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Resistance of Echovirus 11 to ClO(2) Is Associated with Enhanced Host Receptor Use, Altered Entry Routes, and High Fitness
[Image: see text] Waterborne viruses can exhibit resistance to common water disinfectants, yet the mechanisms that allow them to tolerate disinfection are poorly understood. Here, we generated echovirus 11 (E11) with resistance to chlorine dioxide (ClO(2)) by experimental evolution, and we assessed...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607461/ https://www.ncbi.nlm.nih.gov/pubmed/28837336 http://dx.doi.org/10.1021/acs.est.7b03288 |
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author | Zhong, Qingxia Carratalà, Anna Shim, Hyunjin Bachmann, Virginie Jensen, Jeffrey D. Kohn, Tamar |
author_facet | Zhong, Qingxia Carratalà, Anna Shim, Hyunjin Bachmann, Virginie Jensen, Jeffrey D. Kohn, Tamar |
author_sort | Zhong, Qingxia |
collection | PubMed |
description | [Image: see text] Waterborne viruses can exhibit resistance to common water disinfectants, yet the mechanisms that allow them to tolerate disinfection are poorly understood. Here, we generated echovirus 11 (E11) with resistance to chlorine dioxide (ClO(2)) by experimental evolution, and we assessed the associated genotypic and phenotypic traits. ClO(2) resistance emerged after E11 populations were repeatedly reduced (either by ClO(2)-exposure or by dilution) and then regrown in cell culture. The resistance was linked to an improved capacity of E11 to bind to its host cells, which was further attributed to two potential causes: first, the resistant E11 populations possessed mutations that caused amino acid substitutions from ClO(2)-labile to ClO(2)-stable residues in the viral proteins, which likely increased the chemical stability of the capsid toward ClO(2). Second, resistant E11 mutants exhibited the capacity to utilize alternative cell receptors for host binding. Interestingly, the emergence of ClO(2) resistance resulted in an enhanced replicative fitness compared to the less resistant starting population. Overall this study contributes to a better understanding of the mechanism underlying disinfection resistance in waterborne viruses, and processes that drive resistance development. |
format | Online Article Text |
id | pubmed-5607461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-56074612017-09-22 Resistance of Echovirus 11 to ClO(2) Is Associated with Enhanced Host Receptor Use, Altered Entry Routes, and High Fitness Zhong, Qingxia Carratalà, Anna Shim, Hyunjin Bachmann, Virginie Jensen, Jeffrey D. Kohn, Tamar Environ Sci Technol [Image: see text] Waterborne viruses can exhibit resistance to common water disinfectants, yet the mechanisms that allow them to tolerate disinfection are poorly understood. Here, we generated echovirus 11 (E11) with resistance to chlorine dioxide (ClO(2)) by experimental evolution, and we assessed the associated genotypic and phenotypic traits. ClO(2) resistance emerged after E11 populations were repeatedly reduced (either by ClO(2)-exposure or by dilution) and then regrown in cell culture. The resistance was linked to an improved capacity of E11 to bind to its host cells, which was further attributed to two potential causes: first, the resistant E11 populations possessed mutations that caused amino acid substitutions from ClO(2)-labile to ClO(2)-stable residues in the viral proteins, which likely increased the chemical stability of the capsid toward ClO(2). Second, resistant E11 mutants exhibited the capacity to utilize alternative cell receptors for host binding. Interestingly, the emergence of ClO(2) resistance resulted in an enhanced replicative fitness compared to the less resistant starting population. Overall this study contributes to a better understanding of the mechanism underlying disinfection resistance in waterborne viruses, and processes that drive resistance development. American Chemical Society 2017-08-24 2017-09-19 /pmc/articles/PMC5607461/ /pubmed/28837336 http://dx.doi.org/10.1021/acs.est.7b03288 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Zhong, Qingxia Carratalà, Anna Shim, Hyunjin Bachmann, Virginie Jensen, Jeffrey D. Kohn, Tamar Resistance of Echovirus 11 to ClO(2) Is Associated with Enhanced Host Receptor Use, Altered Entry Routes, and High Fitness |
title | Resistance
of Echovirus 11 to ClO(2) Is Associated
with Enhanced Host Receptor Use, Altered Entry Routes, and High Fitness |
title_full | Resistance
of Echovirus 11 to ClO(2) Is Associated
with Enhanced Host Receptor Use, Altered Entry Routes, and High Fitness |
title_fullStr | Resistance
of Echovirus 11 to ClO(2) Is Associated
with Enhanced Host Receptor Use, Altered Entry Routes, and High Fitness |
title_full_unstemmed | Resistance
of Echovirus 11 to ClO(2) Is Associated
with Enhanced Host Receptor Use, Altered Entry Routes, and High Fitness |
title_short | Resistance
of Echovirus 11 to ClO(2) Is Associated
with Enhanced Host Receptor Use, Altered Entry Routes, and High Fitness |
title_sort | resistance
of echovirus 11 to clo(2) is associated
with enhanced host receptor use, altered entry routes, and high fitness |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607461/ https://www.ncbi.nlm.nih.gov/pubmed/28837336 http://dx.doi.org/10.1021/acs.est.7b03288 |
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