Towards facilitated interpretation of shotgun metagenomics long-read sequencing data analyzed with KMA for the detection of bacterial pathogens and their antimicrobial resistance genes

Front Microbiol. 2024 Apr 4:15:1336532. doi: 10.3389/fmicb.2024.1336532. eCollection 2024.

Abstract

Metagenomic sequencing is a promising method that has the potential to revolutionize the world of pathogen detection and antimicrobial resistance (AMR) surveillance in food-producing environments. However, the analysis of the huge amount of data obtained requires performant bioinformatics tools and databases, with intuitive and straightforward interpretation. In this study, based on long-read metagenomics data of chicken fecal samples with a spike-in mock community, we proposed confidence levels for taxonomic identification and AMR gene detection, with interpretation guidelines, to help with the analysis of the output data generated by KMA, a popular k-mer read alignment tool. Additionally, we demonstrated that the completeness and diversity of the genomes present in the reference databases are key parameters for accurate and easy interpretation of the sequencing data. Finally, we explored whether KMA, in a two-step procedure, can be used to link the detected AMR genes to their bacterial host chromosome, both detected within the same long-reads. The confidence levels were successfully tested on 28 metagenomics datasets which were obtained with sequencing of real and spiked samples from fecal (chicken, pig, and buffalo) or food (minced beef and food enzyme products) origin. The methodology proposed in this study will facilitate the analysis of metagenomics sequencing datasets for KMA users. Ultimately, this will contribute to improvements in the rapid diagnosis and surveillance of pathogens and AMR genes in food-producing environments, as prioritized by the EU.

Keywords: KMA; ONT; antimicrobial resistance; bioinformatics; database; metagenomics; pathogens; results interpretation.

Grants and funding

The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. The research that yielded these results was funded by in-kind contribution of Sciensano within the context of JRP12-AMRSH5-FARMED and the Horizon 2020 Research and Innovation program of EU under grant agreement No 773830: One Health European Joint Program. The pig fecal samples used in Experiment E were funded through The environmental REsistome: confluence of Human and Animal Biota in antibiotic resistance spread (REHAB) project funded by the Antimicrobial Resistance Cross-council Initiative supported by the seven research councils (NE/N019989/1) and supported by the National Institute for Health Research Health Protection Research Unit (NIHR HPRU) in Healthcare Associated Infections and Antimicrobial Resistance at the University of Oxford (NIHR200915) in partnership with Public Health England (PHE).