Rapid electrochemical assay for antibiotic and cytotoxic drug susceptibility in microorganisms

• US 6,391,577 B1
• Filed: 03/03/1999
• Issued: 05/21/2002
• Est. Priority Date: 03/03/1999
• Status: Expired due to Fees

• Current Assignee: Mount Sinai Services, Inc.
• Original Assignee: Susan R. Mikkelsen
• Inventors: Ertl, Peter, Mikkelsen, Susan R.
• Primary Examiner(s): GITOMER, RALPH J
• Application Number:
  US09/261,195
• Time in Patent Office: 1,175 Days
• Field of Search: 435/32, 435/4, 435/25, 204/403, 204/431
• US Class Current: 435/32
• CPC Class Codes: C12Q 1/18 Testing for antimicrobial activity of a material

Abstract

This invention presents rapid methods for evaluating the effects of antimicrobial compounds on microorganisms based upon the microorganism'"'"'s ability to transport electrons to an external chemical oxidant (a mediator) that is added to the microorganism sample. The mediator interacts with the terminal components of the respiratory pathway and the extent of its consumption is related to the ability of the microorganism to respire. However, under the assay conditions described herein the extent of mediator consumption is different from the microorganisms'"'"' ability to consume oxygen, due to the addition of metabolizable compounds to the assay mixtures. The consumed mediator is subsequently measured electrochemically (amperometrically or coulometrically) at the working electrode of a standard two-electrode or three-electrode electrochemical cell. The electrochemical signals (change of current or charge with time) obtained with microorganism suspensions incubated in the absence and presence of antimicrobial compounds are significantly different. These signal differences can be used to screen for antimicrobial effectiveness of antibiotic drugs against clinically important multi-drug-resistant organisms, to screen for the presence of unlawful levels of antibiotic compounds in foodstuffs, or to screen potential new antimicrobial compounds for effectiveness against different species of microorganisms.

Claims

1. A method of rapidly assessing susceptibility of a microorganism to a drug selected from the group consisting of an antibiotic and a cytotoxic compound, said method comprising the steps of:

obtaining a test sample of a microorganism;

arresting growth of the microorganism in the test sample;

adding a mediator to a test sample of said microorganism in the presence of said drug;

said mediator being reducible by accepting an electron arising from respiration of the microorganism;

determining variation of the respiration rate of the microorganism over time by electrochemical measurement of mediator reduction in the test sample resulting from microorganism respiration, said variation of the respiration rate being observable over a time period of up to 500 seconds; and

comparing variation of the respiration rate of the test sample with variation of the respiration rate in a control sample of the microorganism not exposed to said drug, thereby assessing susceptibility of the microorganism to the drug.

2. A method as recited in claim 1, wherein the step of adding a mediator to a test sample comprises:

preparing the test sample by combining a cell culture or suspension of the microorganism with a solution of the drug, the combination then being incubated for a fixed time prior to adding the mediator.

3. A method as recited in claim 2, where said mediator comprises at least one compound selected from the group consisting of:

ferricyanide (hexacyanoferrate (III));

dichlorophenol-indophenol (DCIP);

ferrocene and ferrocene derivatives;

methylene blue;

janus green;

tris(bipyridyl)iron (III);

a quinone; and

a phenazine.

4. A method as recited in claim 2, where said drug is selected from the group consisting of:

Penicillin G;

D-Cycloserine;

Vancomycin;

Bacitracin;

Cephalosporin C;

Tetracycline;

Erythromycin;

Chloramphenicol;

Streptomycin;

Nalidixic Acid;

Rifampicin;

Trimethoprim;

Amphotericin;

Nystatin;

EDTA; and

Lysozyme.

5. A method as recited in claim 1, wherein the step of adding a mediator to a test sample comprises:

preparing the test sample by combining a cell culture or suspension of the microorganism with a mediator and a solution of the drug, the combination then being incubated for a fixed time.

6. A method as recited in claim 5, where said mediator comprises at least one compound selected from the group consisting of:

ferricyanide (hexacyanoferrate (III));

dichlorophenol-indophenol (DCIP);

ferrocene and ferrocene derivatives;

methylene blue;

janus green;

tris(bipyridyl)iron (III);

a quinone; and

a phenazine.

7. A method as recited in claim 5, where said drug is selected from the group consisting of:

Penicillin G;

D-Cycloserine;

Vancomycin;

Bacitracin;

Cephalosporin C;

Tetracycline;

Erythromycin;

Chloramphenicol;

Streptomycin;

Nalidixic Acid;

Rifampicin;

Trimethoprim;

Amphotericin;

Nystatin;

EDTA; and

Lysozyme.

8. A method as recited in claim 1, where said mediator comprises at least one compound selected from the group consisting of:

ferricyanide (hexacyanoferrate (III));

dichlorophenol-indophenol (DCIP);

ferrocene and ferrocene derivatives;

methylene blue;

janus green;

tris(bipyridyl)iron (III);

a quinone; and

a phenazine.

9. A method as recited in claim 8, wherein said quinone is selected from the group consisting of benzoquinone, naphthoquinone, menadione, anthraquinone, and substituted derivatives of these.

10. A method as recited in claim 8, wherein said phenazine is selected from the group consisting of phenazine methosulfate and phenazine ethosulfate.

11. A method as recited in claim 1, where said drug is selected from the group consisting of:

Penicillin G;

D-Cycloserine;

Vancomycin;

Bacitracin;

Cephalosporin C;

Tetracycline;

Erythromycin;

Chloramphenicol;

Streptomycin;

Nalidixic Acid;

Rifampicin;

Trimethoprim;

Amphotericin;

Nystatin;

EDTA; and

Lysozyme.

12. A method as recited in claim 1 wherein the variation of the respiration rate is observable over a time period of from 60 to 120 seconds.

13. A method as recited in claim 1 additionally comprising the step of incubation of the mediator with the test sample for up to 20 minutes prior to determining variation of the respiration rate of the microorganism.

14. A method as recited in claim 13 wherein incubation of the mediator with the test sample occurs for up to 10 minutes prior to determining variation of the respiration rate of the microorganism.

15. A method as recited in claim 1 wherein the mediator is reducible by accepting an electron arising from a terminal component of the respiratory pathway of the microorganism.

16. A method of rapidly assessing susceptibility of a microorganism to a drug selected from the group consisting of an antibiotic and a cytotoxic compound, said method comprising the steps of:

obtaining a test sample of a microorganism;

arresting growth of the microorganism in the test sample;

adding a mediator to a test sample of said microorganism in the presence of said drug;

said mediator being reducible by accepting an electron arising from a terminal component of the respiratory pathway of the microorganism;

incubating the mediator with the test sample for up to 20 minutes;

determining variation of the respiration rate of the microorganism over a time by electrochemical measurement of mediator reduction in the test sample resulting from microorganism respiration, said variation of the respiration rate being observable over a time period of from 60 to 120 seconds; and

comparing variation of the respiration rate of the test sample with variation of the respiration rate in a control sample of the microorganism not exposed to said drug, thereby assessing susceptibility of the microorganism to the drug.