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The multicopy sRNA LhrC controls expression of the oligopeptide-binding protein OppA in Listeria monocytogenes
Listeria monocytogenes is the causative agent of the foodborne disease listeriosis. During infection, L. monocytogenes produces an array of non-coding RNAs, including the multicopy sRNA LhrC. These five, nearly identical sRNAs are highly induced in response to cell envelope stress and target the vir...
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Published in: | RNA biology 2015-09, Vol.12 (9), p.985-997 |
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creator | Sievers, Susanne Lund, Anja Menendez-Gil, Pilar Nielsen, Aaraby Storm Mollerup, Maria Lambert Nielsen, Stine Buch Larsson, Pernille Borch-Jensen, Jonas Johansson, Jörgen Kallipolitis, Birgitte Haahr |
description | Listeria monocytogenes is the causative agent of the foodborne disease listeriosis. During infection, L. monocytogenes produces an array of non-coding RNAs, including the multicopy sRNA LhrC. These five, nearly identical sRNAs are highly induced in response to cell envelope stress and target the virulence adhesin lapB at the post-transcriptional level. Here, we demonstrate that LhrC controls expression of additional genes encoding cell envelope-associated proteins with virulence function. Using transcriptomics and proteomics, we identified a set of genes affected by LhrC in response to cell envelope stress. Three targets were significantly down-regulated by LhrC at both the RNA and protein level: lmo2349, tcsA and oppA. All three genes encode membrane-associated proteins: A putative substrate binding protein of an amino acid ABC transporter (Lmo2349); the CD4+ T cell-stimulating antigen TcsA, and the oligopeptide binding protein OppA, of which the latter 2 are required for full virulence of L. monocytogenes. For OppA, we show that LhrC acts by direct base paring to the ribosome binding site of the oppA mRNA, leading to an impediment of its translation and a decreased mRNA level. The sRNA-mRNA interaction depends on 2 of 3 CU-rich regions in LhrC allowing binding of 2 oppA mRNAs to a single LhrC molecule. Finally, we found that LhrC contributes to infection in macrophage-like cells. These findings demonstrate a central role for LhrC in controlling the level of OppA and other virulence-associated cell envelope proteins in response to cell envelope stress. |
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During infection, L. monocytogenes produces an array of non-coding RNAs, including the multicopy sRNA LhrC. These five, nearly identical sRNAs are highly induced in response to cell envelope stress and target the virulence adhesin lapB at the post-transcriptional level. Here, we demonstrate that LhrC controls expression of additional genes encoding cell envelope-associated proteins with virulence function. Using transcriptomics and proteomics, we identified a set of genes affected by LhrC in response to cell envelope stress. Three targets were significantly down-regulated by LhrC at both the RNA and protein level: lmo2349, tcsA and oppA. All three genes encode membrane-associated proteins: A putative substrate binding protein of an amino acid ABC transporter (Lmo2349); the CD4+ T cell-stimulating antigen TcsA, and the oligopeptide binding protein OppA, of which the latter 2 are required for full virulence of L. monocytogenes. For OppA, we show that LhrC acts by direct base paring to the ribosome binding site of the oppA mRNA, leading to an impediment of its translation and a decreased mRNA level. The sRNA-mRNA interaction depends on 2 of 3 CU-rich regions in LhrC allowing binding of 2 oppA mRNAs to a single LhrC molecule. Finally, we found that LhrC contributes to infection in macrophage-like cells. These findings demonstrate a central role for LhrC in controlling the level of OppA and other virulence-associated cell envelope proteins in response to cell envelope stress.</description><identifier>ISSN: 1547-6286</identifier><identifier>ISSN: 1555-8584</identifier><identifier>EISSN: 1555-8584</identifier><identifier>DOI: 10.1080/15476286.2015.1071011</identifier><identifier>PMID: 26176322</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>ABC transporters ; adhesins ; amino acids ; Animals ; antigens ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Base Sequence ; Binding Sites ; Carrier Proteins - genetics ; Carrier Proteins - metabolism ; cell envelope stress ; etiological agents ; foodborne illness ; Gene Dosage ; gene expression ; Gene Expression Profiling ; gene expression regulation ; Gene Expression Regulation, Bacterial ; genes ; Lipoproteins - genetics ; Lipoproteins - metabolism ; Listeria monocytogenes ; Listeria monocytogenes - genetics ; Listeria monocytogenes - metabolism ; listeriosis ; Macrophages - microbiology ; messenger RNA ; Mice ; Mutation ; non-coding RNA ; Nucleic Acid Conformation ; Nucleotide Motifs ; oligopeptides ; Operon ; protein content ; Proteome ; proteomics ; Proteomics - methods ; Research Paper ; ribosomes ; RNA, Messenger - chemistry ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; RNA, Small Untranslated - chemistry ; RNA, Small Untranslated - genetics ; RNA, Small Untranslated - metabolism ; sRNA ; Stress, Physiological - genetics ; Transcriptome ; transcriptomics ; translation (genetics) ; virulence</subject><ispartof>RNA biology, 2015-09, Vol.12 (9), p.985-997</ispartof><rights>2015 Taylor & Francis Group, LLC 2015</rights><rights>2015 Taylor & Francis Group, LLC 2015 Taylor & Francis Group, LLC</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c492t-87f065958a488a08d995ab7e64d5f3f3baa8b0d13a57474d9f634317ce954fc83</citedby><cites>FETCH-LOGICAL-c492t-87f065958a488a08d995ab7e64d5f3f3baa8b0d13a57474d9f634317ce954fc83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615310/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615310/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26176322$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-110203$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Sievers, Susanne</creatorcontrib><creatorcontrib>Lund, Anja</creatorcontrib><creatorcontrib>Menendez-Gil, Pilar</creatorcontrib><creatorcontrib>Nielsen, Aaraby</creatorcontrib><creatorcontrib>Storm Mollerup, Maria</creatorcontrib><creatorcontrib>Lambert Nielsen, Stine</creatorcontrib><creatorcontrib>Buch Larsson, Pernille</creatorcontrib><creatorcontrib>Borch-Jensen, Jonas</creatorcontrib><creatorcontrib>Johansson, Jörgen</creatorcontrib><creatorcontrib>Kallipolitis, Birgitte Haahr</creatorcontrib><title>The multicopy sRNA LhrC controls expression of the oligopeptide-binding protein OppA in Listeria monocytogenes</title><title>RNA biology</title><addtitle>RNA Biol</addtitle><description>Listeria monocytogenes is the causative agent of the foodborne disease listeriosis. During infection, L. monocytogenes produces an array of non-coding RNAs, including the multicopy sRNA LhrC. These five, nearly identical sRNAs are highly induced in response to cell envelope stress and target the virulence adhesin lapB at the post-transcriptional level. Here, we demonstrate that LhrC controls expression of additional genes encoding cell envelope-associated proteins with virulence function. Using transcriptomics and proteomics, we identified a set of genes affected by LhrC in response to cell envelope stress. Three targets were significantly down-regulated by LhrC at both the RNA and protein level: lmo2349, tcsA and oppA. All three genes encode membrane-associated proteins: A putative substrate binding protein of an amino acid ABC transporter (Lmo2349); the CD4+ T cell-stimulating antigen TcsA, and the oligopeptide binding protein OppA, of which the latter 2 are required for full virulence of L. monocytogenes. For OppA, we show that LhrC acts by direct base paring to the ribosome binding site of the oppA mRNA, leading to an impediment of its translation and a decreased mRNA level. The sRNA-mRNA interaction depends on 2 of 3 CU-rich regions in LhrC allowing binding of 2 oppA mRNAs to a single LhrC molecule. Finally, we found that LhrC contributes to infection in macrophage-like cells. These findings demonstrate a central role for LhrC in controlling the level of OppA and other virulence-associated cell envelope proteins in response to cell envelope stress.</description><subject>ABC transporters</subject><subject>adhesins</subject><subject>amino acids</subject><subject>Animals</subject><subject>antigens</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Base Sequence</subject><subject>Binding Sites</subject><subject>Carrier Proteins - genetics</subject><subject>Carrier Proteins - metabolism</subject><subject>cell envelope stress</subject><subject>etiological agents</subject><subject>foodborne illness</subject><subject>Gene Dosage</subject><subject>gene expression</subject><subject>Gene Expression Profiling</subject><subject>gene expression regulation</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>genes</subject><subject>Lipoproteins - genetics</subject><subject>Lipoproteins - metabolism</subject><subject>Listeria monocytogenes</subject><subject>Listeria monocytogenes - genetics</subject><subject>Listeria monocytogenes - metabolism</subject><subject>listeriosis</subject><subject>Macrophages - microbiology</subject><subject>messenger RNA</subject><subject>Mice</subject><subject>Mutation</subject><subject>non-coding RNA</subject><subject>Nucleic Acid Conformation</subject><subject>Nucleotide Motifs</subject><subject>oligopeptides</subject><subject>Operon</subject><subject>protein content</subject><subject>Proteome</subject><subject>proteomics</subject><subject>Proteomics - methods</subject><subject>Research Paper</subject><subject>ribosomes</subject><subject>RNA, Messenger - chemistry</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>RNA, Small Untranslated - chemistry</subject><subject>RNA, Small Untranslated - genetics</subject><subject>RNA, Small Untranslated - metabolism</subject><subject>sRNA</subject><subject>Stress, Physiological - genetics</subject><subject>Transcriptome</subject><subject>transcriptomics</subject><subject>translation (genetics)</subject><subject>virulence</subject><issn>1547-6286</issn><issn>1555-8584</issn><issn>1555-8584</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFkktv1DAUhSMEoqXwE0Beskmx4_cGMRqe0ohKqLC1HMeeMUrsYDst8-_xaKYV3cDqWr7fOfbVPU3zEsFLBAV8gyjhrBPssoOI1iuOIEKPmnNEKW0FFeTx4Ux4e4DOmmc5_4QQMyHp0-asY4gz3HXnTbjeWTAtY_EmznuQv31dgc0urYGJoaQ4ZmB_z8nm7GMA0YFS8Tj6bZztXPxg296HwYctmFMs1gdwNc8rUOvG52KT12CKIZp9iVsbbH7ePHF6zPbFqV403z9-uF5_bjdXn76sV5vWENmVVnAHGZVUaCKEhmKQkuqeW0YG6rDDvdaihwPCmnLCySAdwwQjbqykxBmBL5r26Jtv7bz0ak5-0mmvovbqvf-xUjFt1TItCiHYQVz5t0e-wpMdjK3D6_GB7GEn-J3axhtFGKIYwWrw-mSQ4q_F5qImn40dRx1sXLLqCIFMdoiI_6KIIywpxpJXlB5Rk2LOybr7HyGoDjFQdzFQhxioUwyq7tXf49yr7vZegXdHwAcX06RvYxoHVfR-jMklHYzPCv_7jT-UEsOr</recordid><startdate>20150902</startdate><enddate>20150902</enddate><creator>Sievers, Susanne</creator><creator>Lund, Anja</creator><creator>Menendez-Gil, Pilar</creator><creator>Nielsen, Aaraby</creator><creator>Storm Mollerup, Maria</creator><creator>Lambert Nielsen, Stine</creator><creator>Buch Larsson, Pernille</creator><creator>Borch-Jensen, Jonas</creator><creator>Johansson, Jörgen</creator><creator>Kallipolitis, Birgitte Haahr</creator><general>Taylor & Francis</general><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>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D93</scope></search><sort><creationdate>20150902</creationdate><title>The multicopy sRNA LhrC controls expression of the oligopeptide-binding protein OppA in Listeria monocytogenes</title><author>Sievers, Susanne ; Lund, Anja ; Menendez-Gil, Pilar ; Nielsen, Aaraby ; Storm Mollerup, Maria ; Lambert Nielsen, Stine ; Buch Larsson, Pernille ; Borch-Jensen, Jonas ; Johansson, Jörgen ; Kallipolitis, Birgitte Haahr</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c492t-87f065958a488a08d995ab7e64d5f3f3baa8b0d13a57474d9f634317ce954fc83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>ABC transporters</topic><topic>adhesins</topic><topic>amino acids</topic><topic>Animals</topic><topic>antigens</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Base Sequence</topic><topic>Binding Sites</topic><topic>Carrier Proteins - genetics</topic><topic>Carrier Proteins - metabolism</topic><topic>cell envelope stress</topic><topic>etiological agents</topic><topic>foodborne illness</topic><topic>Gene Dosage</topic><topic>gene expression</topic><topic>Gene Expression Profiling</topic><topic>gene expression regulation</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>genes</topic><topic>Lipoproteins - genetics</topic><topic>Lipoproteins - metabolism</topic><topic>Listeria monocytogenes</topic><topic>Listeria monocytogenes - genetics</topic><topic>Listeria monocytogenes - metabolism</topic><topic>listeriosis</topic><topic>Macrophages - microbiology</topic><topic>messenger RNA</topic><topic>Mice</topic><topic>Mutation</topic><topic>non-coding RNA</topic><topic>Nucleic Acid Conformation</topic><topic>Nucleotide Motifs</topic><topic>oligopeptides</topic><topic>Operon</topic><topic>protein content</topic><topic>Proteome</topic><topic>proteomics</topic><topic>Proteomics - methods</topic><topic>Research Paper</topic><topic>ribosomes</topic><topic>RNA, Messenger - chemistry</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>RNA, Small Untranslated - chemistry</topic><topic>RNA, Small Untranslated - genetics</topic><topic>RNA, Small Untranslated - metabolism</topic><topic>sRNA</topic><topic>Stress, Physiological - genetics</topic><topic>Transcriptome</topic><topic>transcriptomics</topic><topic>translation (genetics)</topic><topic>virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sievers, Susanne</creatorcontrib><creatorcontrib>Lund, Anja</creatorcontrib><creatorcontrib>Menendez-Gil, Pilar</creatorcontrib><creatorcontrib>Nielsen, Aaraby</creatorcontrib><creatorcontrib>Storm Mollerup, Maria</creatorcontrib><creatorcontrib>Lambert Nielsen, Stine</creatorcontrib><creatorcontrib>Buch Larsson, Pernille</creatorcontrib><creatorcontrib>Borch-Jensen, Jonas</creatorcontrib><creatorcontrib>Johansson, Jörgen</creatorcontrib><creatorcontrib>Kallipolitis, Birgitte Haahr</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Umeå universitet</collection><jtitle>RNA biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sievers, Susanne</au><au>Lund, Anja</au><au>Menendez-Gil, Pilar</au><au>Nielsen, Aaraby</au><au>Storm Mollerup, Maria</au><au>Lambert Nielsen, Stine</au><au>Buch Larsson, Pernille</au><au>Borch-Jensen, Jonas</au><au>Johansson, Jörgen</au><au>Kallipolitis, Birgitte Haahr</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The multicopy sRNA LhrC controls expression of the oligopeptide-binding protein OppA in Listeria monocytogenes</atitle><jtitle>RNA biology</jtitle><addtitle>RNA Biol</addtitle><date>2015-09-02</date><risdate>2015</risdate><volume>12</volume><issue>9</issue><spage>985</spage><epage>997</epage><pages>985-997</pages><issn>1547-6286</issn><issn>1555-8584</issn><eissn>1555-8584</eissn><abstract>Listeria monocytogenes is the causative agent of the foodborne disease listeriosis. During infection, L. monocytogenes produces an array of non-coding RNAs, including the multicopy sRNA LhrC. These five, nearly identical sRNAs are highly induced in response to cell envelope stress and target the virulence adhesin lapB at the post-transcriptional level. Here, we demonstrate that LhrC controls expression of additional genes encoding cell envelope-associated proteins with virulence function. Using transcriptomics and proteomics, we identified a set of genes affected by LhrC in response to cell envelope stress. Three targets were significantly down-regulated by LhrC at both the RNA and protein level: lmo2349, tcsA and oppA. All three genes encode membrane-associated proteins: A putative substrate binding protein of an amino acid ABC transporter (Lmo2349); the CD4+ T cell-stimulating antigen TcsA, and the oligopeptide binding protein OppA, of which the latter 2 are required for full virulence of L. monocytogenes. For OppA, we show that LhrC acts by direct base paring to the ribosome binding site of the oppA mRNA, leading to an impediment of its translation and a decreased mRNA level. The sRNA-mRNA interaction depends on 2 of 3 CU-rich regions in LhrC allowing binding of 2 oppA mRNAs to a single LhrC molecule. Finally, we found that LhrC contributes to infection in macrophage-like cells. These findings demonstrate a central role for LhrC in controlling the level of OppA and other virulence-associated cell envelope proteins in response to cell envelope stress.</abstract><cop>United States</cop><pub>Taylor & Francis</pub><pmid>26176322</pmid><doi>10.1080/15476286.2015.1071011</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | ABC transporters adhesins amino acids Animals antigens Bacterial Proteins - genetics Bacterial Proteins - metabolism Base Sequence Binding Sites Carrier Proteins - genetics Carrier Proteins - metabolism cell envelope stress etiological agents foodborne illness Gene Dosage gene expression Gene Expression Profiling gene expression regulation Gene Expression Regulation, Bacterial genes Lipoproteins - genetics Lipoproteins - metabolism Listeria monocytogenes Listeria monocytogenes - genetics Listeria monocytogenes - metabolism listeriosis Macrophages - microbiology messenger RNA Mice Mutation non-coding RNA Nucleic Acid Conformation Nucleotide Motifs oligopeptides Operon protein content Proteome proteomics Proteomics - methods Research Paper ribosomes RNA, Messenger - chemistry RNA, Messenger - genetics RNA, Messenger - metabolism RNA, Small Untranslated - chemistry RNA, Small Untranslated - genetics RNA, Small Untranslated - metabolism sRNA Stress, Physiological - genetics Transcriptome transcriptomics translation (genetics) virulence |
title | The multicopy sRNA LhrC controls expression of the oligopeptide-binding protein OppA in Listeria monocytogenes |
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