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Biology subjects

Wurtzer, S.

Publications and source records attributed to Wurtzer, S..

3 recordsLinked to original sources

Drinking water treatment drastically modifies multi-kingdom water communities, but clinically relevant opportunistic bacterial pathogens persist

Controlling pathogenic microorganisms during water treatment processes is a major public health concern. However, the impact of different water sources and treatment processes on the drinking water microbiome and opportunistic bacterial pathogens remains poorly understood. Here, we report the analyses of two water systems: a river and groundwater source, and their corresponding treated waters, sampled bi-weekly for 6 months. Microbial communities were analysed through a metabarcoding and dPCR workflow coupling universal prokaryotic and eukaryotic primers with genus-targeting primers for Legionella and Pseudomonas to achieve a deep taxonomic resolution. We show that microbial communities in groundwater were more diverse than those in river water and that water treatment affected -diversity. Water treatment had a stronger influence on community composition than water system or seasonal variation. Despite lower bacterial loads, the relative abundance of Legionella, Pseudomonas, and non-tuberculous Mycobacteria (NTM) remained stable or even increased after water treatment, suggesting that conventional treatment processes promote enrichment of specific taxa. Excitingly, the genus-targeting analyses revealed a remarkable and previously uncharacterized diversity of Legionella species. L.pneumophila, pathogenic Pseudomonas clades and P. aeruginosa were detected in all environments, emphasizing their ability to adapt to diverse ecological conditions. Analysis of the eukaryotic fraction emphasized the persistence and emergence of eukaryotic hosts associated with these waterborne opportunistic pathogens. Our findings offer important insights into how water source characteristics and treatment processes influence the composition of the drinking water microbiome, while the high taxonomic resolution achieved for waterborne opportunistic bacterial pathogens underscores their ecological adaptability.

microbiology↗

Lytic bacteriophages active in urine against multi-drug resistant clinically derived Klebsiella pneumoniae causing urinary tract infection

ObjectivesMultidrug-resistant (MDR) Klebsiella pneumoniae is an increasingly important cause of recurrent urinary tract infections (UTIs), particularly in high-risk patients such as those with neurogenic bladder, where therapeutic options are limited. Bacteriophage therapy represents a promising alternative, but pre-clinical models and characterization of phages active against UTI-derived strains remain scarce. We therefore aimed to isolate and characterize bacteriophages targeting a clinical MDR K. pneumoniae strain causing recurrent UTI and evaluate their activity under urinary conditions. MethodsThree bacteriophages were isolated from environmental samples using an ESBL-producing K. pneumoniae clinical isolate obtained from a neurogenic bladder patient. Phages were characterized by genome sequencing, electron microscopy, stability assays, one-step growth curves, and host-range analysis across 79 clinical UTI isolates. Phage activity was quantified in LB medium and human urine using bacterial growth kinetics and a lytic activity score. ResultsThree lytic phages from the former siphoviridae family (EDIRA083, EDIRA088, and EDIRA092) belonging to distinct genera were identified. Genomic analysis confirmed the absence of lysogeny-associated, virulence, or antibiotic-resistance genes. Latent periods ranged from 8 to 40 minutes and burst sizes from 38 to 170 virions per infected bacterium. Host-range analysis revealed narrow activity for EDIRA083 and EDIRA088, whereas EDIRA092 infected 29% of the 79 clinical isolates tested. In liquid phage infection assays, overall lytic activity was consistently higher and more sustained in human urine than in LB, suggesting reduced fitness of resistant mutants under urinary conditions. ConclusionsThese results identify three genetically distinct lytic phages targeting MDR K. pneumoniae and highlight the importance of testing phage activity under infection-relevant conditions. Their activity in urine supports further evaluation of these phages as candidates for therapeutic development against MDR Klebsiella UTI.

microbiology↗

First evidence of SARS-CoV-2 genome detection in zebra mussel (Dreissena polymorpha).

The uses of bivalve molluscs in environmental biomonitoring have recently gained momentum due to their ability to indicate and concentrate human pathogenic microorganisms. In the context of the health crisis caused by the COVID-19 epidemic, the objective of this study was to determine if the SARS-CoV-2 ribonucleic acid genome can be detected in zebra mussels (Dreissena polymorpha) exposed to raw and treated urban wastewaters from two separate plants to support its interest as bioindicator of the SARS-CoV-2 genome contamination in water. The zebra mussels were exposed to treated wastewater through caging at the outlet of two plants located in France, as well as to raw wastewater at laboratory scale in controlled conditions. Within their digestive tissues, our results showed that SARS-CoV-2 genome was detected in zebra mussels, whether in raw and treated wastewaters. Moreover, the detection of the SARS-CoV-2 genome in such bivalve molluscans appeared even with low concentrations in raw wastewaters. This is the first detection of the SARS-CoV-2 genome in the tissues of a sentinel species exposed to raw and treated urban wastewaters. Despite the need for development for quantitative approaches, these results support the importance of such invertebrate organisms, especially zebra mussel, for the active surveillance of pathogenic microorganisms and their indicators in environmental waters. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=71 SRC="FIGDIR/small/446136v1_ufig1.gif" ALT="Figure 1"> View larger version (19K): org.highwire.dtl.DTLVardef@781087org.highwire.dtl.DTLVardef@853128org.highwire.dtl.DTLVardef@5e667forg.highwire.dtl.DTLVardef@19b243e_HPS_FORMAT_FIGEXP M_FIG C_FIG

ecology↗