Topically applied bacteriophage to control multi-drug resistant klebsiella pneumoniae infected wound in a rat model

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorFayez, Mohamed S
dc.contributor.authorHakim, Toka A
dc.contributor.authorAgwa, Mona M
dc.contributor.authorAbdelmoteleb, Mohamed
dc.contributor.authorAly, Rania G
dc.contributor.authorMontaser, Nada N
dc.contributor.authorAbdelsattar, Abdallah S
dc.contributor.authorRezk, Nouran
dc.contributor.authorEl-Shibiny, Ayman
dc.date.accessioned2021-09-12T16:12:42Z
dc.date.available2021-09-12T16:12:42Z
dc.date.issued8/27/2021
dc.descriptionScopusen_US
dc.description.abstract(Background): Multi-drug-resistant Klebsiella pneumoniae (MDR-KP) has steadily grown beyond antibiotic control. Wound infection kills many patients each year, due to the entry of multidrug resistant (MDR) bacterial pathogens into the skin gaps. However, a bacteriophage (phage) is considered to be a potential antibiotic alternative for treating bacterial infections. This research aims at isolating and characterizing a specific phage and evaluate its topical activity against MDR-KP isolated from infected wounds. (Methods): A lytic phage ZCKP8 was isolated by using a clinical isolate KP/15 as a host strain then characterized. Additionally, phage was assessed for its in vitro host range, temperature, ultraviolet (UV), and pH sensitivity. The therapeutic efficiency of phage suspension and a phage-impeded gel vehicle were assessed in vivo against a K. pneumoniae infected wound on a rat model. (Result): The phage produced a clear plaque and was classified as Siphoviridae. The phage inhibited KP/15 growth in vitro in a dose-dependent pattern and it was found to resist high temperature (<70◦C) and was primarily active at pH 5; moreover, it showed UV stability for 45 min. Phage-treated K. pneumoniae inoculated wounds showed the highest healing efficiency by lowering the infection. The quality of the regenerated skin was evidenced via histological examination compared to the untreated control group. (Conclusions): This research represents the evidence of effective phage therapy against MDR-KP. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.en_US
dc.identifier.doihttps://doi.org/10.3390/antibiotics10091048
dc.identifier.otherhttps://doi.org/10.3390/antibiotics10091048
dc.identifier.urihttps://qrgo.page.link/H9pRK
dc.language.isoen_USen_US
dc.publisherMDPIen_US
dc.relation.ispartofseriesAntibiotics;Volume 10, Issue 9September 2021 Article number 1048
dc.subjectBacteriophageen_US
dc.subjectBioinformaticsen_US
dc.subjectGram-negativeen_US
dc.subjectAntibioticsen_US
dc.subjectImmunohistochemical (IHC)en_US
dc.subjectIn vivoen_US
dc.subjectKlebsiella pneumoniaeen_US
dc.subjectMulti-drug resistance (MDR)en_US
dc.subjectPhage characterizationen_US
dc.subjectPhage isolationen_US
dc.subjectPhage therapyen_US
dc.subjectWound healingen_US
dc.subjectWound infectionen_US
dc.titleTopically applied bacteriophage to control multi-drug resistant klebsiella pneumoniae infected wound in a rat modelen_US
dc.typeArticleen_US

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