In vitro activity of minocycline alone or in combination in multidrug-resistant Acinetobacter baumannii isolates
Minocycline (MIN) usually shows good activity against Acinetobacter baumannii strains. The reintroduction to the market of intravenous MIN provides an additional agent to the limited options for the treatment of A. baumannii infections. The activity of MIN as a single agent and in combination with r...
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Veröffentlicht in: | Journal of medical microbiology 2015-10, Vol.64 (10), p.1196-1200 |
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creator | Rodríguez, Carlos Hernan Nastro, Marcela Vay, Carlos Famiglietti, Angela |
description | Minocycline (MIN) usually shows good activity against Acinetobacter baumannii strains. The reintroduction to the market of intravenous MIN provides an additional agent to the limited options for the treatment of A. baumannii infections. The activity of MIN as a single agent and in combination with rifampicin (RIF), colistin (COL) or imipenem (IMI) was evaluated by means of killing curves and 24 h-time-kill curves in five A. baumannii isolates which were selected on the basis of different antimicrobial resistance profiles. MIN showed bacteriostatic activity in three isolates (2 × or 16 × MIC) and bactericidal activity in the other isolates (64 × MIC). In isolates harbouring the tetB gene, the associations studied were always indifferent. However, in isolates not harbouring tetB, the use of MIN in combination showed a rapid synergistic effect (at 4 h) in four out of nine combinations (two with RIF and one each with IMI and COL). At 24 h, this effect was observed in six out of nine combinations (two in each association). MIN in combination with RIF, IMI and COL showed bactericidal synergy in most of the isolates which did not harbour the tetB gene, but the combinations were not synergistic in tetB-positive isolates. |
doi_str_mv | 10.1099/jmm.0.000147 |
format | Article |
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The reintroduction to the market of intravenous MIN provides an additional agent to the limited options for the treatment of A. baumannii infections. The activity of MIN as a single agent and in combination with rifampicin (RIF), colistin (COL) or imipenem (IMI) was evaluated by means of killing curves and 24 h-time-kill curves in five A. baumannii isolates which were selected on the basis of different antimicrobial resistance profiles. MIN showed bacteriostatic activity in three isolates (2 × or 16 × MIC) and bactericidal activity in the other isolates (64 × MIC). In isolates harbouring the tetB gene, the associations studied were always indifferent. However, in isolates not harbouring tetB, the use of MIN in combination showed a rapid synergistic effect (at 4 h) in four out of nine combinations (two with RIF and one each with IMI and COL). At 24 h, this effect was observed in six out of nine combinations (two in each association). MIN in combination with RIF, IMI and COL showed bactericidal synergy in most of the isolates which did not harbour the tetB gene, but the combinations were not synergistic in tetB-positive isolates.</description><identifier>ISSN: 0022-2615</identifier><identifier>EISSN: 1473-5644</identifier><identifier>DOI: 10.1099/jmm.0.000147</identifier><identifier>PMID: 26238719</identifier><language>eng</language><publisher>England</publisher><subject>Acinetobacter baumannii - drug effects ; Acinetobacter baumannii - isolation & purification ; Acinetobacter Infections - microbiology ; Anti-Bacterial Agents - pharmacology ; Drug Interactions ; Humans ; Microbial Sensitivity Tests ; Microbial Viability - drug effects ; Minocycline - pharmacology</subject><ispartof>Journal of medical microbiology, 2015-10, Vol.64 (10), p.1196-1200</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c329t-d87154a8b3adedf3016ba389a4ec5634ebb0f978c154c698b7bb4403db7d8f583</citedby><cites>FETCH-LOGICAL-c329t-d87154a8b3adedf3016ba389a4ec5634ebb0f978c154c698b7bb4403db7d8f583</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3746,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26238719$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rodríguez, Carlos Hernan</creatorcontrib><creatorcontrib>Nastro, Marcela</creatorcontrib><creatorcontrib>Vay, Carlos</creatorcontrib><creatorcontrib>Famiglietti, Angela</creatorcontrib><title>In vitro activity of minocycline alone or in combination in multidrug-resistant Acinetobacter baumannii isolates</title><title>Journal of medical microbiology</title><addtitle>J Med Microbiol</addtitle><description>Minocycline (MIN) usually shows good activity against Acinetobacter baumannii strains. The reintroduction to the market of intravenous MIN provides an additional agent to the limited options for the treatment of A. baumannii infections. The activity of MIN as a single agent and in combination with rifampicin (RIF), colistin (COL) or imipenem (IMI) was evaluated by means of killing curves and 24 h-time-kill curves in five A. baumannii isolates which were selected on the basis of different antimicrobial resistance profiles. MIN showed bacteriostatic activity in three isolates (2 × or 16 × MIC) and bactericidal activity in the other isolates (64 × MIC). In isolates harbouring the tetB gene, the associations studied were always indifferent. However, in isolates not harbouring tetB, the use of MIN in combination showed a rapid synergistic effect (at 4 h) in four out of nine combinations (two with RIF and one each with IMI and COL). At 24 h, this effect was observed in six out of nine combinations (two in each association). MIN in combination with RIF, IMI and COL showed bactericidal synergy in most of the isolates which did not harbour the tetB gene, but the combinations were not synergistic in tetB-positive isolates.</description><subject>Acinetobacter baumannii - drug effects</subject><subject>Acinetobacter baumannii - isolation & purification</subject><subject>Acinetobacter Infections - microbiology</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Drug Interactions</subject><subject>Humans</subject><subject>Microbial Sensitivity Tests</subject><subject>Microbial Viability - drug effects</subject><subject>Minocycline - pharmacology</subject><issn>0022-2615</issn><issn>1473-5644</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kEtLAzEURoMotlZ3riVLF07Nax5ZluKjUHCj65BkMpIySWqSEfrvjbS6uQ849-NyALjFaIkR548755ZoiRDCrD0D81JpVTeMnYM5QoRUpMH1DFyltCtISym_BDPSENq1mM_BfuPht80xQKmzLdMBhgE664M-6NF6A-UYSg0RWg91cMp6mW3wv6ubxmz7OH1W0SSbsvQZrnQ5ykGVOBOhkpOT3lsLbQqjzCZdg4tBjsncnPoCfDw_va9fq-3by2a92laaEp6rvrxXM9kpKnvTDxThRknaccmMrhvKjFJo4G2nC6Ub3qlWKcYQ7VXbd0Pd0QW4P-buY_iaTMrC2aTNOEpvwpQEbgnhhDcEFfThiOoYUopmEPtonYwHgZH4dSyKY4HE0XHB707Jk3Km_4f_pNIfTg56NA</recordid><startdate>201510</startdate><enddate>201510</enddate><creator>Rodríguez, Carlos Hernan</creator><creator>Nastro, Marcela</creator><creator>Vay, Carlos</creator><creator>Famiglietti, Angela</creator><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></search><sort><creationdate>201510</creationdate><title>In vitro activity of minocycline alone or in combination in multidrug-resistant Acinetobacter baumannii isolates</title><author>Rodríguez, Carlos Hernan ; Nastro, Marcela ; Vay, Carlos ; Famiglietti, Angela</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c329t-d87154a8b3adedf3016ba389a4ec5634ebb0f978c154c698b7bb4403db7d8f583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acinetobacter baumannii - drug effects</topic><topic>Acinetobacter baumannii - isolation & purification</topic><topic>Acinetobacter Infections - microbiology</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Drug Interactions</topic><topic>Humans</topic><topic>Microbial Sensitivity Tests</topic><topic>Microbial Viability - drug effects</topic><topic>Minocycline - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rodríguez, Carlos Hernan</creatorcontrib><creatorcontrib>Nastro, Marcela</creatorcontrib><creatorcontrib>Vay, Carlos</creatorcontrib><creatorcontrib>Famiglietti, Angela</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><jtitle>Journal of medical microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rodríguez, Carlos Hernan</au><au>Nastro, Marcela</au><au>Vay, Carlos</au><au>Famiglietti, Angela</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro activity of minocycline alone or in combination in multidrug-resistant Acinetobacter baumannii isolates</atitle><jtitle>Journal of medical microbiology</jtitle><addtitle>J Med Microbiol</addtitle><date>2015-10</date><risdate>2015</risdate><volume>64</volume><issue>10</issue><spage>1196</spage><epage>1200</epage><pages>1196-1200</pages><issn>0022-2615</issn><eissn>1473-5644</eissn><abstract>Minocycline (MIN) usually shows good activity against Acinetobacter baumannii strains. The reintroduction to the market of intravenous MIN provides an additional agent to the limited options for the treatment of A. baumannii infections. The activity of MIN as a single agent and in combination with rifampicin (RIF), colistin (COL) or imipenem (IMI) was evaluated by means of killing curves and 24 h-time-kill curves in five A. baumannii isolates which were selected on the basis of different antimicrobial resistance profiles. MIN showed bacteriostatic activity in three isolates (2 × or 16 × MIC) and bactericidal activity in the other isolates (64 × MIC). In isolates harbouring the tetB gene, the associations studied were always indifferent. However, in isolates not harbouring tetB, the use of MIN in combination showed a rapid synergistic effect (at 4 h) in four out of nine combinations (two with RIF and one each with IMI and COL). At 24 h, this effect was observed in six out of nine combinations (two in each association). MIN in combination with RIF, IMI and COL showed bactericidal synergy in most of the isolates which did not harbour the tetB gene, but the combinations were not synergistic in tetB-positive isolates.</abstract><cop>England</cop><pmid>26238719</pmid><doi>10.1099/jmm.0.000147</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Microbiology Society; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Acinetobacter baumannii - drug effects Acinetobacter baumannii - isolation & purification Acinetobacter Infections - microbiology Anti-Bacterial Agents - pharmacology Drug Interactions Humans Microbial Sensitivity Tests Microbial Viability - drug effects Minocycline - pharmacology |
title | In vitro activity of minocycline alone or in combination in multidrug-resistant Acinetobacter baumannii isolates |
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