Deletion of dltD gene modulates biofilm matrix and acid metabolism to attenuate Streptococcus mutans cariogenicity

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Authors: Jingyun Du, Shan Huang, Yijun Li, Zhoucheng Qiu, Yujia Hao, Jing Huang, Ling Zhan, Shuai Chen, Xiaoyin Huang
Cited by: 0
References: 47

Abstract

Introduction Streptococcus mutans (SM) is one of the key pathogenic bacteria in the occurrence and development of dental caries. Its complex virulence regulation network has become an important target in current ecological caries prevention research. This study explored how dltD attenuates SM cariogenicity using standard strain SM UA159, high-cariogenic clinical strain SM 593, and their dltD deletion/complemented strains. Methods In this study, the clinical serotype C SM 593 clinical strain isolated from caries-active patients (DMFT6), the SM 593 dltD deletion strain ( SM 593- dltD ), and SM 593- dltD complementary strain ( SM 593- dltD-c ) were selected as the experimental strains. Rat caries model was constructed to detect the cariogenicity. Colony forming counting units (CFU) counting was used to detect the colonization ability in vivo . The adhesion ability and surface hydrophobicity of each strain were examined by tube attachment assay and microbial adhesion to hydrocarbons method. Biofilm of each strain was constructed in vitro ., CFU counting and MTT staining were used to analyze the SM biofilm formation. Laser confocal scanning microscope were used to observe the biofilm morphology, live/dead staining distribution. Anthrone-sulfuric acid assay, laser confocal scanning microscope, SYTOX probe assay and BCA protein kit assay were used to detect the extracellular polysaccharide content, extracellular polysaccharide distribution, eDNA content and extracellular protein content of the biofilm. Acid production was examined by detecting the pH of the biofilm supernatant. Potassium iodide assay and lactate dehydrogenase detection kit assay were used to examine intracellular polysaccharides and lactate dehydrogenase activity. CFU counting was used to detect the adaptive acid tolerance ability. Laurdan fluorescent probe was used to examine the cell membranes fluidity under the acidic condition. The expression of genes related to biofilm formation and acid tolerance was detected by RTqPCR. Results In vivo , dltD deletion significantly reduced fissure and proximal caries severity (P

Fields of Study & Subjects

Oral microbiology and periodontitis research Bacterial biofilms and quorum sensing Dental Health and Care Utilization

Publication details

Journal / source
Frontiers in Cellular and Infection Microbiology
Volume
15
Pages
1741359–1741359
Publication date
16 February 2026
Language
EN