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 for treating an acute pathogenic bacterial infection in a subject caused by first bacteria that are E. coli, Pseudomonas aeruginosa or Klebsiella 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 cutting is carried out using a Cas nuclease that is programmed by a guide RNA to cut the target site, wherein the subject has a cancer, wherein the method is carried out no more than 7 days before or after administration of an immunotherapy to the subject, wherein the programmed Cas nuclease treats the infection and the immunotherapy treats the cancer;
wherein:
(a) the immunotherapy comprises administering to the subject an anti-PD-1/PD-L1 axis antibody; and
(b) the cancer is selected from melanoma; renal cell carcinoma; bladder cancer; a solid tumour; non-small cell lung cancer (NSCLC); forehead and neck squamous cell carcinoma (HNSCC); Hodgkin's lymphoma; a cancer that overexpresses PD-L1 and has no mutations in EGFR or in ALK; colorectal cancer and hepatocellular carcinoma.
2. The method of claim 1 , wherein the first bacteria are E. coli.
3. The method of claim 2 , wherein the first bacteria are enterohemorrhagic E. coli (EHEC).
4. The method of claim 1 , wherein the anti-PD-1/PD-L1 axis antibody is selected from the group consisting of pembrolizumab, nivolumab, atezolimumab, avelumab and durvalumab.
5. The method of claim 1 , wherein the treatment of the bacterial infection is carried out simultaneously with the administration of the immunotherapy to the subject.
6. The method of claim 1 , wherein the treatment of the bacterial infection is carried out immediately before or after administering the immunotherapy to the subject.
7. 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.
8. The method of claim 7 , comprising administering a second nucleic acid vector to the subject, wherein the second vector encodes the Cas nuclease.
9. The method of claim 7 , wherein the Cas nuclease is an endogenous Cas nuclease of the first bacteria.
10. The method of claim 7 , wherein the vector is a phage, phagemid, viriophage, virus, plasmid, or transposon.
11. The method of claim 7 , wherein the vector is a conjugative plasmid.
12. The method of claim 11 , wherein the conjugative plasmid is delivered from carrier bacteria.
13. The method of claim 12 , wherein the carrier bacteria are Lactobacillus bacteria.
14. The method of claim 1 , wherein the Cas nuclease is Cas9.
15. The method of claim 1 , wherein the Cas nuclease is Cas3.
16. The method of claim 8 , wherein the Cas nuclease is Cas9.
17. The method of claim 16 , wherein the second vector further comprises a tracrRNA or a DNA encoding a tracrRNA.
18. The method of claim 1 , wherein the treatment of the bacterial infection treats in the subject a disease or condition selected from the group consisting of vaginosis, meningitis, pneumonia, urinary tract infection, cystitis, nephritis, gastroenteritis, a skin infection, impetigo, erysipelas, cellulitis, a dental infection, septicaemia and sepsis, or reduces the risk of the disease or condition in the subject, wherein the disease or condition is mediated by the first bacteria.
19. The method of claim 1 , wherein the guide RNA does not program a Cas nuclease to cut the genome of second bacteria in the subject, 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.