Methods and compositions for the disruption of biofilms
The invention relates to methods of inhibiting biofilm formation or reducing biofilms in a subject or on a device or surface by administering a charged compound such as a polyamino acid to a subject, device or surface. The invention also relates to compositions for inhibiting biofilm formation or reducing biofilms.
1. A method of treating or preventing bacterial keratitis in a subject, comprising administering a polyamino acid selected from the group consisting of polyaspartic acid and polyglutamic acid to a subject or treating a contact lens with a polyamino acid selected from the group consisting of polyaspartic acid and polyglutamic acid, wherein the polyamino acid inhibits or reduces neutrophil-induced biofilm formation associated with bacterial keratitis or associated with the contact lens.
2. The method of claim 1 , wherein the polyamino acid is between 50 and 300 amino acids in length.
3. The method of claim 1 , further comprising administering to the subject a protease inhibitor.
4. The method of claim 1 , further comprising administering to the subject an anti-DNA compound.
5. The method of claim 1 , further comprising administering to a subject a compound that inhibits accumulation of, inhibits necrosis of, or inhibits release of the cellular contents of, cells that undergo necrosis, at or proximal to the site of biofilm formation or the site of infection by a microorganism that forms biofilms.
6. The method of claim 5 , wherein the cells that undergo necrosis are neutrophils.
7. The method of claim 6 wherein the compound inhibits the adherence of, migration to, or the sensing or response to chemoattractants by neutrophils, or inhibits the activity or release of a cytokine, chemokine or chemoattractant that attracts or enhances neutrophil activity.
8. The method of claim 7 , wherein the compound is an anti-inflammatory compound.
9. The method of claim 5 , further comprising administering to the subject an anti-DNA compound.
10. The method of claim 1 , further comprising administering to the subject an anti-mucin compound.
11. The method of claim 1 , wherein the compound is administered when bacterial keratitis is diagnosed or suspected.
12. The method of claim 1 , wherein the compound is administered prior to the treatment of the subject with a process that may cause a biofilm to form in the patient.
13. The method of claim 1 , wherein the compound is administered with a pharmaceutically acceptable carrier.
14. The method of claim 1 , wherein the compound is administered directly to or proximal to the site of biofilm formation or potential therefore.
15. The method of claim 1 , wherein the biofilm forms in connection with bacterial keratitis in an organ, tissue or body system.
16. The method of claim 1 , wherein the biofilm forms on a surface of a tissue, organ or bodily part.
17. The method of claim 5 , wherein the microorganism is Pseudomonas aeruginosa.
18. The method of claim 1 , wherein the contact lens is disposable.
19. The method of claim 1 , wherein the polyamino acid is synthetic polymer.