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 an infection that is associated with septicemia and is caused by first bacteria in a subject, 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 cutting is carried out using a Cas nuclease that is programmed by a guide RNA to cut the target site, wherein the first bacteria are Enterobacteriaceae bacteria selected from the group consisting of Escherichia, Salmonella, Klebsiella, Shigella, Enterobacter and Citrobacter , wherein the subject comprises second bacteria of one or more strains or species that are different from that of the first bacteria, 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.
2. The method of claim 1 , wherein the infection is a urinary tract infection, a lung infection, or a kidney infection.
3. The method of claim 1 , wherein the infection is a urinary tract infection.
4. The method of claim 3 , wherein the first bacteria comprise Escherichia coli cells.
5. The method of claim 4 , wherein the first bacteria are enterohemorrhagic E. coli (EHEC).
6. The method of claim 1 , wherein the infection is a lung infection.
7. The method of claim 6 , wherein the first bacteria comprise E. coli or Klebsiella cells.
8. The method of claim 6 , wherein the first bacteria are Klebsiella pneumoniae cells.
9. The method of claim 1 , wherein and the subject has a compromised immune system.
10. The method of claim 9 , wherein the subject is a cancer patient, a transplant patient, or a patient suffering from a viral infection.
11. The method of claim 9 , wherein the subject is a liver, kidney or lung transplant patient.
12. The method of claim 9 , wherein the subject is on an immunosuppressant medication.
13. The method of claim 9 , wherein the subject has undergone surgery.
14. The method of claim 9 , wherein the subject is suffering from a chronic disease.
15. The method of claim 1 , wherein the first bacteria are comprised by a gut, kidney or lung microbiota of the subject.
16. The method of claim 1 , wherein the subject is a human.
17. The method of claim 16 , wherein at the start of the treatment, the subject has a temperature of <36° C. or >38° C.; a heart rate of >90/min, a respiratory rate of >20 breaths/min or PaCO2<4.3 kPa; and white blood cell count of <4000/mm 3 or >12,000/mm 3 .
18. The method of claim 1 , wherein the Cas nuclease is a Cas3.
19. The method of claim 1 , wherein the Cas nuclease is a Cas9.
20. The method of claim 1 , wherein the method comprises reducing the infection at least 100-fold or at least 1000-fold by the first 30 minutes of the treatment.
21. The method of claim 1 , wherein the method comprises maintaining reduction of the infection by at least 100-fold for at least 60 minutes after exposing the subject to the Cas nuclease and/or the guide RNA.
22. 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.
23. The method of claim 1 , wherein the infection is reduced by at least 90% for 1 hour or more.
24. The method of claim 1 , wherein the infection is durably treated.
25. The method of claim 1 , wherein the method comprises administering the Cas nuclease and/or the guide RNA to the subject at a first time (T1) and at a second time (T2), wherein T2 is at least 1 hour after T1.
26. The method of claim 1 , wherein the method comprises administering to the subject a nucleic acid vector comprising the guide RNA or a DNA encoding the guide RNA.
27. The method of claim 26 , comprising administering a second nucleic acid vector to the subject, wherein the second vector encodes the Cas nuclease.
28. The method of claim 26 , wherein the Cas nuclease is an endogenous Cas nuclease of the first bacteria.