Catecholamine Inotrope Resuscitation of Antibiotic-Damaged Staphylococci and Its Blockade by Specific Receptor Antagonists
The increasing use of antibiotic-coated catheters, such as those containing rifampin or minocycline, has led to a decrease in catheter colonization by staphylococci but not to a decrease in the incidence of catheter-related bloodstream infection (BSI). Because catheters are used for the administrati...
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description | The increasing use of antibiotic-coated catheters, such as those containing rifampin or minocycline, has led to a decrease in catheter colonization by staphylococci but not to a decrease in the incidence of catheter-related bloodstream infection (BSI). Because catheters are used for the administration of catecholamine inotropes to maintain cardiac function, we examined whether 2 commonly employed inotropes, dopamine and norepinephrine, could affect bacterial viability after exposure to rifampin and minocycline. Rifampin inhibition and minocycline inhibition of staphylococcal growth could be reversed by exposure to dopamine or norepinephrine as a result, in part, of catecholamine-mediated increased provision of host-sequestered iron. The simultaneous addition of inotropes with an antibiotic did not affect antibiotic susceptibility. Inotrope-induced growth in bacteria previously exposed to antibiotics was blocked by the inclusion in culture media of specific catecholamine-receptor antagonists. Considered collectively, these results provide a mechanistic basis for understanding how host-related factors, such as inotrope-based therapeutics, may influence the recovery of antibiotic-stressed bacteria in clinical settings |
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Inotrope-induced growth in bacteria previously exposed to antibiotics was blocked by the inclusion in culture media of specific catecholamine-receptor antagonists. Considered collectively, these results provide a mechanistic basis for understanding how host-related factors, such as inotrope-based therapeutics, may influence the recovery of antibiotic-stressed bacteria in clinical settings</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1086/529202</identifier><identifier>PMID: 18419472</identifier><identifier>CODEN: JIDIAQ</identifier><language>eng</language><publisher>Chicago, IL: The University of Chicago Press</publisher><subject>Anti-Bacterial Agents - pharmacology ; Antibiotics ; Bacteria ; Bacteriology ; Biological and medical sciences ; Cardiotonic Agents - pharmacology ; Catecholamines ; Central venous catheterization ; Colony Count, Microbial ; Cultured cells ; Dopamine - pharmacology ; Dopamine antagonists ; Dopamine Antagonists - pharmacology ; Electrolytes ; Fundamental and applied biological sciences. Psychology ; Growth Substances - pharmacology ; Infections ; Iron - metabolism ; Microbial Viability - drug effects ; Microbiology ; Minocycline - pharmacology ; Miscellaneous ; Norepinephrine ; Norepinephrine - pharmacology ; Rifampin - pharmacology ; Staphylococcus ; Staphylococcus - drug effects ; Staphylococcus - growth & development</subject><ispartof>The Journal of infectious diseases, 2008-04, Vol.197 (7), p.1044-1052</ispartof><rights>Copyright 2008 Infectious Diseases Society of America</rights><rights>2008 by the Infectious Diseases Society of America 2008</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-45ac9360ff6e56850dffa1d16ca42c2adc58b97fbbce4d1c849624bf2f5b8e1a3</citedby><cites>FETCH-LOGICAL-c456t-45ac9360ff6e56850dffa1d16ca42c2adc58b97fbbce4d1c849624bf2f5b8e1a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/40253928$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/40253928$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,27924,27925,58017,58250</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20211558$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18419472$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Freestone, Primrose P. E.</creatorcontrib><creatorcontrib>Haigh, Richard D.</creatorcontrib><creatorcontrib>Lyte, Mark</creatorcontrib><title>Catecholamine Inotrope Resuscitation of Antibiotic-Damaged Staphylococci and Its Blockade by Specific Receptor Antagonists</title><title>The Journal of infectious diseases</title><addtitle>The Journal of Infectious Diseases</addtitle><addtitle>The Journal of Infectious Diseases</addtitle><description>The increasing use of antibiotic-coated catheters, such as those containing rifampin or minocycline, has led to a decrease in catheter colonization by staphylococci but not to a decrease in the incidence of catheter-related bloodstream infection (BSI). Because catheters are used for the administration of catecholamine inotropes to maintain cardiac function, we examined whether 2 commonly employed inotropes, dopamine and norepinephrine, could affect bacterial viability after exposure to rifampin and minocycline. Rifampin inhibition and minocycline inhibition of staphylococcal growth could be reversed by exposure to dopamine or norepinephrine as a result, in part, of catecholamine-mediated increased provision of host-sequestered iron. The simultaneous addition of inotropes with an antibiotic did not affect antibiotic susceptibility. Inotrope-induced growth in bacteria previously exposed to antibiotics was blocked by the inclusion in culture media of specific catecholamine-receptor antagonists. Considered collectively, these results provide a mechanistic basis for understanding how host-related factors, such as inotrope-based therapeutics, may influence the recovery of antibiotic-stressed bacteria in clinical settings</description><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibiotics</subject><subject>Bacteria</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Cardiotonic Agents - pharmacology</subject><subject>Catecholamines</subject><subject>Central venous catheterization</subject><subject>Colony Count, Microbial</subject><subject>Cultured cells</subject><subject>Dopamine - pharmacology</subject><subject>Dopamine antagonists</subject><subject>Dopamine Antagonists - pharmacology</subject><subject>Electrolytes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Growth Substances - pharmacology</subject><subject>Infections</subject><subject>Iron - metabolism</subject><subject>Microbial Viability - drug effects</subject><subject>Microbiology</subject><subject>Minocycline - pharmacology</subject><subject>Miscellaneous</subject><subject>Norepinephrine</subject><subject>Norepinephrine - pharmacology</subject><subject>Rifampin - pharmacology</subject><subject>Staphylococcus</subject><subject>Staphylococcus - drug effects</subject><subject>Staphylococcus - growth & development</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFu1DAQhiMEokuBNwC5B7gFbMd24mO7BbqoAkFBQlysycRu3SZxiB2J5enJKquFC-I00synb0b_ZNlTRl8xWqnXkmtO-b1sxWRR5kqx4n62opTznFVaH2WPYryllIpClQ-zI1YJpkXJV9mvNSSLN6GFzveWbPqQxjBY8tnGKaJPkHzoSXDktE--9iF5zM-hg2vbkKsEw822DRgQPYG-IZsUydncuIPGknpLrgaL3nmcdWiHFMadBq5D72OKj7MHDtpon-zrcfb17Zsv64v88uO7zfr0MkchVcqFBNSFos4pK1UlaeMcsIYpBMGRQ4OyqnXp6hqtaBhWQisuasedrCvLoDjOXi7eYQw_JhuT6XxE27bQ2zBFozRjUrHqvyDTpeCV-gvEMcQ4WmeG0Xcwbg2jZvcOs7xjBp_vjVPd2eYPts9_Bl7sAYgIrRuhRx8P3OyYb5O7jScLF6bh38ueLcxtnJM-UIJyWWi-c-TLfA7f_jzMYbwzqixKaS6-fTef5If34mx9bnTxG0-jtjk</recordid><startdate>20080401</startdate><enddate>20080401</enddate><creator>Freestone, Primrose P. 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E. ; Haigh, Richard D. ; Lyte, Mark</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-45ac9360ff6e56850dffa1d16ca42c2adc58b97fbbce4d1c849624bf2f5b8e1a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antibiotics</topic><topic>Bacteria</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>Cardiotonic Agents - pharmacology</topic><topic>Catecholamines</topic><topic>Central venous catheterization</topic><topic>Colony Count, Microbial</topic><topic>Cultured cells</topic><topic>Dopamine - pharmacology</topic><topic>Dopamine antagonists</topic><topic>Dopamine Antagonists - pharmacology</topic><topic>Electrolytes</topic><topic>Fundamental and applied biological sciences. 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E.</creatorcontrib><creatorcontrib>Haigh, Richard D.</creatorcontrib><creatorcontrib>Lyte, Mark</creatorcontrib><collection>Istex</collection><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>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Freestone, Primrose P. 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Because catheters are used for the administration of catecholamine inotropes to maintain cardiac function, we examined whether 2 commonly employed inotropes, dopamine and norepinephrine, could affect bacterial viability after exposure to rifampin and minocycline. Rifampin inhibition and minocycline inhibition of staphylococcal growth could be reversed by exposure to dopamine or norepinephrine as a result, in part, of catecholamine-mediated increased provision of host-sequestered iron. The simultaneous addition of inotropes with an antibiotic did not affect antibiotic susceptibility. Inotrope-induced growth in bacteria previously exposed to antibiotics was blocked by the inclusion in culture media of specific catecholamine-receptor antagonists. 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subjects | Anti-Bacterial Agents - pharmacology Antibiotics Bacteria Bacteriology Biological and medical sciences Cardiotonic Agents - pharmacology Catecholamines Central venous catheterization Colony Count, Microbial Cultured cells Dopamine - pharmacology Dopamine antagonists Dopamine Antagonists - pharmacology Electrolytes Fundamental and applied biological sciences. Psychology Growth Substances - pharmacology Infections Iron - metabolism Microbial Viability - drug effects Microbiology Minocycline - pharmacology Miscellaneous Norepinephrine Norepinephrine - pharmacology Rifampin - pharmacology Staphylococcus Staphylococcus - drug effects Staphylococcus - growth & development |
title | Catecholamine Inotrope Resuscitation of Antibiotic-Damaged Staphylococci and Its Blockade by Specific Receptor Antagonists |
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