
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spelling doaj-e5d65fe8644949b5bdd61f9b9ad33eb02020-11-25T02:24:47ZengFrontiers Media S.A.Frontiers in Cellular and Infection Microbiology2235-29882012-05-01210.3389/fcimb.2012.0006125764O-antigen and virulence profiling of Shiga toxin-producing Escherichia coli by a rapid and cost-effective DNA microarray colorimetric methodBeatriz eQuiñones0Michelle S. Swimley1Koh-Eun eNarm2Ronak N. Patel3Michael B. Cooley4Robert E. Mandrell5United States Department of Agriculture-Agricultural Research ServiceUnited States Department of Agriculture-Agricultural Research ServiceUnited States Department of Agriculture-Agricultural Research ServiceUnited States Department of Agriculture-Agricultural Research ServiceUnited States Department of Agriculture-Agricultural Research ServiceUnited States Department of Agriculture-Agricultural Research ServiceShiga toxin-producing Escherichia coli (STEC) is a leading cause of foodborne illness worldwide. The present study developed the use of DNA microarrays with the ampliPHOX colorimetric method to rapidly detect and genotype STEC strains. A low-density 30-mer oligonucleotide DNA microarray was designed to target O-antigen gene clusters of eleven E. coli serogroups (O26, O45, O91, O103, O104, O111, O113, O121, O128, O145 and O157) that have been associated with the majority of STEC infections. In addition, the DNA microarray targeted eleven virulence genes, encoding adhesins, cytotoxins, proteases, and receptor proteins, which have been implicated in conferring increased ability to cause disease for STEC. Results from the validation experiments demonstrated that this microarray-based colorimetric method allowed for a rapid and accurate genotyping of STEC reference strains from environmental and clinical sources and from distinct geographical locations. Positive hybridization signals were detected only for probes targeting serotype and virulence genes known to be present in the STEC reference strains. Quantification analysis indicated that the mean pixel intensities of the signal for probes targeting O-antigen or virulence genes were at least three times higher when compared to the background. Furthermore, this microarray-based colorimetric method was then employed to genotype a group of E. coli isolates from watershed sediment and animal fecal samples that were collected from an important region for leafy-vegetable production in the central coast of California. The results indicated an accurate identification of O-type and virulence genes in the tested isolates and confirmed that the ampliPHOX colorimetric method with low density DNA microarrays enabled a fast assessment of the virulence potential of STEC using low-cost reagents and instrumentation.http://journal.frontiersin.org/Journal/10.3389/fcimb.2012.00061/fullEscherichia coliShiga Toxinfoodborne pathogenampliPHOXSTECleafy-vegetable production
collection DOAJ
language English
format Article
sources DOAJ
author Beatriz eQuiñones
Michelle S. Swimley
Koh-Eun eNarm
Ronak N. Patel
Michael B. Cooley
Robert E. Mandrell
spellingShingle Beatriz eQuiñones
Michelle S. Swimley
Koh-Eun eNarm
Ronak N. Patel
Michael B. Cooley
Robert E. Mandrell
O-antigen and virulence profiling of Shiga toxin-producing Escherichia coli by a rapid and cost-effective DNA microarray colorimetric method
Frontiers in Cellular and Infection Microbiology
Escherichia coli
Shiga Toxin
foodborne pathogen
ampliPHOX
STEC
leafy-vegetable production
author_facet Beatriz eQuiñones
Michelle S. Swimley
Koh-Eun eNarm
Ronak N. Patel
Michael B. Cooley
Robert E. Mandrell
author_sort Beatriz eQuiñones
title O-antigen and virulence profiling of Shiga toxin-producing Escherichia coli by a rapid and cost-effective DNA microarray colorimetric method
title_short O-antigen and virulence profiling of Shiga toxin-producing Escherichia coli by a rapid and cost-effective DNA microarray colorimetric method
title_full O-antigen and virulence profiling of Shiga toxin-producing Escherichia coli by a rapid and cost-effective DNA microarray colorimetric method
title_fullStr O-antigen and virulence profiling of Shiga toxin-producing Escherichia coli by a rapid and cost-effective DNA microarray colorimetric method
title_full_unstemmed O-antigen and virulence profiling of Shiga toxin-producing Escherichia coli by a rapid and cost-effective DNA microarray colorimetric method
title_sort o-antigen and virulence profiling of shiga toxin-producing escherichia coli by a rapid and cost-effective dna microarray colorimetric method
publisher Frontiers Media S.A.
series Frontiers in Cellular and Infection Microbiology
issn 2235-2988
publishDate 2012-05-01
description Shiga toxin-producing Escherichia coli (STEC) is a leading cause of foodborne illness worldwide. The present study developed the use of DNA microarrays with the ampliPHOX colorimetric method to rapidly detect and genotype STEC strains. A low-density 30-mer oligonucleotide DNA microarray was designed to target O-antigen gene clusters of eleven E. coli serogroups (O26, O45, O91, O103, O104, O111, O113, O121, O128, O145 and O157) that have been associated with the majority of STEC infections. In addition, the DNA microarray targeted eleven virulence genes, encoding adhesins, cytotoxins, proteases, and receptor proteins, which have been implicated in conferring increased ability to cause disease for STEC. Results from the validation experiments demonstrated that this microarray-based colorimetric method allowed for a rapid and accurate genotyping of STEC reference strains from environmental and clinical sources and from distinct geographical locations. Positive hybridization signals were detected only for probes targeting serotype and virulence genes known to be present in the STEC reference strains. Quantification analysis indicated that the mean pixel intensities of the signal for probes targeting O-antigen or virulence genes were at least three times higher when compared to the background. Furthermore, this microarray-based colorimetric method was then employed to genotype a group of E. coli isolates from watershed sediment and animal fecal samples that were collected from an important region for leafy-vegetable production in the central coast of California. The results indicated an accurate identification of O-type and virulence genes in the tested isolates and confirmed that the ampliPHOX colorimetric method with low density DNA microarrays enabled a fast assessment of the virulence potential of STEC using low-cost reagents and instrumentation.
topic Escherichia coli
Shiga Toxin
foodborne pathogen
ampliPHOX
STEC
leafy-vegetable production
url http://journal.frontiersin.org/Journal/10.3389/fcimb.2012.00061/full
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