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Identification of signaling pathways, matrix-digestion enzymes, and motility components controlling Vibrio cholerae biofilm dispersal
by
Fei, Chenyi
, Bassler, Bonnie L.
, Bridges, Andrew A.
in
Adhesins
/ Adhesins, Bacterial - genetics
/ Adhesins, Bacterial - metabolism
/ Anti-Bacterial Agents - pharmacology
/ Bacteria
/ Bacterial Proteins - genetics
/ Bacterial Proteins - metabolism
/ Biodegradation
/ Biofilms
/ Biofilms - drug effects
/ Biofilms - growth & development
/ Biological Sciences
/ Cell adhesion
/ CheY protein
/ Cyclic GMP - analogs & derivatives
/ Cyclic GMP - metabolism
/ Degradation
/ Digestion
/ Disease transmission
/ Dispersal
/ Dispersion
/ Enzymes
/ Enzymes - genetics
/ Enzymes - metabolism
/ Gene Expression Regulation, Bacterial
/ Microbiology
/ Motility
/ Mutation
/ Operon
/ Polysaccharides
/ Porous media
/ Proteins
/ Saccharides
/ Signal Transduction
/ Signaling
/ Swimming
/ Time-Lapse Imaging
/ Vibrio cholerae
/ Vibrio cholerae - drug effects
/ Vibrio cholerae - genetics
/ Vibrio cholerae - pathogenicity
/ Vibrio cholerae - physiology
/ Waterborne diseases
2020
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Identification of signaling pathways, matrix-digestion enzymes, and motility components controlling Vibrio cholerae biofilm dispersal
by
Fei, Chenyi
, Bassler, Bonnie L.
, Bridges, Andrew A.
in
Adhesins
/ Adhesins, Bacterial - genetics
/ Adhesins, Bacterial - metabolism
/ Anti-Bacterial Agents - pharmacology
/ Bacteria
/ Bacterial Proteins - genetics
/ Bacterial Proteins - metabolism
/ Biodegradation
/ Biofilms
/ Biofilms - drug effects
/ Biofilms - growth & development
/ Biological Sciences
/ Cell adhesion
/ CheY protein
/ Cyclic GMP - analogs & derivatives
/ Cyclic GMP - metabolism
/ Degradation
/ Digestion
/ Disease transmission
/ Dispersal
/ Dispersion
/ Enzymes
/ Enzymes - genetics
/ Enzymes - metabolism
/ Gene Expression Regulation, Bacterial
/ Microbiology
/ Motility
/ Mutation
/ Operon
/ Polysaccharides
/ Porous media
/ Proteins
/ Saccharides
/ Signal Transduction
/ Signaling
/ Swimming
/ Time-Lapse Imaging
/ Vibrio cholerae
/ Vibrio cholerae - drug effects
/ Vibrio cholerae - genetics
/ Vibrio cholerae - pathogenicity
/ Vibrio cholerae - physiology
/ Waterborne diseases
2020
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Identification of signaling pathways, matrix-digestion enzymes, and motility components controlling Vibrio cholerae biofilm dispersal
by
Fei, Chenyi
, Bassler, Bonnie L.
, Bridges, Andrew A.
in
Adhesins
/ Adhesins, Bacterial - genetics
/ Adhesins, Bacterial - metabolism
/ Anti-Bacterial Agents - pharmacology
/ Bacteria
/ Bacterial Proteins - genetics
/ Bacterial Proteins - metabolism
/ Biodegradation
/ Biofilms
/ Biofilms - drug effects
/ Biofilms - growth & development
/ Biological Sciences
/ Cell adhesion
/ CheY protein
/ Cyclic GMP - analogs & derivatives
/ Cyclic GMP - metabolism
/ Degradation
/ Digestion
/ Disease transmission
/ Dispersal
/ Dispersion
/ Enzymes
/ Enzymes - genetics
/ Enzymes - metabolism
/ Gene Expression Regulation, Bacterial
/ Microbiology
/ Motility
/ Mutation
/ Operon
/ Polysaccharides
/ Porous media
/ Proteins
/ Saccharides
/ Signal Transduction
/ Signaling
/ Swimming
/ Time-Lapse Imaging
/ Vibrio cholerae
/ Vibrio cholerae - drug effects
/ Vibrio cholerae - genetics
/ Vibrio cholerae - pathogenicity
/ Vibrio cholerae - physiology
/ Waterborne diseases
2020
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Identification of signaling pathways, matrix-digestion enzymes, and motility components controlling Vibrio cholerae biofilm dispersal
Journal Article
Identification of signaling pathways, matrix-digestion enzymes, and motility components controlling Vibrio cholerae biofilm dispersal
2020
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Overview
Bacteria alternate between being free-swimming and existing as members of sessile multicellular communities called biofilms. The biofilm lifecycle occurs in three stages: cell attachment, biofilm maturation, and biofilm dispersal. Vibrio cholerae biofilms are hyperinfectious, and biofilm formation and dispersal are considered central to disease transmission. While biofilm formation is well studied, almost nothing is known about biofilm dispersal. Here, we conducted an imaging screen for V. cholerae mutants that fail to disperse, revealing three classes of dispersal components: signal transduction proteins, matrix-degradation enzymes, and motility factors. Signaling proteins dominated the screen and among them, we focused on an uncharacterized two-component sensory system that we term DbfS/DbfR for dispersal of biofilm sensor/regulator. Phospho-DbfR represses biofilm dispersal. DbfS dephosphorylates and thereby inactivates DbfR, which permits dispersal. Matrix degradation requires two enzymes: LapG, which cleaves adhesins, and RbmB, which digests matrix polysaccharides. Reorientation in swimming direction, mediated by CheY3, is necessary for cells to escape from the porous biofilm matrix. We suggest that these components act sequentially: signaling launches dispersal by terminating matrix production and triggering matrix digestion, and subsequent cell motility permits escape from biofilms. This study lays the groundwork for interventions aimed at modulating V. cholerae biofilm dispersal to ameliorate disease.
Publisher
National Academy of Sciences
Subject
/ Adhesins, Bacterial - genetics
/ Adhesins, Bacterial - metabolism
/ Anti-Bacterial Agents - pharmacology
/ Bacteria
/ Bacterial Proteins - genetics
/ Bacterial Proteins - metabolism
/ Biofilms
/ Biofilms - growth & development
/ Cyclic GMP - analogs & derivatives
/ Enzymes
/ Gene Expression Regulation, Bacterial
/ Motility
/ Mutation
/ Operon
/ Proteins
/ Swimming
/ Vibrio cholerae - drug effects
/ Vibrio cholerae - pathogenicity
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