IP Library Granted Patent US 10,100,369
Granted Patent B2
US 10,100,369 · App. 14/742,367 · Granted Oct 16, 2018

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

Inventors: Richard M. Ozanich (Richland, WA); Janine R. Hutchison (Richland, WA); Kristin D. Victry (Richland, WA); Becky M. Hess (Richland, WA)
Assignee: Battelle Memorial Institute
C12Q1/689C07K14/195C12N1/20C12R1/01
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Quick Facts
Patent No.
US 10,100,369
App. No.
14/742,367
Granted
Oct 16, 2018
Kind
B2
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.

Claims (13)

1. A gene-matched method for enrichment and detection of a microorganism, comprising:

amplifying the microorganism in spent enrichment media, wherein the spent enrichment media is produced by inoculating a suitable growth media with a modified microorganism, wherein the modified microorganism comprises a plurality of silent mutations in at least one target gene, allowing the modified microorganism to grow in the media for a selected period of time, and filtering the media to remove cells of the modified microorganism;

isolating nucleic acid from the amplified microorganism; and

detecting the presence of the microorganism by performing a PCR assay on the isolated nucleic acid using a pair of primers that hybridize with and amplify the target gene of the microorganism, but will not amplify the target gene from the modified microorganism.

2. The method of claim 1 , wherein the microorganism is a bacterial microorganism.

3. The method of claim 2 , wherein the bacterial microorganism is Listeria.

4. The method of claim 3 , wherein the at least one target gene is selected from inlA, inlB, plcA, hylA, actA, plcB, ssrB, ssrA and iap.

5. The method of claim 2 , wherein:

the bacterial microorganism is Bacillus cereus and the target gene is hblC, hblD, hblA, nheA, nheB, nheC, entF, entM or eytK.

6. The method of claim 1 , wherein the microorganism is a fungal microorganism.

7. The method of claim 1 , wherein the microorganism is a protozoan microorganism.

8. The method of claim 2 , wherein the bacterial microorganism is Escherichia coli and the target gene is fedA, stx 2e , faeG, fanA, fasA, est or elt.

9. The method of claim 2 , wherein the bacterial microorganism is Clostridium perfringens and the target gene is plc, pfoA, cola or nahH.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 12, 2016
From: HESS, BECKY M.
To: BATTELLE MEMORIAL INSTITUTE
Reel/Frame 040716/0211 →
CONFIRMATORY LICENSE Recorded Nov 27, 2015
From: BATTELLE MEMORIAL INSTITUTE, PACIFIC NORTHWEST DIVISION
To: U.S. DEPARTMENT OF ENERGY
Reel/Frame 037161/0160 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 1, 2015
From: OZANICH, RICHARD M.; HUTCHISON, JANINE R.; VICTRY, KRISTIN D.
To: BATTELLE MEMORIAL INSTITUTE
Reel/Frame 035989/0757 →
Continuity (2)
Provisional Application 62013998 · Jun 18, 2014
Related Publication 20150368696A1 · Dec 24, 2015