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Профиль

Typas Lab

Профиль Vively

Systems Microbiology @EMBL, combining high-throughput approaches & mechanism in bacteria, antibiotics, microbiome, infection, species diversity, cell envelope https://www.embl.org/groups/typas/

@pilhoferlab.bsky.social @savitski-lab.bsky.social @cibiocm.bsky.social Justin Sonnenburg Erica Sonnenburg @soreklab.bsky.social @baerboletta.bsky.social @jorg-vogel-lab.bsky.social Paul Wilmes @karinaxavierlab.bsky.social Maria Zimmermann-Kogadeeva

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Organisers @lisamaierlab.bsky.social @kiranrpatil.bsky.social @robdfinn.bsky.social @embl.org @events.embl.org Speakers Ami Bhatt @dbikard.bsky.social Xiang Gao kc-huang.bsky.social @jhcepas.bsky.social @microbegrrl.bsky.social @keyfm.bsky.social @microbiome.bsky.social Elisabeth Lowe ...

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Featuring leading voices in microbiome research, with sessions on multi-omics, genetic tools, ecological context functions, and new model species. Focusing on research that moves from descriptive to molecular understanding and functional discoveries.

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Great collaboration inside and outside @embl.org @EMBLHeidelberg with @savitski-lab.bsky.social @zimmermannlab.bsky.social @sarsarela.bsky.social y.social @linairmi.bsky.social Gad Frankel @imperialcollegeldn.bsky.social and others #Microbiome #AntibioticResistance #AMR

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Overall, we demonstrate that specific microbiota compositions affect the fitness of resistant strains through carbohydrate competition, offering a path towards microbiota‑based interventions that actively counter‑select antibiotic-resistant strains without disrupting susceptible community members.

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Mechanistically, glyR mutations upregulate the glycoporin GlyP, improving growth in glycerol-rich niches but carrying costs elsewhere. These mutations are under conditional positive selection in clinical isolates, showing how microbiota context can shape the evolution of resistance.

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We found that E. coli can be a key driver of selection for a high-fitness antibiotic resistant K. pneumoniae strain in complex communities. Higher-order interactions with other community members could enhance or decrease the selective advantage of the resistant mutant.

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We introduce a high-throughput method to quantify resistance-associated fitness costs inside complex gut microbiomes. This lets us identify which microbiota are permissive or restrictive for antibiotic-resistant pathogens.

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@pilhoferlab.bsky.social @savitski-lab.bsky.social @cibiocm.bsky.social Justin Sonnenburg Erica Sonnenburg @soreklab.bsky.social @baerboletta.bsky.social Paul Wilmes @karinaxavierlab.bsky.social Maria Zimmermann Kogadeeva

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Organisers: @lisamaierlab.bsky.social @kiranrpatil.bsky.social @robdfinn.bsky.social @embl.org @events.embl.org Speakers: Ami Bhatt @dbikard.bsky.social Xiang Gao KC Huang @jhcepas.bsky.social @microbegrrl.bsky.social @keyfm.bsky.social @microbiome.bsky.social Elisabeth Lowe

251

Featuring leading voices in microbiome research, with sessions on multi-omics, genetic tools, ecological context functions, and new model species. Focusing on research that moves from descriptive to molecular understanding and functional discoveries.

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Great collaboration inside and outside @embl.org with @kiranrpatil.bsky.social @indraroux.bsky.social @zimmermannlab.bsky.social @zellerlab.bsky.social @EMBLHeidelberg

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We systematically compared essential genes, protein domains & non-coding elements, uncovering toxic modalities & functional redundancy as key aspects of species-specific essentiality.

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