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Parker, M. H.

Publications and source records attributed to Parker, M. H..

2 recordsLinked to original sources

AMR-GNN: A multi-representation graph neural network framework to enable genomic antimicrobial resistance prediction

Whole-genome sequencing (WGS) data are an invaluable resource for understanding antimicrobial resistance (AMR) mechanisms. However, WGS data are high-dimensional and the lack of standardized genomic representations is a key barrier to AMR prediction. To fully explore these high-resolution data, we propose AMR-GNN, a graph deep learning-based framework that integrates multiple genomic representations with graph neural networks (GNN) to enable AMR prediction from genomic sequence data. We tested AMR-GNN with Pseudomonas aeruginosa, a clinically relevant Gram-negative bacterial pathogen known for its complex AMR mechanisms. We demonstrate that AMR-GNN addresses several key problems in AMR prediction with data-driven machine learning (ML) approaches, including using multiple genomic representations to enhance performance, mitigate the influence of clonal relationships, and identify informative biomarkers to provide explainability and generate novel hypotheses. Follow-up validation on the largest publicly available dataset spanning both Gram-negative and Gram-positive pathogens highlights AMR-GNNs broad applicability in detecting AMR in diverse and clinically relevant pathogen-drug combinations.

genomics↗

Wild type domestication: loss of intrinsic metabolic traits concealed by culture in rich media

BackgroundBacteria are typically isolated on rich media to maximise isolation success, removing them from their native evolutionary context. This eliminates selection pressures, enabling otherwise deleterious genomic events to accumulate. Here we present a cautionary tale of these quiet mutations which can persist unnoticed in bacterial culture lines. MethodsWe used a combination of microbiological culture (standard and minimal media conditions), whole genome sequencing and metabolic modelling to investigate putative Klebsiella pneumoniae L-histidine auxotrophs. Additionally, we used genome-scale metabolic modelling to predict auxotrophies among completed public genomes (n=2,637). ResultsTwo sub-populations were identified within a K. pneumoniae frozen stock, differing in their ability to grow in the absence of L-histidine. These sub-populations were the same strain, separated by eight single nucleotide variants and an insertion sequence-mediated deletion of the L-histidine biosynthetic operon. The His- sub-population remained undetected for >10 years despite its in inclusion in independent laboratory experiments. Genome-scale metabolic models predicted 0.8% public genomes contained [≥]1 auxotrophy, with purine/pyrimidine biosynthesis and amino acid metabolism most frequently implicated. DiscussionWe provide a definitive example of the role of standard rich media culture conditions in obscuring biologically relevant mutations i.e. nutrient auxotrophies, and estimate the prevalence of such auxotrophies using public genome collections. While the prevalence is low, it is not insignificant given the thousands of K. pneumoniae that are isolated for global surveillance and research studies each year. Our data serve as a pertinent reminder that rich-media culturing can cause unnoticed wild type domestication.

microbiology↗