Molecular probe technology detects bacteria without culture

<p>Abstract</p> <p>Background</p> <p>Our ultimate goal is to detect the entire human microbiome, in health and in disease, in a single reaction tube, and employing only commercially available reagents. To that end, we adapted molecular inversion probes to detect bacteri...

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Main Authors: Hyman Richard W, St Onge Robert P, Kim Hyunsung, Tamaresis John S, Miranda Molly, Aparicio Ana, Fukushima Marilyn, Pourmand Nader, Giudice Linda C, Davis Ronald W
Format: Article
Language:English
Published: BMC 2012-03-01
Series:BMC Microbiology
Online Access:http://www.biomedcentral.com/1471-2180/12/29
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spelling doaj-4d15bd7da1024c8c921102ed323511a02020-11-25T00:26:04ZengBMCBMC Microbiology1471-21802012-03-011212910.1186/1471-2180-12-29Molecular probe technology detects bacteria without cultureHyman Richard WSt Onge Robert PKim HyunsungTamaresis John SMiranda MollyAparicio AnaFukushima MarilynPourmand NaderGiudice Linda CDavis Ronald W<p>Abstract</p> <p>Background</p> <p>Our ultimate goal is to detect the entire human microbiome, in health and in disease, in a single reaction tube, and employing only commercially available reagents. To that end, we adapted molecular inversion probes to detect bacteria using solely a massively multiplex molecular technology. This molecular probe technology does not require growth of the bacteria in culture. Rather, the molecular probe technology requires only a sequence of forty sequential bases unique to the genome of the bacterium of interest. In this communication, we report the first results of employing our molecular probes to detect bacteria in clinical samples.</p> <p>Results</p> <p>While the assay on Affymetrix GenFlex Tag16K arrays allows the multiplexing of the detection of the bacteria in each clinical sample, one Affymetrix GenFlex Tag16K array must be used for each clinical sample. To multiplex the clinical samples, we introduce a second, independent assay for the molecular probes employing Sequencing by Oligonucleotide Ligation and Detection. By adding one unique oligonucleotide barcode for each clinical sample, we combine the samples after processing, but before sequencing, and sequence them together.</p> <p>Conclusions</p> <p>Overall, we have employed 192 molecular probes representing 40 bacteria to detect the bacteria in twenty-one vaginal swabs as assessed by the Affymetrix GenFlex Tag16K assay and fourteen of those by the Sequencing by Oligonucleotide Ligation and Detection assay. The correlations among the assays were excellent.</p> http://www.biomedcentral.com/1471-2180/12/29
collection DOAJ
language English
format Article
sources DOAJ
author Hyman Richard W
St Onge Robert P
Kim Hyunsung
Tamaresis John S
Miranda Molly
Aparicio Ana
Fukushima Marilyn
Pourmand Nader
Giudice Linda C
Davis Ronald W
spellingShingle Hyman Richard W
St Onge Robert P
Kim Hyunsung
Tamaresis John S
Miranda Molly
Aparicio Ana
Fukushima Marilyn
Pourmand Nader
Giudice Linda C
Davis Ronald W
Molecular probe technology detects bacteria without culture
BMC Microbiology
author_facet Hyman Richard W
St Onge Robert P
Kim Hyunsung
Tamaresis John S
Miranda Molly
Aparicio Ana
Fukushima Marilyn
Pourmand Nader
Giudice Linda C
Davis Ronald W
author_sort Hyman Richard W
title Molecular probe technology detects bacteria without culture
title_short Molecular probe technology detects bacteria without culture
title_full Molecular probe technology detects bacteria without culture
title_fullStr Molecular probe technology detects bacteria without culture
title_full_unstemmed Molecular probe technology detects bacteria without culture
title_sort molecular probe technology detects bacteria without culture
publisher BMC
series BMC Microbiology
issn 1471-2180
publishDate 2012-03-01
description <p>Abstract</p> <p>Background</p> <p>Our ultimate goal is to detect the entire human microbiome, in health and in disease, in a single reaction tube, and employing only commercially available reagents. To that end, we adapted molecular inversion probes to detect bacteria using solely a massively multiplex molecular technology. This molecular probe technology does not require growth of the bacteria in culture. Rather, the molecular probe technology requires only a sequence of forty sequential bases unique to the genome of the bacterium of interest. In this communication, we report the first results of employing our molecular probes to detect bacteria in clinical samples.</p> <p>Results</p> <p>While the assay on Affymetrix GenFlex Tag16K arrays allows the multiplexing of the detection of the bacteria in each clinical sample, one Affymetrix GenFlex Tag16K array must be used for each clinical sample. To multiplex the clinical samples, we introduce a second, independent assay for the molecular probes employing Sequencing by Oligonucleotide Ligation and Detection. By adding one unique oligonucleotide barcode for each clinical sample, we combine the samples after processing, but before sequencing, and sequence them together.</p> <p>Conclusions</p> <p>Overall, we have employed 192 molecular probes representing 40 bacteria to detect the bacteria in twenty-one vaginal swabs as assessed by the Affymetrix GenFlex Tag16K assay and fourteen of those by the Sequencing by Oligonucleotide Ligation and Detection assay. The correlations among the assays were excellent.</p>
url http://www.biomedcentral.com/1471-2180/12/29
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