IP Library Granted Patent US 11,491,210
Granted Patent B2
US 11,491,210 · App. 17/707,074 · Granted Nov 8, 2022

Sequence specific antimicrobials

Inventors: David Bikard (Paris, FR); Luciano Marraffini (Brooklyn, NY)
Assignee: The Rockefeller University
A61K38/465A01N63/00A61K31/713A61K31/7105A61K45/06C12N9/16C12N9/22C12N15/113C12N15/74C12Y301/00C12N2310/10C12N2310/20C12N2795/10331C12N2795/10332C12N2795/10343C12N2795/10371
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Quick Facts
Patent No.
US 11,491,210
App. No.
17/707,074
Granted
Nov 8, 2022
Kind
B2
Abstract

Provided are compositions and methods for selectively reducing the amount of antibiotic resistant and/or virulent bacteria in a mixed bacteria population, or for reducing any other type of unwanted bacteria in a mixed bacteria population. The compositions and methods involve targeting bacteria that are differentiated from other members of the population by at least one unique clustered regularly interspaced short palindromic repeats (CRISPR) targeted DNA sequence. The compositions and methods can be readily adapted to target any bacteria or any bacteria plasmid, or both.

Claims (27)

1. A pharmaceutical composition for selectively killing targeted bacteria in a subject comprising a pharmaceutically acceptable carrier and a clustered regularly interspaced short palindromic repeats (CRISPR) system, wherein the CRISPR system comprises DNA encoding:

i) a Type I, Type II, or Type III CRISPR-associated enzyme; and

ii) a targeting RNA that targets at least one bacterial chromosome at a target site in the bacteria of the subject for selective killing of the targeted bacteria.

2. The pharmaceutical composition of claim 1 , wherein the bacteria is selected from the group consisting of Staphylococcus, Clostridium, Bacillus, Salmonella, Helicobacter pylori, Neisseria gonorrhoeae, Neisseria meningitidis , and Escherichia coli.

3. The pharmaceutical composition of claim 2 , wherein the bacteria is Escherichia coli.

4. The pharmaceutical composition of claim 2 , wherein the bacteria is Staphylococcus aureus.

5. The pharmaceutical composition of claim 4 , wherein the bacteria is a methicillin-resistant Staphylococcus aureus.

6. The pharmaceutical composition of claim 4 , wherein the CRISPR system encodes at least one targeting RNA that targets an S. aureus virulence gene.

7. The pharmaceutical composition of claim 6 , wherein the CRISPR system encodes at least one targeting RNA that targets an enterotoxin sek gene.

8. The pharmaceutical composition of claim 6 , wherein the CRISPR system encodes at least one targeting RNA that targets a mecA gene.

9. The pharmaceutical composition of claim 1 , wherein the CRISPR system encodes at least one targeting RNA that targets a toxin gene.

10. A pharmaceutical composition for selectively killing targeted bacteria in a subject comprising a pharmaceutically acceptable carrier and a clustered regularly interspaced short palindromic repeats (CRISPR) system, wherein the CRISPR system comprises DNA encoding:

i) a Type I, Type II, or Type III CRISPR-associated enzyme; and

ii) a targeting RNA that targets an antibiotic resistance gene on a bacterial plasmid at a target site within the bacterial plasmid in the bacteria of the subject for selective killing of the targeted bacteria in the presence of the antibiotic.

11. The pharmaceutical composition of claim 10 , wherein the bacteria is selected from the group consisting of Staphylococcus, Clostridium, Bacillus, Salmonella, Helicobacter pylori, Neisseria gonorrhoeae, Neisseria meningitidis , and Escherichia coli.

12. The pharmaceutical composition of claim 11 , wherein the bacteria is Staphylococcus aureus.

13. The pharmaceutical composition of claim 12 , wherein the bacteria is a methicillin-resistant Staphylococcus aureus.

14. The pharmaceutical composition of claim 10 , wherein the antibiotic resistance gene confers resistance to a narrow-spectrum beta-lactam antibiotic of the penicillin class of antibiotics.

15. The pharmaceutical composition of claim 14 , wherein the antibiotic resistance gene is a methicillin-resistance gene.

16. A pharmaceutical composition for selectively killing targeted bacteria in a subject comprising a pharmaceutically acceptable carrier and a clustered regularly interspaced short palindromic repeats (CRISPR) system, wherein the CRISPR system comprises DNA encoding:

i) a Type I, Type II, or Type III CRISPR-associated enzyme; and

ii) a targeting RNA that targets a bacterial plasmid comprising an antibiotic resistance gene at a target site within the bacterial plasmid in the bacteria of the subject for selective killing of the targeted bacteria in the presence of the antibiotic.

17. The pharmaceutical composition of claim 16 , wherein the bacteria is selected from the group consisting of Staphylococcus, Clostridium, Bacillus, Salmonella, Helicobacter pylori, Neisseria gonorrhoeae, Neisseria meningitidis , and Escherichia coli.

18. The pharmaceutical composition of claim 17 , wherein the bacteria is Staphylococcus aureus.

19. The pharmaceutical composition of claim 18 , wherein the bacteria is a methicillin-resistant Staphylococcus aureus.

20. The pharmaceutical composition of claim 16 , wherein the antibiotic resistance gene confers resistance to a narrow-spectrum beta-lactam antibiotic of the penicillin class of antibiotics.

21. The pharmaceutical composition of claim 20 , wherein the antibiotic resistance gene is a methicillin-resistance gene.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 30, 2022
From: BIKARD, DAVID
To: THE ROCKEFELLER UNIVERSITY
Reel/Frame 059440/0679 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 30, 2022
From: MARRAFFINI, LUCIANO
To: THE ROCKEFELLER UNIVERSITY
Reel/Frame 059440/0746 →
Continuity (9)
Continuation 17581614 · Jan 21, 2022
Division 17168971 · Feb 5, 2021
Division 17088302 · Nov 3, 2020
Division 17088297 · Nov 3, 2020
Continuation 16877010 · May 18, 2020
Division 15159929 · May 20, 2016
Division 14766675
Provisional Application 61761971 · Feb 7, 2013
Related Publication 20220218797A1 · Jul 14, 2022
Cited By (3)
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