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Competence-Stimulating-Peptide-Dependent Localized Cell Death and Extracellular DNA Production in Streptococcus mutans Biofilms.
Nagasawa, Ryo; Yamamoto, Tatsuya; Utada, Andrew S; Nomura, Nobuhiko; Obana, Nozomu.
Afiliación
  • Nagasawa R; Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan.
  • Yamamoto T; Faculty of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan.
  • Utada AS; Faculty of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan.
  • Nomura N; Microbiology Research Center for Sustainability, University of Tsukuba, Tsukuba, Ibaraki, Japan.
  • Obana N; Faculty of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan nomura.nobuhiko.ge@u.tsukuba.ac.jp obana.nozomu.gb@u.tsukuba.ac.jp.
Appl Environ Microbiol ; 86(23)2020 11 10.
Article en En | MEDLINE | ID: mdl-32948520
ABSTRACT
Extracellular DNA (eDNA) is a biofilm component that contributes to the formation and structural stability of biofilms. Streptococcus mutans, a major cariogenic bacterium, induces eDNA-dependent biofilm formation under specific conditions. Since cell death can result in the release and accumulation of DNA, the dead cells in biofilms are a source of eDNA. However, it remains unknown how eDNA is released from dead cells and is localized within S. mutans biofilms. We focused on cell death induced by the extracellular signaling peptide called competence-stimulating peptide (CSP). We demonstrate that nucleic acid release into the extracellular environment occurs in a subpopulation of dead cells. eDNA production induced by CSP was highly dependent on the lytF gene, which encodes an autolysin. Although lytF expression was induced bimodally by CSP, lytF-expressing cells further divided into surviving cells and eDNA-producing dead cells. Moreover, we found that lytF-expressing cells were abundant near the bottom of the biofilm, even when all cells in the biofilm received the CSP signal. Dead cells and eDNA were also abundantly present near the bottom of the biofilm. The number of lytF-expressing cells in biofilms was significantly higher than that in planktonic cultures, which suggests that adhesion to the substratum surface is important for the induction of lytF expression. The deletion of lytF resulted in reduced adherence to a polystyrene surface. These results suggest that lytF expression and eDNA production induced near the bottom of the biofilm contribute to a firmly attached and structurally stable biofilm.IMPORTANCE Bacterial communities encased by self-produced extracellular polymeric substances (EPSs), known as biofilms, have a wide influence on human health and environmental problems. The importance of biofilm research has increased, as biofilms are the preferred bacterial lifestyle in nature. Furthermore, in recent years it has been noted that the contribution of phenotypic heterogeneity within biofilms requires analysis at the single-cell or subpopulation level to understand bacterial life strategies. In Streptococcus mutans, a cariogenic bacterium, extracellular DNA (eDNA) contributes to biofilm formation. However, it remains unclear how and where the cells produce eDNA within the biofilm. We focused on LytF, an autolysin that is induced by extracellular peptide signals. We used single-cell level imaging techniques to analyze lytF expression in the biofilm population. Here, we show that S. mutans generates eDNA by inducing lytF expression near the bottom of the biofilm, thereby enhancing biofilm adhesion and structural stability.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Streptococcus mutans / ADN Bacteriano / Biopelículas / Matriz Extracelular de Sustancias Poliméricas Idioma: En Revista: Appl Environ Microbiol Año: 2020 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Streptococcus mutans / ADN Bacteriano / Biopelículas / Matriz Extracelular de Sustancias Poliméricas Idioma: En Revista: Appl Environ Microbiol Año: 2020 Tipo del documento: Article País de afiliación: Japón