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Na(+)-Coupled Respiration and Reshaping of Extracellular Polysaccharide Layer Counteract Monensin-Induced Cation Permeability in Prevotella bryantii B(1)4
Monensin is an ionophore for monovalent cations, which is frequently used to prevent ketosis and to enhance performance in dairy cows. Studies have shown the rumen bacteria Prevotella bryantii B(1)4 being less affected by monensin. The present study aimed to reveal more information about the respect...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508442/ https://www.ncbi.nlm.nih.gov/pubmed/34638543 http://dx.doi.org/10.3390/ijms221910202 |
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author | Trautmann, Andrej Schleicher, Lena Pfirrmann, Jana Boldt, Christin Steuber, Julia Seifert, Jana |
author_facet | Trautmann, Andrej Schleicher, Lena Pfirrmann, Jana Boldt, Christin Steuber, Julia Seifert, Jana |
author_sort | Trautmann, Andrej |
collection | PubMed |
description | Monensin is an ionophore for monovalent cations, which is frequently used to prevent ketosis and to enhance performance in dairy cows. Studies have shown the rumen bacteria Prevotella bryantii B(1)4 being less affected by monensin. The present study aimed to reveal more information about the respective molecular mechanisms in P. bryantii, as there is still a lack of knowledge about defense mechanisms against monensin. Cell growth experiments applying increasing concentrations of monensin and incubations up to 72 h were done. Harvested cells were used for label-free quantitative proteomics, enzyme activity measurements, quantification of intracellular sodium and extracellular glucose concentrations and fluorescence microscopy. Our findings confirmed an active cell growth and fermentation activity of P. bryantii B(1)4 despite monensin concentrations up to 60 µM. An elevated abundance and activity of the Na(+)-translocating NADH:quinone oxidoreductase counteracted sodium influx caused by monensin. Cell membranes and extracellular polysaccharides were highly influenced by monensin indicated by a reduced number of outer membrane proteins, an increased number of certain glucoside hydrolases and an elevated concentration of extracellular glucose. Thus, a reconstruction of extracellular polysaccharides in P. bryantii in response to monensin is proposed, which is expected to have a negative impact on the substrate binding capacities of this rumen bacterium. |
format | Online Article Text |
id | pubmed-8508442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85084422021-10-13 Na(+)-Coupled Respiration and Reshaping of Extracellular Polysaccharide Layer Counteract Monensin-Induced Cation Permeability in Prevotella bryantii B(1)4 Trautmann, Andrej Schleicher, Lena Pfirrmann, Jana Boldt, Christin Steuber, Julia Seifert, Jana Int J Mol Sci Article Monensin is an ionophore for monovalent cations, which is frequently used to prevent ketosis and to enhance performance in dairy cows. Studies have shown the rumen bacteria Prevotella bryantii B(1)4 being less affected by monensin. The present study aimed to reveal more information about the respective molecular mechanisms in P. bryantii, as there is still a lack of knowledge about defense mechanisms against monensin. Cell growth experiments applying increasing concentrations of monensin and incubations up to 72 h were done. Harvested cells were used for label-free quantitative proteomics, enzyme activity measurements, quantification of intracellular sodium and extracellular glucose concentrations and fluorescence microscopy. Our findings confirmed an active cell growth and fermentation activity of P. bryantii B(1)4 despite monensin concentrations up to 60 µM. An elevated abundance and activity of the Na(+)-translocating NADH:quinone oxidoreductase counteracted sodium influx caused by monensin. Cell membranes and extracellular polysaccharides were highly influenced by monensin indicated by a reduced number of outer membrane proteins, an increased number of certain glucoside hydrolases and an elevated concentration of extracellular glucose. Thus, a reconstruction of extracellular polysaccharides in P. bryantii in response to monensin is proposed, which is expected to have a negative impact on the substrate binding capacities of this rumen bacterium. MDPI 2021-09-22 /pmc/articles/PMC8508442/ /pubmed/34638543 http://dx.doi.org/10.3390/ijms221910202 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Trautmann, Andrej Schleicher, Lena Pfirrmann, Jana Boldt, Christin Steuber, Julia Seifert, Jana Na(+)-Coupled Respiration and Reshaping of Extracellular Polysaccharide Layer Counteract Monensin-Induced Cation Permeability in Prevotella bryantii B(1)4 |
title | Na(+)-Coupled Respiration and Reshaping of Extracellular Polysaccharide Layer Counteract Monensin-Induced Cation Permeability in Prevotella bryantii B(1)4 |
title_full | Na(+)-Coupled Respiration and Reshaping of Extracellular Polysaccharide Layer Counteract Monensin-Induced Cation Permeability in Prevotella bryantii B(1)4 |
title_fullStr | Na(+)-Coupled Respiration and Reshaping of Extracellular Polysaccharide Layer Counteract Monensin-Induced Cation Permeability in Prevotella bryantii B(1)4 |
title_full_unstemmed | Na(+)-Coupled Respiration and Reshaping of Extracellular Polysaccharide Layer Counteract Monensin-Induced Cation Permeability in Prevotella bryantii B(1)4 |
title_short | Na(+)-Coupled Respiration and Reshaping of Extracellular Polysaccharide Layer Counteract Monensin-Induced Cation Permeability in Prevotella bryantii B(1)4 |
title_sort | na(+)-coupled respiration and reshaping of extracellular polysaccharide layer counteract monensin-induced cation permeability in prevotella bryantii b(1)4 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508442/ https://www.ncbi.nlm.nih.gov/pubmed/34638543 http://dx.doi.org/10.3390/ijms221910202 |
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