Mobilizable antibiotic resistance genes are present in dust microbial communities
The decades-long global trend of urbanization has led to a population that spends increasing amounts of time indoors. Exposure to microbes in buildings, and specifically in dust, is thus also increasing, and has been linked to various health outcomes and to antibiotic resistance genes (ARGs). These...
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description | The decades-long global trend of urbanization has led to a population that spends increasing amounts of time indoors. Exposure to microbes in buildings, and specifically in dust, is thus also increasing, and has been linked to various health outcomes and to antibiotic resistance genes (ARGs). These are most efficiently screened using DNA sequencing, but this method does not determine which microbes are viable, nor does it reveal whether their ARGs can actually disseminate to other microbes. We have thus performed the first study to: 1) examine the potential for ARG dissemination in indoor dust microbial communities, and 2) validate the presence of detected mobile ARGs in viable dust bacteria. Specifically, we integrated 166 dust metagenomes from 43 different buildings. Sequences were assembled, annotated, and screened for potential integrons, transposons, plasmids, and associated ARGs. The same dust samples were further investigated using cultivation and isolate genome and plasmid sequencing. Potential ARGs were detected in dust isolate genomes, and we confirmed their placement on mobile genetic elements using long-read sequencing. We found 183 ARGs, of which 52 were potentially mobile (associated with a putative plasmid, transposon or integron). One dust isolate related to Staphylococcus equorum proved to contain a plasmid carrying an ARG that was detected metagenomically and confirmed through whole genome and plasmid sequencing. This study thus highlights the power of combining cultivation with metagenomics to assess the risk of potentially mobile ARGs for public health. |
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Exposure to microbes in buildings, and specifically in dust, is thus also increasing, and has been linked to various health outcomes and to antibiotic resistance genes (ARGs). These are most efficiently screened using DNA sequencing, but this method does not determine which microbes are viable, nor does it reveal whether their ARGs can actually disseminate to other microbes. We have thus performed the first study to: 1) examine the potential for ARG dissemination in indoor dust microbial communities, and 2) validate the presence of detected mobile ARGs in viable dust bacteria. Specifically, we integrated 166 dust metagenomes from 43 different buildings. Sequences were assembled, annotated, and screened for potential integrons, transposons, plasmids, and associated ARGs. The same dust samples were further investigated using cultivation and isolate genome and plasmid sequencing. Potential ARGs were detected in dust isolate genomes, and we confirmed their placement on mobile genetic elements using long-read sequencing. We found 183 ARGs, of which 52 were potentially mobile (associated with a putative plasmid, transposon or integron). One dust isolate related to Staphylococcus equorum proved to contain a plasmid carrying an ARG that was detected metagenomically and confirmed through whole genome and plasmid sequencing. This study thus highlights the power of combining cultivation with metagenomics to assess the risk of potentially mobile ARGs for public health.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1008211</identifier><identifier>PMID: 31971995</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Air Pollution, Indoor ; Antibiotic resistance ; Antibiotics ; Antimicrobial agents ; Bacteria ; Biology and Life Sciences ; Buildings ; Cattle ; Cultivation ; Datasets ; Deoxyribonucleic acid ; DNA ; DNA sequencing ; Drinking water ; Drug resistance ; Drug Resistance, Microbial - genetics ; Dust ; Ecology and Environmental Sciences ; Engineering ; Environmental engineering ; Environmental Microbiology ; Enzymes ; Gene sequencing ; Gene Transfer, Horizontal ; Genes ; Genes, Bacterial ; Genome, Bacterial ; Genomes ; Indoor air pollution ; Medicine and Health Sciences ; Metagenomics ; Microbial activity ; Microbiomes ; Microbiota - genetics ; Microorganisms ; Pathogens ; Plasmids ; Public health ; Transposons ; Urbanization ; Water treatment</subject><ispartof>PLoS pathogens, 2020-01, Vol.16 (1), p.e1008211</ispartof><rights>2020 Ben Maamar et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Exposure to microbes in buildings, and specifically in dust, is thus also increasing, and has been linked to various health outcomes and to antibiotic resistance genes (ARGs). These are most efficiently screened using DNA sequencing, but this method does not determine which microbes are viable, nor does it reveal whether their ARGs can actually disseminate to other microbes. We have thus performed the first study to: 1) examine the potential for ARG dissemination in indoor dust microbial communities, and 2) validate the presence of detected mobile ARGs in viable dust bacteria. Specifically, we integrated 166 dust metagenomes from 43 different buildings. Sequences were assembled, annotated, and screened for potential integrons, transposons, plasmids, and associated ARGs. The same dust samples were further investigated using cultivation and isolate genome and plasmid sequencing. Potential ARGs were detected in dust isolate genomes, and we confirmed their placement on mobile genetic elements using long-read sequencing. We found 183 ARGs, of which 52 were potentially mobile (associated with a putative plasmid, transposon or integron). One dust isolate related to Staphylococcus equorum proved to contain a plasmid carrying an ARG that was detected metagenomically and confirmed through whole genome and plasmid sequencing. This study thus highlights the power of combining cultivation with metagenomics to assess the risk of potentially mobile ARGs for public health.</description><subject>Air Pollution, Indoor</subject><subject>Antibiotic resistance</subject><subject>Antibiotics</subject><subject>Antimicrobial agents</subject><subject>Bacteria</subject><subject>Biology and Life Sciences</subject><subject>Buildings</subject><subject>Cattle</subject><subject>Cultivation</subject><subject>Datasets</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA sequencing</subject><subject>Drinking water</subject><subject>Drug resistance</subject><subject>Drug Resistance, Microbial - genetics</subject><subject>Dust</subject><subject>Ecology and Environmental Sciences</subject><subject>Engineering</subject><subject>Environmental engineering</subject><subject>Environmental Microbiology</subject><subject>Enzymes</subject><subject>Gene sequencing</subject><subject>Gene Transfer, Horizontal</subject><subject>Genes</subject><subject>Genes, Bacterial</subject><subject>Genome, Bacterial</subject><subject>Genomes</subject><subject>Indoor air pollution</subject><subject>Medicine and Health Sciences</subject><subject>Metagenomics</subject><subject>Microbial activity</subject><subject>Microbiomes</subject><subject>Microbiota - 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Exposure to microbes in buildings, and specifically in dust, is thus also increasing, and has been linked to various health outcomes and to antibiotic resistance genes (ARGs). These are most efficiently screened using DNA sequencing, but this method does not determine which microbes are viable, nor does it reveal whether their ARGs can actually disseminate to other microbes. We have thus performed the first study to: 1) examine the potential for ARG dissemination in indoor dust microbial communities, and 2) validate the presence of detected mobile ARGs in viable dust bacteria. Specifically, we integrated 166 dust metagenomes from 43 different buildings. Sequences were assembled, annotated, and screened for potential integrons, transposons, plasmids, and associated ARGs. The same dust samples were further investigated using cultivation and isolate genome and plasmid sequencing. Potential ARGs were detected in dust isolate genomes, and we confirmed their placement on mobile genetic elements using long-read sequencing. We found 183 ARGs, of which 52 were potentially mobile (associated with a putative plasmid, transposon or integron). One dust isolate related to Staphylococcus equorum proved to contain a plasmid carrying an ARG that was detected metagenomically and confirmed through whole genome and plasmid sequencing. This study thus highlights the power of combining cultivation with metagenomics to assess the risk of potentially mobile ARGs for public health.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>31971995</pmid><doi>10.1371/journal.ppat.1008211</doi><orcidid>https://orcid.org/0000-0002-0966-2014</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Air Pollution, Indoor Antibiotic resistance Antibiotics Antimicrobial agents Bacteria Biology and Life Sciences Buildings Cattle Cultivation Datasets Deoxyribonucleic acid DNA DNA sequencing Drinking water Drug resistance Drug Resistance, Microbial - genetics Dust Ecology and Environmental Sciences Engineering Environmental engineering Environmental Microbiology Enzymes Gene sequencing Gene Transfer, Horizontal Genes Genes, Bacterial Genome, Bacterial Genomes Indoor air pollution Medicine and Health Sciences Metagenomics Microbial activity Microbiomes Microbiota - genetics Microorganisms Pathogens Plasmids Public health Transposons Urbanization Water treatment |
title | Mobilizable antibiotic resistance genes are present in dust microbial communities |
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