The LuxS/AI-2 Quorum-Sensing System of Streptococcus pneumoniae Is Required to Cause Disease, and to Regulate Virulence- and Metabolism-Related Genes in a Rat Model of Middle Ear Infection

• Published in: Frontiers in cellular and infection microbiology 2018-05, Vol.8, p.138-138
• Main Authors: Yadav, Mukesh K, Vidal, Jorge E, Go, Yoon Y, Kim, Shin H, Chae, Sung-Won, Song, Jae-Jun
• Format: Article
• Language: English
• Subjects: Animals; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; biofilm; Biofilms - growth & development; Carbon-Sulfur Lyases - genetics; Carbon-Sulfur Lyases - metabolism; Disease Models, Animal; Ear, Middle - microbiology; Ear, Middle - pathology; Gene Expression Regulation, Bacterial - genetics; Homoserine - analogs & derivatives; Homoserine - genetics; Homoserine - metabolism; Humans; in vivo colonization; Lactones - metabolism; luxS mutation; LuxS/AI-2; Microbiology; Otitis Media - microbiology; Pneumococcal Infections - microbiology; Quorum Sensing; Rats; Rats, Sprague-Dawley; Specific Pathogen-Free Organisms; Streptococcus pneumoniae; Streptococcus pneumoniae - genetics; Streptococcus pneumoniae - pathogenicity; Streptococcus pneumoniae - physiology; Virulence - genetics
• ISSN: 2235-2988; 2235-2988
• DOI: 10.3389/fcimb.2018.00138

colonizes the nasopharynx of children, and from nasopharynx it could migrate to the middle ear and causes acute otitis media (AOM). During colonization and AOM, the pneumococcus forms biofilms. biofilm formation requires a functional LuxS/AI-2 quorum-sensing system. We investigated the role of LuxS/AI-2 signaling in pneumococcal middle ear infection, and identified the genes that are regulated by LuxS/AI-2 during pneumococcal biofilm formation. D39 wild-type and an isogenic D39Δ strain were utilized to evaluate biofilm formation, and colonization and epithelial damage using a microtiter plate assay and a rat model of pneumococcal middle ear infection, respectively. Biofilm structures and colonization and epithelial damage were evaluated at the ultrastructural level by scanning electron microscopy and confocal microscopy. Microarrays were used to investigate the global genes that were regulated by LuxS/AI-2 during biofilm formation. The biofilm biomass and density of D39Δ were significantly ( < 0.05) lower than those of D39 wild-type. SEM and confocal microscopy revealed that D39Δ formed thin biofilms compared with D39 wild-type. The model of middle ear infection showed that D39Δ resulted in ~60% less ( < 0.05) bacterial colonization than the wild-type. SEM analysis of the rat middle ears revealed dense biofilm-like cell debris deposited on the cilia in wild-type D39-infected rats. However, little cell debris was deposited in the middle ears of the D39Δ -inoculated rats, and the cilia were visible. cDNA-microarray analysis revealed 117 differentially expressed genes in D39Δ compared with D39 wild-type. Among the 66 genes encoding putative proteins and previously characterized proteins, 60 were significantly downregulated, whereas 6 were upregulated. Functional annotation revealed that genes involved in DNA replication and repair, ATP synthesis, capsule biosynthesis, cell division, the cell cycle, signal transduction, transcription regulation, competence, virulence, and carbohydrate metabolism were downregulated in the absence of LuxS/AI-2. The LuxS/AI-2 quorum-sensing system is necessary for biofilm formation and the colonization of the ear epithelium, and caused middle ear infection in the rat model. LuxS/AI-2 regulates the expression of the genes involved in virulence and bacterial fitness during pneumococcal biofilm formation.