Functional divergence of MdpS and MdpS2 reveals mucin-targeting strategies in Streptococcus oralis
Fredrik Leo, Jonas Nilsson, Liisa Arike, Sahana Kumar, Emma Hilton, Rolf Lood, David J. Thornton, Gregg A. Duncan, Gunnel Svensäter, Claes Wickström

TL;DR
This study explores how two proteases in Streptococcus oralis help break down mucins, supporting bacterial adaptation in the mouth and influencing biofilm behavior.
Contribution
The study reveals the functional divergence and complementary roles of MdpS and MdpS2 in mucin degradation and biofilm dynamics.
Findings
MdpS2 selectively modulates MUC5B-rich mucus and promotes biofilm dispersal.
MdpS and MdpS2 show overlapping but distinct mucin hydrolysis patterns.
Both proteases are upregulated during late biofilm growth and affect mucus structure.
Abstract
Mucin degradation is essential for understanding oral microbial adaptation, yet the enzymes involved remain incompletely understood. Herein, we have characterised two mucin-degrading proteases, MdpS and MdpS2, from the oral commensal Streptococcus oralis. MdpS2 was characterised using physicochemical assays and substrate profiling and was compared to MdpS. Further Mdp characterisation included structural modelling, and functional assays analysing the gene expression during biofilm growth on salivary MUC5B, enzyme-induced biofilm dispersal, and mucus degradation analysed through nanoLC-MS/MS, sedimentation profiling, and microrheology. MdpS2 shared conformational homology with MdpS despite low sequence identity and showed greater tolerance to pH and sodium chloride. Both genes were significantly upregulated during late stationary biofilm phase. MdpS and MdpS2 hydrolysed MUC5B…
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Taxonomy
TopicsGlycosylation and Glycoproteins Research · Machine Learning in Bioinformatics · Genomics and Phylogenetic Studies
