Please use this identifier to cite or link to this item: https://doi.org/10.3389/fmicb.2017.02200
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dc.titleCharacterization of metagenomes in urban aquatic compartments reveals high prevalence of clinically relevant antibiotic resistance genes in wastewaters
dc.contributor.authorNg C.
dc.contributor.authorTay M.
dc.contributor.authorTan B.
dc.contributor.authorLe T.-H.
dc.contributor.authorHaller L.
dc.contributor.authorChen H.
dc.contributor.authorKoh T.H.
dc.contributor.authorBarkham T.M.S.
dc.contributor.authorGin K.Y.-H.
dc.date.accessioned2020-09-01T00:48:35Z
dc.date.available2020-09-01T00:48:35Z
dc.date.issued2017
dc.identifier.citationNg C., Tay M., Tan B., Le T.-H., Haller L., Chen H., Koh T.H., Barkham T.M.S., Gin K.Y.-H. (2017). Characterization of metagenomes in urban aquatic compartments reveals high prevalence of clinically relevant antibiotic resistance genes in wastewaters. Frontiers in Microbiology 8 (NOV) : 2200. ScholarBank@NUS Repository. https://doi.org/10.3389/fmicb.2017.02200
dc.identifier.issn1664302X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/173759
dc.description.abstractThe dissemination of antimicrobial resistance (AMR) is an escalating problem and a threat to public health. Comparative metagenomics was used to investigate the occurrence of antibiotic resistant genes (ARGs) in wastewater and urban surface water environments in Singapore. Hospital and municipal wastewater (n = 6) were found to have higher diversity and average abundance of ARGs (303 ARG subtypes, 197,816 x/Gb) compared to treated wastewater effluent (n = 2, 58 ARG subtypes, 2,692 x/Gb) and surface water (n = 5, 35 subtypes, 7,985 x/Gb). A cluster analysis showed that the taxonomic composition of wastewaters was highly similar and had a bacterial community composition enriched in gut bacteria (Bacteroides, Faecalibacterium, Bifidobacterium, Blautia, Roseburia, Ruminococcus), the Enterobacteriaceae group (Klebsiella, Aeromonas, Enterobacter) and opportunistic pathogens (Prevotella, Comamonas, Neisseria). Wastewater, treated effluents and surface waters had a shared resistome of 21 ARGs encoding multidrug resistant efflux pumps or resistance to aminoglycoside, macrolide-lincosamide-streptogramins (MLS), quinolones, sulfonamide, and tetracycline resistance which suggests that these genes are wide spread across different environments. Wastewater had a distinctively higher average abundance of clinically relevant, class A beta-lactamase resistant genes (i.e., blaKPC, blaCTX-M, blaSHV, blaTEM). The wastewaters from clinical isolation wards, in particular, had a exceedingly high levels of blaKPC-2 genes (142,200 x/Gb), encoding for carbapenem resistance. Assembled scaffolds (16 and 30 kbp) from isolation ward wastewater samples indicated this gene was located on a Tn3-based transposon (Tn4401), a mobilization element found in Klebsiella pneumonia plasmids. In the longer scaffold, transposable elements were flanked by a toxin-antitoxin (TA) system and other metal resistant genes that likely increase the persistence, fitness and propagation of the plasmid in the bacterial host under conditions of stress. A few bacterial species (Enterobacter cloacae, Klebsiella pneumoniae, Citrobacter freundii, Pseudomonas aeruginosa) that were cultured from the isolation ward wastewaters on CHROMagar media harbored the blaKPC-2 gene. This suggests that hospital wastewaters derived from clinical specialty wards are hotspots for the spread of AMR. Assembled scaffolds of other mobile genetic elements such as IncQ and IncF plasmids bearing quinolone resistance genes (qnrS1, qnrS2) and the class A beta-lactamase gene (blaTEM-1) were recovered in wastewater samples which may aid the transfer of AMR. © 2017 Ng, Tay, Tan, Le, Haller, Chen, Koh, Barkham and Gin.
dc.sourceUnpaywall 20200831
dc.subjectaminoglycoside
dc.subjectantitoxin
dc.subjectbeta lactam antibiotic
dc.subjectbeta lactamase
dc.subjectcarbapenem
dc.subjectlincosamide
dc.subjectmacrolide
dc.subjectquinolone
dc.subjectstreptogramin derivative
dc.subjectsulfonamide
dc.subjectsurface water
dc.subjecttetracycline
dc.subjecttoxin
dc.subjectantibiotic resistance
dc.subjectaquatic environment
dc.subjectArticle
dc.subjectbacterium identification
dc.subjectbacterium isolation
dc.subjectcommunity structure
dc.subjectDNA extraction
dc.subjecteffluent
dc.subjectgene
dc.subjecthospital
dc.subjectintestine flora
dc.subjectmetagenome
dc.subjectmetagenomics
dc.subjectmicrobial community
dc.subjectmultidrug resistance
dc.subjectnonhuman
dc.subjectopen reading frame
dc.subjectphylogeny
dc.subjectplasmid
dc.subjectprevalence
dc.subjecttaxonomy
dc.subjecttransposon
dc.subjecturban area
dc.subjectwaste water
dc.subjectwaste water management
dc.subjectwater analysis
dc.typeArticle
dc.contributor.departmentCIVIL AND ENVIRONMENTAL ENGINEERING
dc.contributor.departmentNUS ENVIRONMENTAL RESEARCH INSTITUTE
dc.contributor.departmentMICROBIOLOGY AND IMMUNOLOGY
dc.description.doi10.3389/fmicb.2017.02200
dc.description.sourcetitleFrontiers in Microbiology
dc.description.volume8
dc.description.issueNOV
dc.description.page2200
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