IP Library Granted Patent US 9,103,788
Granted Patent B2
US 9,103,788 · App. 13/691,511 · Granted Aug 11, 2015

Detection of bacterial contamination in a sample

Inventors: Jon G. Wilkes (Little Rock, AR); Dan Buzatu (Benton, AR); Randal Tucker (Hensley, AR); Thaddeus John Moskal, Jr. (Jonesboro, AR)
Assignees: THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES; VIVIONE BIOSCIENCES, LLC
G01N21/6486G01N21/6428G01N2021/6439G01N2021/6441
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Quick Facts
Patent No.
US 9,103,788
App. No.
13/691,511
Granted
Aug 11, 2015
Kind
B2
Abstract

Methods for detecting one or more target bacteria in a test sample are provided. It is shown herein that photosensitizers combined with intense light exposure reduce fluorescing background due to non-bacterial particles. This permits detection of subsequently labeled target bacterial cells (e.g., using a fluorescently labeled antibody) against a largely black background. In particular examples, the methods include incubating the test sample in a growth medium that permits growth of bacteria present in the sample, contacting the sample with a photo-sensitizer; exposing the sample to light under conditions sufficient for the photo-sensitizer to photobleach contaminating non-bacterial particulates present in the sample. The bacteria can then be substantially separated from the sample, thereby generating an isolated bacterial sample. The method can also include contacting the isolated bacterial sample with a binding agent specific for the one or more target bacteria, and detecting the one or more target bacteria.

Claims (27)

1. A method of detecting one or more target bacteria in a test sample comprising:

incubating the test sample in a bacterial culture medium that permits growth of bacteria present in the test sample;

contacting the bacterial culture medium containing the test sample with a photosensitizing agent;

exposing the bacterial culture medium containing the test sample to infra-red light, visible light, or UV light, under conditions sufficient for the photosensitizing agent to photobleach contaminating or autofluorescing non-bacterial particulates present in the sample;

separating the bacteria from the bacterial culture medium containing the test sample, thereby generating an isolated bacterial sample;

contacting the isolated bacterial sample with a specific binding agent specific for the one or more target bacteria, under conditions sufficient for the specific binding agent to bind to the one or more target bacteria, wherein the specific binding agent is directly or indirectly labeled;

permitting detection of the labeled specific binding agent bound to the one or more target bacteria; and

designating the test sample as containing the one or more target bacteria when the labeled specific binding agent bound to the one or more target bacteria is detected.

2. The method of claim 1 , wherein the bacterial culture medium comprises brain heart infusion medium or tryptic soy broth.

3. The method of claim 1 , wherein the incubation of the test sample is at 37° C. to 45° C. for at least 4 hours.

4. The method of claim 1 , wherein the photosensitizing agent is phloxine B.

5. The method of claim 1 , wherein the exposing the bacterial culture medium containing the test sample to the light comprises the bacterial culture medium containing the test sample to a light intensity of at least 10,000 LUX.

6. The method of claim 1 , wherein the separating the bacteria from the bacterial culture medium containing the test sample comprises pelleting the bacteria.

7. The method of claim 1 , wherein the separating the bacteria from the bacterial culture medium containing the test sample comprises filtering the bacterial culture medium one or more times.

8. The method of claim 1 , wherein the separating the bacteria from the bacterial culture medium containing the test sample comprises centrifuging the bacterial culture medium.

9. The method of claim 1 , wherein the method further comprises contacting the isolated bacterial sample with one or more detergents or surfactants.

10. The method of claim 1 , wherein the specific binding agent is directly or indirectly labeled with a fluorophore.

11. The method of claim 1 , wherein the specific binding agent is directly labeled.

12. The method of claim 1 , wherein the specific binding agent is indirectly labeled, and the method further comprises:

contacting the isolated bacterial sample with a secondary agent specific for the specific binding agent, under conditions sufficient for the secondary agent to bind to the specific binding agent.

13. The method of claim 1 , wherein the specific binding agent is an antibody, peptide nucleic acid (PNA) or an aptamer.

14. The method of claim 12 , wherein the secondary agent is a labeled secondary antibody.

15. The method of claim 1 , wherein the method further comprises:

determining whether the one or more target bacteria detected in the sample are alive or dead.

16. The method of claim 1 , wherein the detecting the one or more target bacteria occurs before the photobleaching deteriorates cell membranes and cell surface epitopes of the one or more target bacteria.

17. The method of claim 1 , wherein the sample is a food sample, patient sample, or environmental sample.

18. The method of claim 1 , wherein the method is completed in 4 hours to 8 hours.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2022
From: APERTURE BIO, LLC; SCION ADVISORS, LLC
To: RENASCENT DIAGNOSTIC, LLC
Reel/Frame 061885/0627 →
CHANGE OF NAME Recorded Oct 15, 2018
From: VIVIONE BIOSCIENCES, LLC
To: APERTURE BIO, LLC
Reel/Frame 047237/0431 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 22, 2013
From: WILKES, JON G.; BUZATU, DAN; TUCKER, RANDAL
To: THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Reel/Frame 029672/0291 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 5, 2012
From: MOSKAL, THADDEUS JOHN, JR.
To: VIVIONE BIOSCIENCES, LLC
Reel/Frame 029409/0516 →
Continuity (2)
Provisional Application 61564926 · Nov 30, 2011
Related Publication 20130137119A1 · May 30, 2013