Biofilms on Hospital Shower Hoses: Characterization and Implications for Nosocomial Infections
Although the source of drinking water (DW) used in hospitals is commonly disinfected, biofilms forming on water pipelines are a refuge for bacteria, including possible pathogens that survive different disinfection strategies. These biofilm communities are only beginning to be explored by culture-ind...
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Veröffentlicht in: | Applied and environmental microbiology 2016-05, Vol.82 (9), p.2872-2883 |
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creator | Soto-Giron, Maria J Rodriguez-R, Luis M Luo, Chengwei Elk, Michael Ryu, Hodon Hoelle, Jill Santo Domingo, Jorge W Konstantinidis, Konstantinos T |
description | Although the source of drinking water (DW) used in hospitals is commonly disinfected, biofilms forming on water pipelines are a refuge for bacteria, including possible pathogens that survive different disinfection strategies. These biofilm communities are only beginning to be explored by culture-independent techniques that circumvent the limitations of conventional monitoring efforts. Hence, theories regarding the frequency of opportunistic pathogens in DW biofilms and how biofilm members withstand high doses of disinfectants and/or chlorine residuals in the water supply remain speculative. The aim of this study was to characterize the composition of microbial communities growing on five hospital shower hoses using both 16S rRNA gene sequencing of bacterial isolates and whole-genome shotgun metagenome sequencing. The resulting data revealed a Mycobacterium-like population, closely related to Mycobacterium rhodesiae and Mycobacterium tusciae, to be the predominant taxon in all five samples, and its nearly complete draft genome sequence was recovered. In contrast, the fraction recovered by culture was mostly affiliated with Proteobacteria, including members of the genera Sphingomonas, Blastomonas, and Porphyrobacter.The biofilm community harbored genes related to disinfectant tolerance (2.34% of the total annotated proteins) and a lower abundance of virulence determinants related to colonization and evasion of the host immune system. Additionally, genes potentially conferring resistance to β-lactam, aminoglycoside, amphenicol, and quinolone antibiotics were detected. Collectively, our results underscore the need to understand the microbiome of DW biofilms using metagenomic approaches. This information might lead to more robust management practices that minimize the risks associated with exposure to opportunistic pathogens in hospitals. |
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E.</contributor><creatorcontrib>Soto-Giron, Maria J ; Rodriguez-R, Luis M ; Luo, Chengwei ; Elk, Michael ; Ryu, Hodon ; Hoelle, Jill ; Santo Domingo, Jorge W ; Konstantinidis, Konstantinos T ; Besser, T. E.</creatorcontrib><description>Although the source of drinking water (DW) used in hospitals is commonly disinfected, biofilms forming on water pipelines are a refuge for bacteria, including possible pathogens that survive different disinfection strategies. These biofilm communities are only beginning to be explored by culture-independent techniques that circumvent the limitations of conventional monitoring efforts. Hence, theories regarding the frequency of opportunistic pathogens in DW biofilms and how biofilm members withstand high doses of disinfectants and/or chlorine residuals in the water supply remain speculative. The aim of this study was to characterize the composition of microbial communities growing on five hospital shower hoses using both 16S rRNA gene sequencing of bacterial isolates and whole-genome shotgun metagenome sequencing. The resulting data revealed a Mycobacterium-like population, closely related to Mycobacterium rhodesiae and Mycobacterium tusciae, to be the predominant taxon in all five samples, and its nearly complete draft genome sequence was recovered. In contrast, the fraction recovered by culture was mostly affiliated with Proteobacteria, including members of the genera Sphingomonas, Blastomonas, and Porphyrobacter.The biofilm community harbored genes related to disinfectant tolerance (2.34% of the total annotated proteins) and a lower abundance of virulence determinants related to colonization and evasion of the host immune system. Additionally, genes potentially conferring resistance to β-lactam, aminoglycoside, amphenicol, and quinolone antibiotics were detected. Collectively, our results underscore the need to understand the microbiome of DW biofilms using metagenomic approaches. This information might lead to more robust management practices that minimize the risks associated with exposure to opportunistic pathogens in hospitals.</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>DOI: 10.1128/aem.03529-15</identifier><identifier>PMID: 26969701</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Bacteria - classification ; Bacteria - genetics ; Bacteria - isolation & purification ; Bacteria - pathogenicity ; Bacterial Physiological Phenomena ; Biofilms - growth & development ; Chlorine ; Cross Infection - genetics ; Cross Infection - microbiology ; Culture Techniques ; Disinfectants - pharmacology ; Disinfection ; DNA, Bacterial - analysis ; Drug Resistance, Bacterial ; Genome, Bacterial ; Hospitals ; Metagenome ; Microbiota - genetics ; Mycobacterium ; Mycobacterium - physiology ; Mycobacterium tusciae ; Ohio ; Phylogeny ; Proteobacteria ; Proteobacteria - physiology ; Public and Environmental Health Microbiology ; RNA, Ribosomal, 16S - genetics ; Sphingomonadaceae - physiology ; Sphingomonas ; Water Microbiology ; Water Supply</subject><ispartof>Applied and environmental microbiology, 2016-05, Vol.82 (9), p.2872-2883</ispartof><rights>Copyright © 2016, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright © 2016, American Society for Microbiology. All Rights Reserved. 2016 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-54c9a9c4594461b0be1f8bde23a59f50fa6772762a3d8fae95861de2ff5122873</citedby><cites>FETCH-LOGICAL-c526t-54c9a9c4594461b0be1f8bde23a59f50fa6772762a3d8fae95861de2ff5122873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4836434/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4836434/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26969701$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Besser, T. E.</contributor><creatorcontrib>Soto-Giron, Maria J</creatorcontrib><creatorcontrib>Rodriguez-R, Luis M</creatorcontrib><creatorcontrib>Luo, Chengwei</creatorcontrib><creatorcontrib>Elk, Michael</creatorcontrib><creatorcontrib>Ryu, Hodon</creatorcontrib><creatorcontrib>Hoelle, Jill</creatorcontrib><creatorcontrib>Santo Domingo, Jorge W</creatorcontrib><creatorcontrib>Konstantinidis, Konstantinos T</creatorcontrib><title>Biofilms on Hospital Shower Hoses: Characterization and Implications for Nosocomial Infections</title><title>Applied and environmental microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>Although the source of drinking water (DW) used in hospitals is commonly disinfected, biofilms forming on water pipelines are a refuge for bacteria, including possible pathogens that survive different disinfection strategies. These biofilm communities are only beginning to be explored by culture-independent techniques that circumvent the limitations of conventional monitoring efforts. Hence, theories regarding the frequency of opportunistic pathogens in DW biofilms and how biofilm members withstand high doses of disinfectants and/or chlorine residuals in the water supply remain speculative. The aim of this study was to characterize the composition of microbial communities growing on five hospital shower hoses using both 16S rRNA gene sequencing of bacterial isolates and whole-genome shotgun metagenome sequencing. The resulting data revealed a Mycobacterium-like population, closely related to Mycobacterium rhodesiae and Mycobacterium tusciae, to be the predominant taxon in all five samples, and its nearly complete draft genome sequence was recovered. In contrast, the fraction recovered by culture was mostly affiliated with Proteobacteria, including members of the genera Sphingomonas, Blastomonas, and Porphyrobacter.The biofilm community harbored genes related to disinfectant tolerance (2.34% of the total annotated proteins) and a lower abundance of virulence determinants related to colonization and evasion of the host immune system. Additionally, genes potentially conferring resistance to β-lactam, aminoglycoside, amphenicol, and quinolone antibiotics were detected. Collectively, our results underscore the need to understand the microbiome of DW biofilms using metagenomic approaches. This information might lead to more robust management practices that minimize the risks associated with exposure to opportunistic pathogens in hospitals.</description><subject>Bacteria - classification</subject><subject>Bacteria - genetics</subject><subject>Bacteria - isolation & purification</subject><subject>Bacteria - pathogenicity</subject><subject>Bacterial Physiological Phenomena</subject><subject>Biofilms - growth & development</subject><subject>Chlorine</subject><subject>Cross Infection - genetics</subject><subject>Cross Infection - microbiology</subject><subject>Culture Techniques</subject><subject>Disinfectants - pharmacology</subject><subject>Disinfection</subject><subject>DNA, Bacterial - analysis</subject><subject>Drug Resistance, Bacterial</subject><subject>Genome, Bacterial</subject><subject>Hospitals</subject><subject>Metagenome</subject><subject>Microbiota - genetics</subject><subject>Mycobacterium</subject><subject>Mycobacterium - physiology</subject><subject>Mycobacterium tusciae</subject><subject>Ohio</subject><subject>Phylogeny</subject><subject>Proteobacteria</subject><subject>Proteobacteria - physiology</subject><subject>Public and Environmental Health Microbiology</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>Sphingomonadaceae - physiology</subject><subject>Sphingomonas</subject><subject>Water Microbiology</subject><subject>Water Supply</subject><issn>0099-2240</issn><issn>1098-5336</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkTtPAzEQhC0EIuHRUaMrKbjg99kUSCHiESlAAbRYjmMTo7tzsC8g-PVcEoigo1qN5tvRrgaAAwR7CGFxom3Vg4RhmSO2AboISpEzQvgm6EIoZY4xhR2wk9ILhJBCLrZBB3PJZQFRFzyd--B8WaUs1Nl1SDPf6DK7n4Z3GxfaptNsMNVRm8ZG_6kb33K6nmTDalZ6s9QpcyFmtyEFEyrfrg9rZ83S2QNbTpfJ7n_PXfB4efEwuM5Hd1fDQX-UG4Z5kzNqpJaGMkkpR2M4tsiJ8cRiopl0DDrNiwIXHGsyEU5byQRHre0cQxiLguyCs1XubD6u7MTYuom6VLPoKx0_VNBe_XVqP1XP4U1RQTgltA04-g6I4XVuU6Mqn4wtS13bME8KFRJKAolA_0AFFoQixlr0eIWaGFKK1q0vQlAt2lP9ixu1bE-hBX74-4s1_FMX-QJ1FZbR</recordid><startdate>20160501</startdate><enddate>20160501</enddate><creator>Soto-Giron, Maria J</creator><creator>Rodriguez-R, Luis M</creator><creator>Luo, Chengwei</creator><creator>Elk, Michael</creator><creator>Ryu, Hodon</creator><creator>Hoelle, Jill</creator><creator>Santo Domingo, Jorge W</creator><creator>Konstantinidis, Konstantinos T</creator><general>American Society for Microbiology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20160501</creationdate><title>Biofilms on Hospital Shower Hoses: Characterization and Implications for Nosocomial Infections</title><author>Soto-Giron, Maria J ; 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E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biofilms on Hospital Shower Hoses: Characterization and Implications for Nosocomial Infections</atitle><jtitle>Applied and environmental microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>2016-05-01</date><risdate>2016</risdate><volume>82</volume><issue>9</issue><spage>2872</spage><epage>2883</epage><pages>2872-2883</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><abstract>Although the source of drinking water (DW) used in hospitals is commonly disinfected, biofilms forming on water pipelines are a refuge for bacteria, including possible pathogens that survive different disinfection strategies. These biofilm communities are only beginning to be explored by culture-independent techniques that circumvent the limitations of conventional monitoring efforts. Hence, theories regarding the frequency of opportunistic pathogens in DW biofilms and how biofilm members withstand high doses of disinfectants and/or chlorine residuals in the water supply remain speculative. The aim of this study was to characterize the composition of microbial communities growing on five hospital shower hoses using both 16S rRNA gene sequencing of bacterial isolates and whole-genome shotgun metagenome sequencing. The resulting data revealed a Mycobacterium-like population, closely related to Mycobacterium rhodesiae and Mycobacterium tusciae, to be the predominant taxon in all five samples, and its nearly complete draft genome sequence was recovered. In contrast, the fraction recovered by culture was mostly affiliated with Proteobacteria, including members of the genera Sphingomonas, Blastomonas, and Porphyrobacter.The biofilm community harbored genes related to disinfectant tolerance (2.34% of the total annotated proteins) and a lower abundance of virulence determinants related to colonization and evasion of the host immune system. Additionally, genes potentially conferring resistance to β-lactam, aminoglycoside, amphenicol, and quinolone antibiotics were detected. Collectively, our results underscore the need to understand the microbiome of DW biofilms using metagenomic approaches. This information might lead to more robust management practices that minimize the risks associated with exposure to opportunistic pathogens in hospitals.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>26969701</pmid><doi>10.1128/aem.03529-15</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bacteria - classification Bacteria - genetics Bacteria - isolation & purification Bacteria - pathogenicity Bacterial Physiological Phenomena Biofilms - growth & development Chlorine Cross Infection - genetics Cross Infection - microbiology Culture Techniques Disinfectants - pharmacology Disinfection DNA, Bacterial - analysis Drug Resistance, Bacterial Genome, Bacterial Hospitals Metagenome Microbiota - genetics Mycobacterium Mycobacterium - physiology Mycobacterium tusciae Ohio Phylogeny Proteobacteria Proteobacteria - physiology Public and Environmental Health Microbiology RNA, Ribosomal, 16S - genetics Sphingomonadaceae - physiology Sphingomonas Water Microbiology Water Supply |
title | Biofilms on Hospital Shower Hoses: Characterization and Implications for Nosocomial Infections |
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