Capsule specificity underpins the biology and translational potential of Klebsiella pneumoniae K16 phages

Abstract Klebsiella pneumoniae species complex (KPSC) is a leading cause of bloodstream infections (BSIs), with capsule diversity complicating vaccine development. Certain capsule types are disproportionately associated with disease, including the under-studied KL16. Here, we isolated and characterised four novel podophages that, despite encoding multiple depolymerases, exhibit strict K16 tropism. We show that selected phage M6 encodes two active depolymerases (K16-Dep46 and K16-Dep47), the first identified for this capsule type and the first example of a phage carrying dual enzymes with conserved substrate specificity. The phages infected all K16 strains tested, including clinical and environmental isolates from Malawi, the UK and Thailand, with diagnostic precision. Purified K16-Dep47 expanded the host range of other phages, enabling M6 to act in concert with capsule-independent phages, as well as with ceftazidime to improve bacterial clearance. These findings define the molecular basis of K16-phage specificity and highlight targeted phage isolation for therapeutic and diagnostic applications.

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Publication Details

Journal
npj Antimicrobials and Resistance
Published
2026-09-11
DOI
https://doi.org/10.1038/s44259-026-00267-8
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Capsule specificity underpins the biology and translational potential of Klebsiella pneumoniae K16 phages

Edward J. Feil, Yunlong Huo, Oliver Pearse, Nathaniel Storey et al.
npj Antimicrobials and Resistance
Bacteriophages and microbial interactions
article

Capsule specificity underpins the biology and translational potential of Klebsiella pneumoniae K16 phages

Edward J. Feil, Yunlong Huo, Oliver Pearse, Nathaniel Storey, Joanne M. Santini, Abid Javed, Matthew B. Avison, Marjorie J. Gibbon, Li Cheng, Maria Stroyakovski, Nicole Stoesser, Allan Zuza, Julie Lavollee, Max J. Cheetham, Paulina Dubiel, Nemean Barber, Samuel Lipworth, Nicholas Feasey
article en

Abstract

Abstract Klebsiella pneumoniae species complex (KPSC) is a leading cause of bloodstream infections (BSIs), with capsule diversity complicating vaccine development. Certain capsule types are disproportionately associated with disease, including the under-studied KL16. Here, we isolated and characterised four novel podophages that, despite encoding multiple depolymerases, exhibit strict K16 tropism. We show that selected phage M6 encodes two active depolymerases (K16-Dep46 and K16-Dep47), the first identified for this capsule type and the first example of a phage carrying dual enzymes with conserved substrate specificity. The phages infected all K16 strains tested, including clinical and environmental isolates from Malawi, the UK and Thailand, with diagnostic precision. Purified K16-Dep47 expanded the host range of other phages, enabling M6 to act in concert with capsule-independent phages, as well as with ceftazidime to improve bacterial clearance. These findings define the molecular basis of K16-phage specificity and highlight targeted phage isolation for therapeutic and diagnostic applications.

npj Antimicrobials and Resistance
University of Liverpool (GB), University of St Andrews (GB), Liverpool School of Tropical Medicine (GB), Malawi-Liverpool-Wellcome Trust Clinical Research Programme (MW), Great Ormond Street Hospital for Children NHS Foundation Trust (GB), The Francis Crick Institute (GB), John Radcliffe Hospital (GB), National Institute for Health and Care Research (GB), University of Bristol (GB), University of Oxford (GB), Oxford BioMedica (United Kingdom) (GB), Institute of Structural and Molecular Biology (GB), Queen Elizabeth Central Hospital (MW), University College London (GB), University of Bath (GB)
National Institute for Health and Care Research, Biotechnology and Biological Sciences Research Council, NIHR Oxford Biomedical Research Centre
Openalex Percentile: Top 11%
Bacteriophages and microbial interactions
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