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Small-Scale Heterogeneity in Drinking Water Biofilms

Biofilm heterogeneity has been characterized on various scales for both natural and engineered ecosystems. This heterogeneity has been attributed to spatial differences in environmental factors. Understanding their impact on localized biofilm heterogeneity in building plumbing systems is important f...

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Autores principales: Neu, Lisa, Proctor, Caitlin R., Walser, Jean-Claude, Hammes, Frederik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828615/
https://www.ncbi.nlm.nih.gov/pubmed/31736893
http://dx.doi.org/10.3389/fmicb.2019.02446
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author Neu, Lisa
Proctor, Caitlin R.
Walser, Jean-Claude
Hammes, Frederik
author_facet Neu, Lisa
Proctor, Caitlin R.
Walser, Jean-Claude
Hammes, Frederik
author_sort Neu, Lisa
collection PubMed
description Biofilm heterogeneity has been characterized on various scales for both natural and engineered ecosystems. This heterogeneity has been attributed to spatial differences in environmental factors. Understanding their impact on localized biofilm heterogeneity in building plumbing systems is important for both management and representative sampling strategies. We assessed heterogeneity within the confined engineered ecosystem of a shower hose by high-resolution sampling (200 individual biofilm sections per hose) on varying scales (μm to m). We postulated that a biofilm grown on a single material under uniform conditions should be homogeneous in its structure, bacterial numbers, and community composition. A biofilm grown for 12 months under controlled laboratory conditions, showed homogeneity on large-scale. However, some small-scale heterogeneity was clearly observed. For example, biofilm thickness of cm-sections varied up to 4-fold, total cell concentrations (TCC) 3-fold, and relative abundance of dominant taxa up to 5-fold. A biofilm grown under real (i.e., uncontrolled) use conditions developed considerably more heterogeneity in all variables which was attributed to more discontinuity in environmental conditions. Interestingly, biofilm communities from both hoses showed comparably low diversity, with <400 taxa each, and only three taxa accounting for 57%, respectively, 73% of the community. This low diversity was attributed to a strong selective pressure, originating in migrating carbon from the flexible hoses as major carbon source. High-resolution sampling strategy enabled detailed analysis of spatial heterogeneity within an individual drinking water biofilm. This study gives insight into biofilm structure and community composition on cm-to m-scale and is useful for decision-making on sampling strategies in biofilm research and monitoring.
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spelling pubmed-68286152019-11-15 Small-Scale Heterogeneity in Drinking Water Biofilms Neu, Lisa Proctor, Caitlin R. Walser, Jean-Claude Hammes, Frederik Front Microbiol Microbiology Biofilm heterogeneity has been characterized on various scales for both natural and engineered ecosystems. This heterogeneity has been attributed to spatial differences in environmental factors. Understanding their impact on localized biofilm heterogeneity in building plumbing systems is important for both management and representative sampling strategies. We assessed heterogeneity within the confined engineered ecosystem of a shower hose by high-resolution sampling (200 individual biofilm sections per hose) on varying scales (μm to m). We postulated that a biofilm grown on a single material under uniform conditions should be homogeneous in its structure, bacterial numbers, and community composition. A biofilm grown for 12 months under controlled laboratory conditions, showed homogeneity on large-scale. However, some small-scale heterogeneity was clearly observed. For example, biofilm thickness of cm-sections varied up to 4-fold, total cell concentrations (TCC) 3-fold, and relative abundance of dominant taxa up to 5-fold. A biofilm grown under real (i.e., uncontrolled) use conditions developed considerably more heterogeneity in all variables which was attributed to more discontinuity in environmental conditions. Interestingly, biofilm communities from both hoses showed comparably low diversity, with <400 taxa each, and only three taxa accounting for 57%, respectively, 73% of the community. This low diversity was attributed to a strong selective pressure, originating in migrating carbon from the flexible hoses as major carbon source. High-resolution sampling strategy enabled detailed analysis of spatial heterogeneity within an individual drinking water biofilm. This study gives insight into biofilm structure and community composition on cm-to m-scale and is useful for decision-making on sampling strategies in biofilm research and monitoring. Frontiers Media S.A. 2019-10-29 /pmc/articles/PMC6828615/ /pubmed/31736893 http://dx.doi.org/10.3389/fmicb.2019.02446 Text en Copyright © 2019 Neu, Proctor, Walser and Hammes. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Neu, Lisa
Proctor, Caitlin R.
Walser, Jean-Claude
Hammes, Frederik
Small-Scale Heterogeneity in Drinking Water Biofilms
title Small-Scale Heterogeneity in Drinking Water Biofilms
title_full Small-Scale Heterogeneity in Drinking Water Biofilms
title_fullStr Small-Scale Heterogeneity in Drinking Water Biofilms
title_full_unstemmed Small-Scale Heterogeneity in Drinking Water Biofilms
title_short Small-Scale Heterogeneity in Drinking Water Biofilms
title_sort small-scale heterogeneity in drinking water biofilms
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828615/
https://www.ncbi.nlm.nih.gov/pubmed/31736893
http://dx.doi.org/10.3389/fmicb.2019.02446
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