Publication:
Citywide metagenomic surveillance of food centres reveals local microbial signatures and antibiotic resistance gene enrichment

dc.contributor.coauthorTeo JJY
dc.contributor.coauthorHo EXP
dc.contributor.coauthorNg AHQ
dc.contributor.coauthorHow SHC
dc.contributor.coauthorChng KR
dc.contributor.coauthorFau'di MT
dc.contributor.coauthorAung KT
dc.contributor.coauthorNagarajan N.
dc.contributor.kuauthorAteş, Yiğit Can
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.date.accessioned2025-09-10T05:01:37Z
dc.date.available2025-09-09
dc.date.issued2025
dc.description.abstractThe distribution of microorganisms in built environments with high human traffic, such as food centres, can potentially have a significant impact on public health, particularly in the context of increasing worldwide incidence of food and fomite-related outbreaks. In many major Asian cities, public food centres are central to daily food consumption, yet there is a lack of baseline knowledge about their environmental microbiomes. We performed a city-wide metagenomic survey of food-centre microbiomes in Singapore, covering 16 centres and 240 samples, to map the abundances of microbial (bacteria, archaea, fungi, viruses) and non-microbial DNA across two timepoints. Food-centre microbiomes were found to be enriched in food-related DNA signatures compared to other environments, such as hospitals and offices, with specific food-microbe associations (e.g., Enterobacteriaceae and fish) and food DNA providing a partial explanation for the microbial profiles observed (44% of variation explained). Machine learning analysis identified a small set of microbial species (n = 22) that serve as highly accurate (>80%) location-specific signatures for various food centres, some of which persist even after 3 years. Profiling of antibiotic resistance genes (ARGs) and pathogens identified a surprising enrichment of ARGs in food centres relative to other non-healthcare environments (>2.5×), and an order of magnitude enrichment of key pathogenic species (e.g., Klebsiella pneumoniae, Enterobacter spp) even compared to hospital environments. These results highlight the contribution of diverse biotic and abiotic factors in shaping the unique microbiome profiles of different food-centre environments, and the potential for using metagenomic surveillance to understand the risk for infections and antibiotic resistance gene transmission.
dc.description.fulltextYes
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyPubMed
dc.description.openaccessGold OA
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.versionPublished Version
dc.identifier.doi10.1038/s44259-025-00132-0
dc.identifier.eissn2731-8745
dc.identifier.embargoNo
dc.identifier.filenameinventorynoIR06581
dc.identifier.issue1
dc.identifier.pubmed40629022
dc.identifier.quartileN/A
dc.identifier.urihttps://doi.org/10.1038/s44259-025-00132-0
dc.identifier.urihttps://hdl.handle.net/20.500.14288/30539
dc.identifier.volume3
dc.identifier.wos001636561700001
dc.language.isoeng
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofNPJ Antimicrob Resist
dc.relation.openaccessYes
dc.rightsCC BY-NC-ND (Attribution-NonCommercial-NoDerivs)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleCitywide metagenomic surveillance of food centres reveals local microbial signatures and antibiotic resistance gene enrichment
dc.typeJournal Article
dspace.entity.typePublication
person.familyNameAteş
person.givenNameYiğit Can
relation.isParentOrgUnitOfPublication8e756b23-2d4a-4ce8-b1b3-62c794a8c164
relation.isParentOrgUnitOfPublication.latestForDiscovery8e756b23-2d4a-4ce8-b1b3-62c794a8c164

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