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PPAD Activity Promotes Outer Membrane Vesicle Biogenesis and Surface Translocation by Porphyromonas gingivalis

Many bacteria switch between a sessile and a motile mode in response to environmental and host-related signals. , an oral anaerobe implicated in the etiology of chronic periodontal disease, has long been described as a nonmotile bacterium. And yet, recent studies have shown that under certain condit...

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Published in:Journal of bacteriology 2021-01, Vol.203 (4), p.1
Main Authors: Vermilyea, Danielle M, Moradali, M Fata, Kim, Hey-Min, Davey, Mary E
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Kim, Hey-Min
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description Many bacteria switch between a sessile and a motile mode in response to environmental and host-related signals. , an oral anaerobe implicated in the etiology of chronic periodontal disease, has long been described as a nonmotile bacterium. And yet, recent studies have shown that under certain conditions, is capable of surface translocation. Considering these findings, this work aimed to increase our understanding of how transitions between sessile growth and surface migration. Here, we show that the peptidylarginine deiminase secreted by (PPAD), an enzyme previously shown to be upregulated during surface translocation and to constrain biofilm formation, promotes surface translocation. In the absence of PPAD, the production of outer membrane vesicles (OMVs) was drastically reduced. In turn, there was a reduction in gingipain-mediated proteolysis and a reduced zone of hydration around the site of inoculation. Transcriptome sequencing (RNA-Seq) and metabolomics analyses also showed that these changes corresponded to a shift in arginine metabolism. Overall, this report provides new evidence for the functional relevance of PPAD and proteases, as well as the importance of PPAD activity in OMV biogenesis and release. Our findings support the model that citrullination is a critical mechanism during lifestyle transition between surface-attached growth and surface translocation by modulating OMV-mediated proteolysis and arginine metabolism. Gram-negative bacteria produce nanosized OMVs that are actively released into their surroundings. The oral anaerobe is prolific in OMV production, and many of the proteins packaged in these vesicles are proteolytic or protein-modifying enzymes. This includes key virulence determinants, such as the gingipains and PPAD (a unique peptidylarginine deiminase). Here, we show that PPAD activity (citrullination) is involved in OMV biogenesis. The study revealed an unusual mechanism that allows this bacterium to transform its surroundings. Since OMVs are detected in circulation and in systemic tissues, our study results also support the notion that PPAD activity may be a key factor in the correlation between periodontitis and systemic diseases, further supporting the idea of PPAD as an important therapeutic target.
doi_str_mv 10.1128/JB.00343-20
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And yet, recent studies have shown that under certain conditions, is capable of surface translocation. Considering these findings, this work aimed to increase our understanding of how transitions between sessile growth and surface migration. Here, we show that the peptidylarginine deiminase secreted by (PPAD), an enzyme previously shown to be upregulated during surface translocation and to constrain biofilm formation, promotes surface translocation. In the absence of PPAD, the production of outer membrane vesicles (OMVs) was drastically reduced. In turn, there was a reduction in gingipain-mediated proteolysis and a reduced zone of hydration around the site of inoculation. Transcriptome sequencing (RNA-Seq) and metabolomics analyses also showed that these changes corresponded to a shift in arginine metabolism. Overall, this report provides new evidence for the functional relevance of PPAD and proteases, as well as the importance of PPAD activity in OMV biogenesis and release. Our findings support the model that citrullination is a critical mechanism during lifestyle transition between surface-attached growth and surface translocation by modulating OMV-mediated proteolysis and arginine metabolism. Gram-negative bacteria produce nanosized OMVs that are actively released into their surroundings. The oral anaerobe is prolific in OMV production, and many of the proteins packaged in these vesicles are proteolytic or protein-modifying enzymes. This includes key virulence determinants, such as the gingipains and PPAD (a unique peptidylarginine deiminase). Here, we show that PPAD activity (citrullination) is involved in OMV biogenesis. The study revealed an unusual mechanism that allows this bacterium to transform its surroundings. 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Our findings support the model that citrullination is a critical mechanism during lifestyle transition between surface-attached growth and surface translocation by modulating OMV-mediated proteolysis and arginine metabolism. Gram-negative bacteria produce nanosized OMVs that are actively released into their surroundings. The oral anaerobe is prolific in OMV production, and many of the proteins packaged in these vesicles are proteolytic or protein-modifying enzymes. This includes key virulence determinants, such as the gingipains and PPAD (a unique peptidylarginine deiminase). Here, we show that PPAD activity (citrullination) is involved in OMV biogenesis. The study revealed an unusual mechanism that allows this bacterium to transform its surroundings. 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source American Society for Microbiology; PubMed (Medline)
subjects Arginine
Bacteria
Bacteriology
Biofilms
Biosynthesis
Citrulline
Etiology
Gene expression
Gene sequencing
Gingipain
Gram-negative bacteria
Inoculation
Membrane vesicles
Membranes
Metabolism
Metabolomics
Periodontal disease
Periodontal diseases
Periodontitis
Porphyromonas gingivalis
Protein-arginine deiminase
Proteins
Proteolysis
Research Article
Ribonucleic acid
RNA
Sessile species
Therapeutic targets
Transcriptomes
Translocation
Vesicles
Virulence
title PPAD Activity Promotes Outer Membrane Vesicle Biogenesis and Surface Translocation by Porphyromonas gingivalis
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