IP Library Granted Patent US 9,310,365
Granted Patent B2
US 9,310,365 · App. 13/639,450 · Granted Apr 12, 2016

Method of diagnosing and treating melioidosis

Inventors: Thomas Kozel (Reno, NV); David Aucoin (Reno, NC)
Assignee: The Board of Regents of the Nevada System of Higher Education, on behalf of the University of Nevada, Reno
G01N33/56911C07K16/1214G01N2333/21G01N2800/52
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Quick Facts
Patent No.
US 9,310,365
App. No.
13/639,450
Granted
Apr 12, 2016
Kind
B2
Abstract

Non-invasive methods are provided herein for the diagnosis of melioidosis with specific antibodies capable of detecting molecules associated with melioidosis in a biological fluid, such as urine or serum. These molecules can be identified using proteomic methods, including but not limited to antibody based methods, such as an enzyme-linked immunosorbant assay (ELISA), a radioimmunoassay (RIA), or a lateral flow immunoassay. Methods of inducing an immune response to melioidosis are also disclosed. The methods include the use of the immunogenic melioidosis polypeptides, nucleic acids encoding these polypeptides, and/or viral vectors encoding an immunogenic melioidosis polypeptide, alone or in conjunction with other agents, such as traditional melioidosis therapies. Also disclosed are methods for treating a subject having melioidosis. These methods include inducing an immune response to melioidosis and/or using an inhibitory nucleic acid, such as a siRNA or antisense molecule, to decrease a melioidosis associated molecule expression in order to treat melioidosis.

Claims (21)

1. A method of diagnosing a subject with melioidosis, comprising:

detecting, with an antibody produced by immunizing an animal with a melioidosis-associated antigen, by laboratory immunoassay, the melioidosis-associated antigen in a sample obtained from a subject exhibiting one or more signs or symptoms associated with melioidosis or a subject known to be at risk of acquiring melioidosis so as to obtain laboratory assay results regarding the presence of the melioidosis-associated antigen in the sample, wherein the melioidosis-associated antigen is a capsular polysaccharide (CPS) comprising an unbranched homopolymer of 6-deoxy-D-manno-heptose; and

providing laboratory assay results thereby diagnosing whether the subject has melioidosis.

2. The method of claim 1 , further comprising comparing detection of the melioidosis-associated antigen in the sample obtained from the subject exhibiting one or more signs or symptoms associated with melioidosis to a control, wherein increased detection of the melioidosis-associated antigen relative to a control indicates that the subject has melioidosis.

3. The method of claim 2 , wherein the method is used for diagnosing a subject with acute melioidosis.

4. The method of claim 2 , wherein detecting at least one melioidosis-associated antigen comprises using a lateral flow device.

5. The method of claim 1 , wherein the method is used for detecting any condition or disease associated with B. mallei, B. pseudomallei, B. thailandensis or a combination thereof.

6. The method of claim 1 , wherein the sample is a urine sample.

7. A method of monitoring the efficacy of a melioidosis therapy, comprising:

detecting, with an antibody produced by immunizing an animal with a melioidosis-associated antigen, by laboratory immunoassay, the melioidosis-associated antigen in a sample obtained from a subject that has been administered a meliodosis therapy, wherein the melioidosis-associated antigen is a capsular polysaccharide (CPS) comprising an unbranched homopolymer of 6-deoxy-D-manno-heptose;

comparing detection of the melioidosis-associated antigen in the sample obtained from the subject to a reference sample;

providing laboratory assay results thereby monitoring the efficacy of the melioidosis therapy.

8. The method of claim 7 , wherein the method is used for monitoring any condition or disease associated with B. mallei, B. pseudomallei, B. thailandensis or a combination thereof.

9. The method of claim 7 , wherein the reference sample is a sample from a subject with melioidosis.

10. The method of claim 7 , wherein the reference sample is a sample from a subject that does not have melioidosis.

11. The method of claim 1 , wherein the antibody is produced by a hybridoma created from the immunized animal.

12. The method of claim 7 , wherein the antibody is produced by a hybridoma created from the immunized animal.

13. The method of claim 1 , wherein detecting comprises detecting a plurality of melioidosis-associated antigens.

14. The method of claim 7 , wherein detecting comprises detecting a plurality of melioidosis-associated antigens.

15. The method of claim 1 , wherein the antibody is a monoclonal antibody.

16. The method of claim 7 , wherein the antibody is a monoclonal antibody.

Assignments (1)
CONFIRMATORY LICENSE Recorded Nov 1, 2012
From: UNIVERSITY OF NEVADA RENO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029229/0532 →
Continuity (3)
Provisional Application 61323236 · Apr 12, 2010
Provisional Application 61452388 · Mar 14, 2011
Related Publication 20130028927A1 · Jan 31, 2013