Orientia tsutsugamushi Is Highly Susceptible to the RNA Polymerase Switch Region Inhibitor Corallopyronin A In Vitro and In Vivo

Scrub typhus is a potentially lethal infection caused by the obligate intracellular bacterium Reports on the emergence of doxycycline-resistant strains highlight the urgent need to develop novel antiinfectives against scrub typhus. Corallopyronin A (CorA) is a novel α-pyrone compound synthesized by...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Antimicrobial agents and chemotherapy 2018-04, Vol.62 (4)
Hauptverfasser: Kock, Fredericke, Hauptmann, Matthias, Osterloh, Anke, Schäberle, Till F, Poppert, Sven, Frickmann, Hagen, Menzel, Klaus-Dieter, Peschel, Gundela, Pfarr, Kenneth, Schiefer, Andrea, König, Gabriele M, Hoerauf, Achim, Fleischer, Bernhard, Keller, Christian
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 4
container_start_page
container_title Antimicrobial agents and chemotherapy
container_volume 62
creator Kock, Fredericke
Hauptmann, Matthias
Osterloh, Anke
Schäberle, Till F
Poppert, Sven
Frickmann, Hagen
Menzel, Klaus-Dieter
Peschel, Gundela
Pfarr, Kenneth
Schiefer, Andrea
König, Gabriele M
Hoerauf, Achim
Fleischer, Bernhard
Keller, Christian
description Scrub typhus is a potentially lethal infection caused by the obligate intracellular bacterium Reports on the emergence of doxycycline-resistant strains highlight the urgent need to develop novel antiinfectives against scrub typhus. Corallopyronin A (CorA) is a novel α-pyrone compound synthesized by the myxobacterium that was characterized as a noncompetitive inhibitor of the switch region of the bacterial RNA polymerase (RNAP). We investigated the antimicrobial action of CorA against the human-pathogenic Karp strain of and The MIC of CorA against was remarkably low (0.0078 μg/ml), 16-fold lower than that against In the lethal intraperitoneal mouse infection model, a minimum daily dose of 100 μg CorA protected 100% of infected mice. Two days of treatment were sufficient to confer protection. In contrast to BALB/c mice, SCID mice succumbed to the infection despite treatment with CorA or tetracycline, suggesting that antimicrobial treatment required synergistic action of the adaptive immune response. Similar to tetracycline, CorA did not prevent latent infection of However, latency was not caused by acquisition of antimicrobial resistance, since reisolated from latently infected BALB/c mice remained fully susceptible to CorA. No mutations were found in the CorA-binding regions of the β and β' RNAP subunit genes and Inhibition of the RNAP switch region of by CorA is therefore a novel and highly potent target for antimicrobial therapy for scrub typhus.
doi_str_mv 10.1128/AAC.01732-17
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5913972</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1990488853</sourcerecordid><originalsourceid>FETCH-LOGICAL-a418t-65fc646e3f0f76932342a1cb51d1a0d30b56dda71d7e6d12d4e21a59be40419b3</originalsourceid><addsrcrecordid>eNp1UU1v1DAQtRCILgs3zshHkJri78QXpGhF6UoVRS1wtZzY2bhK7MV2ivbGT8ewpYID0mhGo3l6M28eAC8xOsOYNG_bdnOGcE1JhetHYIWRbCrBpXgMVggJUbEGsRPwLKVbVHou0VNwQiTlDZF8BX5cRWd9dhrmtJTY6XlJo4PbBC_cbpwO8GZJvd1n100W5gDzaOH1xxZ-CtNhtlEnC2--u9yP8NruXPBw60fXuRwi3ISopynsDzF452FbRvCryzFA7c2xuQvPwZNBT8m-uK9r8OX8_efNRXV59WG7aS8rzXCTi6KhF0xYOqChFpISyojGfcexwRoZijoujNE1NrUVBhPDLMGay84yxLDs6Bq8O_Lul262pi-iy3VqH92s40EF7dS_E-9GtQt3iktMZU0Kwet7ghi-LTZlNbvymWnS3oYlKSwlYk3TcFqgp0doH0NK0Q4PazBSv0xTxTT12zRV0hq8OcJ1mom6DUv05RP_w776W8YD8R9H6U9WUKDC</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1990488853</pqid></control><display><type>article</type><title>Orientia tsutsugamushi Is Highly Susceptible to the RNA Polymerase Switch Region Inhibitor Corallopyronin A In Vitro and In Vivo</title><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Kock, Fredericke ; Hauptmann, Matthias ; Osterloh, Anke ; Schäberle, Till F ; Poppert, Sven ; Frickmann, Hagen ; Menzel, Klaus-Dieter ; Peschel, Gundela ; Pfarr, Kenneth ; Schiefer, Andrea ; König, Gabriele M ; Hoerauf, Achim ; Fleischer, Bernhard ; Keller, Christian</creator><creatorcontrib>Kock, Fredericke ; Hauptmann, Matthias ; Osterloh, Anke ; Schäberle, Till F ; Poppert, Sven ; Frickmann, Hagen ; Menzel, Klaus-Dieter ; Peschel, Gundela ; Pfarr, Kenneth ; Schiefer, Andrea ; König, Gabriele M ; Hoerauf, Achim ; Fleischer, Bernhard ; Keller, Christian</creatorcontrib><description>Scrub typhus is a potentially lethal infection caused by the obligate intracellular bacterium Reports on the emergence of doxycycline-resistant strains highlight the urgent need to develop novel antiinfectives against scrub typhus. Corallopyronin A (CorA) is a novel α-pyrone compound synthesized by the myxobacterium that was characterized as a noncompetitive inhibitor of the switch region of the bacterial RNA polymerase (RNAP). We investigated the antimicrobial action of CorA against the human-pathogenic Karp strain of and The MIC of CorA against was remarkably low (0.0078 μg/ml), 16-fold lower than that against In the lethal intraperitoneal mouse infection model, a minimum daily dose of 100 μg CorA protected 100% of infected mice. Two days of treatment were sufficient to confer protection. In contrast to BALB/c mice, SCID mice succumbed to the infection despite treatment with CorA or tetracycline, suggesting that antimicrobial treatment required synergistic action of the adaptive immune response. Similar to tetracycline, CorA did not prevent latent infection of However, latency was not caused by acquisition of antimicrobial resistance, since reisolated from latently infected BALB/c mice remained fully susceptible to CorA. No mutations were found in the CorA-binding regions of the β and β' RNAP subunit genes and Inhibition of the RNAP switch region of by CorA is therefore a novel and highly potent target for antimicrobial therapy for scrub typhus.</description><identifier>ISSN: 0066-4804</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/AAC.01732-17</identifier><identifier>PMID: 29358295</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Anti-Bacterial Agents ; DNA-Directed RNA Polymerases ; Lactones ; Orientia tsutsugamushi ; Scrub Typhus ; Susceptibility</subject><ispartof>Antimicrobial agents and chemotherapy, 2018-04, Vol.62 (4)</ispartof><rights>Copyright © 2018 American Society for Microbiology.</rights><rights>Copyright © 2018 American Society for Microbiology. 2018 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a418t-65fc646e3f0f76932342a1cb51d1a0d30b56dda71d7e6d12d4e21a59be40419b3</citedby><cites>FETCH-LOGICAL-a418t-65fc646e3f0f76932342a1cb51d1a0d30b56dda71d7e6d12d4e21a59be40419b3</cites><orcidid>0000-0003-4873-249X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913972/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913972/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29358295$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kock, Fredericke</creatorcontrib><creatorcontrib>Hauptmann, Matthias</creatorcontrib><creatorcontrib>Osterloh, Anke</creatorcontrib><creatorcontrib>Schäberle, Till F</creatorcontrib><creatorcontrib>Poppert, Sven</creatorcontrib><creatorcontrib>Frickmann, Hagen</creatorcontrib><creatorcontrib>Menzel, Klaus-Dieter</creatorcontrib><creatorcontrib>Peschel, Gundela</creatorcontrib><creatorcontrib>Pfarr, Kenneth</creatorcontrib><creatorcontrib>Schiefer, Andrea</creatorcontrib><creatorcontrib>König, Gabriele M</creatorcontrib><creatorcontrib>Hoerauf, Achim</creatorcontrib><creatorcontrib>Fleischer, Bernhard</creatorcontrib><creatorcontrib>Keller, Christian</creatorcontrib><title>Orientia tsutsugamushi Is Highly Susceptible to the RNA Polymerase Switch Region Inhibitor Corallopyronin A In Vitro and In Vivo</title><title>Antimicrobial agents and chemotherapy</title><addtitle>Antimicrob Agents Chemother</addtitle><addtitle>Antimicrob Agents Chemother</addtitle><description>Scrub typhus is a potentially lethal infection caused by the obligate intracellular bacterium Reports on the emergence of doxycycline-resistant strains highlight the urgent need to develop novel antiinfectives against scrub typhus. Corallopyronin A (CorA) is a novel α-pyrone compound synthesized by the myxobacterium that was characterized as a noncompetitive inhibitor of the switch region of the bacterial RNA polymerase (RNAP). We investigated the antimicrobial action of CorA against the human-pathogenic Karp strain of and The MIC of CorA against was remarkably low (0.0078 μg/ml), 16-fold lower than that against In the lethal intraperitoneal mouse infection model, a minimum daily dose of 100 μg CorA protected 100% of infected mice. Two days of treatment were sufficient to confer protection. In contrast to BALB/c mice, SCID mice succumbed to the infection despite treatment with CorA or tetracycline, suggesting that antimicrobial treatment required synergistic action of the adaptive immune response. Similar to tetracycline, CorA did not prevent latent infection of However, latency was not caused by acquisition of antimicrobial resistance, since reisolated from latently infected BALB/c mice remained fully susceptible to CorA. No mutations were found in the CorA-binding regions of the β and β' RNAP subunit genes and Inhibition of the RNAP switch region of by CorA is therefore a novel and highly potent target for antimicrobial therapy for scrub typhus.</description><subject>Anti-Bacterial Agents</subject><subject>DNA-Directed RNA Polymerases</subject><subject>Lactones</subject><subject>Orientia tsutsugamushi</subject><subject>Scrub Typhus</subject><subject>Susceptibility</subject><issn>0066-4804</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1UU1v1DAQtRCILgs3zshHkJri78QXpGhF6UoVRS1wtZzY2bhK7MV2ivbGT8ewpYID0mhGo3l6M28eAC8xOsOYNG_bdnOGcE1JhetHYIWRbCrBpXgMVggJUbEGsRPwLKVbVHou0VNwQiTlDZF8BX5cRWd9dhrmtJTY6XlJo4PbBC_cbpwO8GZJvd1n100W5gDzaOH1xxZ-CtNhtlEnC2--u9yP8NruXPBw60fXuRwi3ISopynsDzF452FbRvCryzFA7c2xuQvPwZNBT8m-uK9r8OX8_efNRXV59WG7aS8rzXCTi6KhF0xYOqChFpISyojGfcexwRoZijoujNE1NrUVBhPDLMGay84yxLDs6Bq8O_Lul262pi-iy3VqH92s40EF7dS_E-9GtQt3iktMZU0Kwet7ghi-LTZlNbvymWnS3oYlKSwlYk3TcFqgp0doH0NK0Q4PazBSv0xTxTT12zRV0hq8OcJ1mom6DUv05RP_w776W8YD8R9H6U9WUKDC</recordid><startdate>20180401</startdate><enddate>20180401</enddate><creator>Kock, Fredericke</creator><creator>Hauptmann, Matthias</creator><creator>Osterloh, Anke</creator><creator>Schäberle, Till F</creator><creator>Poppert, Sven</creator><creator>Frickmann, Hagen</creator><creator>Menzel, Klaus-Dieter</creator><creator>Peschel, Gundela</creator><creator>Pfarr, Kenneth</creator><creator>Schiefer, Andrea</creator><creator>König, Gabriele M</creator><creator>Hoerauf, Achim</creator><creator>Fleischer, Bernhard</creator><creator>Keller, Christian</creator><general>American Society for Microbiology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4873-249X</orcidid></search><sort><creationdate>20180401</creationdate><title>Orientia tsutsugamushi Is Highly Susceptible to the RNA Polymerase Switch Region Inhibitor Corallopyronin A In Vitro and In Vivo</title><author>Kock, Fredericke ; Hauptmann, Matthias ; Osterloh, Anke ; Schäberle, Till F ; Poppert, Sven ; Frickmann, Hagen ; Menzel, Klaus-Dieter ; Peschel, Gundela ; Pfarr, Kenneth ; Schiefer, Andrea ; König, Gabriele M ; Hoerauf, Achim ; Fleischer, Bernhard ; Keller, Christian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a418t-65fc646e3f0f76932342a1cb51d1a0d30b56dda71d7e6d12d4e21a59be40419b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Anti-Bacterial Agents</topic><topic>DNA-Directed RNA Polymerases</topic><topic>Lactones</topic><topic>Orientia tsutsugamushi</topic><topic>Scrub Typhus</topic><topic>Susceptibility</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kock, Fredericke</creatorcontrib><creatorcontrib>Hauptmann, Matthias</creatorcontrib><creatorcontrib>Osterloh, Anke</creatorcontrib><creatorcontrib>Schäberle, Till F</creatorcontrib><creatorcontrib>Poppert, Sven</creatorcontrib><creatorcontrib>Frickmann, Hagen</creatorcontrib><creatorcontrib>Menzel, Klaus-Dieter</creatorcontrib><creatorcontrib>Peschel, Gundela</creatorcontrib><creatorcontrib>Pfarr, Kenneth</creatorcontrib><creatorcontrib>Schiefer, Andrea</creatorcontrib><creatorcontrib>König, Gabriele M</creatorcontrib><creatorcontrib>Hoerauf, Achim</creatorcontrib><creatorcontrib>Fleischer, Bernhard</creatorcontrib><creatorcontrib>Keller, Christian</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Antimicrobial agents and chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kock, Fredericke</au><au>Hauptmann, Matthias</au><au>Osterloh, Anke</au><au>Schäberle, Till F</au><au>Poppert, Sven</au><au>Frickmann, Hagen</au><au>Menzel, Klaus-Dieter</au><au>Peschel, Gundela</au><au>Pfarr, Kenneth</au><au>Schiefer, Andrea</au><au>König, Gabriele M</au><au>Hoerauf, Achim</au><au>Fleischer, Bernhard</au><au>Keller, Christian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Orientia tsutsugamushi Is Highly Susceptible to the RNA Polymerase Switch Region Inhibitor Corallopyronin A In Vitro and In Vivo</atitle><jtitle>Antimicrobial agents and chemotherapy</jtitle><stitle>Antimicrob Agents Chemother</stitle><addtitle>Antimicrob Agents Chemother</addtitle><date>2018-04-01</date><risdate>2018</risdate><volume>62</volume><issue>4</issue><issn>0066-4804</issn><eissn>1098-6596</eissn><abstract>Scrub typhus is a potentially lethal infection caused by the obligate intracellular bacterium Reports on the emergence of doxycycline-resistant strains highlight the urgent need to develop novel antiinfectives against scrub typhus. Corallopyronin A (CorA) is a novel α-pyrone compound synthesized by the myxobacterium that was characterized as a noncompetitive inhibitor of the switch region of the bacterial RNA polymerase (RNAP). We investigated the antimicrobial action of CorA against the human-pathogenic Karp strain of and The MIC of CorA against was remarkably low (0.0078 μg/ml), 16-fold lower than that against In the lethal intraperitoneal mouse infection model, a minimum daily dose of 100 μg CorA protected 100% of infected mice. Two days of treatment were sufficient to confer protection. In contrast to BALB/c mice, SCID mice succumbed to the infection despite treatment with CorA or tetracycline, suggesting that antimicrobial treatment required synergistic action of the adaptive immune response. Similar to tetracycline, CorA did not prevent latent infection of However, latency was not caused by acquisition of antimicrobial resistance, since reisolated from latently infected BALB/c mice remained fully susceptible to CorA. No mutations were found in the CorA-binding regions of the β and β' RNAP subunit genes and Inhibition of the RNAP switch region of by CorA is therefore a novel and highly potent target for antimicrobial therapy for scrub typhus.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>29358295</pmid><doi>10.1128/AAC.01732-17</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-4873-249X</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0066-4804
ispartof Antimicrobial agents and chemotherapy, 2018-04, Vol.62 (4)
issn 0066-4804
1098-6596
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5913972
source EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Anti-Bacterial Agents
DNA-Directed RNA Polymerases
Lactones
Orientia tsutsugamushi
Scrub Typhus
Susceptibility
title Orientia tsutsugamushi Is Highly Susceptible to the RNA Polymerase Switch Region Inhibitor Corallopyronin A In Vitro and In Vivo
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T14%3A26%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Orientia%20tsutsugamushi%20Is%20Highly%20Susceptible%20to%20the%20RNA%20Polymerase%20Switch%20Region%20Inhibitor%20Corallopyronin%20A%20In%20Vitro%20and%20In%20Vivo&rft.jtitle=Antimicrobial%20agents%20and%20chemotherapy&rft.au=Kock,%20Fredericke&rft.date=2018-04-01&rft.volume=62&rft.issue=4&rft.issn=0066-4804&rft.eissn=1098-6596&rft_id=info:doi/10.1128/AAC.01732-17&rft_dat=%3Cproquest_pubme%3E1990488853%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1990488853&rft_id=info:pmid/29358295&rfr_iscdi=true