Agnès Cottalorda1, Marie Leoz1, Sandrine Dahyot1,2, François Gravey3, Maxime Grand1, Thomas Froidure1, Fabien Aujoulat4, Simon Le Hello3, Estelle Jumas-Bilak4, Martine Pestel-Caron1,2. 1. Normandie Université, UNIROUEN, Groupe de Recherche sur l'Adapatation Microbienne (GRAM 2.0 EA2656), Rouen, France. 2. Department of Bacteriology, Rouen University Hospital, Normandie Université, UNIROUEN, Groupe de Recherche sur l'Adapatation Microbienne (GRAM 2.0 EA2656), Rouen, France. 3. Normandie Université, UNICAEN, Groupe de Recherche sur l'Adapatation Microbienne (GRAM 2.0 EA2656), Caen, France. 4. Team Pathogènes Hydriques Santé Environnement, UMR 5569 HydroSciences Montpellier, Unité de Bactériologie, UFR Pharmacie, University of Montpellier, Montpellier, France.
Abstract
BACKGROUND: Pseudomonas aeruginosa is responsible for up to 10% of healthcare associated urinary tract infections (UTI), which can be difficult to treat and can lead to bacterial persistence. While numerous whole genome sequencing (WGS) analyses have explored within-host genomic adaptation and microevolution of P. aeruginosa during cystic fibrosis (CF) infections, little is known about P. aeruginosa adaptation to the urinary tract. RESULTS: Whole genome sequencing was performed on 108 P. aeruginosa urinary isolates, representing up to five isolates collected from 2 to 5 successive urine samples from seven patients hospitalized in a French hospital over 48-488 days. Clone type single nucleotide polymorphisms (ctSNPs) analysis revealed that each patient was colonized by a single clone type (<6000 SNPs between two isolates) at a given time and over time. However, 0-126 SNPs/genome/year were detected over time. Furthermore, large genomic deletions (1-5% of the genome) were identified in late isolates from three patients. For 2 of them, a convergent deletion of 70 genes was observed. Genomic adaptation (SNPs and deletion) occurred preferentially in genes encoding transcriptional regulators, two-component systems, and carbon compound catabolism. This genomic adaptation was significantly associated with a reduced fitness, particularly in artificial urine medium, but no strict correlation was identified between genomic adaptation and biofilm formation. CONCLUSION: This study provides the first insight into P. aeruginosa within-host evolution in the urinary tract. It was driven by mutational mechanisms and genomic deletions and could lead to phenotypic changes in terms of fitness and biofilm production. Further metabolomic and phenotypic analyses are needed to describe in-depth genotype-phenotype associations in this complex and dynamic host-environment.
BACKGROUND: Pseudomonas aeruginosa is responsible for up to 10% of healthcare associated urinary tract infections (UTI), which can be difficult to treat and can lead to bacterial persistence. While numerous whole genome sequencing (WGS) analyses have explored within-host genomic adaptation and microevolution of P. aeruginosa during cystic fibrosis (CF) infections, little is known about P. aeruginosa adaptation to the urinary tract. RESULTS: Whole genome sequencing was performed on 108 P. aeruginosa urinary isolates, representing up to five isolates collected from 2 to 5 successive urine samples from seven patients hospitalized in a French hospital over 48-488 days. Clone type single nucleotide polymorphisms (ctSNPs) analysis revealed that each patient was colonized by a single clone type (<6000 SNPs between two isolates) at a given time and over time. However, 0-126 SNPs/genome/year were detected over time. Furthermore, large genomic deletions (1-5% of the genome) were identified in late isolates from three patients. For 2 of them, a convergent deletion of 70 genes was observed. Genomic adaptation (SNPs and deletion) occurred preferentially in genes encoding transcriptional regulators, two-component systems, and carbon compound catabolism. This genomic adaptation was significantly associated with a reduced fitness, particularly in artificial urine medium, but no strict correlation was identified between genomic adaptation and biofilm formation. CONCLUSION: This study provides the first insight into P. aeruginosa within-host evolution in the urinary tract. It was driven by mutational mechanisms and genomic deletions and could lead to phenotypic changes in terms of fitness and biofilm production. Further metabolomic and phenotypic analyses are needed to describe in-depth genotype-phenotype associations in this complex and dynamic host-environment.
Authors: Gabriel Cabot; Laura Zamorano; Bartolomé Moyà; Carlos Juan; Alfonso Navas; Jesús Blázquez; Antonio Oliver Journal: Antimicrob Agents Chemother Date: 2016-01-04 Impact factor: 5.191
Authors: Petra Tielen; Daniel Wibberg; Jochen Blom; Nathalie Rosin; Ann-Kathrin Meyer; Boyke Bunk; Max Schobert; Reinhilde Tüpker; Sarah Schatschneider; Christian Rückert; Andreas Albersmeier; Alexander Goesmann; Frank-Jörg Vorhölter; Dieter Jahn; Alfred Pühler Journal: Genome Announc Date: 2014-01-23
Authors: Daniel Wibberg; Petra Tielen; Jochen Blom; Nathalie Rosin; Max Schobert; Reinhilde Tüpker; Sarah Schatschneider; Dominik Spilker; Andreas Albersmeier; Alexander Goesmann; Frank-Jörg Vorhölter; Alfred Pühler; Dieter Jahn Journal: Genome Announc Date: 2014-03-13
Authors: Frank-Jörg Vorhölter; Petra Tielen; Daniel Wibberg; Maike Narten; Max Schobert; Reinhilde Tüpker; Jochen Blom; Sarah Schatschneider; Anika Winkler; Andreas Albersmeier; Alexander Goesmann; Alfred Pühler; Dieter Jahn Journal: Genome Announc Date: 2015-03-12