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Antibiotic mixture effects on growth of the leaf-shredding stream detritivore Gammarus fossarum

Pharmaceuticals contribute greatly to human and animal health. Given their specific biological targets, pharmaceuticals pose a significant environmental risk by affecting organisms and ecosystem processes, including leaf-litter decomposition. Although litter decomposition is a central process in for...

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Autores principales: Bundschuh, Mirco, Hahn, Torsten, Gessner, Mark O., Schulz, Ralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420384/
https://www.ncbi.nlm.nih.gov/pubmed/28285374
http://dx.doi.org/10.1007/s10646-017-1787-2
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author Bundschuh, Mirco
Hahn, Torsten
Gessner, Mark O.
Schulz, Ralf
author_facet Bundschuh, Mirco
Hahn, Torsten
Gessner, Mark O.
Schulz, Ralf
author_sort Bundschuh, Mirco
collection PubMed
description Pharmaceuticals contribute greatly to human and animal health. Given their specific biological targets, pharmaceuticals pose a significant environmental risk by affecting organisms and ecosystem processes, including leaf-litter decomposition. Although litter decomposition is a central process in forest streams, the consequences of exposure to pharmaceuticals remain poorly known. The present study assessed the impact of antibiotics as an important class of pharmaceuticals on the growth of the leaf-shredding amphipod Gammarus fossarum over 24 days. Exposure scenarios involved an antibiotic mixture (i.e. sulfamethoxazole, trimethoprim, erythromycin-H(2)O, roxithromycin, clarithromycin) at 0, 2 and 200 µg/L to assess impacts resulting from exposure to both water and food. The antibiotics had no effect on either leaf-associated fungal biomass or bacterial abundance. However, modification of leaf quality (e.g. through shifts in leaf-associated microbial communities) may have triggered faster growth of gammarids (assessed in terms of body mass gain) at the low antibiotic concentration relative to the control. At 200 µg/L, however, gammarid growth was not stimulated. This outcome might be due to a modified ability of the gut microflora to assimilate nutrients and carbon. Furthermore, the observed lack of increases in the diameter of the gammarids’ peduncles, despite an increase in gammarid mass, suggests antibiotic-induced effects in the moulting cycle. Although the processes responsible for the observed effects have not yet been identified, these results suggest a potential role of food-quality, gammarid gut microflora and alteration in the moulting cycle in mediating impacts of antibiotics on these detritivores and the leaf decomposition process in streams.
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spelling pubmed-54203842017-05-22 Antibiotic mixture effects on growth of the leaf-shredding stream detritivore Gammarus fossarum Bundschuh, Mirco Hahn, Torsten Gessner, Mark O. Schulz, Ralf Ecotoxicology Article Pharmaceuticals contribute greatly to human and animal health. Given their specific biological targets, pharmaceuticals pose a significant environmental risk by affecting organisms and ecosystem processes, including leaf-litter decomposition. Although litter decomposition is a central process in forest streams, the consequences of exposure to pharmaceuticals remain poorly known. The present study assessed the impact of antibiotics as an important class of pharmaceuticals on the growth of the leaf-shredding amphipod Gammarus fossarum over 24 days. Exposure scenarios involved an antibiotic mixture (i.e. sulfamethoxazole, trimethoprim, erythromycin-H(2)O, roxithromycin, clarithromycin) at 0, 2 and 200 µg/L to assess impacts resulting from exposure to both water and food. The antibiotics had no effect on either leaf-associated fungal biomass or bacterial abundance. However, modification of leaf quality (e.g. through shifts in leaf-associated microbial communities) may have triggered faster growth of gammarids (assessed in terms of body mass gain) at the low antibiotic concentration relative to the control. At 200 µg/L, however, gammarid growth was not stimulated. This outcome might be due to a modified ability of the gut microflora to assimilate nutrients and carbon. Furthermore, the observed lack of increases in the diameter of the gammarids’ peduncles, despite an increase in gammarid mass, suggests antibiotic-induced effects in the moulting cycle. Although the processes responsible for the observed effects have not yet been identified, these results suggest a potential role of food-quality, gammarid gut microflora and alteration in the moulting cycle in mediating impacts of antibiotics on these detritivores and the leaf decomposition process in streams. Springer US 2017-03-11 2017 /pmc/articles/PMC5420384/ /pubmed/28285374 http://dx.doi.org/10.1007/s10646-017-1787-2 Text en © The Author(s) 2017 This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Bundschuh, Mirco
Hahn, Torsten
Gessner, Mark O.
Schulz, Ralf
Antibiotic mixture effects on growth of the leaf-shredding stream detritivore Gammarus fossarum
title Antibiotic mixture effects on growth of the leaf-shredding stream detritivore Gammarus fossarum
title_full Antibiotic mixture effects on growth of the leaf-shredding stream detritivore Gammarus fossarum
title_fullStr Antibiotic mixture effects on growth of the leaf-shredding stream detritivore Gammarus fossarum
title_full_unstemmed Antibiotic mixture effects on growth of the leaf-shredding stream detritivore Gammarus fossarum
title_short Antibiotic mixture effects on growth of the leaf-shredding stream detritivore Gammarus fossarum
title_sort antibiotic mixture effects on growth of the leaf-shredding stream detritivore gammarus fossarum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420384/
https://www.ncbi.nlm.nih.gov/pubmed/28285374
http://dx.doi.org/10.1007/s10646-017-1787-2
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