Estimating the fitness cost and benefit of antimicrobial resistance from pathogen genomic data

Author:

Helekal David1,Keeling Matt2ORCID,Grad Yonatan H.3ORCID,Didelot Xavier4ORCID

Affiliation:

1. Centre for Doctoral Training in Mathematics for Real-World Systems, University of Warwick, Coventry, UK

2. Mathematics Institute and School of Life Sciences, University of Warwick, Coventry, UK

3. Department of Immunology and Infectious Diseases, TH Chan School of Public Health, Harvard University, Boston, MA, USA

4. School of Life Sciences and Department of Statistics, University of Warwick, Coventry, UK

Abstract

Increasing levels of antibiotic resistance in many bacterial pathogen populations are a major threat to public health. Resistance to an antibiotic provides a fitness benefit when the bacteria are exposed to this antibiotic, but resistance also often comes at a cost to the resistant pathogen relative to susceptible counterparts. We lack a good understanding of these benefits and costs of resistance for many bacterial pathogens and antibiotics, but estimating them could lead to better use of antibiotics in a way that reduces or prevents the spread of resistance. Here, we propose a new model for the joint epidemiology of susceptible and resistant variants, which includes explicit parameters for the cost and benefit of resistance. We show how Bayesian inference can be performed under this model using phylogenetic data from susceptible and resistant lineages and that by combining data from both we are able to disentangle and estimate the resistance cost and benefit parameters separately. We applied our inferential methodology to several simulated datasets to demonstrate good scalability and accuracy. We analysed a dataset of Neisseria gonorrhoeae genomes collected between 2000 and 2013 in the USA. We found that two unrelated lineages resistant to fluoroquinolones shared similar epidemic dynamics and resistance parameters. Fluoroquinolones were abandoned for the treatment of gonorrhoea due to increasing levels of resistance, but our results suggest that they could be used to treat a minority of around 10% of cases without causing resistance to grow again.

Funder

Public Health Research Programme

Engineering and Physical Sciences Research Council

Publisher

The Royal Society

Subject

Biomedical Engineering,Biochemistry,Biomaterials,Bioengineering,Biophysics,Biotechnology

Reference58 articles.

1. CDC. 2013 Antibiotic resistance threats in the United States, 2013. CS239559-B. Atlanta, GA: CDC. See https://www.cdc.gov/drugresistance/pdf/ar-threats-2013-508.pdf.

2. O’Neill J. 2016 Tackling drug-resistant infections globally: final report and recommendations. London, UK: Wellcome Trust/HM Government.

3. Global burden of bacterial antimicrobial resistance in 2019: a systematic analysis

4. Targeting virulence: a new paradigm for antimicrobial therapy

5. Evaluating treatment protocols to prevent antibiotic resistance

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