Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/3953
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dc.contributor.authorBegović, Jelenaen_US
dc.contributor.authorJovčić, Brankoen_US
dc.contributor.authorPapić-Obradović, Milenaen_US
dc.contributor.authorVeljović, Katarinaen_US
dc.contributor.authorLukić, Jovankaen_US
dc.contributor.authorKojić, Milanen_US
dc.contributor.authorTopisirović, Ljubišaen_US
dc.date.accessioned2021-04-16T12:54:38Z-
dc.date.available2021-04-16T12:54:38Z-
dc.date.issued2013-
dc.identifier.issn0944-5013-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/3953-
dc.description.abstractStaphylococcus epidermidis strains were isolated from the expressed human breast milk (EHM) of 14 healthy donor mothers. Genetic diversity was evaluated using RAPD-PCR REP-PCR and pulse-field gel electrophoresis (PFGE). PFGE allowed the best discrimination of the isolates, since it provided for the greatest diversity of the analyzed genomes. Among the S. epidermidis strains, resistance to gentamicin, tetracycline, erythromycin, clindamycin or vancomycin was detected, whilst four isolates were multiresistant. The results from our study demonstrate that staphylococci from EHM could be reservoirs of resistance genes, since we showed that tetK could be transferred from EHM staphylococci to Gram-negative Escherichia coli. Most of the staphylococcal strains displayed excellent proteolytic and lipolytic activities. Additionally, the presence of ica genes, which was related to their ability to form a biofilm on tissue culture plates, and the presence of virulence factors including autolysin/adhesin AtLE, point to their pathogenic potential.en_US
dc.language.isoenen_US
dc.relation.ispartofMicrobiological Researchen_US
dc.relation.ispartofseries168 (2013) (2);77-83-
dc.subjectHuman breast milken_US
dc.subjectS. epidermidisen_US
dc.subjectAntibiotic susceptibilityen_US
dc.subjectVirulenceen_US
dc.titleGenotypic diversity and virulent factors of Staphylococcus epidermidis isolated from human breast milken_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.micres.2012.09.004-
dc.identifier.pmid23098640-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.grantfulltextrestricted-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.orcid0000-0002-9500-3786-
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