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Molecular dissection of box jellyfish venom cytotoxicity highlights an effective venom antidote
The box jellyfish Chironex fleckeri is extremely venomous, and envenoming causes tissue necrosis, extreme pain and death within minutes after severe exposure. Despite rapid and potent venom action, basic mechanistic insight is lacking. Here we perform molecular dissection of a jellyfish venom-induce...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491561/ https://www.ncbi.nlm.nih.gov/pubmed/31040274 http://dx.doi.org/10.1038/s41467-019-09681-1 |
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author | Lau, Man-Tat Manion, John Littleboy, Jamie B. Oyston, Lisa Khuong, Thang M. Wang, Qiao-Ping Nguyen, David T. Hesselson, Daniel Seymour, Jamie E. Neely, G. Gregory |
author_facet | Lau, Man-Tat Manion, John Littleboy, Jamie B. Oyston, Lisa Khuong, Thang M. Wang, Qiao-Ping Nguyen, David T. Hesselson, Daniel Seymour, Jamie E. Neely, G. Gregory |
author_sort | Lau, Man-Tat |
collection | PubMed |
description | The box jellyfish Chironex fleckeri is extremely venomous, and envenoming causes tissue necrosis, extreme pain and death within minutes after severe exposure. Despite rapid and potent venom action, basic mechanistic insight is lacking. Here we perform molecular dissection of a jellyfish venom-induced cell death pathway by screening for host components required for venom exposure-induced cell death using genome-scale lenti-CRISPR mutagenesis. We identify the peripheral membrane protein ATP2B1, a calcium transporting ATPase, as one host factor required for venom cytotoxicity. Targeting ATP2B1 prevents venom action and confers long lasting protection. Informatics analysis of host genes required for venom cytotoxicity reveal pathways not previously implicated in cell death. We also discover a venom antidote that functions up to 15 minutes after exposure and suppresses tissue necrosis and pain in mice. These results highlight the power of whole genome CRISPR screening to investigate venom mechanisms of action and to rapidly identify new medicines. |
format | Online Article Text |
id | pubmed-6491561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64915612019-05-02 Molecular dissection of box jellyfish venom cytotoxicity highlights an effective venom antidote Lau, Man-Tat Manion, John Littleboy, Jamie B. Oyston, Lisa Khuong, Thang M. Wang, Qiao-Ping Nguyen, David T. Hesselson, Daniel Seymour, Jamie E. Neely, G. Gregory Nat Commun Article The box jellyfish Chironex fleckeri is extremely venomous, and envenoming causes tissue necrosis, extreme pain and death within minutes after severe exposure. Despite rapid and potent venom action, basic mechanistic insight is lacking. Here we perform molecular dissection of a jellyfish venom-induced cell death pathway by screening for host components required for venom exposure-induced cell death using genome-scale lenti-CRISPR mutagenesis. We identify the peripheral membrane protein ATP2B1, a calcium transporting ATPase, as one host factor required for venom cytotoxicity. Targeting ATP2B1 prevents venom action and confers long lasting protection. Informatics analysis of host genes required for venom cytotoxicity reveal pathways not previously implicated in cell death. We also discover a venom antidote that functions up to 15 minutes after exposure and suppresses tissue necrosis and pain in mice. These results highlight the power of whole genome CRISPR screening to investigate venom mechanisms of action and to rapidly identify new medicines. Nature Publishing Group UK 2019-04-30 /pmc/articles/PMC6491561/ /pubmed/31040274 http://dx.doi.org/10.1038/s41467-019-09681-1 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lau, Man-Tat Manion, John Littleboy, Jamie B. Oyston, Lisa Khuong, Thang M. Wang, Qiao-Ping Nguyen, David T. Hesselson, Daniel Seymour, Jamie E. Neely, G. Gregory Molecular dissection of box jellyfish venom cytotoxicity highlights an effective venom antidote |
title | Molecular dissection of box jellyfish venom cytotoxicity highlights an effective venom antidote |
title_full | Molecular dissection of box jellyfish venom cytotoxicity highlights an effective venom antidote |
title_fullStr | Molecular dissection of box jellyfish venom cytotoxicity highlights an effective venom antidote |
title_full_unstemmed | Molecular dissection of box jellyfish venom cytotoxicity highlights an effective venom antidote |
title_short | Molecular dissection of box jellyfish venom cytotoxicity highlights an effective venom antidote |
title_sort | molecular dissection of box jellyfish venom cytotoxicity highlights an effective venom antidote |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491561/ https://www.ncbi.nlm.nih.gov/pubmed/31040274 http://dx.doi.org/10.1038/s41467-019-09681-1 |
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