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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
Main Authors: Hu, Ying, Kwan, Brian W., Osbourne, Devon O., Benedik, Michael J., Wood, Thomas K.
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Language:English
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creator Hu, Ying
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Benedik, Michael J.
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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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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 &amp; Sons Ltd</rights><rights>2014 Society for Applied Microbiology and John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2015 Society for Applied Microbiology and John Wiley &amp; 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. 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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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