Persistence of the oral probiotic Streptococcus salivarius M18 is dose dependent and megaplasmid transfer can augment their bacteriocin production and adhesion characteristics

PLoS One. 2013 Jun 13;8(6):e65991. doi: 10.1371/journal.pone.0065991. Print 2013.

Abstract

Bacteriocin-producing probiotic Streptococcus salivarius M18 offers beneficial modulatory capabilities within the oral microbiome, apparently through potent inhibitory activity against potentially deleterious bacteria, such as Streptococcus pyogenes. The oral cavity persistence of S. salivarius M18 was investigated in 75 subjects receiving four different doses for 28 days. Sixty per cent of the subjects already had some inhibitor-producing S. salivarius in their saliva prior to probiotic intervention. Strain M18's persistence was dependent upon the dose, but not the period of administration. Culture analysis indicated that in some individuals the introduced strain had almost entirely replaced the indigenous S. salivarius, though the total numbers of the species did not increase. Selected subjects showing either high or low probiotic persistence had their salivary populations profiled using Illumina sequencing of the V6 region of the 16S rRNA gene. Analysis indicated that while certain bacterial phenotypes were markedly modulated, the overall composition of the oral microbiome was not modified by the probiotic treatment. Megaplasmids encoding bacteriocins and adhesion factors were transferred in vitro to generate a transconjugant S. salivarius exhibiting enhanced antimicrobial production and binding capabilities to HEp-2 cells. Since no widespread perturbation of the existing indigenous microbiota was associated with oral instillation and given its antimicrobial activity against potentially pathogenic streptococci, it appears that application of probiotic strain M18 offers potential low impact alternative to classical antibiotic prophylaxis. For candidate probiotic strains having relatively poor antimicrobial or adhesive properties, unique derivatives displaying improved probiotic performance may be engineered in vitro by megaplasmid transfer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Adhesion / genetics*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Bacteriocins / biosynthesis*
  • Bacteriocins / genetics*
  • Cell Line
  • Conjugation, Genetic
  • Humans
  • Microbiota
  • Mouth / microbiology
  • Plasmids / genetics*
  • Probiotics / administration & dosage*
  • RNA, Ribosomal, 16S / genetics
  • Saliva / microbiology
  • Sequence Analysis, DNA
  • Streptococcus / classification
  • Streptococcus / genetics*
  • Streptococcus / metabolism*

Substances

  • Bacterial Proteins
  • Bacteriocins
  • RNA, Ribosomal, 16S

Grants and funding

The study was proposed by BLIS Technologies Ltd to gain further insight into the persistence properties of the organism. The company provided the lozenges for the study but did not fund the analysis of the samples collected at the university or the in vitro components of the study. Analysis and other experiments were supported by funds for University of Otago Post Graduates and by the Canadian Research and Development Centre for Probiotics at the Lawson Health Research Institute. The funders had some role in study design, assisted by providing personnel to collect raw data, but did not have a role in the analysis, decision to publish, or preparation of the manuscript (other than for final proof reading purposes).