The streptococcal inhibitor of complement (SIC) protects Streptococcus pyogenes from bacteriocin-like inhibitory substance (BLIS) from Streptococcus salivarius.
Minami. Masaaki M; Ohmori. Daisuke D; Tatsuno. Ichiro I; Isaka. Masanori M; Kawamura. Yoshiaki Y; Ohta. Michio M; Hasegawa. Tadao T
Key Findings
- BLIS‑positive S. salivarius creates larger inhibition zones against S. pyogenes than BLIS‑negative strains
- SIC protein levels drop when S. pyogenes is exposed to BLIS‑containing broth
- SIC‑deficient S. pyogenes mutants are more vulnerable to BLIS
Practical Outcomes
- The findings hint that boosting beneficial oral bacteria like S. salivarius might help natural antimicrobial peptides such as LL‑37 work better against harmful microbes, but the research is limited to petri‑dish experiments and doesn’t provide a direct protocol for humans.
Summary
The study shows that a friendly mouth bacterium (Streptococcus salivarius) makes a substance (BLIS) that can weaken a defense protein (SIC) used by the harmful throat bug (Streptococcus pyogenes). When SIC is reduced, the natural antimicrobial peptide LL‑37 works better against the bad bacteria. This was seen in lab dishes, not in people.
Abstract
Streptococcus salivarius inhibits the growth of Streptococcus pyogenes in vitro. Streptococcus pyogenes has various virulence factors, including the streptococcus inhibitor of complement (SIC). Although SIC inhibits the activity of the peptides LL-37 and NAP1, the relationship between SIC and the bacteriocin-like inhibitory substance (BLIS) has not been elucidated. Here, we evaluated whether S. salivarius BLIS affects S. pyogenes SIC. We created three deltasic mutant strains from three S. pyogenes strains and performed deferred antagonism assays. The test strains were BLIS-positive S. salivarius JCM5707 and BLIS-negative S. salivarius NCU12. Deferred antagonism assays with JCM5707 showed that the inhibitory zones in the three deltasic mutant strains were wider than those in the three wild-type strains. Streptococcus pyogenes was cultured in BLIS-containing broth and the change in SIC in the supernatant was assessed by two-dimensional gel electrophoresis (2-DE). The 2-DE analysis of S. pyogenes exoproteins with the JCM5707 supernatant showed reduced SIC compared with those without the JCM5707 supernatant. Changes in sic mRNA levels affected by S. salivarius BLIS were evaluated by a reverse transcriptase-PCR. The sic mRNA level was affected more by the BLIS-positive S. salivarius than by the BLIS-negative strain. Our result indicates that SIC plays a role in the inhibition of S. salivarius BLIS.
Study Information
pubmed
2009
2009-09-01T00:00:00.000Z
10.1111/j.1574-6968.2009.01696.x
7
24