Selectively altering microbiota for immune modulation
The invention relates to methods of modulating immune cells in a patient by altering microbiota of the patient. The invention also relates to methods of modulating treatments or therapies in a subject organism by altering microbiota of the subject. The invention also relates to cell populations, systems, arrays, cells, RNA, kits and other means for effecting this. In an example, advantageously selective targeting of a particular species in a human gut microbiota using guided nucleic acid modification is carried out to effect the alteration.
1. A method of treating or reducing the progression of an infection that is associated with sepsis or septic shock and is caused by pathogenic host cells of Escherichia coli, Staphylococcus, Streptococcus, Mycobacterium, Haemophilus or Pseudomonas in a human or animal subject, the method comprising selective targeting of the pathogenic host cells, wherein the host cells are comprised by a microbiota in the subject, wherein the method comprising:
a. contacting the microbiota with an engineered nucleic acid sequence for producing a host modifying (HM) crRNA, and
b. producing the HM-crRNA in a host cell,
wherein the HM-crRNA is operable with a Cas nuclease in the host cell to form a HM-CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas system, and wherein the HM-crRNA comprises a sequence that is capable of hybridizing to a target sequence of the host cell to guide the Cas nuclease to the target sequence in the host cell, whereby the target sequence is modified by the HM-CRISPR/Cas system and the host cell is killed or growth of the host cell is reduced,
wherein the microbiota comprises a second species of bacteria that is different from the species of the pathogenic host cells, and
wherein growth of the second species of bacteria is not substantially reduced, thereby reducing the proportion of host cells in the microbiota.
2. The method of claim 1 , wherein the microbiota is selected from the group consisting of a gut microbiota, skin microbiota, oral cavity microbiota, throat microbiota, hair microbiota, armpit microbiota, rectal microbiota, anal microbiota, ocular microbiota, nasal microbiota, tongue microbiota, liver microbiota, scrotal microbiota, mammary gland microbiota, ear microbiota, organ microbiota and dental microbiota.
3. The method of claim 1 , wherein the microbiota is a kidney microbiota, urethra microbiota, vaginal microbiota or penile microbiota.
4. The method of claim 1 , wherein the microbiota is a kidney microbiota.
5. The method of claim 1 , wherein the microbiota is a urethra microbiota.
6. The method of claim 1 , wherein the microbiota is a lung microbiota.
7. The method of claim 1 , wherein the Cas is a Cas3, Cas9 or Cpf1.
8. The method of claim 1 , wherein the engineered nucleic acid sequence is administered intravenously to the subject.
9. The method of claim 2 , wherein the engineered nucleic acid sequence is administered intravenously to the subject.
10. The method of claim 6 , wherein the engineered nucleic acid sequence is administered by inhalation to the subject.
11. The method of claim 1 , wherein each HM-crRNA is comprised by a single guide RNA (sgRNA).
12. The method of claim 1 , wherein the nucleic acid sequence encoding the HM-crRNA is under a constitutive promoter.
13. The method of claim 1 , wherein the Cas is a wild-type host cell endogenous Cas3 and/or CASCADE Cas.
14. The method of claim 1 , wherein the nucleic acid sequence is comprised by a vector, wherein the vector is a virus, phage, prophage or conjugative plasmid.
15. A method of treating or reducing the progression of an infection that is associated with sepsis or septic shock and is caused by pathogenic host cells of Escherichia coli in a human or animal subject, the method comprising selective targeting of the pathogenic host cells, wherein the host cells are comprised by a microbiota in the subject, wherein the method comprising:
a. contacting the microbiota with an engineered nucleic acid sequence for producing a host modifying (HM) crRNA, and
b. producing the HM-crRNA in a host cell,
wherein the HM-crRNA is operable with a Cas nuclease in the host cell to form a HM-CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas system, and wherein the HM-crRNA comprises a sequence that is capable of hybridizing to a target sequence of the host cell to guide the Cas nuclease to the target sequence in the host cell, whereby the target sequence is modified by the HM-CRISPR/Cas system and the host cell is killed or growth of the host cell is reduced,
wherein the microbiota comprises a second species of bacteria that is different from the species of the pathogenic host cells, and
wherein growth of the second species of bacteria is not substantially reduced, thereby reducing the proportion of host cells in the microbiota; and
wherein the microbiota is a kidney microbiota or urethra microbiota.
16. The method of claim 15 , wherein the HM-crRNA is comprised by a single guide RNA (sgRNA).
17. The method of claim 15 , wherein the engineered nucleic acid sequence is administered intravenously to the subject.
18. The method of claim 15 , wherein the engineered nucleic acid sequence is administered by inhalation to the subject.
19. The method of claim 15 , wherein the nucleic acid sequence encoding the HM-crRNA is under a constitutive promoter.
20. The method of claim 15 , wherein the Cas is a wild-type host cell endogenous Cas3 and/or CASCADE Cas.
21. The method of claim 1 , wherein the engineered nucleic acid sequence is comprised by a vector, wherein the vector is a virus, phage, prophage or conjugative plasmid.
22. The method of claim 15 , wherein the Cas is a wild-type host cell endogenous Cas9.
23. The method of claim 1 , wherein growth of the pathogenic host cells is inhibited by at least 1000 fold.
24. The method of claim 15 , wherein growth of the pathogenic host cells inhibited by at least 1000 fold.