IP Library Granted Patent US 9,140,698
Granted Patent B2
US 9,140,698 · App. 14/009,724 · Granted Sep 22, 2015

Modulating bacterial MAM polypeptides in pathogenic disease

Inventors: Kim Orth (Dallas, TX); Hyeilin Ham (Dallas, TX); Anne-Marie Krachler (Malvern, GB)
Assignee: The Board of Regents of the University of Texas System
G01N33/554A23L1/3014A61K35/74A61K35/741A61K38/164G01N33/56911G01N2333/195
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Quick Facts
Patent No.
US 9,140,698
App. No.
14/009,724
Granted
Sep 22, 2015
Kind
B2
Abstract

The disclosure relates to methods and compositions for preventing or inhibiting pathogenic bacterial infections in a subject caused by pathogenic bacteria expressing a multivalent adhesion molecule (MAM) polypeptide by administering to a subject a composition comprising a MAM polypeptide or a non-pathogenic bacterium expressing a MAM polypeptide, or a combination thereof.

Claims (26)

1. A method of preventing or inhibiting a pathogenic bacterial infection in a subject caused by a pathogenic bacterium expressing a multivalent adhesion molecule (MAM) polypeptide, comprising administering to said subject a composition comprising a non-pathogenic bacterium expressing a MAM polypeptide comprising at least 6 mce repeat regions.

2. The method of claim 1 , wherein said pathogenic bacterium is Gram-negative.

3. The method of claim 2 , wherein said pathogenic bacterium is selected from the group consisting of Vibrio parahaemolyticus, Vibrio cholerae, Yersinia pseutotuberculosis , and enteropathogenic Escherichia coli.

4. The method of claim 1 , wherein said non-pathogenic bacterium expresses a native MAM polypeptide.

5. The method of claim 1 , wherein said non-pathogenic bacterium expresses a heterologous MAM polypeptide.

6. The method of claim 5 , wherein said non-pathogenic bacterium comprises a gene encoding a MAM polypeptide in an extrachromosomal self-replicating vector.

7. The method of claim 5 , wherein said non-pathogenic bacterium comprises a gene encoding a MAM polypeptide integrated into a chromosome of said non-pathogenic bacterium.

8. The method of claim 1 , wherein said composition further comprises a probiotic.

9. The method of claim 8 , wherein said composition is administered orally.

10. The method of claim 8 , wherein said composition is selected from the group consisting of milk, yogurt, curd, cheese, fermented milks, milk based fermented products, ice-creams, fermented cereal based products, milk based powders, infant formulae, pet food, a tablet, a liquid bacterial suspension, dried oral supplement and wet oral supplement.

11. The method of claim 1 , wherein said composition is administered topically.

12. The method of claim 11 , wherein said subject has suffered a burn injury.

13. The method of claim 11 , wherein said composition is formulated as a cream, a gel, a salve, an ointment or a powder.

14. The method of claim 11 , wherein said composition is comprised in or disposed on a wound dressing.

15. The method of claim 1 , wherein said composition is comprises in or disposed on a surgical mesh or implantable device.

16. A method of preventing or inhibiting a pathogenic bacterial infection in a subject caused by a pathogenic bacterium expressing a multivalent adhesion molecule (MAM) polypeptide, comprising administering to said subject a composition comprising a MAM peptide or protein comprising at least 6 mce repeat regions coupled to a carrier.

17. The method of claim 16 , wherein said pathogenic bacterium is Gram-negative.

18. The method of claim 17 , wherein said pathogenic bacterium is selected from the group consisting of Vibrio parahaemolyticus, Vibrio cholerae, Yersinia pseutotuberculosis , and enteropathogenic Escherichia coli.

19. The method of claim 16 , wherein said carrier is a particle or bead.

20. A method for identifying or quantifying phosphatidic acid on a membrane comprising contacting a membrane with a peptide or polypeptide comprising a multivalent adhesion molecule (MAM) mce repeat region.

21. The method of claim 20 , wherein said membrane is part of an intact cell.

22. The method of claim 1 , wherein the number of mce repeats is 6.

23. The method of claim 1 , wherein the number of mce repeats is 7.

24. The method of claim 16 , wherein the number of mce repeats is 6.

25. The method of claim 16 , wherein the number of mce repeats is 7.

26. The method of claim 16 , wherein said carrier is a liposome, a nanoparticle, a nanoshell, a nanocluster or a quantum dot.

Assignments (2)
CONFIRMATORY LICENSE Recorded Mar 2, 2022
From: UT SOUTHWESTERN MEDICAL CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 059292/0643 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 17, 2013
From: ORTH, KIM; HAM, HYEILIN; KRACHLER, ANNE-MARIE
To: THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 031802/0822 →
Continuity (2)
Provisional Application 61472440 · Apr 6, 2011
Related Publication 20140093477A1 · Apr 3, 2014