Murine macrophage transcriptional and functional responses to Bacillus anthracis edema toxin
Edema toxin (EdTx), which is a combination of edema factor and a binding moiety (protective antigen), is produced by Bacillus anthracis, the etiological agent of anthrax. EdTx is an adenylyl cyclase enzyme that converts adenosine triphosphate to adenosine-3′,5′-monophosphate, resulting in interstiti...
Gespeichert in:
Veröffentlicht in: | Microbial pathogenesis 2006-08, Vol.41 (2), p.96-110 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 110 |
---|---|
container_issue | 2 |
container_start_page | 96 |
container_title | Microbial pathogenesis |
container_volume | 41 |
creator | Comer, Jason E. Galindo, Cristi L. Zhang, Fan Wenglikowski, Autumn M. Bush, Katie L. Garner, Harold R. Peterson, Johnny W. Chopra, Ashok K. |
description | Edema toxin (EdTx), which is a combination of edema factor and a binding moiety (protective antigen), is produced by
Bacillus anthracis, the etiological agent of anthrax. EdTx is an adenylyl cyclase enzyme that converts adenosine triphosphate to adenosine-3′,5′-monophosphate, resulting in interstitial edema seen in anthrax patients. We used GeneChip analysis to examine global transcriptional profiles of EdTx-treated RAW 264.7 murine macrophage-like cells and identified 71 and 259 genes whose expression was significantly altered by the toxin at 3 and 6
h, respectively. Alteration in the expression levels of selected genes was confirmed by real time-reverse transcriptase polymerase chain reaction. The genes with up-regulated expression in macrophages in response to EdTx-treatment were known to be involved in inflammatory responses, regulation of apoptosis, adhesion, immune cell activation, and transcription regulation. Additionally, GeneChip analysis results implied that EdTx-induced activation of activator protein-1 (AP-1) and CAAAT/enhancer-binding protein-beta (C/EBP-
β). Gel shift assays were therefore performed, and an increase in the activities of both of these transcription factors was observed within 30
min. EdTx also inhibited tumor necrosis factor alpha production and crippled the phagocytic ability of the macrophages. This is the first report detailing the host cell global transcriptional responses to EdTx. |
doi_str_mv | 10.1016/j.micpath.2006.05.001 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68762792</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0882401006000751</els_id><sourcerecordid>68762792</sourcerecordid><originalsourceid>FETCH-LOGICAL-c424t-f5aa1b6940f12efbacd70f952c7404a9090a5178b852ec4d752478843b288d843</originalsourceid><addsrcrecordid>eNqFkM1u1TAQRi0EoreFRwBlA7uEsWM7zgrRCgpSERvYIVkTZ8L1VeIEO0Hw9ri6kbrsavRpzvzoMPaKQ8WB63enavJuwfVYCQBdgaoA-BN24NDqkgswT9kBjBGlBA4X7DKlEwC0sm6fswuujdQN1wf28-sWfaBiQhfn5Yi_qFgjhuSiX1Y_BxwLDH0xbMHtMVJa5pAoFetcXKPz47ilDK3HmEMqqKcJc--vDy_YswHHRC_3esV-fPr4_eZzefft9svNh7vSSSHXclCIvNOthIELGjp0fQNDq4RrJEhsoQVUvDGdUYKc7BslZGOMrDthTJ_rFXt73rvE-fdGabWTT47GEQPNW7LaNFo0rXgU5G1dK9A6g-oMZispRRrsEv2E8Z_lYO_925Pd_dt7_xaUzf7z3Ov9wNZN1D9M7cIz8GYHMDkch-w6S3vgDGhRg8nc-zNH2dsfT9Em5yk46n0kt9p-9o-88h-G8ab1</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19335066</pqid></control><display><type>article</type><title>Murine macrophage transcriptional and functional responses to Bacillus anthracis edema toxin</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Comer, Jason E. ; Galindo, Cristi L. ; Zhang, Fan ; Wenglikowski, Autumn M. ; Bush, Katie L. ; Garner, Harold R. ; Peterson, Johnny W. ; Chopra, Ashok K.</creator><creatorcontrib>Comer, Jason E. ; Galindo, Cristi L. ; Zhang, Fan ; Wenglikowski, Autumn M. ; Bush, Katie L. ; Garner, Harold R. ; Peterson, Johnny W. ; Chopra, Ashok K.</creatorcontrib><description>Edema toxin (EdTx), which is a combination of edema factor and a binding moiety (protective antigen), is produced by
Bacillus anthracis, the etiological agent of anthrax. EdTx is an adenylyl cyclase enzyme that converts adenosine triphosphate to adenosine-3′,5′-monophosphate, resulting in interstitial edema seen in anthrax patients. We used GeneChip analysis to examine global transcriptional profiles of EdTx-treated RAW 264.7 murine macrophage-like cells and identified 71 and 259 genes whose expression was significantly altered by the toxin at 3 and 6
h, respectively. Alteration in the expression levels of selected genes was confirmed by real time-reverse transcriptase polymerase chain reaction. The genes with up-regulated expression in macrophages in response to EdTx-treatment were known to be involved in inflammatory responses, regulation of apoptosis, adhesion, immune cell activation, and transcription regulation. Additionally, GeneChip analysis results implied that EdTx-induced activation of activator protein-1 (AP-1) and CAAAT/enhancer-binding protein-beta (C/EBP-
β). Gel shift assays were therefore performed, and an increase in the activities of both of these transcription factors was observed within 30
min. EdTx also inhibited tumor necrosis factor alpha production and crippled the phagocytic ability of the macrophages. This is the first report detailing the host cell global transcriptional responses to EdTx.</description><identifier>ISSN: 0882-4010</identifier><identifier>EISSN: 1096-1208</identifier><identifier>DOI: 10.1016/j.micpath.2006.05.001</identifier><identifier>PMID: 16846716</identifier><identifier>CODEN: MIPAEV</identifier><language>eng</language><publisher>Oxford: Elsevier India Pvt Ltd</publisher><subject>Animals ; Antigens, Bacterial - pharmacology ; Bacillus anthracis ; Bacillus anthracis - genetics ; Bacillus anthracis - metabolism ; Bacterial Infections - microbiology ; Bacterial Toxins - pharmacology ; Biological and medical sciences ; cAMP ; CCAAT-Enhancer-Binding Protein-beta - biosynthesis ; CCAAT-Enhancer-Binding Protein-beta - genetics ; Cyclic AMP - metabolism ; Cytokine production ; Cytokines - biosynthesis ; Cytokines - genetics ; Edema toxin ; Fundamental and applied biological sciences. Psychology ; Gel shift ; Macrophages ; Macrophages - drug effects ; Macrophages - metabolism ; Macrophages - physiology ; Mice ; Microarray Analysis - methods ; Microarrays ; Microbiology ; Phagocytes - immunology ; Phagocytes - metabolism ; Phagocytosis ; Polymerase Chain Reaction - methods ; Transcription Factor AP-1 - biosynthesis ; Transcription Factor AP-1 - genetics ; Transcription Factors - biosynthesis ; Transcription Factors - genetics ; Transcription, Genetic - drug effects ; Up-Regulation - drug effects</subject><ispartof>Microbial pathogenesis, 2006-08, Vol.41 (2), p.96-110</ispartof><rights>2006 Elsevier Ltd</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-f5aa1b6940f12efbacd70f952c7404a9090a5178b852ec4d752478843b288d843</citedby><cites>FETCH-LOGICAL-c424t-f5aa1b6940f12efbacd70f952c7404a9090a5178b852ec4d752478843b288d843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.micpath.2006.05.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18062308$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16846716$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Comer, Jason E.</creatorcontrib><creatorcontrib>Galindo, Cristi L.</creatorcontrib><creatorcontrib>Zhang, Fan</creatorcontrib><creatorcontrib>Wenglikowski, Autumn M.</creatorcontrib><creatorcontrib>Bush, Katie L.</creatorcontrib><creatorcontrib>Garner, Harold R.</creatorcontrib><creatorcontrib>Peterson, Johnny W.</creatorcontrib><creatorcontrib>Chopra, Ashok K.</creatorcontrib><title>Murine macrophage transcriptional and functional responses to Bacillus anthracis edema toxin</title><title>Microbial pathogenesis</title><addtitle>Microb Pathog</addtitle><description>Edema toxin (EdTx), which is a combination of edema factor and a binding moiety (protective antigen), is produced by
Bacillus anthracis, the etiological agent of anthrax. EdTx is an adenylyl cyclase enzyme that converts adenosine triphosphate to adenosine-3′,5′-monophosphate, resulting in interstitial edema seen in anthrax patients. We used GeneChip analysis to examine global transcriptional profiles of EdTx-treated RAW 264.7 murine macrophage-like cells and identified 71 and 259 genes whose expression was significantly altered by the toxin at 3 and 6
h, respectively. Alteration in the expression levels of selected genes was confirmed by real time-reverse transcriptase polymerase chain reaction. The genes with up-regulated expression in macrophages in response to EdTx-treatment were known to be involved in inflammatory responses, regulation of apoptosis, adhesion, immune cell activation, and transcription regulation. Additionally, GeneChip analysis results implied that EdTx-induced activation of activator protein-1 (AP-1) and CAAAT/enhancer-binding protein-beta (C/EBP-
β). Gel shift assays were therefore performed, and an increase in the activities of both of these transcription factors was observed within 30
min. EdTx also inhibited tumor necrosis factor alpha production and crippled the phagocytic ability of the macrophages. This is the first report detailing the host cell global transcriptional responses to EdTx.</description><subject>Animals</subject><subject>Antigens, Bacterial - pharmacology</subject><subject>Bacillus anthracis</subject><subject>Bacillus anthracis - genetics</subject><subject>Bacillus anthracis - metabolism</subject><subject>Bacterial Infections - microbiology</subject><subject>Bacterial Toxins - pharmacology</subject><subject>Biological and medical sciences</subject><subject>cAMP</subject><subject>CCAAT-Enhancer-Binding Protein-beta - biosynthesis</subject><subject>CCAAT-Enhancer-Binding Protein-beta - genetics</subject><subject>Cyclic AMP - metabolism</subject><subject>Cytokine production</subject><subject>Cytokines - biosynthesis</subject><subject>Cytokines - genetics</subject><subject>Edema toxin</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gel shift</subject><subject>Macrophages</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - metabolism</subject><subject>Macrophages - physiology</subject><subject>Mice</subject><subject>Microarray Analysis - methods</subject><subject>Microarrays</subject><subject>Microbiology</subject><subject>Phagocytes - immunology</subject><subject>Phagocytes - metabolism</subject><subject>Phagocytosis</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Transcription Factor AP-1 - biosynthesis</subject><subject>Transcription Factor AP-1 - genetics</subject><subject>Transcription Factors - biosynthesis</subject><subject>Transcription Factors - genetics</subject><subject>Transcription, Genetic - drug effects</subject><subject>Up-Regulation - drug effects</subject><issn>0882-4010</issn><issn>1096-1208</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1u1TAQRi0EoreFRwBlA7uEsWM7zgrRCgpSERvYIVkTZ8L1VeIEO0Hw9ri6kbrsavRpzvzoMPaKQ8WB63enavJuwfVYCQBdgaoA-BN24NDqkgswT9kBjBGlBA4X7DKlEwC0sm6fswuujdQN1wf28-sWfaBiQhfn5Yi_qFgjhuSiX1Y_BxwLDH0xbMHtMVJa5pAoFetcXKPz47ilDK3HmEMqqKcJc--vDy_YswHHRC_3esV-fPr4_eZzefft9svNh7vSSSHXclCIvNOthIELGjp0fQNDq4RrJEhsoQVUvDGdUYKc7BslZGOMrDthTJ_rFXt73rvE-fdGabWTT47GEQPNW7LaNFo0rXgU5G1dK9A6g-oMZispRRrsEv2E8Z_lYO_925Pd_dt7_xaUzf7z3Ov9wNZN1D9M7cIz8GYHMDkch-w6S3vgDGhRg8nc-zNH2dsfT9Em5yk46n0kt9p-9o-88h-G8ab1</recordid><startdate>20060801</startdate><enddate>20060801</enddate><creator>Comer, Jason E.</creator><creator>Galindo, Cristi L.</creator><creator>Zhang, Fan</creator><creator>Wenglikowski, Autumn M.</creator><creator>Bush, Katie L.</creator><creator>Garner, Harold R.</creator><creator>Peterson, Johnny W.</creator><creator>Chopra, Ashok K.</creator><general>Elsevier India Pvt Ltd</general><general>Elsevier</general><scope>IQODW</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>7QL</scope><scope>7U7</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20060801</creationdate><title>Murine macrophage transcriptional and functional responses to Bacillus anthracis edema toxin</title><author>Comer, Jason E. ; Galindo, Cristi L. ; Zhang, Fan ; Wenglikowski, Autumn M. ; Bush, Katie L. ; Garner, Harold R. ; Peterson, Johnny W. ; Chopra, Ashok K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c424t-f5aa1b6940f12efbacd70f952c7404a9090a5178b852ec4d752478843b288d843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Antigens, Bacterial - pharmacology</topic><topic>Bacillus anthracis</topic><topic>Bacillus anthracis - genetics</topic><topic>Bacillus anthracis - metabolism</topic><topic>Bacterial Infections - microbiology</topic><topic>Bacterial Toxins - pharmacology</topic><topic>Biological and medical sciences</topic><topic>cAMP</topic><topic>CCAAT-Enhancer-Binding Protein-beta - biosynthesis</topic><topic>CCAAT-Enhancer-Binding Protein-beta - genetics</topic><topic>Cyclic AMP - metabolism</topic><topic>Cytokine production</topic><topic>Cytokines - biosynthesis</topic><topic>Cytokines - genetics</topic><topic>Edema toxin</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gel shift</topic><topic>Macrophages</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - metabolism</topic><topic>Macrophages - physiology</topic><topic>Mice</topic><topic>Microarray Analysis - methods</topic><topic>Microarrays</topic><topic>Microbiology</topic><topic>Phagocytes - immunology</topic><topic>Phagocytes - metabolism</topic><topic>Phagocytosis</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Transcription Factor AP-1 - biosynthesis</topic><topic>Transcription Factor AP-1 - genetics</topic><topic>Transcription Factors - biosynthesis</topic><topic>Transcription Factors - genetics</topic><topic>Transcription, Genetic - drug effects</topic><topic>Up-Regulation - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Comer, Jason E.</creatorcontrib><creatorcontrib>Galindo, Cristi L.</creatorcontrib><creatorcontrib>Zhang, Fan</creatorcontrib><creatorcontrib>Wenglikowski, Autumn M.</creatorcontrib><creatorcontrib>Bush, Katie L.</creatorcontrib><creatorcontrib>Garner, Harold R.</creatorcontrib><creatorcontrib>Peterson, Johnny W.</creatorcontrib><creatorcontrib>Chopra, Ashok K.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Microbial pathogenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Comer, Jason E.</au><au>Galindo, Cristi L.</au><au>Zhang, Fan</au><au>Wenglikowski, Autumn M.</au><au>Bush, Katie L.</au><au>Garner, Harold R.</au><au>Peterson, Johnny W.</au><au>Chopra, Ashok K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Murine macrophage transcriptional and functional responses to Bacillus anthracis edema toxin</atitle><jtitle>Microbial pathogenesis</jtitle><addtitle>Microb Pathog</addtitle><date>2006-08-01</date><risdate>2006</risdate><volume>41</volume><issue>2</issue><spage>96</spage><epage>110</epage><pages>96-110</pages><issn>0882-4010</issn><eissn>1096-1208</eissn><coden>MIPAEV</coden><abstract>Edema toxin (EdTx), which is a combination of edema factor and a binding moiety (protective antigen), is produced by
Bacillus anthracis, the etiological agent of anthrax. EdTx is an adenylyl cyclase enzyme that converts adenosine triphosphate to adenosine-3′,5′-monophosphate, resulting in interstitial edema seen in anthrax patients. We used GeneChip analysis to examine global transcriptional profiles of EdTx-treated RAW 264.7 murine macrophage-like cells and identified 71 and 259 genes whose expression was significantly altered by the toxin at 3 and 6
h, respectively. Alteration in the expression levels of selected genes was confirmed by real time-reverse transcriptase polymerase chain reaction. The genes with up-regulated expression in macrophages in response to EdTx-treatment were known to be involved in inflammatory responses, regulation of apoptosis, adhesion, immune cell activation, and transcription regulation. Additionally, GeneChip analysis results implied that EdTx-induced activation of activator protein-1 (AP-1) and CAAAT/enhancer-binding protein-beta (C/EBP-
β). Gel shift assays were therefore performed, and an increase in the activities of both of these transcription factors was observed within 30
min. EdTx also inhibited tumor necrosis factor alpha production and crippled the phagocytic ability of the macrophages. This is the first report detailing the host cell global transcriptional responses to EdTx.</abstract><cop>Oxford</cop><pub>Elsevier India Pvt Ltd</pub><pmid>16846716</pmid><doi>10.1016/j.micpath.2006.05.001</doi><tpages>15</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0882-4010 |
ispartof | Microbial pathogenesis, 2006-08, Vol.41 (2), p.96-110 |
issn | 0882-4010 1096-1208 |
language | eng |
recordid | cdi_proquest_miscellaneous_68762792 |
source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Animals Antigens, Bacterial - pharmacology Bacillus anthracis Bacillus anthracis - genetics Bacillus anthracis - metabolism Bacterial Infections - microbiology Bacterial Toxins - pharmacology Biological and medical sciences cAMP CCAAT-Enhancer-Binding Protein-beta - biosynthesis CCAAT-Enhancer-Binding Protein-beta - genetics Cyclic AMP - metabolism Cytokine production Cytokines - biosynthesis Cytokines - genetics Edema toxin Fundamental and applied biological sciences. Psychology Gel shift Macrophages Macrophages - drug effects Macrophages - metabolism Macrophages - physiology Mice Microarray Analysis - methods Microarrays Microbiology Phagocytes - immunology Phagocytes - metabolism Phagocytosis Polymerase Chain Reaction - methods Transcription Factor AP-1 - biosynthesis Transcription Factor AP-1 - genetics Transcription Factors - biosynthesis Transcription Factors - genetics Transcription, Genetic - drug effects Up-Regulation - drug effects |
title | Murine macrophage transcriptional and functional responses to Bacillus anthracis edema toxin |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T08%3A28%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Murine%20macrophage%20transcriptional%20and%20functional%20responses%20to%20Bacillus%20anthracis%20edema%20toxin&rft.jtitle=Microbial%20pathogenesis&rft.au=Comer,%20Jason%20E.&rft.date=2006-08-01&rft.volume=41&rft.issue=2&rft.spage=96&rft.epage=110&rft.pages=96-110&rft.issn=0882-4010&rft.eissn=1096-1208&rft.coden=MIPAEV&rft_id=info:doi/10.1016/j.micpath.2006.05.001&rft_dat=%3Cproquest_cross%3E68762792%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=19335066&rft_id=info:pmid/16846716&rft_els_id=S0882401006000751&rfr_iscdi=true |