IP Library Granted Patent US 11,491,209
Granted Patent B2
US 11,491,209 · App. 17/707,049 · 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 11,491,209
App. No.
17/707,049
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 (30)

1. A pharmaceutical composition for killing targeted bacteria in a mixed bacterial population comprising:

a pharmaceutically acceptable carrier and

a packaged, recombinant phagemid that is packaged in a phage capsid,

wherein the packaged phagemid comprises 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; and

wherein, upon contacting a bacterial population containing the at least one bacterial chromosome with the pharmaceutical composition, the phagemid is introduced into bacteria in the bacterial population,

wherein subsequent to the introduction of the phagemid, the targeting RNA and the CRISPR-associated enzyme are expressed in the bacteria into which the phagemid is introduced,

wherein the expressed CRISPR-associated enzyme cleaves the bacterial chromosome at the target site of the targeting RNA, and

wherein the cleavage of the bacterial chromosome at the target site kills the 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, Escherichia coli , and any combination thereof.

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. A pharmaceutical composition for killing targeted bacteria in a mixed bacterial population comprising:

a pharmaceutically acceptable carrier and

a packaged, recombinant phagemid that is packaged in a phage capsid,

wherein the packaged phagemid comprises 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 plasmid at a target site within the plasmid;

wherein, upon contacting a bacterial population containing the at least one antibiotic resistance gene on a plasmid with the pharmaceutical composition, the phagemid is introduced into bacteria in the bacterial population,

wherein the targeting RNA and the CRISPR-associated enzyme are expressed in the bacteria into which the phagemid is introduced,

wherein the expressed CRISPR-associated enzyme cleaves the antibiotic resistance gene on a plasmid at the target site within the plasmid, and

wherein the cleavage of the bacterial plasmid at the target site kills the bacteria in the presence of the antibiotic.

7. The pharmaceutical composition of claim 6 , wherein the bacteria is selected from the group consisting of Staphylococcus, Clostridium, Bacillus, Salmonella, Helicobacter pylori, Neisseria gonorrhoeae, Neisseria meningitidis, Escherichia coli , and any combination thereof.

8. The pharmaceutical composition of claim 7 , wherein the bacteria is Escherichia coli.

9. The pharmaceutical composition of claim 7 , wherein the bacteria is Staphylococcus aureus.

10. The pharmaceutical composition of claim 9 , wherein the bacteria is a methicillin-resistant Staphylococcus aureus.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 30, 2022
From: BIKARD, DAVID
To: THE ROCKEFELLER UNIVERSITY
Reel/Frame 059440/0348 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 30, 2022
From: MARRAFFINI, LUCIANO
To: THE ROCKEFELLER UNIVERSITY
Reel/Frame 059440/0384 →
Continuity (10)
Division 15159929 · May 20, 2016
Division 14766675
Division 17707049
Continuation 17581614 · Jan 21, 2022
Continuation 16877010 · May 18, 2020
Division 17088297 · Nov 3, 2020
Division 17088302 · Nov 3, 2020
Division 17168971 · Feb 5, 2021
Provisional Application 61761971 · Feb 7, 2013
Related Publication 20220218795A1 · Jul 14, 2022
Cited By (3)
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