A metagenomic survey of global antimicrobial resistance

dc.contributor.authorBerkman, Aaron Yehuda
dc.contributor.supervisorDe Maayer, Pieter
dc.date.accessioned2026-07-10T12:32:44Z
dc.date.issued2025-02
dc.descriptionA dissertation submitted in fulfilment of the requirements for the degree Master of Science, to the Faculty of Science, School of Molecular and Cell Biology,, University of the Witwatersrand, Johannesburg, 2025
dc.description.abstractAntimicrobial resistance (AMR) poses a major global health threat, yet understanding of environmental reservoirs remains limited. This study analysed 1,758 metagenomes to assess microbial species and antimicrobial resistance gene (ARG) diversity across global soil and aquatic environments. Using Kraken2 for taxonomic classification and DeepARG for ARG identification, coupled with diversity analyses, this research revealed distinct patterns in microbial and antibiotic resistance gene profiles. Microbial communities showed similar overall diversity between soil and aquatic environments (Shannon indices: 5.409 and 5.410 respectively) but exhibited distinct structural patterns. Urban wastewater demonstrated the highest microbial diversity in aquatic settings (Shannon index: 5.43), while cold biomes showed highest diversity in soils (Shannon index: 5.63). ARG profiles revealed different patterns, with soil environments showing higher median diversity (4.68) compared to aquatic environments (4.52). Notably, anthropogenic soils exhibited the highest ARG diversity (Shannon index: 5.71) despite reduced microbial diversity, highlighting human activity's role in ARG proliferation. The soil core resistome was substantially larger than aquatic (179 vs 113 ARGs), with 101 shared ARGs between environments. ESKAPE pathogens were most prevalent in human-impacted environments, reaching 8.32% in groundwater and 8.23% in temperate soils. This comprehensive analysis reveals how environmental conditions and human activities distinctly shape microbial communities and their associated resistomes. These findings underscore the urgent need for integrated AMR surveillance beyond clinical settings and highlight critical intervention points for mitigating the spread of antibiotic resistance, particularly in agricultural and urban environments where human activities substantially influence resistance patterns.
dc.description.sponsorshipUniversity of the Witwatersrand, Johannesburg - Postgraduate Merit Award (PMA)
dc.description.submitterMMM2026
dc.facultyFaculty of Science
dc.identifier0009-0009-1345-6887
dc.identifier.citationBerkman, Aaron Yehuda. (2025). A metagenomic survey of global antimicrobial resistance. [Master's dissertation, University of the Witwatersrand, Johannesburg]. WIReDSpace. https://hdl.handle.net/10539/49561
dc.identifier.urihttps://hdl.handle.net/10539/49561
dc.language.isoen
dc.publisherUniversity of the Witwatersrand, Johannesburg
dc.rights©2025 University of the Witwatersrand, Johannesburg. All rights reserved. The copyright in this work vests in the University of the Witwatersrand, Johannesburg. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of University of the Witwatersrand, Johannesburg.
dc.rights.holderUniversity of the Witwatersrand, Johannesburg
dc.schoolSchool of Molecular and Cell Biology
dc.subjectAntimicrobial resistance
dc.subjectEnvironmental resistome
dc.subjectESKAPE pathogens
dc.subjectMetagenomics
dc.subjectMicrobial diversity
dc.subjectCore resistome
dc.subjectEnvironmental reservoirs
dc.subjectAnthropogenic impact
dc.subjectSoil microbiome
dc.subjectAquatic microbiome
dc.subjectUCTD
dc.subject.primarysdgSDG-9: Industry, innovation and infrastructure
dc.subject.secondarysdgSDG-3: Good health and well-being
dc.titleA metagenomic survey of global antimicrobial resistance
dc.typeDissertation

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