IP Library Granted Patent US 12,214,002
Granted Patent B2
US 12,214,002 · App. 16/760,757 · Granted Feb 4, 2025

Compositions and methods for treating antibiotic resistance

Inventors: Christopher Burton Ford (Swampscott, MA); Jessica Bryant (Cambridge, MA); Edward J. O'Brien (Arlington, MA)
Assignee: Seres Therapeutics, Inc.
A61K35/742A61P31/04
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Quick Facts
Patent No.
US 12,214,002
App. No.
16/760,757
Granted
Feb 4, 2025
Kind
B2
Abstract

The present invention relates to compositions and methods for reducing the carriage of antibiotic resistance genes.

Claims (36)

1. A method of reducing an abundance of at least one antibiotic-resistance gene in the microbiome of a mammalian subject in need thereof, comprising administering to the subject a therapeutically effective amount of a composition comprising a combination of bacteria, the combination comprising Blautia wexlerae and Anaerotruncus colihominis , wherein after the administration of the composition, the abundance of the at least one antibiotic-resistance gene in the microbiome of the subject is reduced as compared to a corresponding subject who did not receive the administration of the composition, wherein the at least one antibiotic-resistance gene is capable of conferring resistance to beta-lactam antibiotics and at least one additional antibiotic drug class, and wherein:

(a) the Blautia wexlerae comprises a 16S rDNA sequence that is at least 97% identical to the 16S rDNA sequence set forth in any one of SEQ ID NOs: 104-110 and 255; and

(b) the Anaerotruncus colihominis comprises a 16S rDNA sequence that is at least 97% identical to the 16S rDNA sequence set forth in any one of SEQ ID NOs: 89-92.

2. A method of treating a mammalian subject at risk for or diagnosed with an undesirable level of bacteria that are resistant to multiple antibiotic drug classes, comprising administering to the subject a therapeutically effective amount of a composition comprising a combination of bacteria, wherein the combination comprises Blautia wexlerae and Anaerotruncus colihominis , wherein the undesirable level is a level significantly greater than that in a healthy subject population and the multiple antibiotic drug classes comprise beta-lactam antibiotics and at least one additional antibiotic drug class, and wherein:

(a) the Blautia wexlerae comprises a 16S rDNA sequence that is at least 97% identical to the 16S rDNA sequence set forth in any one of SEQ ID NOs: 104-110 and 255; and

(b) the Anaerotruncus colihominis comprises a 16S rDNA sequence that is at least 97% identical to the 16S rDNA sequence set forth in any one of SEQ ID NOs: 89-92.

3. The method of claim 1 , wherein the composition comprises 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20 or more bacterial species.

4. The method of claim 1 , wherein the bacteria are in a spore form, a vegetative form, or a mixed vegetative form and spore form.

5. The method of claim 1 , wherein, prior to the administration, the subject has been unresponsive to antibiotic treatment, has or is at risk of developing Clostridium difficile infection, or has or is at risk of developing colitis.

6. The method of claim 1 , wherein:

(a) the Blautia wexlerae comprises a 16S rDNA sequence that is at least 98% identical to the 16S rDNA sequence set forth in any one of SEQ ID NOs: 104-110 and 255; and

(b) the Anaerotruncus colihominis comprises a 16S rDNA sequence that is at least 98% identical to the 16S rDNA sequence set forth in any one of SEQ ID NOs: 89-92.

7. The method of claim 1 , wherein:

(a) the Blautia wexlerae comprises a 16S rDNA sequence that is at least 99% identical to the 16S rDNA sequence set forth in any one of SEQ ID NOs: 104-110 and 255; and

(b) the Anaerotruncus colihominis comprises a 16S rDNA sequence that is at least 99% identical to the 16S rDNA sequence set forth in any one of SEQ ID NOs: 89-92.

8. The method of claim 1 , wherein:

(a) the Blautia wexlerae comprises the 16S rDNA sequence set forth in any one of SEQ ID NOs: 104-110 and 255; and

(b) the Anaerotruncus colihominis comprises the 16S rDNA sequence set forth in any one of SEQ ID NOs: 89-92.

9. The method of claim 2 , wherein:

(a) the Blautia wexlerae comprises a 16S rDNA sequence that is at least 98% identical to the 16S rDNA sequence set forth in any one of SEQ ID NOs: 104-110 and 255; and

(b) the Anaerotruncus colihominis comprises a 16S rDNA sequence that is at least 98% identical to the 16S rDNA sequence set forth in any one of SEQ ID NOs: 89-92.

10. The method of claim 2 , wherein:

(a) the Blautia wexlerae comprises a 16S rDNA sequence that is at least 99% identical to the 16S rDNA sequence set forth in any one of SEQ ID NOs: 104-110 and 255; and

(b) the Anaerotruncus colihominis comprises a 16S rDNA sequence that is at least 99% identical to the 16S rDNA sequence set forth in any one of SEQ ID NOs: 89-92.

11. The method of claim 2 , wherein:

(a) the Blautia wexlerae comprises the 16S rDNA sequence set forth in any one of SEQ ID NOs: 104-110 and 255; and

(b) the Anaerotruncus colihominis comprises the 16S rDNA sequence set forth in any one of SEQ ID NOs: 89-92.

12. The method of claim 2 , wherein the composition comprises 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20 or more bacterial species.

13. The method of claim 2 , wherein the bacteria are in a spore form, a vegetative form, or a mixed vegetative form and spore form.

14. The method of claim 1 , wherein the bacteria are cultured.

15. The method of claim 2 , wherein the bacteria are cultured.

16. The method of claim 1 , wherein the composition is administered to the subject via oral delivery, colonoscopic delivery, or nasogastric delivery.

17. The method of claim 2 , wherein the composition is administered to the subject via oral delivery, colonoscopic delivery, or nasogastric delivery.

18. The method of claim 1 , wherein the abundance of 2, 3, 4, 5, 6, 7, 8, 9, 10, or more antibiotic-resistance genes in the microbiome of the subject is reduced as compared to the corresponding subject who did not receive the administration of the composition.

19. The method of claim 1 , wherein the at least one additional antibiotic drug class is selected from aminocoumarin antibiotic, aminoglycoside antibiotic, cephalosporin, cephamycin, fluoroquinolone antibiotic, glycylcycline, macrolide antibiotic, nitroimidazole antibiotic, nucleoside antibiotic, penam, peptide antibiotic, phenicol antibiotic, rifamycin antibiotic, benzalkonium chloride, monobactam, penem, streptogramin antibiotic, rhodamine, triclosan, lincosamide antibiotic, acridine dye, carbapenem, tetracycline antibiotic, and fosfomycin.

20. The method of claim 2 , wherein the at least one additional antibiotic drug class is selected from aminocoumarin antibiotic, aminoglycoside antibiotic, cephalosporin, cephamycin, fluoroquinolone antibiotic, glycylcycline, macrolide antibiotic, nitroimidazole antibiotic, nucleoside antibiotic, penam, peptide antibiotic, phenicol antibiotic, rifamycin antibiotic, benzalkonium chloride, monobactam, penem, streptogramin antibiotic, rhodamine, triclosan, lincosamide antibiotic, acridine dye, carbapenem, tetracycline antibiotic, and fosfomycin.

Assignments (4)
CROSS-LICENSE AGREEMENT Recorded Mar 30, 2026
From: SERES THERAPEUTICS, INC.
To: SOCIÉTÉ DES PRODUITS NESTLÉ S.A.
Reel/Frame 075314/0554 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 19, 2024
From: FORD, CHRISTOPHER BURTON; BRYANT, JESSICA; O'BRIEN, EDWARD J.
To: SERES THERAPEUTICS, INC.
Reel/Frame 069642/0583 →
RELEASE OF SECURITY INTEREST Recorded Sep 30, 2024
From: OAKTREE FUND ADMINISTRATION, LLC, AS ADMINISTRATIVE AGENT
To: SERES THERAPEUTICS, INC.
Reel/Frame 069082/0849 →
SECURITY INTEREST Recorded Apr 27, 2023
From: SERES THERAPEUTICS, INC.
To: OAKTREE FUND ADMINISTRATION, LLC
Reel/Frame 063485/0542 →
Continuity (3)
Provisional Application 62578698 · Oct 30, 2017
Provisional Application 62741346 · Oct 4, 2018
Related Publication 20200353018A1 · Nov 12, 2020
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