Hinrich Schulenburg Y

This paper develops a population-genetics model to study how host-associated microbes can assist in population rescue during environmental change, identifying two microbial contributions that shape rescue outcomes.

This study investigates how resistance to different antibiotics affects virulence in Pseudomonas aeruginosa, finding antibiotic-specific trade-offs between resistance and virulence.

This study shows that large population size accelerates ivermectin resistance in C. elegans, with unexpected cross-resistance to emodepside and sexual recombination playing a role.

The paper identifies negative hysteresis as a robust phenomenon in Pseudomonas aeruginosa that enhances antibiotic efficacy through increased aminoglycoside uptake after beta-lactam treatment.

This study uses a population genetic model to show that androdioecious C. elegans populations adapt rapidly to drug selection and exhibit high genetic diversity.

This study shows that β-lactam resistance in Haemophilus influenzae leads to fitness costs and collateral sensitivities, with unpredictable evolutionary outcomes.

The paper identifies sphingolipids from a bacterial PKS as mediators of microbiota protection against pathogens in C. elegans.

This study shows that resistance variation and bacterial interactions influence the adaptation of a genetically diverse Pseudomonas aeruginosa population to antibiotic treatment.

The paper characterizes new Pseudobdellovibrionaceae strains, revealing genomic features and evolutionary insights into bacterial predation modes.

This study shows that the fungus Barnettozyma californica can be ingested by C. elegans and, when combined with E. coli, enhances population growth and alters foraging behavior, suggesting a genetic basis for host-fungus-bacteria interactions.

The paper uses metabolic modeling to predict precision prebiotics that specifically enhance the abundance of a beneficial microbiome species in C. elegans.

The paper uses a multi-parental recombinant inbred line population in C. elegans to study gene expression variation and identifies eQTLs and trans-bands affecting gene expression.

This study develops a multi-parent recombinant inbred line population of C. elegans to improve QTL mapping resolution and identify novel QTLs for life-history traits.