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      Targeted surveillance strategies for efficient detection of novel antibiotic resistance variants

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          Abstract

          Genotype-based diagnostics for antibiotic resistance represent a promising alternative to empiric therapy, reducing inappropriate antibiotic use. However, because such assays infer resistance based on known genetic markers, their utility will wane with the emergence of novel resistance. Maintenance of these diagnostics will therefore require surveillance to ensure early detection of novel resistance variants, but efficient strategies to do so remain undefined. We evaluate the efficiency of targeted sampling approaches informed by patient and pathogen characteristics in detecting antibiotic resistance and diagnostic escape variants in Neisseria gonorrhoeae, a pathogen associated with a high burden of disease and antibiotic resistance and the development of genotype-based diagnostics. We show that patient characteristic-informed sampling is not a reliable strategy for efficient variant detection. In contrast, sampling informed by pathogen characteristics, such as genomic diversity and genomic background, is significantly more efficient than random sampling in identifying genetic variants associated with resistance and diagnostic escape.

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          Most cited references60

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          Anthropological and socioeconomic factors contributing to global antimicrobial resistance: a univariate and multivariable analysis

          Understanding of the factors driving global antimicrobial resistance is limited. We analysed antimicrobial resistance and antibiotic consumption worldwide versus many potential contributing factors.
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            Evolutionary history and global spread of the Mycobacterium tuberculosis Beijing lineage.

            Mycobacterium tuberculosis strains of the Beijing lineage are globally distributed and are associated with the massive spread of multidrug-resistant (MDR) tuberculosis in Eurasia. Here we reconstructed the biogeographical structure and evolutionary history of this lineage by genetic analysis of 4,987 isolates from 99 countries and whole-genome sequencing of 110 representative isolates. We show that this lineage initially originated in the Far East, from where it radiated worldwide in several waves. We detected successive increases in population size for this pathogen over the last 200 years, practically coinciding with the Industrial Revolution, the First World War and HIV epidemics. Two MDR clones of this lineage started to spread throughout central Asia and Russia concomitantly with the collapse of the public health system in the former Soviet Union. Mutations identified in genes putatively under positive selection and associated with virulence might have favored the expansion of the most successful branches of the lineage.
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              Aligning Sequence Reads, Clone Sequences and Assembly Contigs with BWA-MEM

              H. Li, Li, H Li (2013)
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                Author and article information

                Contributors
                Role: Senior Editor
                Role: Reviewing Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                30 June 2020
                2020
                : 9
                : e56367
                Affiliations
                [1 ]Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health BostonUnited States
                [2 ]Department of Microbiology and Immunology, The University of Melbourne at The Peter Doherty Institute for Infection and Immunity MelbourneAustralia
                [3 ]Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard T.H. Chan School of Public Health BostonUnited States
                [4 ]Division of Infectious Diseases, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School BostonUnited States
                McGill University Canada
                University of New South Wales Australia
                University of New South Wales Australia
                Kirby Institute, UNSW Sydney Australia
                Kirby Institute, UNSW Sydney Australia
                Author information
                https://orcid.org/0000-0003-1372-1301
                https://orcid.org/0000-0003-3062-7800
                https://orcid.org/0000-0001-6255-690X
                https://orcid.org/0000-0001-7363-6665
                https://orcid.org/0000-0003-1504-9213
                https://orcid.org/0000-0001-5646-1314
                Article
                56367
                10.7554/eLife.56367
                7326491
                32602459
                334b963a-276b-4c26-aa9b-2624f9d5731a
                © 2020, Hicks et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 25 February 2020
                : 17 May 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000060, National Institute of Allergy and Infectious Diseases (NIAID);
                Award ID: R01AI132606
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Research Article
                Epidemiology and Global Health
                Microbiology and Infectious Disease
                Custom metadata
                Sampling informed by pathogen genomic data may facilitate more efficient detection of novel antibiotic resistance than random sampling.

                Life sciences
                antibiotic resistance,diagnostic,surveillance,neisseria gonorrhoeae,other
                Life sciences
                antibiotic resistance, diagnostic, surveillance, neisseria gonorrhoeae, other

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