<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Stracy M</submitter><funding>European Research Council</funding><funding>Wellcome Trust</funding><funding>NIGMS NIH HHS</funding><pagination>889-894</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7612469</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>375(6583)</volume><pubmed_abstract>Treatment of bacterial infections currently focuses on choosing an antibiotic that matches a pathogen's susceptibility, with less attention paid to the risk that even susceptibility-matched treatments can fail as a result of resistance emerging in response to treatment. Combining whole-genome sequencing of 1113 pre- and posttreatment bacterial isolates with machine-learning analysis of 140,349 urinary tract infections and 7365 wound infections, we found that treatment-induced emergence of resistance could be predicted and minimized at the individual-patient level. Emergence of resistance was common and driven not by de novo resistance evolution but by rapid reinfection with a different strain resistant to the prescribed antibiotic. As most infections are seeded from a patient's own microbiota, these resistance-gaining recurrences can be predicted using the patient's past infection history and minimized by machine learning-personalized antibiotic recommendations, offering a means to reduce the emergence and spread of resistant pathogens.</pubmed_abstract><journal>Science (New York, N.Y.)</journal><pubmed_title>Minimizing treatment-induced emergence of antibiotic resistance in bacterial infections.</pubmed_title><pmcid>PMC7612469</pmcid><funding_grant_id>204684</funding_grant_id><funding_grant_id>281891</funding_grant_id><funding_grant_id>R01 GM081617</funding_grant_id><funding_grant_id>204684/Z/16/Z</funding_grant_id><pubmed_authors>Wolf T</pubmed_authors><pubmed_authors>Kishony R</pubmed_authors><pubmed_authors>Katz R</pubmed_authors><pubmed_authors>Amer Y</pubmed_authors><pubmed_authors>Herzel E</pubmed_authors><pubmed_authors>Yelin I</pubmed_authors><pubmed_authors>Koren G</pubmed_authors><pubmed_authors>Chodick G</pubmed_authors><pubmed_authors>Stracy M</pubmed_authors><pubmed_authors>Foxman B</pubmed_authors><pubmed_authors>Shalev V</pubmed_authors><pubmed_authors>Parizade M</pubmed_authors><pubmed_authors>Rimler G</pubmed_authors><pubmed_authors>Kuint J</pubmed_authors><pubmed_authors>Snitser O</pubmed_authors></additional><is_claimable>false</is_claimable><name>Minimizing treatment-induced emergence of antibiotic resistance in bacterial infections.</name><description>Treatment of bacterial infections currently focuses on choosing an antibiotic that matches a pathogen's susceptibility, with less attention paid to the risk that even susceptibility-matched treatments can fail as a result of resistance emerging in response to treatment. Combining whole-genome sequencing of 1113 pre- and posttreatment bacterial isolates with machine-learning analysis of 140,349 urinary tract infections and 7365 wound infections, we found that treatment-induced emergence of resistance could be predicted and minimized at the individual-patient level. Emergence of resistance was common and driven not by de novo resistance evolution but by rapid reinfection with a different strain resistant to the prescribed antibiotic. As most infections are seeded from a patient's own microbiota, these resistance-gaining recurrences can be predicted using the patient's past infection history and minimized by machine learning-personalized antibiotic recommendations, offering a means to reduce the emergence and spread of resistant pathogens.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2025-04-04T02:24:01.364Z</modification><creation>2025-04-04T02:24:01.364Z</creation></dates><accession>S-EPMC7612469</accession><cross_references><pubmed>35201862</pubmed><doi>10.1126/science.abg9868</doi></cross_references></HashMap>