Cargando…
Disruption of Metapopulation Structure Reduces Tasmanian Devil Facial Tumour Disease Spread at the Expense of Abundance and Genetic Diversity
Metapopulation structure plays a fundamental role in the persistence of wildlife populations. It can also drive the spread of infectious diseases and transmissible cancers such as the Tasmanian devil facial tumour disease (DFTD). While disrupting this structure can reduce disease spread, it can also...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8705368/ https://www.ncbi.nlm.nih.gov/pubmed/34959547 http://dx.doi.org/10.3390/pathogens10121592 |
_version_ | 1784621928944762880 |
---|---|
author | Durrant, Rowan Hamede, Rodrigo Wells, Konstans Lurgi, Miguel |
author_facet | Durrant, Rowan Hamede, Rodrigo Wells, Konstans Lurgi, Miguel |
author_sort | Durrant, Rowan |
collection | PubMed |
description | Metapopulation structure plays a fundamental role in the persistence of wildlife populations. It can also drive the spread of infectious diseases and transmissible cancers such as the Tasmanian devil facial tumour disease (DFTD). While disrupting this structure can reduce disease spread, it can also impair host resilience by disrupting gene flow and colonisation dynamics. Using an individual-based metapopulation model we investigated the synergistic effects of host dispersal, disease transmission rate and inter-individual contact distance for transmission, on the spread and persistence of DFTD from local to regional scales. Disease spread, and the ensuing population declines, are synergistically determined by individuals’ dispersal, disease transmission rate and within-population mixing. Transmission rates can be magnified by high dispersal and inter-individual transmission distance. The isolation of local populations effectively reduced metapopulation-level disease prevalence but caused severe declines in metapopulation size and genetic diversity. The relative position of managed (i.e., isolated) local populations had a significant effect on disease prevalence, highlighting the importance of considering metapopulation structure when implementing metapopulation-scale disease control measures. Our findings suggest that population isolation is not an ideal management method for preventing disease spread in species inhabiting already fragmented landscapes, where genetic diversity and extinction risk are already a concern. |
format | Online Article Text |
id | pubmed-8705368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87053682021-12-25 Disruption of Metapopulation Structure Reduces Tasmanian Devil Facial Tumour Disease Spread at the Expense of Abundance and Genetic Diversity Durrant, Rowan Hamede, Rodrigo Wells, Konstans Lurgi, Miguel Pathogens Article Metapopulation structure plays a fundamental role in the persistence of wildlife populations. It can also drive the spread of infectious diseases and transmissible cancers such as the Tasmanian devil facial tumour disease (DFTD). While disrupting this structure can reduce disease spread, it can also impair host resilience by disrupting gene flow and colonisation dynamics. Using an individual-based metapopulation model we investigated the synergistic effects of host dispersal, disease transmission rate and inter-individual contact distance for transmission, on the spread and persistence of DFTD from local to regional scales. Disease spread, and the ensuing population declines, are synergistically determined by individuals’ dispersal, disease transmission rate and within-population mixing. Transmission rates can be magnified by high dispersal and inter-individual transmission distance. The isolation of local populations effectively reduced metapopulation-level disease prevalence but caused severe declines in metapopulation size and genetic diversity. The relative position of managed (i.e., isolated) local populations had a significant effect on disease prevalence, highlighting the importance of considering metapopulation structure when implementing metapopulation-scale disease control measures. Our findings suggest that population isolation is not an ideal management method for preventing disease spread in species inhabiting already fragmented landscapes, where genetic diversity and extinction risk are already a concern. MDPI 2021-12-08 /pmc/articles/PMC8705368/ /pubmed/34959547 http://dx.doi.org/10.3390/pathogens10121592 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Durrant, Rowan Hamede, Rodrigo Wells, Konstans Lurgi, Miguel Disruption of Metapopulation Structure Reduces Tasmanian Devil Facial Tumour Disease Spread at the Expense of Abundance and Genetic Diversity |
title | Disruption of Metapopulation Structure Reduces Tasmanian Devil Facial Tumour Disease Spread at the Expense of Abundance and Genetic Diversity |
title_full | Disruption of Metapopulation Structure Reduces Tasmanian Devil Facial Tumour Disease Spread at the Expense of Abundance and Genetic Diversity |
title_fullStr | Disruption of Metapopulation Structure Reduces Tasmanian Devil Facial Tumour Disease Spread at the Expense of Abundance and Genetic Diversity |
title_full_unstemmed | Disruption of Metapopulation Structure Reduces Tasmanian Devil Facial Tumour Disease Spread at the Expense of Abundance and Genetic Diversity |
title_short | Disruption of Metapopulation Structure Reduces Tasmanian Devil Facial Tumour Disease Spread at the Expense of Abundance and Genetic Diversity |
title_sort | disruption of metapopulation structure reduces tasmanian devil facial tumour disease spread at the expense of abundance and genetic diversity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8705368/ https://www.ncbi.nlm.nih.gov/pubmed/34959547 http://dx.doi.org/10.3390/pathogens10121592 |
work_keys_str_mv | AT durrantrowan disruptionofmetapopulationstructurereducestasmaniandevilfacialtumourdiseasespreadattheexpenseofabundanceandgeneticdiversity AT hamederodrigo disruptionofmetapopulationstructurereducestasmaniandevilfacialtumourdiseasespreadattheexpenseofabundanceandgeneticdiversity AT wellskonstans disruptionofmetapopulationstructurereducestasmaniandevilfacialtumourdiseasespreadattheexpenseofabundanceandgeneticdiversity AT lurgimiguel disruptionofmetapopulationstructurereducestasmaniandevilfacialtumourdiseasespreadattheexpenseofabundanceandgeneticdiversity |