Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/5516
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dc.contributor.authorObradović, Minaen_US
dc.contributor.authorMalešević, Milkaen_US
dc.contributor.authorDi Luca, Mariagraziaen_US
dc.contributor.authorKekić, Dušanen_US
dc.contributor.authorGajić, Inaen_US
dc.contributor.authorMcAuliffe, Oliviaen_US
dc.contributor.authorNeve, Horsten_US
dc.contributor.authorStanisavljević, Nemanjaen_US
dc.contributor.authorVukotić, Goranen_US
dc.contributor.authorKojić, Milanen_US
dc.date.accessioned2023-03-09T13:38:24Z-
dc.date.available2023-03-09T13:38:24Z-
dc.date.issued2023-02-25-
dc.identifier.issn1999-4915-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/5516-
dc.description.abstractKlebsiella pneumoniae is a global health threat and bacteriophages are a potential solution in combating pandrug-resistant K. pneumoniae infections. Two lytic phages, LASTA and SJM3, active against several pandrug-resistant, nosocomial strains of K. pneumoniae were isolated and characterized. Their host range is narrow and latent period is particularly long; however, their lysogenic nature was refuted using both bioinformatic and experimental approaches. Genome sequence analysis clustered them with only two other phages into the new genus Lastavirus. Genomes of LASTA and SJM3 differ in only 13 base pairs, mainly located in tail fiber genes. Individual phages, as well as their cocktail, demonstrated significant bacterial reduction capacity in a time-dependent manner, yielding up to 4 log reduction against planktonic, and up to 2.59 log on biofilm-embedded, cells. Bacteria emerging from the contact with the phages developed resistance and achieved numbers comparable to the growth control after 24 h. The resistance to the phage seems to be of a transient nature and varies significantly between the two phages, as resistance to LASTA remained constant while resensitization to SJM3 was more prominent. Albeit with very few differences, SJM3 performed better than LASTA overall; however, more investigation is needed in order to consider them for therapeutic application.en_US
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.relation.ispartofVirusesen_US
dc.subjectLastavirusen_US
dc.subjectLytic bacteriophageen_US
dc.subjectKlebsiella pneumoniaeen_US
dc.subjectTail fiberen_US
dc.subjectPhage resistanceen_US
dc.titleIsolation, Characterization, Genome Analysis and Host Resistance Development of Two Novel Lastavirus Phages Active against Pandrug-Resistant Klebsiella pneumoniaeen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/v15030628-
dc.description.rankM22en_US
dc.description.impact5.818en_US
dc.description.startpage628en_US
dc.description.volume15en_US
dc.description.issue3en_US
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeArticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.orcid0000-0001-9343-6214-
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