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Traits of a mussel transmissible cancer are reminiscent of a parasitic life style
Some cancers have evolved the ability to spread from host to host by transmission of cancerous cells. These rare biological entities can be considered parasites with a host-related genome. Still, we know little about their specific adaptation to a parasitic lifestyle. MtrBTN2 is one of the few linea...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8677744/ https://www.ncbi.nlm.nih.gov/pubmed/34916573 http://dx.doi.org/10.1038/s41598-021-03598-w |
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author | Burioli, E. A. V. Hammel, M. Bierne, N. Thomas, F. Houssin, M. Destoumieux-Garzón, D. Charrière, G. M. |
author_facet | Burioli, E. A. V. Hammel, M. Bierne, N. Thomas, F. Houssin, M. Destoumieux-Garzón, D. Charrière, G. M. |
author_sort | Burioli, E. A. V. |
collection | PubMed |
description | Some cancers have evolved the ability to spread from host to host by transmission of cancerous cells. These rare biological entities can be considered parasites with a host-related genome. Still, we know little about their specific adaptation to a parasitic lifestyle. MtrBTN2 is one of the few lineages of transmissible cancers known in the animal kingdom. Reported worldwide, MtrBTN2 infects marine mussels. We isolated MtrBTN2 cells circulating in the hemolymph of cancerous mussels and investigated their phenotypic traits. We found that MtrBTN2 cells had remarkable survival capacities in seawater, much higher than normal hemocytes. With almost 100% cell survival over three days, they increase significantly their chances to infect neighboring hosts. MtrBTN2 also triggered an aggressive cancerous process: proliferation in mussels was ~ 17 times higher than normal hemocytes (mean doubling time of ~ 3 days), thereby favoring a rapid increase of intra-host population size. MtrBTN2 appears to induce host castration, thereby favoring resources re-allocation to the parasites and increasing the host carrying capacity. Altogether, our results highlight a series of traits of MtrBTN2 consistent with a marine parasitic lifestyle that may have contributed to the success of its persistence and dissemination in different mussel populations across the globe. |
format | Online Article Text |
id | pubmed-8677744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86777442021-12-20 Traits of a mussel transmissible cancer are reminiscent of a parasitic life style Burioli, E. A. V. Hammel, M. Bierne, N. Thomas, F. Houssin, M. Destoumieux-Garzón, D. Charrière, G. M. Sci Rep Article Some cancers have evolved the ability to spread from host to host by transmission of cancerous cells. These rare biological entities can be considered parasites with a host-related genome. Still, we know little about their specific adaptation to a parasitic lifestyle. MtrBTN2 is one of the few lineages of transmissible cancers known in the animal kingdom. Reported worldwide, MtrBTN2 infects marine mussels. We isolated MtrBTN2 cells circulating in the hemolymph of cancerous mussels and investigated their phenotypic traits. We found that MtrBTN2 cells had remarkable survival capacities in seawater, much higher than normal hemocytes. With almost 100% cell survival over three days, they increase significantly their chances to infect neighboring hosts. MtrBTN2 also triggered an aggressive cancerous process: proliferation in mussels was ~ 17 times higher than normal hemocytes (mean doubling time of ~ 3 days), thereby favoring a rapid increase of intra-host population size. MtrBTN2 appears to induce host castration, thereby favoring resources re-allocation to the parasites and increasing the host carrying capacity. Altogether, our results highlight a series of traits of MtrBTN2 consistent with a marine parasitic lifestyle that may have contributed to the success of its persistence and dissemination in different mussel populations across the globe. Nature Publishing Group UK 2021-12-16 /pmc/articles/PMC8677744/ /pubmed/34916573 http://dx.doi.org/10.1038/s41598-021-03598-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Burioli, E. A. V. Hammel, M. Bierne, N. Thomas, F. Houssin, M. Destoumieux-Garzón, D. Charrière, G. M. Traits of a mussel transmissible cancer are reminiscent of a parasitic life style |
title | Traits of a mussel transmissible cancer are reminiscent of a parasitic life style |
title_full | Traits of a mussel transmissible cancer are reminiscent of a parasitic life style |
title_fullStr | Traits of a mussel transmissible cancer are reminiscent of a parasitic life style |
title_full_unstemmed | Traits of a mussel transmissible cancer are reminiscent of a parasitic life style |
title_short | Traits of a mussel transmissible cancer are reminiscent of a parasitic life style |
title_sort | traits of a mussel transmissible cancer are reminiscent of a parasitic life style |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8677744/ https://www.ncbi.nlm.nih.gov/pubmed/34916573 http://dx.doi.org/10.1038/s41598-021-03598-w |
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