IP Library Granted Patent US 9,334,503
Granted Patent B2
US 9,334,503 · App. 14/151,601 · Granted May 10, 2016

Commensal bacteria as singal mediators within a mammalian host

Inventors: John C. March (Ithaca, NY); Franklin Faping Duan (Ithaca, NY)
Assignee: Cornell University
C12N15/74A23K1/008A23K1/009A61K38/164A61K38/22A61K38/26C07K14/4705C07K14/605A61K35/12C07H21/04C12N15/75C12N2510/00
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Quick Facts
Patent No.
US 9,334,503
App. No.
14/151,601
Granted
May 10, 2016
Kind
B2
Abstract

Genetically engineered cells and microorganisms are provided for preventing or ameliorating diseases through genetically engineered quorum signaling. Therapeutic methods for using the cells and microorganisms to prevent or ameliorate diseases are also provided. The genetically engineered cells or microorganisms can be engineered to express a signal and used to interrupt the signaling-dependent virulence of an invading pathogen. The cells or microorganisms can be used to provide signal-dependent expression of a desirable gene in order to interrupt, prevent, and/or ameliorate a disease of mammals, such as parasitic diseases, infectious diseases, autoimmune diseases and genetic disorders.

Claims (24)

1. A method of treating diabetes in a mammalian host comprising:

administering to the gastrointestinal tract of mammalian host a recombinant enteric commensal bacterium comprising a recombinant nucleic acid encoding a signal that comprises a mammalian insulin secretion-stimulating peptide glucagon-like peptide 1 (GLP-1), wherein:

the recombinant nucleic acid encoding the signal is under the control of a promoter,

the signal is expressed and secreted by the recombinant enteric commensal bacterium in the gastrointestinal tract of the mammalian host, and

the signal stimulates glucose-responsive insulin production in the mammalian host.

2. The method according to claim 1 , wherein the bacterium is a species of Pseudomonas, Bacteroides, Lactobacillus, Lactococcus, Bacillus, Proteus, Bifidobacterium, Streptococcus, Staphylococcus , or Corynebacterium.

3. The method of claim 1 wherein the commensal bacteria is a strain of Lactobacillus.

4. The method of claim 3 wherein the glucagon-like peptide 1 is GLP-1(1-37).

5. The method of claim 4 wherein the diabetes is Type I diabetes.

6. The method of claim 1 wherein the glucagon-like peptide 1 is GLP-1(1-37).

7. The method of claim 6 wherein the diabetes is Type I diabetes.

8. The method of claim 1 wherein the diabetes is Type I diabetes.

9. A method of treating diabetes in a human comprising:

administering to the gastrointestinal tract of the human a recombinant enteric commensal bacterium comprising a recombinant nucleic acid encoding a signal that comprises mammalian insulin secretion-stimulating peptide glucagon-like peptide 1 (GLP-1), wherein:

the recombinant nucleic acid encoding the signal is under the control of a promoter,

the signal is expressed and secreted by the recombinant enteric commensal bacterium in the gastrointestinal tract of the human, and

the signal stimulates glucose-responsive insulin production in the human.

10. The method according to claim 9 , wherein the bacterium is a species of Pseudomonas, Bacteroides, Lactobacillus, Lactococcus, Bacillus, Proteus, Bifidobacterium, Streptococcus, Staphylococcus , or Corynebacterium.

11. The method of claim 9 wherein the commensal bacteria is a strain of Lactobacillus.

12. The method of claim 11 wherein the glucagon-like peptide 1 is GLP-1(1-37).

13. The method of claim 12 wherein the diabetes is Type I diabetes.

14. The method of claim 9 wherein the glucagon-like peptide 1 peptide is GLP-1(1-37).

15. The method of claim 14 wherein the diabetes is Type I diabetes.

16. The method of claim 9 wherein the diabetes is Type I diabetes.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 7, 2015
From: MARCH, JOHN C.; DUAN, FRANKLIN FAPING
To: CORNELL UNIVERSITY
Reel/Frame 036805/0863 →
Continuity (3)
Continuation 12937176
Provisional Application 61043426 · Apr 9, 2008
Related Publication 20140234256A1 · Aug 21, 2014