High frequency body site translocation of nosocomial Pseudomonas aeruginosa

Lewis W. S. Fisher, Harry A. Thorpe, Davide Sassera, Jukka Corander and Josephine M. Bryant ()
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Lewis W. S. Fisher: Wellcome Sanger Institute, Parasites and Microbes
Harry A. Thorpe: University of Oslo, Department of Biostatistics, Faculty of Medicine
Davide Sassera: University of Pavia, Department of Biology and Biotechnology
Jukka Corander: Wellcome Sanger Institute, Parasites and Microbes
Josephine M. Bryant: Wellcome Sanger Institute, Parasites and Microbes

Nature Communications, 2025, vol. 16, issue 1, 1-9

Abstract: Abstract Pseudomonas aeruginosa is an important nosocomial pathogen which can cause serious infections across diverse anatomic locations. Infections can spread within an individual to different body sites, but the rate and directionality of this process is unknown. Here, we explore within-host diversity as well as the body site translocation dynamics using de-convoluted metagenomic P. aeruginosa reads from 256 hospital patients sampled at both respiratory and gut sites. Of the 84 patients where P. aeruginosa genomes could be recovered, there were 27 cases where the same P. aeruginosa clone was detected across multiple body sites. Using a simulation approach, we find that the majority of body site sharing is likely due to within-patient translocation of clones rather than independent acquisition from the hospital environment. Using ancestral reconstruction, we predict that most clones likely occupied a respiratory niche, and that the probable direction of clone transmission is lung-to-gut. Analysis of within-patient variation highlights strong enrichment of mutations in genes associated with antimicrobial resistance, irrespective of sample type. We report significantly more translocation than has been previously reported and highlight that lower respiratory tract infections can result in persistent gut colonisation of P. aeruginosa, a major risk factor for sepsis in vulnerable patients.

Date: 2025
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DOI: 10.1038/s41467-025-66088-x

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