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...

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Veröffentlicht in:Microbial pathogenesis 2006-08, Vol.41 (2), p.96-110
Hauptverfasser: Comer, Jason E., Galindo, Cristi L., Zhang, Fan, Wenglikowski, Autumn M., Bush, Katie L., Garner, Harold R., Peterson, Johnny W., Chopra, Ashok K.
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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
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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. 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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>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=18062308$$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. 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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. 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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>
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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
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