Topical application of CRISPR-modified bacteria to treat acne vulgaris
Compositions, systems and methods of improving the health of the microbiome of an individual's skin relate to the provision of skin contacting formulations containing beneficial bacteria and other microbe components to foster the growth and maintenance of a healthy skin microbiome. Embodiments include methods for treating an individual suffering from acne vulgaris by topically administering a composition that includes live bacteria selected from the group consisting of L. reuteri, L. johnsonii, L. crispatus, C. acnes , and Nitrosomonas eutropha , that have been modified by using a using a clustered regularly interspaced short palindromic repeats (CRISPR) CRISPR associated protein (Cas) system or a CRISPR from Prevotella and Francisella 1(Cpf1) system to reduce the production of a virulence factor of the bacteria.
1. A method of reducing the likelihood of a skin condition comprising acne vulgaris that causes skin inflammation in an individual human being, said method comprising: administering a therapeutically effective amount of a bacterial formulation comprising at least one of a live bacteria selected from the group consisting of Lactobacillus reuteri, Lactobacillus johnsonii, Lactobacillus crispatus, Cutibacterium acnes , and Nitrosomonas eutropha , said bacterial formulation comprising a lotion, ointment or gel adapted to be rubbed onto a region of an individual's skin, wherein at least some bacteria in the bacterial formulation have been modified by using a using a clustered regularly interspaced short palindromic repeats (CRISPR) CRISPR associated protein (Cas) system or a CRISPR from Prevotella and Francisella 1(Cpf1) system to reduce the production of a virulence factor by at least one of said live bacteria in said bacterial formulation.
2. The method as set forth in claim 1 , wherein the live bacteria is Cutibacterium acnes.
3. The method as set forth in claim 2 , wherein the Cutibacterium acne has the expression of at least one virulence factor gene modified using a CRISPR system, said virulence factors gene selected from the group consisting of virulence factor genes involved in cell adhesion, mediation of inflammation, tissue invasion, and the synthesis of capsule polysaccharides.
4. The method as set forth in claim 2 , wherein the Cutibacterium acnes has the expression of at least one virulence factor gene modified using a CRISPR system, said virulence factors gene selected from the group consisting of virulence factor genes that encode sialidases, neuraminidases, endoglycoceramidases, adhesins, thermal shock proteins, Christie-Atkins-Munch-Petersen (CAMP) factors, and lipases.
5. The method as set forth in claim 2 , wherein the Cutibacterium acnes has the expression of at least one virulence factor gene modified using a CRISPR system, said virulence factors gene selected from the group consisting of virulence factor genes that encode adhesin dermatan-sulfate (DsA1 and DsA2), CAMP factors, polyunsaturated fatty acid isomerase, HtaA iron acquisition protein and GehA lipase, and heat shock proteins.
6. The method as set forth in claim 2 , wherein the Cutibacterium acnes is modified to enhance the production by C. acnes to produce short-chain fatty acids (SCFA) selected from the group consisting of propionate, acetate, butyrate and valerate.
7. The method as set forth in claim 6 , wherein the SCFA production by C. acnes suppresses the growth of Staphylococcus aureus in an amount to reduce the colonization of S. aureus on the skin.
8. The method as set forth in claim 6 , wherein the SCFA production inhibits biofilm formation by S. epidermidis.
9. The method as set forth in claim 6 , wherein the Cutibacterium acnes is modified via a CRISPR system to increase production of butyrate to achieve beneficial skin conditions.
10. The method as set forth in claim 2 , wherein the Cutibacterium acnes is modified via a CRISPR system to increase production of butyrate to achieve beneficial skin conditions.
11. The method as set forth in claim 2 , wherein the Cutibacterium acnes is modified using a CRISPR system to produce increased levels of porphyrins in an amount sufficient to positively affect other members of the skin microbiome.
12. A method for treating an individual suffering from acne vulgaris, comprising,
using a clustered regularly interspaced short palindromic repeats (CRISPR) CRISPR associated protein (Cas), selectively killing or retarding the growth of a pathogenic bacteria within the individual, said pathogenic bacteria selected from the group consisting of Staphylococcus aureus; Pseudomonas aeruginosa; Klebsiella; Streptoccocus; Salmonella; Shigella; Mycobacterium tuberculosis; Enterococcus; E coli; Clostridium; Neisseria gonorrhoeae; Acinetobacter baumannii ; and Campylobacter , and enhancing the growth of a beneficial bacteria in the individual selected from the group consisting of C. acnes, Akkermansia, Bacteroides, Bifidobacterium, Fusobacterium, Coprococcus, Lactobacillus, Propionibacterium, Ruminococcus, Veillonella, Prevotella , and Streptococcus bacteria.
13. The method of claim 12 , wherein the individual has skin cancer and the method further comprises administering to the individual an immune checkpoint inhibitor selected from the group consisting of nivolumab, dostarlimab, pembrolizumab, pidilizumab, AMP-224, AMP-514, STI-A1110, RG-7446, BMS-936559, MEDI-4736, AUR-012 and STI-A1010.
14. The method of claim 12 , wherein the individual has skin cancer and the method further comprises administering to the individual an immune checkpoint inhibitor that specifically binds to an immune checkpoint protein selected from the group consisting of CTLA4, PD-1, PD-L1, PD-L2, A2AR, B7-H3, B7-H4, BTLA, KIR, LAG3, TIM-3 and VISTA; and wherein the immune checkpoint inhibitor is selected from the group consisting of nivolumab, pembrolizumab, pidilizumab, AMP-224, AMP-514, STI-A1110, TSR-042, RG-7446, BMS-936559, MEDI-4736, AUR-012 and STI-A1010.h.
15. The method as set forth in claim 12 , wherein said CRISPR Cas system comprises Cas3 and is delivered using a bacteriophage.
16. The method as set forth in claim 12 , wherein using the CRISPR-Cas system, said pathogenic bacteria are killed while sparing other commensal bacteria.
17. The method as set forth in claim 12 , further comprising administering at least two probiotic strains to the individual's skin, said at least two probiotic strains being either live or heat-killed and selected from the group consisting of Cutibacterium, Staphylococcus, Corynebacterium, Micrococcus spp., Actinobacteria, Proteobacteria, and Firmicutes.
18. The method as set forth in claim 12 , further comprising administering to the individual's skin at least one probiotic strain that does not upregulate innate immune response genes selected from the group consisting of CXCL1, CXCL3, CXCL8, CXCL10.
19. The method as set forth in claim 12 , further comprising administering to the individual's skin at least one probiotic strain that does not upregulate innate immune response genes selected from the group consisting of IL10RA, PTGS2, F2RL1, TRIM29, TRAF4, LGALS3, CD55, TRIMS, CASP4, IFNGR1, ADA, NOD1, NOS2, and APP.
20. The method as set forth in claim 12 , wherein using CRISPR-Cas systems, said pathogenic bacteria are killed while sparing other commensal bacteria, said commensal bacteria selected from the group consisting of C. acnes, Faecalibacterium prausnitzii, Bifidobacterium, Lachnospira, Veillonella, Coprococcus, Akkermansia muciniphila and Rothia.