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High-efficiency electroporation of chytrid fungi
Two species of parasitic fungi from the phylum Chytridiomycota (chytrids) are annihilating global amphibian populations. These chytrid species—Batrachochytrium dendrobatidis and B. salamandrivorans—have high rates of mortality and transmission. Upon establishing infection in amphibians, chytrids rap...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493940/ https://www.ncbi.nlm.nih.gov/pubmed/32934254 http://dx.doi.org/10.1038/s41598-020-71618-2 |
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author | Swafford, Andrew J. M. Hussey, Shane P. Fritz-Laylin, Lillian K. |
author_facet | Swafford, Andrew J. M. Hussey, Shane P. Fritz-Laylin, Lillian K. |
author_sort | Swafford, Andrew J. M. |
collection | PubMed |
description | Two species of parasitic fungi from the phylum Chytridiomycota (chytrids) are annihilating global amphibian populations. These chytrid species—Batrachochytrium dendrobatidis and B. salamandrivorans—have high rates of mortality and transmission. Upon establishing infection in amphibians, chytrids rapidly multiply within the skin and disrupt their hosts’ vital homeostasis mechanisms. Current disease models suggest that chytrid fungi locate and infect their hosts during a motile, unicellular ‘zoospore’ life stage. Moreover, other chytrid species parasitize organisms from across the tree of life, making future epidemics in new hosts a likely possibility. Efforts to mitigate the damage and spread of chytrid disease have been stymied by the lack of knowledge about basic chytrid biology and tools with which to test molecular hypotheses about disease mechanisms. To overcome this bottleneck, we have developed high-efficiency delivery of molecular payloads into chytrid zoospores using electroporation. Our electroporation protocols result in payload delivery to between 75 and 97% of living cells of three species: B. dendrobatidis, B. salamandrivorans, and a non-pathogenic relative, Spizellomyces punctatus. This method lays the foundation for molecular genetic tools needed to establish ecological mitigation strategies and answer broader questions in evolutionary and cell biology. |
format | Online Article Text |
id | pubmed-7493940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74939402020-09-16 High-efficiency electroporation of chytrid fungi Swafford, Andrew J. M. Hussey, Shane P. Fritz-Laylin, Lillian K. Sci Rep Article Two species of parasitic fungi from the phylum Chytridiomycota (chytrids) are annihilating global amphibian populations. These chytrid species—Batrachochytrium dendrobatidis and B. salamandrivorans—have high rates of mortality and transmission. Upon establishing infection in amphibians, chytrids rapidly multiply within the skin and disrupt their hosts’ vital homeostasis mechanisms. Current disease models suggest that chytrid fungi locate and infect their hosts during a motile, unicellular ‘zoospore’ life stage. Moreover, other chytrid species parasitize organisms from across the tree of life, making future epidemics in new hosts a likely possibility. Efforts to mitigate the damage and spread of chytrid disease have been stymied by the lack of knowledge about basic chytrid biology and tools with which to test molecular hypotheses about disease mechanisms. To overcome this bottleneck, we have developed high-efficiency delivery of molecular payloads into chytrid zoospores using electroporation. Our electroporation protocols result in payload delivery to between 75 and 97% of living cells of three species: B. dendrobatidis, B. salamandrivorans, and a non-pathogenic relative, Spizellomyces punctatus. This method lays the foundation for molecular genetic tools needed to establish ecological mitigation strategies and answer broader questions in evolutionary and cell biology. Nature Publishing Group UK 2020-09-15 /pmc/articles/PMC7493940/ /pubmed/32934254 http://dx.doi.org/10.1038/s41598-020-71618-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Swafford, Andrew J. M. Hussey, Shane P. Fritz-Laylin, Lillian K. High-efficiency electroporation of chytrid fungi |
title | High-efficiency electroporation of chytrid
fungi |
title_full | High-efficiency electroporation of chytrid
fungi |
title_fullStr | High-efficiency electroporation of chytrid
fungi |
title_full_unstemmed | High-efficiency electroporation of chytrid
fungi |
title_short | High-efficiency electroporation of chytrid
fungi |
title_sort | high-efficiency electroporation of chytrid
fungi |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493940/ https://www.ncbi.nlm.nih.gov/pubmed/32934254 http://dx.doi.org/10.1038/s41598-020-71618-2 |
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