Egyszerű nézet

dc.contributor.author Kádár, Béla
dc.contributor.author Kocsis, Béla
dc.contributor.author Kristóf, Katalin
dc.contributor.author Tóth, Ákos
dc.contributor.author Szabó, Dóra
dc.date.accessioned 2018-06-26T06:31:42Z
dc.date.available 2018-06-26T06:31:42Z
dc.date.issued 2015
dc.identifier 84953300697
dc.identifier.citation pagination=501-508; journalVolume=62; journalIssueNumber=4; journalTitle=ACTA MICROBIOLOGICA ET IMMUNOLOGICA HUNGARICA;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/5466
dc.identifier.uri doi:10.1556/030.62.2015.4.12
dc.description.abstract In this study susceptibility to different antimicrobial peptides was investigated on colistin-susceptible and colistin-resistant identical pulsotype strains of KPC-2 producing Klebsiella pneumoniae ST258 as well as colistin-susceptible and colistin-resistant Enterobacter asburiae strains isolated from clinical samples. In our test, bacteria were exposed to 50 mg/ml lactoferrin, lysozyme and protamine - cationic antimicrobial peptides belonging to innate immune system and having structural similarity to polymyxins - in separate reactions. After 18 hours incubation of colonies were counted. 40% of colistin-resistant K. pneumoniae strains and 97% of colistin-susceptible counterpart strains were lysed by protamine whereas 87% and 100% colony forming unit decrease by lysozyme was seen, respectively. In the case of colistin-resistant E. asburiae strains 1 log10 cell count increase were observed after treatment with lysozyme and 1.56 log10 after lactoferrin exposure compared to the initial number whereas the colistin-susceptible showed no relevant cell count increase. Our findings suggest that acquired colistin-resistance in Enterobacteriaceae is associated with tolerance against antimicrobial peptides.
dc.relation.ispartof urn:issn:1217-8950
dc.title Effect of antimicrobial peptides on colistin-susceptible and colistin-resistant strains of Klebsiella pneumoniae and Enterobacter asburiae
dc.type Journal Article
dc.date.updated 2018-05-28T06:29:57Z
dc.language.rfc3066 en
dc.identifier.mtmt 2987548
dc.identifier.wos 000366946500012
dc.identifier.pubmed 26689883
dc.contributor.department SE/AOK/I/Orvosi Mikrobiológiai Intézet
dc.contributor.department SE/AOK/I/Laboratóriumi Medicina Intézet
dc.contributor.institution Semmelweis Egyetem


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