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Removal of Waterborne Viruses by Tetrahymena pyriformis Is Virus-Specific and Coincides with Changes in Protist Swimming Speed

[Image: see text] Biological treatment of waterborne viruses, specifically grazing of viruses by protists, can enhance microbial water quality while avoiding the production of toxic byproducts and high energy costs. However, tangible applications are limited by the lack of understanding of the under...

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Autores principales: Olive, Margot, Moerman, Felix, Fernandez-Cassi, Xavier, Altermatt, Florian, Kohn, Tamar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988290/
https://www.ncbi.nlm.nih.gov/pubmed/35258957
http://dx.doi.org/10.1021/acs.est.1c05518
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author Olive, Margot
Moerman, Felix
Fernandez-Cassi, Xavier
Altermatt, Florian
Kohn, Tamar
author_facet Olive, Margot
Moerman, Felix
Fernandez-Cassi, Xavier
Altermatt, Florian
Kohn, Tamar
author_sort Olive, Margot
collection PubMed
description [Image: see text] Biological treatment of waterborne viruses, specifically grazing of viruses by protists, can enhance microbial water quality while avoiding the production of toxic byproducts and high energy costs. However, tangible applications are limited by the lack of understanding of the underlying mechanisms. Here, we examined the feeding behavior of Tetrahymena pyriformis ciliates on 13 viruses, including bacteriophages, enteric viruses, and respiratory viruses. Significant differences in virus removal by T. pyriformis were observed, ranging from no removal (Qbeta, coxsackievirus B5) to ≥2.7 log(10) (JC polyomavirus) after 48 h of co-incubation of the protist with the virus. Removal rates were conserved even when protists were co-incubated with multiple viruses simultaneously. Video analysis revealed that the extent of virus removal was correlated with an increase in the protists’ swimming speed, a behavioral trait consistent with the protists’ response to the availability of food. Protistan feeding may be driven by a virus’ hydrophobicity but was independent of virus size or the presence of a lipid envelope.
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spelling pubmed-89882902022-04-08 Removal of Waterborne Viruses by Tetrahymena pyriformis Is Virus-Specific and Coincides with Changes in Protist Swimming Speed Olive, Margot Moerman, Felix Fernandez-Cassi, Xavier Altermatt, Florian Kohn, Tamar Environ Sci Technol [Image: see text] Biological treatment of waterborne viruses, specifically grazing of viruses by protists, can enhance microbial water quality while avoiding the production of toxic byproducts and high energy costs. However, tangible applications are limited by the lack of understanding of the underlying mechanisms. Here, we examined the feeding behavior of Tetrahymena pyriformis ciliates on 13 viruses, including bacteriophages, enteric viruses, and respiratory viruses. Significant differences in virus removal by T. pyriformis were observed, ranging from no removal (Qbeta, coxsackievirus B5) to ≥2.7 log(10) (JC polyomavirus) after 48 h of co-incubation of the protist with the virus. Removal rates were conserved even when protists were co-incubated with multiple viruses simultaneously. Video analysis revealed that the extent of virus removal was correlated with an increase in the protists’ swimming speed, a behavioral trait consistent with the protists’ response to the availability of food. Protistan feeding may be driven by a virus’ hydrophobicity but was independent of virus size or the presence of a lipid envelope. American Chemical Society 2022-03-08 2022-04-05 /pmc/articles/PMC8988290/ /pubmed/35258957 http://dx.doi.org/10.1021/acs.est.1c05518 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Olive, Margot
Moerman, Felix
Fernandez-Cassi, Xavier
Altermatt, Florian
Kohn, Tamar
Removal of Waterborne Viruses by Tetrahymena pyriformis Is Virus-Specific and Coincides with Changes in Protist Swimming Speed
title Removal of Waterborne Viruses by Tetrahymena pyriformis Is Virus-Specific and Coincides with Changes in Protist Swimming Speed
title_full Removal of Waterborne Viruses by Tetrahymena pyriformis Is Virus-Specific and Coincides with Changes in Protist Swimming Speed
title_fullStr Removal of Waterborne Viruses by Tetrahymena pyriformis Is Virus-Specific and Coincides with Changes in Protist Swimming Speed
title_full_unstemmed Removal of Waterborne Viruses by Tetrahymena pyriformis Is Virus-Specific and Coincides with Changes in Protist Swimming Speed
title_short Removal of Waterborne Viruses by Tetrahymena pyriformis Is Virus-Specific and Coincides with Changes in Protist Swimming Speed
title_sort removal of waterborne viruses by tetrahymena pyriformis is virus-specific and coincides with changes in protist swimming speed
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988290/
https://www.ncbi.nlm.nih.gov/pubmed/35258957
http://dx.doi.org/10.1021/acs.est.1c05518
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