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Le-Bury, P.

Publications and source records attributed to Le-Bury, P..

3 recordsLinked to original sources

Yersinia pestis lipoprotein SlyB promotes plague pathogenesis via envelope stress tolerance

Yersinia pestis, the etiological agent of plague, persists in an enzootic cycle involving mammals and fleas, requiring constant outer membrane (OM) adaptation to disparate host environments. One such pathway involves the glycine zipper 2TM domain-containing protein SlyB, a central component of the OM stress response and PhoPQ virulence pathway. While the OM is critical for virulence, the role of the OM lipoprotein SlyB in Y. pestis ecology and pathogenesis remains unknown. We show by phylogenetic analyses that slyB paralogs expanded in environmental bacteria, whereas the canonical slyB gene was under negative selective pressure during Y. pestis speciation from Yersinia pseudotuberculosis. Using rodent and flea infection models recapitulating Y. pestis natural history, we demonstrate that SlyB is specifically required to resist the mammalian immune system at 37{degrees}C, including neutrophil-mediated antimicrobial activity during lymph node colonization, but is dispensable in septicemic plague in rodents. Strikingly, SlyB is not required for flea colonization and resistance to the antimicrobial-peptide-based immunity of arthropods at lower temperatures. SlyB-dependent OM stress tolerance reveals a mechanism by which Y. pestis establishes bubonic plague, in line with its critical lipopolysaccharide structural switch. Our findings identify SlyB as an evolutionarily fine-tuned component of the Y. pestis envelope that mediates immune escape upon infection of mammalian hosts through maintenance of structural integrity.

microbiology↗

In-host evolution of Yersinia enterocolitica during a chronic human infection

Following a pacemaker implantation, a 75-years-old patient suffered from five successive bacteremia episodes between in 1999 and 2013 despite long-term antibiotic treatment, with intermittent vegetation apparition on the device atrial lead. Four blood isolates, identified as Yersinia enterocolitica bioserotype 4/O:3, were further genetically and phenotypically characterized. Phylogenetic reconstruction showed that the patient was chronically infected by the same strain, which evolved within the host for 14 years. Single-nucleotide polymorphism (SNP) analysis indicates that the last two isolates evolved in parallel and formed two independent lineages within the host. Pan-genome analysis and genome comparison showed that their common evolution was characterized by 41 small insertion/deletion events, loss of three large DNA fragments and mutations in 140 genes. A phylogenetic analysis by maximum likelihood identified two genes presenting a positive selection signal, suggesting that these mutations provided a survival advantage to bacteria during chronic infection. Quinolone resistance in the last two isolates was acquired through a so far undescribed deletion in the gyrA gene. Mass-spectrometry analysis revealed a strong proteome remodeling in the last two isolates which was correlated with a truncation in the stringent response regulator DksA. A reduced carbon, energy and purine metabolism supports their severe growth defects in vitro. 3rd-generation cephalosporin resistance of the last isolate was correlated with a truncation of OmpF, the main porin translocating antibiotics through the outer-membrane, as well as an increased production of BlaA and AmpC {beta}-lactamases. This is the first report of genetic and phenotypic changes associated to within-host adaptation of a pathogenic Yersinia species under antibiotic pressure.

microbiology↗

Dual proteomic signature of immune cells and Yersinia pestis upon blood infection

Emerging and reemerging infectious diseases represent major public health concerns. The urgent need for infection control measures requires deep understanding of molecular pathogenesis. Global approaches to study biological systems such as mass-spectrometry based proteomics benefited from groundbreaking physical and bioinformatical technological developments over recent years. However, dual proteomic study of highly pathogenic microorganisms and their hosts in complex matrices encountered during infection remains challenging due to high protein dynamic range of samples and requirements imposed in biosafety level 3 or 4 laboratories. Here, we constructed a dual proteomic pipeline of Yersinia pestis in human blood and plasma, mirroring bacteremic phase of plague. We provide the most complete Y. pestis proteome revealing a major reshaping of important bacterial path-ways such as methionine biosynthesis and iron acquisition in human plasma. Remarkably, proteomic profiling in human blood highlights a greater Yersinia outer proteins intoxication of monocytes than neutrophils. Our study unravels global expression changes and points to a specific pathogenic signature during infection, paving the way for future exploration of proteomes in the complex context of host-pathogen interactions. Subject CategoriesMicrobiology, Virology and Host Pathogen Interaction, Proteomics

systems biology↗