Treating and preventing microbial infections
The invention provides methods for treating or preventing microbial (eg, bacterial) infections and means for performing these methods. In particular, treatment of infections requiring rapid and durable therapy is made possible, such as for treating acute conditions such as septicemia, sepsis, SIRS or septic shock. The invention is particularly useful, for example, for treatment of microbes such as for environmental, food and beverage use. The invention relates inter alia to methods of controlling microbiologically influenced corrosion (MIC) or biofouling of a substrate or fluid in an industrial or domestic system. The invention also useful for the treatment of pathogenic bacterial infections in subjects receiving a treatment for a disease or condition, such as a transplant or a treatment for cancer, a viral infection or an autoimmune disease.
1. A method of treating or reducing the risk of an acute infection in a human or animal subject in need of a transplant or that has been administered a transplant, wherein the infection is caused by first bacteria of a first pathogenic species or strain of Escherichia coli ( E. coli ) bacteria, the method comprising selectively killing the first bacteria comprised by the subject by cutting a target site comprised by the genomes of the first bacteria,
wherein the method comprises administering to the subject a nucleic acid sequence comprising or encoding a guide RNA,
wherein the guide RNA hybridizes to the target site to guide a Cas nuclease to cut the target site, thereby killing the first bacteria, and
wherein the transplant is a tissue, organ or stem cell transplant.
2. The method of claim 1 , wherein the transplant is a heart, liver, kidney, lung, or hematopoietic stem cell transplant.
3. The method of claim 1 , wherein the treatment of the infection is carried out simultaneously with the administration of the transplant to the subject.
4. The method of claim 1 , wherein the treatment of the infection is carried out immediately before the administration of the transplant to the subject.
5. The method of claim 1 , wherein the treatment of the infection is carried out immediately after the administration of the transplant to the subject.
6. The method of claim 4 , wherein the treatment of the infection is carried out no more than 7 days before the administration of the transplant.
7. The method of claim 5 , wherein the treatment of the infection is carried out no more than 7 days after the administration of the transplant.
8. The method of claim 1 , wherein the first bacteria are resistant to an antibiotic selected from the group consisting of cephalosporin and carbapenem.
9. The method of claim 1 , wherein the first bacteria are resistant to an antibiotic selected from the group consisting of Aminoglycosides, Ampicillin, Amoxicillin, Amoxicillin or clavulanic acid, Carbapenems, Piperacillin or tazobactam, Quinolones, Tetracyclines, Chloramphenicol, Ticarcillin, Trimethoprim or sulfamethoxazole, penicillin, streptomycin, oxytetracycline and potentiated sulfonamides.
10. The method of claim 1 , wherein the subject has been administered an immunosuppressant drug, or is on a course of an immunosuppressant drug.
11. The method of claim 1 , wherein the subject comprises second bacteria of one or more strains or species that are different from the first strain or species, wherein the genomes of the second bacteria do not comprise the target site, wherein the genomes of the second bacteria are not cut by the Cas nuclease in the subject, whereby second bacteria survive in the presence of the Cas nuclease in the subject.
12. The method of claim 11 , wherein the second bacteria are selected from the group consisting of Akkermansia, Alistipes, Bacteroides, Barnesiella, Bifidobacterium, Clostridium, Collinsella, Enterococcus, Fusobacterium, Lactobacillus, Propionibacterium, Ruminococcus , Segmented filamentous bacteria (SFB), Veillonella, Prevotella, Escherichia and Streptococcus bacteria.
13. The method of claim 1 , wherein the nucleic acid sequence comprising or encoding the guide RNA is a nucleic acid vector comprising the guide RNA or a DNA encoding the guide RNA.
14. The method of claim 1 , comprising administering a second nucleic acid sequence to the subject, wherein the second nucleic acid sequence encodes the Cas nuclease.
15. The method of claim 1 , wherein the Cas nuclease is an endogenous Cas nuclease of the first bacteria.
16. The method of claim 1 , wherein the nucleic acid sequence is administered in a vector that is a phage, phagemid, viriophage, virus, plasmid, or transposon.
17. The method of claim 16 , wherein the vector is a phagemid.
18. The method of claim 1 , wherein the Cas nuclease is Cas9.
19. The method of claim 1 , wherein the Cas nuclease is Cas3.
20. The method of claim 1 , wherein the method comprises reducing the infection by at least 100-fold by the first 30 minutes of the treatment.
21. The method of claim 1 , wherein the method comprises reducing the infection by at least 1000-fold by the first 30 minutes of the treatment.
22. The method of claim 1 , wherein the method comprises maintaining reduction of the infection by at least 100-fold for at least 180 minutes after exposing the subject to the Cas nuclease and/or the guide RNA.
23. The method of claim 20 , wherein the reduction of the infection persists for at least 30 minutes immediately after the first 30 minutes of the treatment.
24. The method of claim 1 , wherein the infection is reduced by at least 90% for 1 hour or more.
25. The method of claim 1 , wherein the method comprises maintaining reduction of the infection by at least 1000-fold for at least 180 minutes after exposing the subject to the Cas nuclease and/or the guide RNA.
26. The method of claim 1 , wherein the method comprises administering the Cas nuclease and/or the nucleic acid sequence comprising or encoding the guide RNA to the subject at a first time (T1) and at a second time (T2), wherein T2 is at least 3 hours after T1.
27. The method of claim 1 , wherein the first bacteria are comprised by gut microbiota or urethra microbiota.
28. The method of claim 21 , wherein the reduction in infection persists for at least 60 minutes immediately after the first 30 minutes of treatment.
29. The method of claim 10 , wherein the method comprises reducing the infection by at least 100-fold by the first 30 minutes of the treatment.
30. The method of claim 10 , wherein the method comprises reducing the infection by at least 1000-fold by the first 30 minutes of the treatment.
31. The method of claim 10 , wherein the method comprises administering the Cas nuclease and/or the nucleic acid sequence comprising or encoding the guide RNA to the subject at a first time (T1) and at a second time (T2), wherein T2 is at least 3 hours after T2.