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Title: Gene-matched enrichment and polymerase chain reaction for rapid detection of microorganisms

Abstract

A method for amplifying and detecting microorganisms, such as species of Listeria, is described. The method utilizes gene-matched enrichment media and PCR-based detection. The enrichment media is spent media produced using a modified microorganism containing a plurality of mutations in a selected gene such that the modified microorganism does not contain the PCR signature. Thus, PCR detects only the amplified microorganism of interest, not the modified microorganism. Exemplary methods and kits for amplification and detection of Listeria species are described.

Inventors:
; ; ;
Issue Date:
Research Org.:
Pacific Northwest National Laboratory (PNNL), Richland, WA (United States)
Sponsoring Org.:
USDOE
OSTI Identifier:
1489680
Patent Number(s):
10100369
Application Number:
14/742,367
Assignee:
Battelle Memorial Institute (Richland, WA)
Patent Classifications (CPCs):
C - CHEMISTRY C07 - ORGANIC CHEMISTRY C07K - PEPTIDES
C - CHEMISTRY C12 - BIOCHEMISTRY C12N - MICROORGANISMS OR ENZYMES
DOE Contract Number:  
AC05-76RL01830
Resource Type:
Patent
Resource Relation:
Patent File Date: 2015 Jun 17
Country of Publication:
United States
Language:
English
Subject:
59 BASIC BIOLOGICAL SCIENCES

Citation Formats

Ozanich, Richard M., Hutchison, Janine R., Victry, Kristin D., and Hess, Becky M. Gene-matched enrichment and polymerase chain reaction for rapid detection of microorganisms. United States: N. p., 2018. Web.
Ozanich, Richard M., Hutchison, Janine R., Victry, Kristin D., & Hess, Becky M. Gene-matched enrichment and polymerase chain reaction for rapid detection of microorganisms. United States.
Ozanich, Richard M., Hutchison, Janine R., Victry, Kristin D., and Hess, Becky M. Tue . "Gene-matched enrichment and polymerase chain reaction for rapid detection of microorganisms". United States. https://www.osti.gov/servlets/purl/1489680.
@article{osti_1489680,
title = {Gene-matched enrichment and polymerase chain reaction for rapid detection of microorganisms},
author = {Ozanich, Richard M. and Hutchison, Janine R. and Victry, Kristin D. and Hess, Becky M.},
abstractNote = {A method for amplifying and detecting microorganisms, such as species of Listeria, is described. The method utilizes gene-matched enrichment media and PCR-based detection. The enrichment media is spent media produced using a modified microorganism containing a plurality of mutations in a selected gene such that the modified microorganism does not contain the PCR signature. Thus, PCR detects only the amplified microorganism of interest, not the modified microorganism. Exemplary methods and kits for amplification and detection of Listeria species are described.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {Tue Oct 16 00:00:00 EDT 2018},
month = {Tue Oct 16 00:00:00 EDT 2018}
}

Works referenced in this record:

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Multiple point mutations in virulence genes explain the low virulence of Listeria monocytogenes field strains
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The inlA Gene of Listeria monocytogenesLO28 Harbors a Nonsense Mutation Resulting in Release of Internalin
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Catellibacterium nectariphilum gen. nov., sp. nov., which requires a diffusible compound from a strain related to the genus Sphingomonas for vigorous growth
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