Hetero- and adaptive resistance to polymyxin B in OXA-23-producing carbapenem-resistant Acinetobacter baumannii isolates

Detalhes bibliográficos
Autor(a) principal: Barin, Juliana
Data de Publicação: 2013
Outros Autores: Martins, Andreza Francisco, Heineck, Bianca Lúcia, Barth, Afonso Luis, Zavascki, Alexandre Prehn
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/80348
Resumo: Background: Resistance rates to polymyxin B in surveillance studies have been very low despite its increasing use worldwide as the last resort therapy for multidrug-resistant Gram-negative bacilli. However, two other resistance phenotypes, hetero- and adaptive resistance, have been reported to polymyxin. We aimed to investigate the presence of polymyxin B hetero- and adaptive resistance and evaluate its stability in carbapenem-resistant Acinetobacter baumannii (CRAB) clinical isolates. Methods: CRAB isolates were recovered from hospitalized patients at three Brazilian hospitals. Hetero-resistance was determined by population analysis profile (PAP). Adaptive resistance was evaluated after serial daily passages of isolates in Luria-Bertani broth containing increasing polymyxin B concentrations. MICs of polymyxin B of colonies growing at the highest polymyxin B concentration were further determined after daily sub-cultured in antibiotic-free medium and after storage at −80°C, in some selected isolates. Results: Eighty OXA-23-producing CRAB isolates were typed resulting in 15 distinct clones. Twenty-nine randomly selected isolates (at least one from each clone) were selected for hetero- resistance evaluation: 26 (90%) presented growth of subpopulations with higher polymyxin B MIC than the original one in PAP. No isolate has grown at polymyxin B concentrations higher than 2 mg/L. Polymyxin B MICs of subpopulations remained higher than the original population after daily passages on antibiotic-free medium but returned to the same or similar levels after storage. Twenty-two of the 29 isolates (at least one from each clone) were evaluated for adaptive resistance: 12 (55%) presented growth in plates containing 64 mg/L of polymyxin B. Polymyxin B MICs decreased after daily passages on antibiotic-free medium and returned to the same levels after storage. Conclusions: The presence of subpopulations with higher polymyxin B MIC was extremely common and high-level adaptive resistance was very frequent in CRAB isolates.
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spelling Barin, JulianaMartins, Andreza FranciscoHeineck, Bianca LúciaBarth, Afonso LuisZavascki, Alexandre Prehn2013-11-13T01:47:02Z20131476-0711http://hdl.handle.net/10183/80348000904684Background: Resistance rates to polymyxin B in surveillance studies have been very low despite its increasing use worldwide as the last resort therapy for multidrug-resistant Gram-negative bacilli. However, two other resistance phenotypes, hetero- and adaptive resistance, have been reported to polymyxin. We aimed to investigate the presence of polymyxin B hetero- and adaptive resistance and evaluate its stability in carbapenem-resistant Acinetobacter baumannii (CRAB) clinical isolates. Methods: CRAB isolates were recovered from hospitalized patients at three Brazilian hospitals. Hetero-resistance was determined by population analysis profile (PAP). Adaptive resistance was evaluated after serial daily passages of isolates in Luria-Bertani broth containing increasing polymyxin B concentrations. MICs of polymyxin B of colonies growing at the highest polymyxin B concentration were further determined after daily sub-cultured in antibiotic-free medium and after storage at −80°C, in some selected isolates. Results: Eighty OXA-23-producing CRAB isolates were typed resulting in 15 distinct clones. Twenty-nine randomly selected isolates (at least one from each clone) were selected for hetero- resistance evaluation: 26 (90%) presented growth of subpopulations with higher polymyxin B MIC than the original one in PAP. No isolate has grown at polymyxin B concentrations higher than 2 mg/L. Polymyxin B MICs of subpopulations remained higher than the original population after daily passages on antibiotic-free medium but returned to the same or similar levels after storage. Twenty-two of the 29 isolates (at least one from each clone) were evaluated for adaptive resistance: 12 (55%) presented growth in plates containing 64 mg/L of polymyxin B. Polymyxin B MICs decreased after daily passages on antibiotic-free medium and returned to the same levels after storage. Conclusions: The presence of subpopulations with higher polymyxin B MIC was extremely common and high-level adaptive resistance was very frequent in CRAB isolates.application/pdfengAnnals of Clinical Microbiology and Antimicrobials. London : BioMed Central, 2013. Vol. 12, no. 15 (Jul. 2013), 5 p.Acinetobacter baumanniiColistinaPolimixina BPolymyxinsPolymyxin BColistinHetero-resistanceAdaptive resistanceMultidrug-resistanceCarbapenemaseHetero- and adaptive resistance to polymyxin B in OXA-23-producing carbapenem-resistant Acinetobacter baumannii isolatesEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL000904684.pdf000904684.pdfTexto completo (inglês)application/pdf133004http://www.lume.ufrgs.br/bitstream/10183/80348/1/000904684.pdf20d0907a10065f2b32e0f11ff00dee95MD51TEXT000904684.pdf.txt000904684.pdf.txtExtracted Texttext/plain22176http://www.lume.ufrgs.br/bitstream/10183/80348/2/000904684.pdf.txtac6a2fa37baecfc335175ef31c6db1b3MD52THUMBNAIL000904684.pdf.jpg000904684.pdf.jpgGenerated Thumbnailimage/jpeg1832http://www.lume.ufrgs.br/bitstream/10183/80348/3/000904684.pdf.jpg3a0d7aae3bb42340cf1ac210d6568415MD5310183/803482018-10-05 08:11:41.971oai:www.lume.ufrgs.br:10183/80348Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2018-10-05T11:11:41Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Hetero- and adaptive resistance to polymyxin B in OXA-23-producing carbapenem-resistant Acinetobacter baumannii isolates
title Hetero- and adaptive resistance to polymyxin B in OXA-23-producing carbapenem-resistant Acinetobacter baumannii isolates
spellingShingle Hetero- and adaptive resistance to polymyxin B in OXA-23-producing carbapenem-resistant Acinetobacter baumannii isolates
Barin, Juliana
Acinetobacter baumannii
Colistina
Polimixina B
Polymyxins
Polymyxin B
Colistin
Hetero-resistance
Adaptive resistance
Multidrug-resistance
Carbapenemase
title_short Hetero- and adaptive resistance to polymyxin B in OXA-23-producing carbapenem-resistant Acinetobacter baumannii isolates
title_full Hetero- and adaptive resistance to polymyxin B in OXA-23-producing carbapenem-resistant Acinetobacter baumannii isolates
title_fullStr Hetero- and adaptive resistance to polymyxin B in OXA-23-producing carbapenem-resistant Acinetobacter baumannii isolates
title_full_unstemmed Hetero- and adaptive resistance to polymyxin B in OXA-23-producing carbapenem-resistant Acinetobacter baumannii isolates
title_sort Hetero- and adaptive resistance to polymyxin B in OXA-23-producing carbapenem-resistant Acinetobacter baumannii isolates
author Barin, Juliana
author_facet Barin, Juliana
Martins, Andreza Francisco
Heineck, Bianca Lúcia
Barth, Afonso Luis
Zavascki, Alexandre Prehn
author_role author
author2 Martins, Andreza Francisco
Heineck, Bianca Lúcia
Barth, Afonso Luis
Zavascki, Alexandre Prehn
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Barin, Juliana
Martins, Andreza Francisco
Heineck, Bianca Lúcia
Barth, Afonso Luis
Zavascki, Alexandre Prehn
dc.subject.por.fl_str_mv Acinetobacter baumannii
Colistina
Polimixina B
topic Acinetobacter baumannii
Colistina
Polimixina B
Polymyxins
Polymyxin B
Colistin
Hetero-resistance
Adaptive resistance
Multidrug-resistance
Carbapenemase
dc.subject.eng.fl_str_mv Polymyxins
Polymyxin B
Colistin
Hetero-resistance
Adaptive resistance
Multidrug-resistance
Carbapenemase
description Background: Resistance rates to polymyxin B in surveillance studies have been very low despite its increasing use worldwide as the last resort therapy for multidrug-resistant Gram-negative bacilli. However, two other resistance phenotypes, hetero- and adaptive resistance, have been reported to polymyxin. We aimed to investigate the presence of polymyxin B hetero- and adaptive resistance and evaluate its stability in carbapenem-resistant Acinetobacter baumannii (CRAB) clinical isolates. Methods: CRAB isolates were recovered from hospitalized patients at three Brazilian hospitals. Hetero-resistance was determined by population analysis profile (PAP). Adaptive resistance was evaluated after serial daily passages of isolates in Luria-Bertani broth containing increasing polymyxin B concentrations. MICs of polymyxin B of colonies growing at the highest polymyxin B concentration were further determined after daily sub-cultured in antibiotic-free medium and after storage at −80°C, in some selected isolates. Results: Eighty OXA-23-producing CRAB isolates were typed resulting in 15 distinct clones. Twenty-nine randomly selected isolates (at least one from each clone) were selected for hetero- resistance evaluation: 26 (90%) presented growth of subpopulations with higher polymyxin B MIC than the original one in PAP. No isolate has grown at polymyxin B concentrations higher than 2 mg/L. Polymyxin B MICs of subpopulations remained higher than the original population after daily passages on antibiotic-free medium but returned to the same or similar levels after storage. Twenty-two of the 29 isolates (at least one from each clone) were evaluated for adaptive resistance: 12 (55%) presented growth in plates containing 64 mg/L of polymyxin B. Polymyxin B MICs decreased after daily passages on antibiotic-free medium and returned to the same levels after storage. Conclusions: The presence of subpopulations with higher polymyxin B MIC was extremely common and high-level adaptive resistance was very frequent in CRAB isolates.
publishDate 2013
dc.date.accessioned.fl_str_mv 2013-11-13T01:47:02Z
dc.date.issued.fl_str_mv 2013
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/80348
dc.identifier.issn.pt_BR.fl_str_mv 1476-0711
dc.identifier.nrb.pt_BR.fl_str_mv 000904684
identifier_str_mv 1476-0711
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url http://hdl.handle.net/10183/80348
dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Annals of Clinical Microbiology and Antimicrobials. London : BioMed Central, 2013. Vol. 12, no. 15 (Jul. 2013), 5 p.
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