eprintid: 10204379
rev_number: 6
eprint_status: archive
userid: 699
dir: disk0/10/20/43/79
datestamp: 2025-02-06 17:06:15
lastmod: 2025-02-06 17:06:15
status_changed: 2025-02-06 17:06:15
type: article
metadata_visibility: show
sword_depositor: 699
creators_name: Phitchayapak, Wintachai
creators_name: Santini, Joanne
creators_name: Renuka, Thonguppatham
creators_name: Maria, Stroyakovski
creators_name: Komwit, Surachat
creators_name: Apirchart, Atipairin
title: Isolation, Characterization, and Anti-Biofilm Activity of a Novel Kaypoctavirus Against K24 Capsular Type, Multidrug-Resistant Klebsiella pneumoniae Clinical Isolates
ispublished: pub
divisions: UCL
divisions: B02
divisions: C08
divisions: D09
divisions: G03
keywords: Antibacterial activity; bacteriophage; biofilms; K24 capsular type; Klebsiella pneumoniae; phage therapy
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abstract: The significant outbreak of multidrug-resistant Klebsiella pneumoniae has emerged as a primary global concern associated with high morbidity and mortality rates. Certain strains of K. pneumoniae are highly resistant to most antibiotics available in clinical practice, exacerbating the challenge of bacterial infections. Methods: Phage vB_KpnP_PW7 (vKPPW7) was isolated and characterized. Its morphology, stability, adsorption rate, one-step growth curve, lytic activity, whole-genome sequence analysis, and antibacterial and antibiofilm activities were evaluated. Results: The virulent phage has a 73,658 bp linear dsDNA genome and was classified as a new species of the genus Kaypoctavirus, subfamily Enquatrovirinae, and family Schitoviridae. Phage vKPPW7 has a high adsorption rate, a short latent period, and a large burst size. The phage showed activity against 18 K. pneumoniae isolates with the K24 capsular type but was unable to lyse K. pneumoniae isolates whose capsular type was not classified as K24. Additionally, phage vKPPW7 demonstrated strong stability across various temperatures and pH values. The phage exhibited antibacterial activity, and scanning electron microscopy (SEM) confirmed its ability to lyse MDR K. pneumoniae with the K24 capsular type. Furthermore, phage vKPPW7 effectively removed preformed biofilm and prevented biofilm formation, resulting in reduced biofilm biomass and biofilm viability compared to controls. The architecture of phage-treated biofilms was confirmed under SEM. Conclusions: These findings suggest that phage vKPPW7 holds promise for development as a therapeutic or biocontrol agent.
date: 2025-02-05
date_type: published
publisher: MDPI AG
official_url: https://www.mdpi.com/2079-6382/14/2/157
oa_status: green
full_text_type: pub
language: eng
primo: open
primo_central: open_green
verified: verified_manual
elements_id: 2358241
doi: 10.3390/antibiotics14020157
lyricists_name: Santini, Giovanna
lyricists_id: JMSAN31
actors_name: Santini, Giovanna
actors_id: JMSAN31
actors_role: owner
full_text_status: public
publication: Antibiotics
volume: 14
number: 2
article_number: 157
citation:        Phitchayapak, Wintachai;    Santini, Joanne;    Renuka, Thonguppatham;    Maria, Stroyakovski;    Komwit, Surachat;    Apirchart, Atipairin;      (2025)    Isolation, Characterization, and Anti-Biofilm Activity of a Novel Kaypoctavirus Against K24 Capsular Type, Multidrug-Resistant Klebsiella pneumoniae Clinical Isolates.                   Antibiotics , 14  (2)    , Article 157.  10.3390/antibiotics14020157 <https://doi.org/10.3390/antibiotics14020157>.       Green open access   
 
document_url: https://discovery.ucl.ac.uk/id/eprint/10204379/1/antibiotics-14-00157.pdf