Chimeric bacteriophage lysin with activity against
The present disclosure relates to chimeric bacteriophage lysins useful for the identification and/or reduction of staphylococcal populations. For example, a chimeric bacteriophage lysin was engineered and shown to effectively kill all strains of staphylococci tested including antibiotic resistant methicillin-resistant S. aureus (MRSA) and vancomycin-resistant Staphylococcus aureus (VISA).
1. A chimeric bacteriophage lysin comprising a catalytic domain of a first Staphylococcus -specific phage lysin bound to the binding domain of another second Staphylococcus -specific phage lysin, wherein the binding domain has the polypeptide sequence of SEQ ID NO:1 and the catalytic domain is the Twort endopeptidase domain and comprises amino acids 1-186 of SEQ ID NO:2, wherein the chimeric lysin comprises the polypeptide sequence of SEQ ID NO: 2 or a variant thereof having at least 90% amino acid sequence identity to SEQ ID NO: 2, and wherein said chimeric lysin or variant has killing activity against Staphylococcus aureus and is capable of binding specifically to staphylococci.
2. The chimeric lysin of claim 1 , wherein said variant has at least 95% amino acid sequence identity to SEQ ID NO: 2 and is capable of binding specifically to staphylococci and has killing activity against Staphylococcus aureus.
3. The chimeric lysin of claim 1 , wherein the chimeric lysin has the polypeptide sequence of SEQ ID NO:2.
4. The chimeric lysin of claim 1 , wherein the chimeric lysin has killing activity against methicillin-resistant and methicillin-sensitive strains of S. aureus.
5. The chimeric lysin of claim 1 having killing activity against multiple staphylococcal species.
6. The chimeric lysin of claim 5 , wherein the chimeric lysin kills Staphylococcus epidermidis.
7. The chimeric lysin of claim 1 having killing activity against Staphylococcal bacteria over a pH range of 4-10.
8. The chimeric lysin of claim 1 , where the chimeric lysin has a solubility of at least 3 mg/mL in phosphate buffered saline (PBS).
9. An anti-microbial composition for sanitizing or decontaminating porous or non-porous surfaces comprising the chimeric lysin of any of claims 1 , 2 or 3 .
10. A method for decontaminating inanimate surfaces suspected of containing infectious staphylococci bacteria comprising treatment of said surfaces with a bacteriocidal or bacteriostatically effective amount of the composition of claim 9 .
11. A pharmaceutical composition comprising the chimeric lysin of any of claims 1 , 2 or 3 and a pharmaceutically acceptable carrier.
12. The pharmaceutical composition of claim 11 further comprising one or more bacteriostatic or bacteriocidal agents.
13. The pharmaceutical composition of claim 11 further comprising one or more antibiotic.
14. The pharmaceutical composition of claim 11 which is formulated for topical, ocular, nasal, pulmonary, buccal, parenteral, oral, vaginal or rectal administration.
15. A method of treating a mammal with a staphylococcal infection comprising administering to said mammal the chimeric bacteriophage lysin of any of claims 1 , 2 or 3 .
16. A method of treating a mammal with a staphylococcal infection comprising administering to said mammal the pharmaceutical composition of claim 11 .
17. A method of treating a mammal with a staphylococcal infection comprising administering to said mammal the pharmaceutical composition of claim 12 .
18. A method of decolonizing staphylococci in a mammal colonized by staphylococci comprising administering to said mammal the chimeric bacteriophage lysin of any of claims 1 , 2 or 3 .
19. The method of claim 15 , wherein the chimeric lysin selectively binds to staphylococcal bacteria in the presence of one or more additional bacteria selected from the group consisting of: E coli, B. cereus and P. aeruginosa.
20. A method of treating a mammal with a staphylococcal infection comprising administering to said mammal the pharmaceutical composition of claim 13 .
21. The method of claim 16 , wherein the chimeric lysine selectively binds to staphylococcal bacteria in the presence of one or more additional bacteria selected from the group consisting of: E coli, B. cereus and P. aeruginosa.
22. The method of claim 17 , wherein the chimeric lysine selectively binds to staphylococcal bacteria in the presence of one or more additional bacteria selected from the group consisting of: E coli, B. cereus and P. aeruginosa.
23. The method of claim 20 , wherein the chimeric lysine selectively binds to staphylococcal bacteria in the presence of one or more additional bacteria selected from the group consisting of: E coli, B. cereus and P. aeruginosa.