Toxin-Antitoxin systems eliminate defective cells and preserve symmetry in Bacillus subtilis biofilms
Summary Toxin‐antitoxin modules are gene pairs encoding a toxin and its antitoxin, and are found on the chromosomes of many bacteria, including pathogens. Here, we characterize the specific contribution of the TxpA and YqcG toxins in elimination of defective cells from developing Bacillus subtilis b...
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Veröffentlicht in: | Environmental microbiology 2016-12, Vol.18 (12), p.5032-5047 |
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creator | Bloom-Ackermann, Zohar Steinberg, Nitai Rosenberg, Gili Oppenheimer-Shaanan, Yaara Pollack, Dan Ely, Shir Storzi, Nimrod Levy, Asaf Kolodkin-Gal, Ilana |
description | Summary
Toxin‐antitoxin modules are gene pairs encoding a toxin and its antitoxin, and are found on the chromosomes of many bacteria, including pathogens. Here, we characterize the specific contribution of the TxpA and YqcG toxins in elimination of defective cells from developing Bacillus subtilis biofilms. On nutrient limitation, defective cells accumulated in the biofilm breaking its symmetry. Deletion of the toxins resulted in accumulation of morphologically abnormal cells, and interfered with the proper development of the multicellular community. Dual physiological responses are of significance for TxpA and YqcG activation: nitrogen deprivation enhances the transcription of both TxpA and YqcG toxins, and simultaneously sensitizes the biofilm cells to their activity. Furthermore, we demonstrate that while both toxins when overexpressed affect the morphology of the developing biofilm, the toxin TxpA can act to lyse and dissolve pre‐established B. subtilis biofilms. |
doi_str_mv | 10.1111/1462-2920.13471 |
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Toxin‐antitoxin modules are gene pairs encoding a toxin and its antitoxin, and are found on the chromosomes of many bacteria, including pathogens. Here, we characterize the specific contribution of the TxpA and YqcG toxins in elimination of defective cells from developing Bacillus subtilis biofilms. On nutrient limitation, defective cells accumulated in the biofilm breaking its symmetry. Deletion of the toxins resulted in accumulation of morphologically abnormal cells, and interfered with the proper development of the multicellular community. Dual physiological responses are of significance for TxpA and YqcG activation: nitrogen deprivation enhances the transcription of both TxpA and YqcG toxins, and simultaneously sensitizes the biofilm cells to their activity. Furthermore, we demonstrate that while both toxins when overexpressed affect the morphology of the developing biofilm, the toxin TxpA can act to lyse and dissolve pre‐established B. subtilis biofilms.</description><identifier>ISSN: 1462-2912</identifier><identifier>EISSN: 1462-2920</identifier><identifier>DOI: 10.1111/1462-2920.13471</identifier><identifier>PMID: 27450630</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Antitoxins - genetics ; Antitoxins - metabolism ; Bacillus subtilis ; Bacillus subtilis - genetics ; Bacillus subtilis - growth & development ; Bacillus subtilis - physiology ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Bacterial Toxins - genetics ; Bacterial Toxins - metabolism ; Biofilms ; Biofilms - growth & development ; Genes</subject><ispartof>Environmental microbiology, 2016-12, Vol.18 (12), p.5032-5047</ispartof><rights>2016 Society for Applied Microbiology and John Wiley & Sons Ltd</rights><rights>2016 Society for Applied Microbiology and John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1462-2920.13471$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1462-2920.13471$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27450630$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bloom-Ackermann, Zohar</creatorcontrib><creatorcontrib>Steinberg, Nitai</creatorcontrib><creatorcontrib>Rosenberg, Gili</creatorcontrib><creatorcontrib>Oppenheimer-Shaanan, Yaara</creatorcontrib><creatorcontrib>Pollack, Dan</creatorcontrib><creatorcontrib>Ely, Shir</creatorcontrib><creatorcontrib>Storzi, Nimrod</creatorcontrib><creatorcontrib>Levy, Asaf</creatorcontrib><creatorcontrib>Kolodkin-Gal, Ilana</creatorcontrib><title>Toxin-Antitoxin systems eliminate defective cells and preserve symmetry in Bacillus subtilis biofilms</title><title>Environmental microbiology</title><addtitle>Environ Microbiol</addtitle><description>Summary
Toxin‐antitoxin modules are gene pairs encoding a toxin and its antitoxin, and are found on the chromosomes of many bacteria, including pathogens. Here, we characterize the specific contribution of the TxpA and YqcG toxins in elimination of defective cells from developing Bacillus subtilis biofilms. On nutrient limitation, defective cells accumulated in the biofilm breaking its symmetry. Deletion of the toxins resulted in accumulation of morphologically abnormal cells, and interfered with the proper development of the multicellular community. Dual physiological responses are of significance for TxpA and YqcG activation: nitrogen deprivation enhances the transcription of both TxpA and YqcG toxins, and simultaneously sensitizes the biofilm cells to their activity. Furthermore, we demonstrate that while both toxins when overexpressed affect the morphology of the developing biofilm, the toxin TxpA can act to lyse and dissolve pre‐established B. subtilis biofilms.</description><subject>Antitoxins - genetics</subject><subject>Antitoxins - metabolism</subject><subject>Bacillus subtilis</subject><subject>Bacillus subtilis - genetics</subject><subject>Bacillus subtilis - growth & development</subject><subject>Bacillus subtilis - physiology</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bacterial Toxins - genetics</subject><subject>Bacterial Toxins - metabolism</subject><subject>Biofilms</subject><subject>Biofilms - growth & development</subject><subject>Genes</subject><issn>1462-2912</issn><issn>1462-2920</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkT1v2zAQhomgRT7czNkKAl2yqOGnKI2ukTgu3GRx25EgpRPAhJIcUUqsfx8qTj1kKhfeHZ_3cMcXoQtKvtN4rqhIWcJyFlMuFD1Cp4fKp0NM2Qk6C-GBEKq4IsfohCkhScrJKYJNu3NNMm96108RDmPooQ4YvKtdY3rAJVRQ9O4ZcAHeB2yaEm87CNDFUhjrGvpuxFH6wxTO-yHgMNjeeRewdW3lfB2-oM-V8QHO3-8Z-n1zvVncJuv75WoxXyeO54omeVlaTvJCWmWtVYLmhijOFWOiUhkUMqsMBZmyUlSWxn2lkbmhLBVpwYXM-Axd7vtuu_ZpgNDr2oVpatNAOwRNM5mLLIuN_wNlqeKMpiyi3z6gD-3QNXGRqSElQgohIvX1nRpsDaXedq423aj__XUE5B54cR7GwzslerJST2bpyTj9ZqW-_rV6C6Iu2etcdGZ30JnuUccJldR_75b654IvNn9kqiV_BV1Knjc</recordid><startdate>201612</startdate><enddate>201612</enddate><creator>Bloom-Ackermann, Zohar</creator><creator>Steinberg, Nitai</creator><creator>Rosenberg, Gili</creator><creator>Oppenheimer-Shaanan, Yaara</creator><creator>Pollack, Dan</creator><creator>Ely, Shir</creator><creator>Storzi, Nimrod</creator><creator>Levy, Asaf</creator><creator>Kolodkin-Gal, Ilana</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QH</scope><scope>7QL</scope><scope>7ST</scope><scope>7T7</scope><scope>7TN</scope><scope>7U9</scope><scope>7UA</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>201612</creationdate><title>Toxin-Antitoxin systems eliminate defective cells and preserve symmetry in Bacillus subtilis biofilms</title><author>Bloom-Ackermann, Zohar ; 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Toxin‐antitoxin modules are gene pairs encoding a toxin and its antitoxin, and are found on the chromosomes of many bacteria, including pathogens. Here, we characterize the specific contribution of the TxpA and YqcG toxins in elimination of defective cells from developing Bacillus subtilis biofilms. On nutrient limitation, defective cells accumulated in the biofilm breaking its symmetry. Deletion of the toxins resulted in accumulation of morphologically abnormal cells, and interfered with the proper development of the multicellular community. Dual physiological responses are of significance for TxpA and YqcG activation: nitrogen deprivation enhances the transcription of both TxpA and YqcG toxins, and simultaneously sensitizes the biofilm cells to their activity. Furthermore, we demonstrate that while both toxins when overexpressed affect the morphology of the developing biofilm, the toxin TxpA can act to lyse and dissolve pre‐established B. subtilis biofilms.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>27450630</pmid><doi>10.1111/1462-2920.13471</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antitoxins - genetics Antitoxins - metabolism Bacillus subtilis Bacillus subtilis - genetics Bacillus subtilis - growth & development Bacillus subtilis - physiology Bacterial Proteins - genetics Bacterial Proteins - metabolism Bacterial Toxins - genetics Bacterial Toxins - metabolism Biofilms Biofilms - growth & development Genes |
title | Toxin-Antitoxin systems eliminate defective cells and preserve symmetry in Bacillus subtilis biofilms |
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