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Mice Against Ticks: an experimental community-guided effort to prevent tick-borne disease by altering the shared environment
Mice Against Ticks is a community-guided ecological engineering project that aims to prevent tick-borne disease by using CRISPR-based genome editing to heritably immunize the white-footed mice (Peromyscus leucopus) responsible for infecting many ticks in eastern North America. Introducing antibody-e...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452264/ https://www.ncbi.nlm.nih.gov/pubmed/30905296 http://dx.doi.org/10.1098/rstb.2018.0105 |
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author | Buchthal, Joanna Evans, Sam Weiss Lunshof, Jeantine Telford, Sam R. Esvelt, Kevin M. |
author_facet | Buchthal, Joanna Evans, Sam Weiss Lunshof, Jeantine Telford, Sam R. Esvelt, Kevin M. |
author_sort | Buchthal, Joanna |
collection | PubMed |
description | Mice Against Ticks is a community-guided ecological engineering project that aims to prevent tick-borne disease by using CRISPR-based genome editing to heritably immunize the white-footed mice (Peromyscus leucopus) responsible for infecting many ticks in eastern North America. Introducing antibody-encoding resistance alleles into the local mouse population is anticipated to disrupt the disease transmission cycle for decades. Technology development is shaped by engagement with community members and visitors to the islands of Nantucket and Martha's Vineyard, including decisions at project inception about which types of disease resistance to pursue. This engagement process has prompted the researchers to use only white-footed mouse DNA if possible, meaning the current project will not involve gene drive. Instead, engineered mice would be released in the spring when the natural population is low, a plan unlikely to increase total numbers above the normal maximum in autumn. Community members are continually asked to share their suggestions and concerns, a process that has already identified potential ecological consequences unanticipated by the research team that will likely affect implementation. As an early example of CRISPR-based ecological engineering, Mice Against Ticks aims to start small and simple by working with island communities whose mouse populations can be lastingly immunized without gene drive. This article is part of a discussion meeting issue ‘The ecology and evolution of prokaryotic CRISPR-Cas adaptive immune systems’. |
format | Online Article Text |
id | pubmed-6452264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-64522642019-04-18 Mice Against Ticks: an experimental community-guided effort to prevent tick-borne disease by altering the shared environment Buchthal, Joanna Evans, Sam Weiss Lunshof, Jeantine Telford, Sam R. Esvelt, Kevin M. Philos Trans R Soc Lond B Biol Sci Articles Mice Against Ticks is a community-guided ecological engineering project that aims to prevent tick-borne disease by using CRISPR-based genome editing to heritably immunize the white-footed mice (Peromyscus leucopus) responsible for infecting many ticks in eastern North America. Introducing antibody-encoding resistance alleles into the local mouse population is anticipated to disrupt the disease transmission cycle for decades. Technology development is shaped by engagement with community members and visitors to the islands of Nantucket and Martha's Vineyard, including decisions at project inception about which types of disease resistance to pursue. This engagement process has prompted the researchers to use only white-footed mouse DNA if possible, meaning the current project will not involve gene drive. Instead, engineered mice would be released in the spring when the natural population is low, a plan unlikely to increase total numbers above the normal maximum in autumn. Community members are continually asked to share their suggestions and concerns, a process that has already identified potential ecological consequences unanticipated by the research team that will likely affect implementation. As an early example of CRISPR-based ecological engineering, Mice Against Ticks aims to start small and simple by working with island communities whose mouse populations can be lastingly immunized without gene drive. This article is part of a discussion meeting issue ‘The ecology and evolution of prokaryotic CRISPR-Cas adaptive immune systems’. The Royal Society 2019-05-13 2019-03-25 /pmc/articles/PMC6452264/ /pubmed/30905296 http://dx.doi.org/10.1098/rstb.2018.0105 Text en © 2019 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Articles Buchthal, Joanna Evans, Sam Weiss Lunshof, Jeantine Telford, Sam R. Esvelt, Kevin M. Mice Against Ticks: an experimental community-guided effort to prevent tick-borne disease by altering the shared environment |
title | Mice Against Ticks: an experimental community-guided effort to prevent tick-borne disease by altering the shared environment |
title_full | Mice Against Ticks: an experimental community-guided effort to prevent tick-borne disease by altering the shared environment |
title_fullStr | Mice Against Ticks: an experimental community-guided effort to prevent tick-borne disease by altering the shared environment |
title_full_unstemmed | Mice Against Ticks: an experimental community-guided effort to prevent tick-borne disease by altering the shared environment |
title_short | Mice Against Ticks: an experimental community-guided effort to prevent tick-borne disease by altering the shared environment |
title_sort | mice against ticks: an experimental community-guided effort to prevent tick-borne disease by altering the shared environment |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452264/ https://www.ncbi.nlm.nih.gov/pubmed/30905296 http://dx.doi.org/10.1098/rstb.2018.0105 |
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