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Toxin YafQ increases persister cell formation by reducing indole signalling
Summary Persister cells survive antibiotic and other environmental stresses by slowing metabolism. Since toxins of toxin/antitoxin (TA) systems have been postulated to be responsible for persister cell formation, we investigated the influence of toxin YafQ of the YafQ/DinJ Escherichia coli TA system...
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Published in: | Environmental microbiology 2015-04, Vol.17 (4), p.1275-1285 |
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creator | Hu, Ying Kwan, Brian W. Osbourne, Devon O. Benedik, Michael J. Wood, Thomas K. |
description | Summary
Persister cells survive antibiotic and other environmental stresses by slowing metabolism. Since toxins of toxin/antitoxin (TA) systems have been postulated to be responsible for persister cell formation, we investigated the influence of toxin YafQ of the YafQ/DinJ Escherichia coli TA system on persister cell formation. Under stress, YafQ alters metabolism by cleaving transcripts with in‐frame 5′‐AAA‐G/A‐3′ sites. Production of YafQ increased persister cell formation with multiple antibiotics, and by investigating changes in protein expression, we found that YafQ reduced tryptophanase levels (TnaA mRNA has 16 putative YafQ cleavage sites). Consistently, TnaA mRNA levels were also reduced by YafQ. Tryptophanase is activated in the stationary phase by the stationary‐phase sigma factor RpoS, which was also reduced dramatically upon production of YafQ. Tryptophanase converts tryptophan into indole, and as expected, indole levels were reduced by the production of YafQ. Corroborating the effect of YafQ on persistence, addition of indole reduced persistence. Furthermore, persistence increased upon deleting tnaA, and persistence decreased upon adding tryptophan to the medium to increase indole levels. Also, YafQ production had a much smaller effect on persistence in a strain unable to produce indole. Therefore, YafQ increases persistence by reducing indole, and TA systems are related to cell signalling. |
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Persister cells survive antibiotic and other environmental stresses by slowing metabolism. Since toxins of toxin/antitoxin (TA) systems have been postulated to be responsible for persister cell formation, we investigated the influence of toxin YafQ of the YafQ/DinJ Escherichia coli TA system on persister cell formation. Under stress, YafQ alters metabolism by cleaving transcripts with in‐frame 5′‐AAA‐G/A‐3′ sites. Production of YafQ increased persister cell formation with multiple antibiotics, and by investigating changes in protein expression, we found that YafQ reduced tryptophanase levels (TnaA mRNA has 16 putative YafQ cleavage sites). Consistently, TnaA mRNA levels were also reduced by YafQ. Tryptophanase is activated in the stationary phase by the stationary‐phase sigma factor RpoS, which was also reduced dramatically upon production of YafQ. Tryptophanase converts tryptophan into indole, and as expected, indole levels were reduced by the production of YafQ. Corroborating the effect of YafQ on persistence, addition of indole reduced persistence. Furthermore, persistence increased upon deleting tnaA, and persistence decreased upon adding tryptophan to the medium to increase indole levels. Also, YafQ production had a much smaller effect on persistence in a strain unable to produce indole. Therefore, YafQ increases persistence by reducing indole, and TA systems are related to cell signalling.</description><identifier>ISSN: 1462-2912</identifier><identifier>EISSN: 1462-2920</identifier><identifier>DOI: 10.1111/1462-2920.12567</identifier><identifier>PMID: 25041421</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Antitoxins - genetics ; Bacterial Proteins - metabolism ; Bacterial Toxins - genetics ; Bacterial Toxins - metabolism ; Escherichia coli ; Escherichia coli - genetics ; Escherichia coli - pathogenicity ; Escherichia coli Proteins - genetics ; Escherichia coli Proteins - metabolism ; Indoles - analysis ; Manufacturing cells ; Metabolism ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Sigma Factor - metabolism ; Signal Transduction ; Tryptophan - chemistry ; Tryptophanase - biosynthesis ; Tryptophanase - genetics ; Tryptophanase - metabolism</subject><ispartof>Environmental microbiology, 2015-04, Vol.17 (4), p.1275-1285</ispartof><rights>2014 Society for Applied Microbiology and John Wiley & Sons Ltd</rights><rights>2014 Society for Applied Microbiology and John Wiley & Sons Ltd.</rights><rights>Copyright © 2015 Society for Applied Microbiology and John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4837-da0980930a8dff5985c47e174c362bf7ac6a4ea8c0c158316f32f4ba09ecb693</citedby><cites>FETCH-LOGICAL-c4837-da0980930a8dff5985c47e174c362bf7ac6a4ea8c0c158316f32f4ba09ecb693</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25041421$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hu, Ying</creatorcontrib><creatorcontrib>Kwan, Brian W.</creatorcontrib><creatorcontrib>Osbourne, Devon O.</creatorcontrib><creatorcontrib>Benedik, Michael J.</creatorcontrib><creatorcontrib>Wood, Thomas K.</creatorcontrib><title>Toxin YafQ increases persister cell formation by reducing indole signalling</title><title>Environmental microbiology</title><addtitle>Environ Microbiol</addtitle><description>Summary
Persister cells survive antibiotic and other environmental stresses by slowing metabolism. Since toxins of toxin/antitoxin (TA) systems have been postulated to be responsible for persister cell formation, we investigated the influence of toxin YafQ of the YafQ/DinJ Escherichia coli TA system on persister cell formation. Under stress, YafQ alters metabolism by cleaving transcripts with in‐frame 5′‐AAA‐G/A‐3′ sites. Production of YafQ increased persister cell formation with multiple antibiotics, and by investigating changes in protein expression, we found that YafQ reduced tryptophanase levels (TnaA mRNA has 16 putative YafQ cleavage sites). Consistently, TnaA mRNA levels were also reduced by YafQ. Tryptophanase is activated in the stationary phase by the stationary‐phase sigma factor RpoS, which was also reduced dramatically upon production of YafQ. Tryptophanase converts tryptophan into indole, and as expected, indole levels were reduced by the production of YafQ. Corroborating the effect of YafQ on persistence, addition of indole reduced persistence. Furthermore, persistence increased upon deleting tnaA, and persistence decreased upon adding tryptophan to the medium to increase indole levels. Also, YafQ production had a much smaller effect on persistence in a strain unable to produce indole. Therefore, YafQ increases persistence by reducing indole, and TA systems are related to cell signalling.</description><subject>Antitoxins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bacterial Toxins - genetics</subject><subject>Bacterial Toxins - metabolism</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - pathogenicity</subject><subject>Escherichia coli Proteins - genetics</subject><subject>Escherichia coli Proteins - metabolism</subject><subject>Indoles - analysis</subject><subject>Manufacturing cells</subject><subject>Metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Sigma Factor - metabolism</subject><subject>Signal Transduction</subject><subject>Tryptophan - chemistry</subject><subject>Tryptophanase - biosynthesis</subject><subject>Tryptophanase - genetics</subject><subject>Tryptophanase - metabolism</subject><issn>1462-2912</issn><issn>1462-2920</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFkTtPwzAUhS0EgvKY2VAkFpZQv2I7I6KlIF5CqkBMluPYlSFNit2I9t_jUNqBpV7se_2dI_seAE4RvERx9RFlOMU5jiXOGN8BvU1nd3NG-AAchvABIeKEw31wgDNIEcWoB-7HzcLVybuyL4mrtTcqmJDMjA8uzI1PtKmqxDZ-quauqZNimXhTttrVk4iXTWWS4Ca1qqrYOQZ7VlXBnPztR2B8Mxxf36YPz6O766uHVFNBeFoqmAuYE6hEaW2Wi0xTbhCnmjBcWK40U9QooaFGmSCIWYItLaLK6ILl5AhcrGxnvvlqTZjLqQvdO1VtmjZIxDNCGcux2I4yjjDCEJGInv9DP5rWx591FMtFHBmGkeqvKO2bELyxcubdVPmlRFB2ichu5rKbv_xNJCrO_nzbYmrKDb-OIALZCvh2lVlu85PDx7u1cbrSdUEtNjrlP2W85Zl8exrJfABHrwOCpSA_CDmifQ</recordid><startdate>201504</startdate><enddate>201504</enddate><creator>Hu, Ying</creator><creator>Kwan, Brian W.</creator><creator>Osbourne, Devon O.</creator><creator>Benedik, Michael J.</creator><creator>Wood, Thomas K.</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>AAYXX</scope><scope>CITATION</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>201504</creationdate><title>Toxin YafQ increases persister cell formation by reducing indole signalling</title><author>Hu, Ying ; Kwan, Brian W. ; Osbourne, Devon O. ; Benedik, Michael J. ; Wood, Thomas K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4837-da0980930a8dff5985c47e174c362bf7ac6a4ea8c0c158316f32f4ba09ecb693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Antitoxins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Bacterial Toxins - genetics</topic><topic>Bacterial Toxins - metabolism</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - pathogenicity</topic><topic>Escherichia coli Proteins - genetics</topic><topic>Escherichia coli Proteins - metabolism</topic><topic>Indoles - analysis</topic><topic>Manufacturing cells</topic><topic>Metabolism</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Sigma Factor - metabolism</topic><topic>Signal Transduction</topic><topic>Tryptophan - chemistry</topic><topic>Tryptophanase - biosynthesis</topic><topic>Tryptophanase - genetics</topic><topic>Tryptophanase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Ying</creatorcontrib><creatorcontrib>Kwan, Brian W.</creatorcontrib><creatorcontrib>Osbourne, Devon O.</creatorcontrib><creatorcontrib>Benedik, Michael J.</creatorcontrib><creatorcontrib>Wood, Thomas K.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aqualine</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Oceanic Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Water Resources Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Environmental microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Ying</au><au>Kwan, Brian W.</au><au>Osbourne, Devon O.</au><au>Benedik, Michael J.</au><au>Wood, Thomas K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Toxin YafQ increases persister cell formation by reducing indole signalling</atitle><jtitle>Environmental microbiology</jtitle><addtitle>Environ Microbiol</addtitle><date>2015-04</date><risdate>2015</risdate><volume>17</volume><issue>4</issue><spage>1275</spage><epage>1285</epage><pages>1275-1285</pages><issn>1462-2912</issn><eissn>1462-2920</eissn><abstract>Summary
Persister cells survive antibiotic and other environmental stresses by slowing metabolism. Since toxins of toxin/antitoxin (TA) systems have been postulated to be responsible for persister cell formation, we investigated the influence of toxin YafQ of the YafQ/DinJ Escherichia coli TA system on persister cell formation. Under stress, YafQ alters metabolism by cleaving transcripts with in‐frame 5′‐AAA‐G/A‐3′ sites. Production of YafQ increased persister cell formation with multiple antibiotics, and by investigating changes in protein expression, we found that YafQ reduced tryptophanase levels (TnaA mRNA has 16 putative YafQ cleavage sites). Consistently, TnaA mRNA levels were also reduced by YafQ. Tryptophanase is activated in the stationary phase by the stationary‐phase sigma factor RpoS, which was also reduced dramatically upon production of YafQ. Tryptophanase converts tryptophan into indole, and as expected, indole levels were reduced by the production of YafQ. Corroborating the effect of YafQ on persistence, addition of indole reduced persistence. Furthermore, persistence increased upon deleting tnaA, and persistence decreased upon adding tryptophan to the medium to increase indole levels. Also, YafQ production had a much smaller effect on persistence in a strain unable to produce indole. Therefore, YafQ increases persistence by reducing indole, and TA systems are related to cell signalling.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>25041421</pmid><doi>10.1111/1462-2920.12567</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antitoxins - genetics Bacterial Proteins - metabolism Bacterial Toxins - genetics Bacterial Toxins - metabolism Escherichia coli Escherichia coli - genetics Escherichia coli - pathogenicity Escherichia coli Proteins - genetics Escherichia coli Proteins - metabolism Indoles - analysis Manufacturing cells Metabolism RNA, Messenger - genetics RNA, Messenger - metabolism Sigma Factor - metabolism Signal Transduction Tryptophan - chemistry Tryptophanase - biosynthesis Tryptophanase - genetics Tryptophanase - metabolism |
title | Toxin YafQ increases persister cell formation by reducing indole signalling |
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