Method and system for addressing adverse effects on the oral microbiome and restoring gingival health caused by sodium lauryl sulphate exposure
A method and system to address the adverse effects on an individual's oral microbiome with the objective of restoring gingival health caused by exposure to sodium lauryl sulfate. Certain embodiments of the present invention facilitate the growth of desired bacteria in a human's mouth to reduce the likelihood of dental caries, halitosis, canker sores, and other oral diseases. Probiotic bacterial, bioactive flavonoid, xylitol and zinc compound compositions, provide effective prevention and treatment options, especially while precluding the use of sodium lauryl sulfate so as to reduce adverse consequences it has on gingival health.
1. A method for reducing the likelihood of developing dental caries and halitosis, comprising:
providing to an oral cavity of an individual subject:
a first bacterial composition comprising beneficial bacteria adapted to form a biofilm, said beneficial bacteria comprising a bacterium of the genus Rothia;
a second composition comprising:
an oral probiotic comprising at least two of the following bacteria: Lactobacillus brevis CD2, Streptococcus sanguinis BCC23, Lactobacillus acidophilus, Lactobacillus bulgaricus, Lactobacillus johnsonii, Bifidobacterium bifidum, Enterococcus faecium, Lactobacillus rhamnosus, Lactobacillus plantarum, Lactobacillus reuteri, Lactobacillus paracasei, Lactobacillus casei, Lachnospira, Veillonella, Faecalibacterium and Prevotella;
at least one zinc-based compound selected from the group consisting of zinc acetate, zinc chloride, zinc citrate, and zinc sulphate; and
at least one bioactive flavonoid selected from the group consisting of baicalein, naringenin, catechins, quercetin, trans-resveratrol, luteolin, kaempferol, hesperidin, hesperetin, naringin, diosmin, rutin, nobiletin, and tangeretin; and
wherein the oral probiotic lowers the pH of the individual subject's oral cavity in an amount sufficient to disrupt the formation of biofilms by pathogenic bacteria.
2. The method of claim 1 , wherein the step of providing comprises topically administering said second composition in the form of one of a toothpaste, mouth wash, chewing gum, oral strip, extruded chew and jerky chew.
3. The method of claim 1 , further comprising, using a clustered regularly interspaced short palindromic repeats (CRIPSR)-CRISPR associated protein (Cas) system or a CRISPR from Prevotella and Franscisella 1 (Cpf1a) system, selectively killing pathogenic bacteria in the individual subject's oral cavity.
4. The method of claim 1 , wherein said step of providing the first bacterial composition is performed after the individual subject has cleaned their teeth with a toothpaste devoid of sodium lauryl sulphate (SLS).
5. The method of claim 1 , wherein said second composition comprises Veillonella bacteria.
6. The method of claim 1 , wherein said second composition further comprises breath freshening components.
7. The method as set forth in claim 1 , further comprising providing at least one bacteria that has been modified by employment of a CRISPR-Cas or Cpf1 system to remove a virulence factor selected from the group consisting of gelatinase and hemolysin.
8. The method as set forth in claim 1 , wherein the individual subject is a human.
9. The method as set forth in claim 1 , wherein the individual subject is a canine.
10. The method as set forth in claim 1 , wherein the first bacterial composition and the second are combined.
11. A method for reducing the likelihood of developing dental caries and halitosis, comprising:
providing to an oral cavity of an individual subject:
a first bacterial composition comprising beneficial bacteria adapted to form a biofilm, said beneficial bacteria comprising a bacterium of the genus Rothia , and wherein said bacterial composition does not inhibit growth of a bacterium of species Lactobacillus salivarius ; said step of providing performed after the individual subject has cleaned their teeth with a toothpaste devoid of sodium lauryl sulphate (SLS);
a second composition comprising:
an oral probiotic comprising at least two of the following bacteria: Lactobacillus brevis CD2, Streptococcus sanguinis BCC23, Lactobacillus acidophilus, Lactobacillus bulgaricus, Lactobacillus johnsonii, Bifidobacterium bifidum, Enterococcus faecium, Lactobacillus rhamnosus, Lactobacillus plantarum, Lactobacillus reuteri, Lactobacillus paracasei, Lactobacillus casei, Lachnospira, Veillonella, Faecalibacterium and Prevotella;
at least one zinc-based compound selected from the group consisting of zinc acetate, zinc chloride, zinc citrate, and zinc sulphate; and
at least one bioactive flavonoid selected from the group consisting of baicalein, naringenin, catechins, quercetin, trans-resveratrol, Luteolin, kaempferol, hesperidin, hesperetin, naringin, diosmin, rutin, nobiletin, and tangeretin; and
wherein the halitosis is caused by a pathogenic bacteria that generates volatile sulfur compounds comprising one of methylmercaptan and hydrogen sulfite.
12. The method as set forth in claim 11 , further comprising using a clustered regularly interspaced short palindromic repeats (CRIPSR)-CRISPR associated protein (Cas) system or a CRISPR from Prevotella and Franscisella 1 (Cpf1a) system, selectively killing pathogenic bacteria in the individual subject's oral cavity.
13. The method as set forth in claim 11 , wherein said pathogenic bacteria is Porphyromonas gingivalis.
14. The method as set forth in claim 11 , wherein the individual subject is a human.
15. The method as set forth in claim 14 , wherein the individual subject is a canine.
16. A method for reducing the likelihood of developing dental caries and halitosis, comprising:
providing to an oral cavity of an individual subject:
a first bacterial composition comprising beneficial bacteria adapted to form a biofilm, said beneficial bacteria comprising a bacterium of the genus Rothia , and wherein said bacterial composition does not inhibit growth of a bacterium of species Lactobacillus salivarius ; said step of providing performed after the individual subject has cleaned their teeth;
a second composition comprising:
an oral probiotic comprising at least two of the following bacteria: Lactobacillus brevis CD2, Streptococcus sanguinis BCC23, Lactobacillus rhamnosus, Lactobacillus plantarum, Lactobacillus reuteri, Lactobacillus casei strain Shirota, and Veillonella;
at least one zinc-based compound selected from the group consisting of zinc acetate, zinc chloride, zinc citrate, and zinc sulphate; and
at least one bioactive flavonoid selected from the group consisting of quercetin, nobiletin, tangeretin; and xylitol; and
wherein said step of providing the first bacterial composition is performed after the individual subject has cleaned their teeth with a toothpaste devoid of sodium lauryl sulphate (SLS).
17. The method of claim 1 , wherein said second composition is in the form of one of a toothpaste, mouth wash, gargle solution, nose spray, mouth spray, throat spray, chewing gum, hydrogel, oral strip, and oral cream.
18. The method of claim 1 , wherein said oral probiotic comprises Lactobacillus casei , strain Shirota.
19. The method as set forth in claim 16 , further comprising providing at least one bacteria that has been modified by employment of a CRISPR-Cas or Cpf1 system to remove a virulence factor selected from the group consisting of gelatinase and hemolysin.
20. The method of claim 16 , further comprising, using a clustered regularly interspaced short palindromic repeats (CRIPSR)-CRISPR associated protein (Cas) system or a CRISPR from Prevotella and Franscisella 1 (Cpf1a) system, selectively killing pathogenic bacteria in the individual subject's oral cavity.