A genomic data resource for predicting antimicrobial resistance from laboratory-derived antimicrobial susceptibility phenotypes

Author:

VanOeffelen Margo1,Nguyen Marcus23,Aytan-Aktug Derya4,Brettin Thomas25,Dietrich Emily M25,Kenyon Ronald W6,Machi Dustin6,Mao Chunhong6,Olson Robert23,Pusch Gordon D1,Shukla Maulik23,Stevens Rick57ORCID,Vonstein Veronika1,Warren Andrew S6,Wattam Alice R36,Yoo Hyunseung23,Davis James J238ORCID

Affiliation:

1. Fellowship for Interpretation of Genomes, Burr Ridge, IL, USA

2. University of Chicago Consortium for Advanced Science and Engineering, University of Chicago, Chicago, IL, USA

3. Data Science and Learning Division, Argonne National Laboratory, Argonne, IL, USA

4. National Food Institute, Technical University of Denmark, Kgs. Lyngby, Denmark

5. Computing Environment and Life Sciences, Argonne National Laboratory, Argonne, IL, USA

6. Biocomplexity Institute and Initiative, University of Virginia, Virginia, USA

7. Department of Computer Science, University of Chicago, Chicago, IL, USA

8. Northwestern Argonne Institute for Science and Engineering, Evanston, IL, USA

Abstract

Abstract Antimicrobial resistance (AMR) is a major global health threat that affects millions of people each year. Funding agencies worldwide and the global research community have expended considerable capital and effort tracking the evolution and spread of AMR by isolating and sequencing bacterial strains and performing antimicrobial susceptibility testing (AST). For the last several years, we have been capturing these efforts by curating data from the literature and data resources and building a set of assembled bacterial genome sequences that are paired with laboratory-derived AST data. This collection currently contains AST data for over 67 000 genomes encompassing approximately 40 genera and over 100 species. In this paper, we describe the characteristics of this collection, highlighting areas where sampling is comparatively deep or shallow, and showing areas where attention is needed from the research community to improve sampling and tracking efforts. In addition to using the data to track the evolution and spread of AMR, it also serves as a useful starting point for building machine learning models for predicting AMR phenotypes. We demonstrate this by describing two machine learning models that are built from the entire dataset to show where the predictive power is comparatively high or low. This AMR metadata collection is freely available and maintained on the Bacterial and Viral Bioinformatics Center (BV-BRC) FTP site ftp://ftp.bvbrc.org/RELEASE_NOTES/PATRIC_genomes_AMR.txt.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Information Systems

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