Nutrients and Pharmaceuticals Structure Bacterial Core Communities in Urban and Montane Stream Biofilms
Bacteria in stream biofilms contribute to stream biogeochemical processes and are potentially sensitive to the substantial levels of pollution entering urban streams. To examine the effects of contaminants on stream biofilm bacteria in situ, we exposed growing biofilms to experimental additions of n...
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doaj-139c82e8d4ba4867993de2a762e07ee42020-11-25T04:01:38ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2020-10-011110.3389/fmicb.2020.526545526545Nutrients and Pharmaceuticals Structure Bacterial Core Communities in Urban and Montane Stream BiofilmsElizabeth M. Ogata0Michelle A. Baker1Emma J. Rosi2Trevor B. Smart3Donald Long4Zachary T. Aanderud5Department of Biology and Ecology Center, Utah State University, Logan, UT, United StatesDepartment of Biology and Ecology Center, Utah State University, Logan, UT, United StatesCary Institute of Ecosystem Studies, Millbrook, NY, United StatesDepartment of Plant and Wildlife Sciences, Brigham Young University, Provo, UT, United StatesDepartment of Biology, Southern Utah University, Cedar City, UT, United StatesDepartment of Plant and Wildlife Sciences, Brigham Young University, Provo, UT, United StatesBacteria in stream biofilms contribute to stream biogeochemical processes and are potentially sensitive to the substantial levels of pollution entering urban streams. To examine the effects of contaminants on stream biofilm bacteria in situ, we exposed growing biofilms to experimental additions of nutrients [nitrogen (N), phosphorus (P), and iron (Fe)], pharmaceuticals (caffeine and diphenhydramine), nutrients plus pharmaceuticals, or no contaminants using contaminant exposure substrates (CES) in three catchments in northern Utah. We performed our study at montane and urban sites to examine the influence of existing pollution on biofilm response. We identified bacterial core communities (core) for each contaminant treatment at each land-use type (e.g., nutrient addition montane bacterial core, nutrient addition urban bacterial core, pharmaceutical addition montane bacterial core) by selecting all taxa found in at least 75% of the samples belonging to each specific grouping. Montane and urban land-use distinguished bacterial cores, while nutrients and pharmaceuticals had subtle, but nonetheless distinct effects. Nutrients enhanced the dominance of already abundant copiotrophs [i.e., Pseudomonadaceae (Gammaproteobacteria) and Comamonadaceae (Betaproteobacteria)] within bacterial cores at montane and urban sites. In contrast, pharmaceuticals fostered species-rich bacterial cores containing unique contaminant-degrading taxa within Pseudomonadaceae and Anaerolineaceae (Chloroflexi). Surprisingly, even at urban sites containing ambient pharmaceutical pollution, pharmaceutical additions increased bacterial core richness, specifically within DR-16 (Betaproteobacteria), WCHB1-32 (Bacteroidetes), and Leptotrichiaceae (Fusobacteria). Nutrients exerted greater selective force than pharmaceuticals in nutrient plus pharmaceutical addition treatments, creating bacterial cores more closely resembling those under nutrient rather than pharmaceutical addition, and promoting unique Oscillatoriales (Cyanobacteria) taxa in urban streams. Our results show that additions of N, P, and Fe intensified the dominance of already abundant copiotrophs, while additions of caffeine and diphenhydramine enabled unique taxa associated with contaminant degradation to participate in bacterial cores. Further, biofilm bacteria at urban sites remained sensitive to pharmaceuticals commonly present in waters, suggesting a dynamic interplay among pharmaceutical pollution, bacterial diversity, and contaminant degradation.https://www.frontiersin.org/article/10.3389/fmicb.2020.526545/fullwater qualitystream biofilmsnutrientspharmaceuticalsbacteriacontaminant diffusing substrate |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Elizabeth M. Ogata Michelle A. Baker Emma J. Rosi Trevor B. Smart Donald Long Zachary T. Aanderud |
spellingShingle |
Elizabeth M. Ogata Michelle A. Baker Emma J. Rosi Trevor B. Smart Donald Long Zachary T. Aanderud Nutrients and Pharmaceuticals Structure Bacterial Core Communities in Urban and Montane Stream Biofilms Frontiers in Microbiology water quality stream biofilms nutrients pharmaceuticals bacteria contaminant diffusing substrate |
author_facet |
Elizabeth M. Ogata Michelle A. Baker Emma J. Rosi Trevor B. Smart Donald Long Zachary T. Aanderud |
author_sort |
Elizabeth M. Ogata |
title |
Nutrients and Pharmaceuticals Structure Bacterial Core Communities in Urban and Montane Stream Biofilms |
title_short |
Nutrients and Pharmaceuticals Structure Bacterial Core Communities in Urban and Montane Stream Biofilms |
title_full |
Nutrients and Pharmaceuticals Structure Bacterial Core Communities in Urban and Montane Stream Biofilms |
title_fullStr |
Nutrients and Pharmaceuticals Structure Bacterial Core Communities in Urban and Montane Stream Biofilms |
title_full_unstemmed |
Nutrients and Pharmaceuticals Structure Bacterial Core Communities in Urban and Montane Stream Biofilms |
title_sort |
nutrients and pharmaceuticals structure bacterial core communities in urban and montane stream biofilms |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Microbiology |
issn |
1664-302X |
publishDate |
2020-10-01 |
description |
Bacteria in stream biofilms contribute to stream biogeochemical processes and are potentially sensitive to the substantial levels of pollution entering urban streams. To examine the effects of contaminants on stream biofilm bacteria in situ, we exposed growing biofilms to experimental additions of nutrients [nitrogen (N), phosphorus (P), and iron (Fe)], pharmaceuticals (caffeine and diphenhydramine), nutrients plus pharmaceuticals, or no contaminants using contaminant exposure substrates (CES) in three catchments in northern Utah. We performed our study at montane and urban sites to examine the influence of existing pollution on biofilm response. We identified bacterial core communities (core) for each contaminant treatment at each land-use type (e.g., nutrient addition montane bacterial core, nutrient addition urban bacterial core, pharmaceutical addition montane bacterial core) by selecting all taxa found in at least 75% of the samples belonging to each specific grouping. Montane and urban land-use distinguished bacterial cores, while nutrients and pharmaceuticals had subtle, but nonetheless distinct effects. Nutrients enhanced the dominance of already abundant copiotrophs [i.e., Pseudomonadaceae (Gammaproteobacteria) and Comamonadaceae (Betaproteobacteria)] within bacterial cores at montane and urban sites. In contrast, pharmaceuticals fostered species-rich bacterial cores containing unique contaminant-degrading taxa within Pseudomonadaceae and Anaerolineaceae (Chloroflexi). Surprisingly, even at urban sites containing ambient pharmaceutical pollution, pharmaceutical additions increased bacterial core richness, specifically within DR-16 (Betaproteobacteria), WCHB1-32 (Bacteroidetes), and Leptotrichiaceae (Fusobacteria). Nutrients exerted greater selective force than pharmaceuticals in nutrient plus pharmaceutical addition treatments, creating bacterial cores more closely resembling those under nutrient rather than pharmaceutical addition, and promoting unique Oscillatoriales (Cyanobacteria) taxa in urban streams. Our results show that additions of N, P, and Fe intensified the dominance of already abundant copiotrophs, while additions of caffeine and diphenhydramine enabled unique taxa associated with contaminant degradation to participate in bacterial cores. Further, biofilm bacteria at urban sites remained sensitive to pharmaceuticals commonly present in waters, suggesting a dynamic interplay among pharmaceutical pollution, bacterial diversity, and contaminant degradation. |
topic |
water quality stream biofilms nutrients pharmaceuticals bacteria contaminant diffusing substrate |
url |
https://www.frontiersin.org/article/10.3389/fmicb.2020.526545/full |
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