Evidence map›Paper›PMID 41254584›Full record

ArticleBMC biology2025

Insights into the molecular determinants of host specificity in Pseudomonas aeruginosa-infecting phages: a structural and functional analysis of tail fibre proteins.

Aleksandra Zalewska, Agata Jurczak-Kurek, Magdalena Kwiatek, Heejoon Myung, Marcin Górniak

Abstract read
In one paragraph

Article in BMC biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
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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.

Aleksandra ZalewskaDepartment of Evolutionary Genetics and Biosystematics, University of Gdańsk, Gdańsk, Poland.
Agata Jurczak-KurekDepartment of Evolutionary Genetics and Biosystematics, University of Gdańsk, Gdańsk, Poland. agata.jurczak-kurek@ug.edu.pl.
Magdalena KwiatekMilitary Institute of Hygiene and Epidemiology, Biological Threats Identification and Countermeasure Centre, Puławy, Poland.
Heejoon MyungDepartment of Bioscience and Biotechnology, Hankuk University of Foreign Studies, Gyung-Gi-Do, Yong-In, South Korea.
Marcin GórniakDepartment of Evolutionary Genetics and Biosystematics, University of Gdańsk, Gdańsk, Poland. marcin.gorniak@ug.edu.pl.

Funding

Faculty of Biology, University of Gdansk 539-D200-B086-23
6 · The paper itself

Abstract

backgroundBacteriophages and bacteria frequently occupy the same ecological niches, driving complex and dynamic host-virus interactions. In Pseudomonas aeruginosa, phages from the Migulavirinae subfamily, tail fibre proteins (TFPs) are crucial to host recognition. These proteins, located within the phage tail structure, are subject to frequent recombination and may play a key role in shaping host range. This study investigates the molecular basis of host specificity in Litunavirus and Luzseptimavirus phages, focusing on the structure and variation of their TFPs.

resultsHost spectrum analysis divided phages into three categories; however, contrary to expectations, no direct correlation was found between TFP recombination history and host range, most likely because subsequent single amino acid changes in the pyocin knob regions, critical for adsorption, altered the host spectrum after the recombination event. Notably, phages sharing highly similar pyocin knob 2 domain architectures displayed identical host spectra, suggesting a strong link between this region and host specificity. Despite high sequence variability, all TFPs adopted a conserved trimeric fold with five regions: N-terminal, GrpE-like, GDSL-like with a carbohydrate-binding module, pyocin knob, and C-terminal. Structural similarities to bacterial PilA and pyocins were noted. Variation in the pyocin knob region, especially substitutions involving polar residues, was partially correlated with host range, likely via hydrogen bonding with the O-antigen. The GrpE-like domain resembled type IV pili, suggesting a role in reversible attachment, while the GDSL-like domain may support enzymatic processing of the O-antigen.

conclusionsOur findings support a multi-step adsorption mechanism of Migulavirinae phages, initiated by random encounters with the bacterial surface, followed by specific, stable interactions between the pyocin knob region and the bacterial lipopolysaccharide (LPS) O-antigen. Final stabilization involves additional interactions with the LPS core region. While the GrpE-like domain may contribute to transient stabilization near the surface, its structural similarity to PilA suggests a possible evolutionary convergence rather than a direct pilus-binding function. Despite high sequence variability, TFPs maintain conserved structural features, allowing for modular adaptations that precisely adjust host specificity. Importantly, the lack of a direct link between TFP recombination and host range suggests that factors beyond recombination influence phage host specificity.

Indexed as

Host SpecificityPseudomonas aeruginosaPseudomonas PhagesViral Tail ProteinsViral Tail ProteinsBacteriophagesHost spectrumPhage adsorptionPhage-host interactionsProtein modellingPseudomonas aeruginosaReceptor-binding proteinTail fibre proteins

Identifiers

PMID41254584
PMCPMC12625404

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.