Engineered enzymatically active bacteriophage and methods for dispersing biofilms
View Patent ↗The present invention is directed to engineered enzymatically active bacteriophages that are both capable of killing the bacteria by lysis and dispersing the bacterial biofilm because they have been also engineered to express biofilm-degrading enzymes, particularly dispersin B (DspB), an enzyme that hydrolyzes β-1,6-N-acetyl-D-glucosamine, a crucial adhesion molecule needed for biofilm formation and integrity in Staphylococcus and E. coli , including E. coli K-12, as well as clinical isolates.
1. A method of dispersing a bacterial biofilm on a surface comprising administering to said surface a genetically engineered lytic T7 bacteriophage wherein the bacteriophage comprises a nucleic acid encoding dispersin B enzyme operably linked to a strong promoter and a nucleic acid encoding a protein to enhance or expand infectivity and or replication capacity of the lytic T7 bacteriophage, wherein the nucleic acid encoding the protein to enhance or expand infectivity and or replication capacity of the lytic T7 bacteriophage encodes T3 1.2 protein.
2. The method of claim 1 , wherein the strong promoter is T7 φ10.
3. The method of claim 1 , wherein the biofilm is a mature biofilm.
4. The method of claim 1 , wherein the biofilm comprises β-1,6-N-acetyl-D-glucosamine.
5. The method of claim 4 further comprising a step of prior to administering the bacteriophage, determining if the biofilm comprises β-1,6-N-acetyl-D-glucosamine, and if it does, then administering the engineered lytic bacteriophage.
6. The method of claim 1 , wherein the biofilm is formed by— Staphylococcus and E. coli , including E. coli K-12 strain, and clinical isolates of E. coli.
7. The method of claim 1 , wherein the administering is performed once.
8. The method of claim 1 , wherein the administering is performed before, after or concurrently with an antibiotic or antimicrobial agent.
9. The method of claim 1 , wherein the administering is performed before, after or concurrently with a biofilm degrading chemical.
10. The method of claim 1 , wherein the phage further comprises a terminator sequence.