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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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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. |
format | Online Article Text |
id | pubmed-8988290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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