Sequence specific antimicrobials
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.
1. A pharmaceutical composition for killing targeted bacteria in a mixed bacterial population comprising:
a pharmaceutically acceptable carrier and a clustered regularly interspaced short palindromic repeats (CRISPR) system packaged in a phage,
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 CRISPR system is introduced into bacteria in the bacterial population,
wherein subsequent to the introduction of the CRISPR system, the targeting RNA and the CRISPR-associated enzyme are expressed in the bacteria into which the CRISPR system 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 phage can infect different types of bacteria in a mixed bacteria population.
3. The pharmaceutical composition of claim 1 , wherein the phage is specific for a bacterial strain selected from Streptococcus, Staphylococcus, Clostridium, Bacillus, Salmonella, Helicobacter pylori, Neisseria gonorrhoeae, Neisseria meningitidis , and Escherichia coli.
4. The pharmaceutical composition of claim 1 , wherein the phage is specific for Staphylococcus aureus.
5. The pharmaceutical composition of claim 1 , wherein the phage is a staphylococcal phiNM1 phage.
6. The pharmaceutical composition of claim 1 , wherein the phage is specific for Escherichia coli.
7. The pharmaceutical composition of claim 1 , wherein the Cas nuclease is a Type II Cas nuclease.
8. The pharmaceutical composition of claim 1 , wherein the Cas nuclease is Cas 9 .
9. A pharmaceutical composition for killing targeted bacteria in a mixed bacterial population comprising:
a pharmaceutically acceptable carrier and a clustered regularly interspaced short palindromic repeats (CRISPR) system packaged in a phage,
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;
wherein, upon contacting a bacterial population containing the antibiotic resistance gene on the bacterial plasmid with the pharmaceutical composition, the CRISPR system is introduced into bacteria in the bacterial population,
wherein subsequent to the introduction of the CRISPR system, the targeting RNA and the CRISPR-associated enzyme are expressed in the bacteria into which the CRISPR system is introduced,
wherein the expressed CRISPR-associated enzyme cleaves the antibiotic resistance gene on a bacterial plasmid at the target site within the bacterial plasmid, and wherein the cleavage of the bacterial plasmid at the target site kills the bacteria in the presence of the antibiotic.
10. The pharmaceutical composition of claim 9 , wherein the phage can infect different types of bacteria in a mixed bacteria population.
11. The pharmaceutical composition of claim 9 , wherein the phage is specific for a bacterial strain selected from Streptococcus, Staphylococcus, Clostridium, Bacillus, Salmonella, Helicobacter pylori, Neisseria gonorrhoeae, Neisseria meningitidis , and Escherichia coli.
12. The pharmaceutical composition of claim 9 , wherein the phage is specific for Staphylococcus aureus.
13. The pharmaceutical composition of claim 9 , wherein the phage is a staphylococcal phiNM 1 phage.
14. The pharmaceutical composition of claim 9 , wherein the phage is specific for Escherichia coli.
15. The pharmaceutical composition of claim 9 , wherein the Cas nuclease is a Type II Cas nuclease.
16. The pharmaceutical composition of claim 9 , wherein the Cas nuclease is Cas9.
17. The pharmaceutical composition of claim 9 , wherein the antibiotic resistance gene confers resistance to a narrow-spectrum beta-lactam antibiotic of the penicillin class of antibiotics.
18. The pharmaceutical composition of claim 9 , wherein the antibiotic resistance gene is a methicillin-resistance gene.