Sample processing for DNA chip array-based analysis of enterohemorrhagic <it>Escherichia coli </it>(EHEC)
<p>Abstract</p> <p>Background</p> <p>Exploitation of DNA-based analyses of microbial pathogens, and especially simultaneous typing of several virulence-related genes in bacteria is becoming an important objective of public health these days.</p> <p>Results&l...
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doaj-c5495835624a4622b1737a2a221395472020-11-24T20:47:08ZengBMCMicrobial Cell Factories1475-28592008-10-01712910.1186/1475-2859-7-29Sample processing for DNA chip array-based analysis of enterohemorrhagic <it>Escherichia coli </it>(EHEC)Enfors Sven-OlofWegrzyn GrzegorzBasselet PascalGabig-Ciminska Magdalena<p>Abstract</p> <p>Background</p> <p>Exploitation of DNA-based analyses of microbial pathogens, and especially simultaneous typing of several virulence-related genes in bacteria is becoming an important objective of public health these days.</p> <p>Results</p> <p>A procedure for sample processing for a confirmative analysis of enterohemorrhagic <it>Escherichia coli </it>(EHEC) on a single colony with DNA chip array was developed and is reported here. The protocol includes application of fragmented genomic DNA from ultrasonicated colonies. The sample processing comprises first 2.5 min of ultrasonic treatment, DNA extraction (2×), and afterwards additional 5 min ultrasonication. Thus, the total sample preparation time for a confirmative analysis of EHEC is nearly 10 min. Additionally, bioinformatic revisions were performed in order to design PCR primers and array probes specific to most conservative regions of the EHEC-associated genes. Six strains with distinct pathogenic properties were selected for this study. At last, the EHEC chip array for a parallel and simultaneous detection of genes <it>etpC</it>-<it>stx1</it>-<it>stx2</it>-<it>eae </it>was designed and examined. This should permit to sense all currently accessible variants of the selected sequences in EHEC types and subtypes.</p> <p>Conclusion</p> <p>In order to implement the DNA chip array-based analysis for direct EHEC detection the sample processing was established in course of this work. However, this sample preparation mode may also be applied to other types of EHEC DNA-based sensing systems.</p> http://www.microbialcellfactories.com/content/7/1/29 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Enfors Sven-Olof Wegrzyn Grzegorz Basselet Pascal Gabig-Ciminska Magdalena |
spellingShingle |
Enfors Sven-Olof Wegrzyn Grzegorz Basselet Pascal Gabig-Ciminska Magdalena Sample processing for DNA chip array-based analysis of enterohemorrhagic <it>Escherichia coli </it>(EHEC) Microbial Cell Factories |
author_facet |
Enfors Sven-Olof Wegrzyn Grzegorz Basselet Pascal Gabig-Ciminska Magdalena |
author_sort |
Enfors Sven-Olof |
title |
Sample processing for DNA chip array-based analysis of enterohemorrhagic <it>Escherichia coli </it>(EHEC) |
title_short |
Sample processing for DNA chip array-based analysis of enterohemorrhagic <it>Escherichia coli </it>(EHEC) |
title_full |
Sample processing for DNA chip array-based analysis of enterohemorrhagic <it>Escherichia coli </it>(EHEC) |
title_fullStr |
Sample processing for DNA chip array-based analysis of enterohemorrhagic <it>Escherichia coli </it>(EHEC) |
title_full_unstemmed |
Sample processing for DNA chip array-based analysis of enterohemorrhagic <it>Escherichia coli </it>(EHEC) |
title_sort |
sample processing for dna chip array-based analysis of enterohemorrhagic <it>escherichia coli </it>(ehec) |
publisher |
BMC |
series |
Microbial Cell Factories |
issn |
1475-2859 |
publishDate |
2008-10-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Exploitation of DNA-based analyses of microbial pathogens, and especially simultaneous typing of several virulence-related genes in bacteria is becoming an important objective of public health these days.</p> <p>Results</p> <p>A procedure for sample processing for a confirmative analysis of enterohemorrhagic <it>Escherichia coli </it>(EHEC) on a single colony with DNA chip array was developed and is reported here. The protocol includes application of fragmented genomic DNA from ultrasonicated colonies. The sample processing comprises first 2.5 min of ultrasonic treatment, DNA extraction (2×), and afterwards additional 5 min ultrasonication. Thus, the total sample preparation time for a confirmative analysis of EHEC is nearly 10 min. Additionally, bioinformatic revisions were performed in order to design PCR primers and array probes specific to most conservative regions of the EHEC-associated genes. Six strains with distinct pathogenic properties were selected for this study. At last, the EHEC chip array for a parallel and simultaneous detection of genes <it>etpC</it>-<it>stx1</it>-<it>stx2</it>-<it>eae </it>was designed and examined. This should permit to sense all currently accessible variants of the selected sequences in EHEC types and subtypes.</p> <p>Conclusion</p> <p>In order to implement the DNA chip array-based analysis for direct EHEC detection the sample processing was established in course of this work. However, this sample preparation mode may also be applied to other types of EHEC DNA-based sensing systems.</p> |
url |
http://www.microbialcellfactories.com/content/7/1/29 |
work_keys_str_mv |
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