Genomic Prediction of Antimicrobial Resistance: Ready or Not, Here It Comes!

Author:

Ransom Eric M1,Potter Robert F2,Dantas Gautam1234,Burnham Carey-Ann D135

Affiliation:

1. Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO

2. The Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO

3. Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO

4. Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO

5. Departments of Pediatrics and Medicine, Washington University School of Medicine, St. Louis, MO

Abstract

Abstract Background Next-generation sequencing (NGS) technologies are being used to predict antimicrobial resistance. The field is evolving rapidly and transitioning out of the research setting into clinical use. Clinical laboratories are evaluating the accuracy and utility of genomic resistance prediction, including methods for NGS, downstream bioinformatic pipeline components, and the clinical settings in which this type of testing should be offered. Content We describe genomic sequencing as it pertains to predicting antimicrobial resistance in clinical isolates and samples. We elaborate on current methodologies and workflows to perform this testing and summarize the current state of genomic resistance prediction in clinical settings. To highlight this aspect, we include 3 medically relevant microorganism exemplars: Mycobacterium tuberculosis, Staphylococcus aureus, and Neisseria gonorrhoeae. Last, we discuss the future of genomic-based resistance detection in clinical microbiology laboratories. Summary Antimicrobial resistance prediction by genomic approaches is in its infancy for routine patient care. Genomic approaches have already added value to the current diagnostic testing landscape in specific circumstances and will play an increasingly important role in diagnostic microbiology. Future advancements will shorten turnaround time, reduce costs, and improve our analysis and interpretation of clinically actionable results.

Funder

BioFire

Publisher

Oxford University Press (OUP)

Subject

Biochemistry, medical,Clinical Biochemistry

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