IP Library Granted Patent US 11,918,631
Granted Patent B2
US 11,918,631 · App. 15/159,929 · Granted Mar 5, 2024

Sequence specific antimicrobials

Inventors: David Bikard (New York, NY); Luciano Marraffini (New York, NY)
Assignee: THE ROCKEFELLER UNIVERSITY
A61K38/465A01N63/00A61K31/7105A61K31/713A61K45/06C12N9/16C12N9/22C12N15/113C12N15/74C12Y301/00C12N2310/10C12N2310/20C12N2795/10331C12N2795/10332C12N2795/10343C12N2795/10371
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Quick Facts
Patent No.
US 11,918,631
App. No.
15/159,929
Granted
Mar 5, 2024
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 (14)

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

providing a pharmaceutical composition comprising a pharmaceutically acceptable carrier and packaged, recombinant phagemids that are packaged in phage capsids,

wherein the packaged phagemids comprise a clustered regularly interspaced short palindromic repeats (CRISPR) system,

wherein the CRISPR system comprises DNA encoding: i) a type II CRISPR-associated enzyme; and ii) a targeting RNA that targets at least one bacterial chromosome at a target site; and

contacting the bacterial population with the pharmaceutical composition,

wherein the contacting with the pharmaceutical composition introduces at least some of the phagemids into at least some of the bacteria in the bacterial population,

wherein subsequent to the introduction of the phagemids, the bacteria into which the phagemid is introduced expresses the targeting RNA and the type II CRISPR-associated enzyme,

wherein the expressed type II 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 method of claim 1 , wherein the type II CRISPR-associated enzyme is a Cas9 enzyme.

3. The method of claim 2 , wherein the Cas9 enzyme is a Streptococcus pyogenes Cas9.

4. The method of claim 1 , further comprising detecting the killing of bacteria by the pharmaceutical composition.

5. The method of claim 1 , wherein the bacteria that are killed are Staphylococcus aureus.

6. The method of claim 5 , wherein the bacteria a that are killed are methicillin-resistant Staphylococcus aureus.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 11, 2020
From: BIKARD, DAVID
To: THE ROCKEFELLER UNIVERSITY
Reel/Frame 052086/0031 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 11, 2020
From: MARRAFFINI, LUCIANO
To: THE ROCKEFELLER UNIVERSITY
Reel/Frame 052086/0261 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 11, 2020
From: BIKARD, DAVID
To: THE ROCKEFELLER UNIVERSITY
Reel/Frame 052086/0350 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 11, 2020
From: MARRAFFINI, LUCIANO
To: THE ROCKEFELLER UNIVERSITY
Reel/Frame 052086/0413 →
Continuity (3)
Division 14766675
Provisional Application 61761971 · Feb 7, 2013
Related Publication 20160324938A1 · Nov 10, 2016
Cited By (2)
US 12,246,061 US 12,285,467