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dc.contributor.authorHassan, M
dc.contributor.authorDiep, DB
dc.contributor.authorJavadzadeh, Y
dc.contributor.authorDastmalchi, S
dc.contributor.authorNes, IF
dc.contributor.authorSharifi, Y
dc.contributor.authorYari, S
dc.contributor.authorFarajnia, S
dc.contributor.authorLotfipour, F
dc.date.accessioned2018-08-26T08:05:19Z
dc.date.available2018-08-26T08:05:19Z
dc.date.issued2012
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/49793
dc.description.abstractThe aim of the project was to isolate and characterize bacteriocin-producing enterococci, as well as determine the prevalence of enterocin structural genes in 187 enterococcal clinical isolates from the northwest of Iran. The isolates were screened for antibacterial activity against 15 different indicator strains. The proteinaceous nature of the antimicrobial substances was confirmed by sensitivity to proteinase K; their stability to heat treatment was tested at 60 degrees C and 100 degrees C for 20 and 10 min, respectively. The PCR method was applied to detect previously identified enterocin genes. Our results showed that 38 (20.3%) of the enterococcal isolates were considered to be potential bacteriocinogenic strains. Furthermore, genes encoding diverse bacteriocin are highly distributed among clinical enterococci, and the strains with multi-bacteriocin genes displayed high antimicrobial activity. Enterocin A, enterolysin A, and enterocin L50A/B were the most abundant structural genes detected in bacteriocinogenic strains. This work is the first survey on the prevalence of bacteriocin genes among clinical enterococci in Iran that has isolated a strain with high antimicrobial activity and sensitivity to clinically relevant antibiotics.
dc.language.isoEnglish
dc.relation.ispartofCANADIAN JOURNAL OF MICROBIOLOGY
dc.subjectprevalence
dc.subjectgenes
dc.subjectbacteriocin
dc.subjectenterococci
dc.subjectclinical
dc.titlePrevalence of bacteriocin activities and bacteriocin-encoding genes in enterococcal clinical isolates in Iran
dc.typeArticle
dc.citation.volume58
dc.citation.issue4
dc.citation.spage359
dc.citation.epage368
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1139/W11-136


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