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Goeker, M.

Publications and source records attributed to Goeker, M..

3 recordsLinked to original sources

Large Language Model-assisted text mining reveals bacterial pathogen diversity

Compiling and characterising the diversity of bacterial pathogens of humans is a critical challenge to tackle infection risk, especially in the context of global antimicrobial resistance, climate change, and changing demographics. Here, we present a scalable, automated pipeline that harnesses large language models (LLMs) to systematically mine the biomedical literature for information of human pathogenicity across the bacterial domain. By interrogating tens of thousands of PubMed abstracts we identify 1,222 species with at least one abstract documenting human infection, of which 783 species are supported by 3 or more abstracts and are regarded as "confirmed pathogens". We extract, summarise, visualise and interpret data on infection contexts using both expert-curated LLM prompts and unsupervised text vectorisation. We show that these methods enable fine-grained trait mapping across taxa, including quantifying the degree of specialism or generalism in body site specificity for different taxa and the classification of pathogen species into 75 "pathogen types". An objective measure of the rate at which species are reported in the literature coupled to species clustering offers insights into the drivers of pathogen emergence. Our LLM-driven strategy generates an open, updatable, evidence-based catalogue of bacterial human pathogens and their ecological and clinical traits, providing a foundation for public health surveillance, diagnostics, and predictive modelling. This work demonstrates the potential of AI-assisted literature synthesis to transform our understanding of microbial diversity, including its impact on human health.

microbiology↗

Ancestral regulatory mechanisms specify conserved midbrain circuitry in arthropods and vertebrates

Corresponding attributes of neural development and function suggest arthropod and vertebrate brains may have an evolutionarily conserved organization. However, the underlying mechanisms have remained elusive. Here we identify a gene regulatory and character identity network defining the deutocerebral-tritocerebral boundary (DTB) in Drosophila. We show this network comprises genes homologous to those directing midbrain-hindbrain boundary (MHB) formation in vertebrates and their closest chordate relatives. Genetic tracing reveals that the embryonic DTB gives rise to adult midbrain circuits that in flies control auditory and vestibular information processing and motor coordination, as do MHB-derived circuits in vertebrates. DTB-specific gene expression and function is directed by cis-regulatory elements (CREs) of developmental control genes that include homologs of mammalian Zinc finger of the cerebellum and Purkinje cell protein 4. Moreover, Drosophila DTB-specific CREs correspond to regulatory sequences of human ENGRAILED-2, PAX-2 and DACHSHUND-1 that direct MHB-specific expression in the embryonic mouse brain. Together, these findings imply ancestral regulatory mechanisms mediating the genetic specification of midbrain-cerebellar circuitry for balance and motor control that may predated the radiation of cephalic nervous systems across the animal kingdom.

neuroscience↗

VICTOR: Genome-based Phylogeny and Classification of Prokaryotic Viruses

Bacterial and archaeal viruses (\"phages\") play an enormous role in global life cycles and have recently regained importance as therapeutic agents to fight serious infections by multi-resistant bacterial strains. Nevertheless, taxonomic classification of phages is up to now only insufficiently informed by genome sequencing. Despite thousands of publicly available phage genomes, it still needs to be investigated how this wealth of information can be used for the fast, universal and accurate classification of phages. The Genome BLAST Distance Phylogeny (GBDP) approach is a truly whole-genome method currently used for in silico DNA: DNA hybridization and phylogenetic inference from prokaryotic genomes. Based on the principles of phylogenetic systematics, we here established GBDP for phage phylogeny and classification, using the common subset of genome-sequenced and officially classified phages. Trees inferred with the best GBDP variants showed only few deviations from the official phage classification, which were uniformly due to incorrectly annotated GenBank entries. Except for low resolution at the family level, the majority of taxa was well supported as monophyletic. Clustering genome sequences with distance thresholds optimized for the agreement with the classification turned out to be phylogenetically reasonable. Accordingly modifying genera and species is taxonomically optional but would yield more uniform sequence divergence as well as stronger branch support. Analysing an expanded data set containing > 4000 phage genomes from public databases allowed for extrapolating regarding the number, composition and host specificity of future phage taxa. The selected methods are implemented in an easy-to-use web service \"VICTOR\" freely available at http://ggdc.dsmz.de/victor.php.

evolutionary biology↗