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Purification of a High Molecular Mass Protein in Streptococcus mutans
Published on: September 14, 2019
Impact of Modified Lactoperoxidase Systems on Glycolytic Metabolism and Virulence Factors in Streptococcus mutans
Marcin Rafał Magacz1, Anna Skalniak2, Paweł Mamica1
1Department of Medical Diagnostics, Faculty of Pharmacy, Jagiellonian University Medical College, Medyczna 9, 30-688 Kraków, Poland.
Abstract:
The lactoperoxidase system (LpoS) is an enzymatic antimicrobial mechanism of saliva that oxidizes (pseudo)halide substrates to reactive compounds capable of limiting microbial growth. This study evaluated how different LpoS variants-utilizing iodide (LpoS-I-), thiocyanate (LpoS-SCN-), selenocyanate (LpoS-SeCN-), and a thiocyanate-iodide mixture (LpoS-SCN- + I-)-affect virulence, metabolism, and biofilm structure in Streptococcus mutans. Using qRT-PCR, pyruvate assays, MTT reduction, and confocal microscopy, we found that LpoS-I- most effectively reduced atpD and ldh expression, impaired acid tolerance, and decreased lactate and pyruvate production. LpoS-SCN- and LpoS-SeCN- also downregulated atpD and gtfB, although LpoS-SeCN- upregulated ldh. Despite minimal structural biofilm disruption, LpoS-I- markedly inhibited intracellular and extracellular pyruvate accumulation, suggesting altered glycolytic flux. These findings indicate that iodide-based LPO systems modulate key metabolic and regulatory pathways in S. mutans and may hold potential for inclusion in anticaries oral formulations.
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