Characterization of <i>Klebsiella</i> phages PMBT12, PMBT63, and PMBT64 with functional insights into a Hoc-like, mucin-interacting protein of phage PMBT63

ABSTRACT Three novel Klebsiella phages, PMBT12, PMBT63, and PMBT64, were isolated and characterized. The phages revealed distinct morphologies, phylogenetic backgrounds, and a high degree of genomic divergence. PMBT12 and PMBT64 exhibited narrow host ranges, whereas PMBT63 demonstrated a broader host range across the tested Klebsiella strains with diverse sequence and capsule types. PMBT63 possesses a large genome that approaches the size of jumbo T4-like phages, encodes 16 tRNAs, and exhibits high thermal stability up to 70°C. A conserved Hoc-like protein in PMBT63 was identified and structurally characterized, showing a highly conserved genomic context across diverse Enterobacteriaceae phages. Computational analyses predicted putative mucin-binding sites within this protein, which was corroborated experimentally by enhanced phage retention on mucin-coated surfaces. IMPORTANCE These findings identify Klebsiella phage PMBT63 as a promising candidate for therapeutic applications. It also highlights the importance of characterizing phages for potential phage-mucin interactions, which may influence their persistence and function within the gastrointestinal tract.

Authors

Institutions

Publication Details

Journal
Microbiology Spectrum
Published
2026-06-29
DOI
https://doi.org/10.1128/spectrum.00536-26
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Characterization of Klebsiella phages PMBT12, PMBT63, and PMBT64 with functional insights into a Hoc-like, mucin-interacting protein of phage PMBT63

Erik Brinks, Charles M. A. P. Franz, Frank Hille, Gyu‐Sung Cho et al.
Microbiology Spectrum
Bacteriophages and microbial interactions
article

Characterization of Klebsiella phages PMBT12, PMBT63, and PMBT64 with functional insights into a Hoc-like, mucin-interacting protein of phage PMBT63

Erik Brinks, Charles M. A. P. Franz, Frank Hille, Gyu‐Sung Cho, Anna Ewertz
article en

Abstract

ABSTRACT Three novel Klebsiella phages, PMBT12, PMBT63, and PMBT64, were isolated and characterized. The phages revealed distinct morphologies, phylogenetic backgrounds, and a high degree of genomic divergence. PMBT12 and PMBT64 exhibited narrow host ranges, whereas PMBT63 demonstrated a broader host range across the tested Klebsiella strains with diverse sequence and capsule types. PMBT63 possesses a large genome that approaches the size of jumbo T4-like phages, encodes 16 tRNAs, and exhibits high thermal stability up to 70°C. A conserved Hoc-like protein in PMBT63 was identified and structurally characterized, showing a highly conserved genomic context across diverse Enterobacteriaceae phages. Computational analyses predicted putative mucin-binding sites within this protein, which was corroborated experimentally by enhanced phage retention on mucin-coated surfaces. IMPORTANCE These findings identify Klebsiella phage PMBT63 as a promising candidate for therapeutic applications. It also highlights the importance of characterizing phages for potential phage-mucin interactions, which may influence their persistence and function within the gastrointestinal tract.

Microbiology Spectrum
Max Rubner Institut (DE)
Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 8%
Bacteriophages and microbial interactions
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.