Bacteriophage PAK_P3 genome structuration and dynamics during infection of Pseudomonas aeruginosa reveal specific interaction patterns

While the dynamic changes in genome organization in cellular organisms have been well described, the three-dimensional (3D) folding of phage genomes during the infection of their host is extremely limited. Understanding how phage genomes fold, invade, and rearrange the genome of their host to functionally organize the optimal expression of their genes remains unknown. Here, we explore the spatial dynamics of the virulent double-stranded DNA phage PAK_P3 during infection of its host Pseudomonas aeruginosa and reveal how its genome rapidly decondenses to adopt a specific 3D organization that reflects its transcriptional program. Concomitantly, the host genome decondenses as gene expression wanes and transcription-induced domains vanish. We also uncover specific contacts of the phage genome with host chromosome, showing how the phage genome exploits the spatial genome architecture of its host to succeed in its infection cycle. Our data highlight an unprecedented level of genome folding and gene expression regulation during a viral infection.

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Publication Details

Journal
Science Advances
Published
2026-08-26
DOI
https://doi.org/10.1126/sciadv.aef2512
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Bacteriophage PAK_P3 genome structuration and dynamics during infection of Pseudomonas aeruginosa reveal specific interaction patterns

Fabien Girard, Pauline Misson, Quentin Lamy-Besnier, Romain Koszul et al.
Science Advances
Bacteriophages and microbial interactions
article

Bacteriophage PAK_P3 genome structuration and dynamics during infection of Pseudomonas aeruginosa reveal specific interaction patterns

Fabien Girard, Pauline Misson, Quentin Lamy-Besnier, Romain Koszul, Martial Marbouty, Laurent Debarbieux, Devon E. Conti, Amaury Bignaud, Agnès Thierry
article en

Abstract

While the dynamic changes in genome organization in cellular organisms have been well described, the three-dimensional (3D) folding of phage genomes during the infection of their host is extremely limited. Understanding how phage genomes fold, invade, and rearrange the genome of their host to functionally organize the optimal expression of their genes remains unknown. Here, we explore the spatial dynamics of the virulent double-stranded DNA phage PAK_P3 during infection of its host Pseudomonas aeruginosa and reveal how its genome rapidly decondenses to adopt a specific 3D organization that reflects its transcriptional program. Concomitantly, the host genome decondenses as gene expression wanes and transcription-induced domains vanish. We also uncover specific contacts of the phage genome with host chromosome, showing how the phage genome exploits the spatial genome architecture of its host to succeed in its infection cycle. Our data highlight an unprecedented level of genome folding and gene expression regulation during a viral infection.

Science AdvancesVol. 12(35)
Centre National de la Recherche Scientifique (FR), Institut Pasteur (FR), Université Sorbonne Nouvelle (FR), Université Paris Cité (FR), Sorbonne Université (FR), University of Oxford (GB), Department of Genomes & Genetics (FR)
Ministère de l'Enseignement supérieur, de la Recherche et de l'Innovation, Agence Nationale de la Recherche, H2020 European Research Council
Openalex Percentile: Top 10%
Bacteriophages and microbial interactions
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