Evidence map›Paper›PMID 41514414›Full record

ArticleBMC microbiology2026

Multidimensional characterization of a novel porcine Klebsiella pneumoniae phage Pkp-1.

Shenghui Wan, Nana Li, Yanfang Li, Yan Liang, Yonggang Qu

Abstract read
In one paragraph

Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Shenghui WanCollege of Animal Science and Technology, Shihezi University, Shihezi, 832003, China.
Nana LiCollege of Animal Science and Technology, Shihezi University, Shihezi, 832003, China.
Yanfang LiCollege of Animal Science and Technology, Shihezi University, Shihezi, 832003, China.
Yan LiangCollege of Animal Science and Technology, Shihezi University, Shihezi, 832003, China. liangyan@shzu.edu.cn.
Yonggang QuCollege of Animal Science and Technology, Shihezi University, Shihezi, 832003, China. quyonggang@shzu.edu.cn.

Funding

The Natural Science Support Program Project of Xinjiang Production and Construction Corps 2024DA007the Shihezi University Technology Transfer and Promotion Program CGZH202309
6 · The paper itself

Abstract

backgroundIn recent years, the inappropriate use of antibiotics has led to the widespread emergence of multidrug-resistant Klebsiella pneumoniae (MDR-K. pneumoniae), resulting in infections that are increasingly challenging to manage clinically. Bacteriophages (phages) are emerging as promising alternatives to antibiotics. This study aimed to isolate and characterize lytic phages targeting MDR-K. pneumoniae, providing biological resources and experimental data for phage-based control of MDR-K. pneumoniae infections.

resultsA lytic phage, designated vB_KpnA_Pkp-1 (Pkp-1), was successfully isolated. TEM revealed that Pkp-1 belongs to the Caudoviricetes class, featuring an icosahedral head (62 ± 2 nm) and a short tail (17 ± 1 nm), with plaques displaying clear centers and translucent halos. Pkp-1 exhibited strict specificity for porcine-derived ST967 K. pneumoniae isolates. Its optimal MOI was 0.00001, with a latent period of 25 min and a burst size of 108 PFU/cell. Pkp-1 demonstrated high stability at 40 °C-60 °C and pH 4.0-11.0, effectively inhibiting planktonic bacteria and suppressing/eradicating biofilms. Genomic analysis revealed a 38,455 bp dsDNA genome with 48 open reading frames (ORFs), functions of 30 proteins were predicted (e.g., DNA polymerase, tail fiber), while the remaining 18 proteins were annotated as hypothetical. Genomic analysis confirmed the absence of virulence, lysogeny-related, and antibiotic resistance genes. Pkp-1 shared high identity with phages phi1_146013 (98.71%) and P7124 (97.25%). Recombination analysis revealed 19 recombination events, with two specifically located within the tail protein gene. Notably, this tail protein gene exhibits significant divergence from those of other classified Kayfunavirus phages.

conclusionThe lytic phage Pkp-1 represents a novel recombinant chimera within the Kayfunavirus genus, characterized by rapid replication, strict host specificity, environmental resilience, potent bactericidal activity, and biofilm clearance capability. The significant divergence of its tail protein from other Kayfunavirus phages suggests unique adaptive evolution. It represents a novel recombinant chimeric phage of the genus Kayfunavirus, with multiple recombination events in its genome. Its tail protein exhibits significant differences from those of other phages in the genus Kayfunavirus, indicating that it possesses adaptive evolutionary characteristics. These attributes position Pkp-1 as a potential biocontrol agent against MDR-K. pneumoniae infections, particularly in livestock and clinical settings. Further studies on in vivo efficacy and safety are warranted.

Indexed as

BacteriophagesKlebsiella pneumoniaeAnimalsBiofilmsCaudoviralesDNA, ViralGenome, ViralHost SpecificityHydrogen-Ion ConcentrationKlebsiella InfectionsPhylogenySwineTemperatureViral ProteinsDNA, ViralViral ProteinsBiofilm clearanceGenome-wide analysisLytic phageMultidrug-resistant K. pneumonia

Identifiers

PMID41514414
PMCPMC12911343

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.