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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 |
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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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, 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.</description><identifier>ISSN: 0021-9193</identifier><identifier>EISSN: 1098-5530</identifier><identifier>DOI: 10.1128/JB.00343-20</identifier><identifier>PMID: 33257525</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>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</subject><ispartof>Journal of bacteriology, 2021-01, Vol.203 (4), p.1</ispartof><rights>Copyright © 2021 Vermilyea et al.</rights><rights>Copyright American Society for Microbiology Feb 2021</rights><rights>Copyright © 2021 Vermilyea et al. 2021 Vermilyea et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a442t-e1d8c916362ec471238a9a97be1139d996189a55e33aebf2e5ed3c02b7233b253</citedby><cites>FETCH-LOGICAL-a442t-e1d8c916362ec471238a9a97be1139d996189a55e33aebf2e5ed3c02b7233b253</cites><orcidid>0000-0001-8129-0537</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.asm.org/doi/pdf/10.1128/JB.00343-20$$EPDF$$P50$$Gasm2$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.asm.org/doi/full/10.1128/JB.00343-20$$EHTML$$P50$$Gasm2$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,27924,27925,52751,52752,52753,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33257525$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Comstock, Laurie E</contributor><contributor>Comstock, Laurie E.</contributor><creatorcontrib>Vermilyea, Danielle M</creatorcontrib><creatorcontrib>Moradali, M Fata</creatorcontrib><creatorcontrib>Kim, Hey-Min</creatorcontrib><creatorcontrib>Davey, Mary E</creatorcontrib><title>PPAD Activity Promotes Outer Membrane Vesicle Biogenesis and Surface Translocation by Porphyromonas gingivalis</title><title>Journal of bacteriology</title><addtitle>J Bacteriol</addtitle><addtitle>J Bacteriol</addtitle><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.</description><subject>Arginine</subject><subject>Bacteria</subject><subject>Bacteriology</subject><subject>Biofilms</subject><subject>Biosynthesis</subject><subject>Citrulline</subject><subject>Etiology</subject><subject>Gene expression</subject><subject>Gene sequencing</subject><subject>Gingipain</subject><subject>Gram-negative bacteria</subject><subject>Inoculation</subject><subject>Membrane vesicles</subject><subject>Membranes</subject><subject>Metabolism</subject><subject>Metabolomics</subject><subject>Periodontal disease</subject><subject>Periodontal diseases</subject><subject>Periodontitis</subject><subject>Porphyromonas gingivalis</subject><subject>Protein-arginine deiminase</subject><subject>Proteins</subject><subject>Proteolysis</subject><subject>Research Article</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Sessile species</subject><subject>Therapeutic targets</subject><subject>Transcriptomes</subject><subject>Translocation</subject><subject>Vesicles</subject><subject>Virulence</subject><issn>0021-9193</issn><issn>1098-5530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNptkUtr3DAURkVpSKZpVt0XQTeF4kRP29oUZtI2DxIy0LRbIct3Jgq2NJXsgfn31eTZlKzERYdzHx9CHyg5pJTVR-ezQ0K44AUjb9CEElUXUnLyFk0IYbRQVPE99C6lW0KoEJLtoj3OmawkkxPk5_PpNzy1g1u7YYPnMfRhgISvxgEivoS-icYD_g3J2Q7wzIUl-FwkbHyLf45xYSzg6wylLlgzuOBxkz0hrm42W5k3CS-dX7q16Vx6j3YWpktw8PDuo18_vl8fnxYXVydnx9OLwgjBhgJoW1tFS14ysKKijNdGGVU1QClXrVIlrZWREjg30CwYSGi5JaypGOcNk3wffb33rsamh9aCH6Lp9Cq63sSNDsbplz_e3ehlWOuqFpXkdRZ8fhDE8GeENOjeJQtdl68RxqSZKEsiSCVoRj_9h96GMfq8XqbqSpTbW2fqyz1lY0gpwuJpGEr0Nkd9PtN3OWpGntub1LNn3-vox39XfdI-Zsz_AlympX8</recordid><startdate>20210125</startdate><enddate>20210125</enddate><creator>Vermilyea, Danielle M</creator><creator>Moradali, M Fata</creator><creator>Kim, Hey-Min</creator><creator>Davey, Mary E</creator><general>American Society for Microbiology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8129-0537</orcidid></search><sort><creationdate>20210125</creationdate><title>PPAD Activity Promotes Outer Membrane Vesicle Biogenesis and Surface Translocation by Porphyromonas gingivalis</title><author>Vermilyea, Danielle M ; Moradali, M Fata ; Kim, Hey-Min ; Davey, Mary E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a442t-e1d8c916362ec471238a9a97be1139d996189a55e33aebf2e5ed3c02b7233b253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Arginine</topic><topic>Bacteria</topic><topic>Bacteriology</topic><topic>Biofilms</topic><topic>Biosynthesis</topic><topic>Citrulline</topic><topic>Etiology</topic><topic>Gene expression</topic><topic>Gene sequencing</topic><topic>Gingipain</topic><topic>Gram-negative bacteria</topic><topic>Inoculation</topic><topic>Membrane vesicles</topic><topic>Membranes</topic><topic>Metabolism</topic><topic>Metabolomics</topic><topic>Periodontal disease</topic><topic>Periodontal diseases</topic><topic>Periodontitis</topic><topic>Porphyromonas gingivalis</topic><topic>Protein-arginine deiminase</topic><topic>Proteins</topic><topic>Proteolysis</topic><topic>Research Article</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Sessile species</topic><topic>Therapeutic targets</topic><topic>Transcriptomes</topic><topic>Translocation</topic><topic>Vesicles</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vermilyea, Danielle M</creatorcontrib><creatorcontrib>Moradali, M Fata</creatorcontrib><creatorcontrib>Kim, Hey-Min</creatorcontrib><creatorcontrib>Davey, Mary E</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of bacteriology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vermilyea, Danielle M</au><au>Moradali, M Fata</au><au>Kim, Hey-Min</au><au>Davey, Mary E</au><au>Comstock, Laurie E</au><au>Comstock, Laurie E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PPAD Activity Promotes Outer Membrane Vesicle Biogenesis and Surface Translocation by Porphyromonas gingivalis</atitle><jtitle>Journal of bacteriology</jtitle><stitle>J Bacteriol</stitle><addtitle>J Bacteriol</addtitle><date>2021-01-25</date><risdate>2021</risdate><volume>203</volume><issue>4</issue><spage>1</spage><pages>1-</pages><issn>0021-9193</issn><eissn>1098-5530</eissn><abstract>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.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>33257525</pmid><doi>10.1128/JB.00343-20</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0001-8129-0537</orcidid><oa>free_for_read</oa></addata></record> |
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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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