Cargando…
Host age structure reshapes parasite symbiosis: collaboration begets pathogens, competition begets virulent mutualists
BACKGROUND: Symbiotic relationships are ubiquitous in the biosphere. Inter-species symbiosis is impacted by intra-specific distinctions, in particular, those defined by the age structure of a population. Older individuals compete with younger individuals for resources despite being less likely to re...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652831/ https://www.ncbi.nlm.nih.gov/pubmed/36371206 http://dx.doi.org/10.1186/s13062-022-00343-9 |
_version_ | 1784828560464150528 |
---|---|
author | Portner, Carsten O. S. Rong, Edward G. Ramirez, Jared A. Wolf, Yuri I. Bosse, Angelique P. Koonin, Eugene V. Rochman, Nash D. |
author_facet | Portner, Carsten O. S. Rong, Edward G. Ramirez, Jared A. Wolf, Yuri I. Bosse, Angelique P. Koonin, Eugene V. Rochman, Nash D. |
author_sort | Portner, Carsten O. S. |
collection | PubMed |
description | BACKGROUND: Symbiotic relationships are ubiquitous in the biosphere. Inter-species symbiosis is impacted by intra-specific distinctions, in particular, those defined by the age structure of a population. Older individuals compete with younger individuals for resources despite being less likely to reproduce, diminishing the fitness of the population. Conversely, however, older individuals can support the reproduction of younger individuals, increasing the population fitness. Parasitic relationships are commonly age structured, typically, more adversely affecting older hosts. RESULTS: We employ mathematical modeling to explore the differential effects of collaborative or competitive host age structures on host-parasite relationships. A classical epidemiological compartment model is constructed with three disease states: susceptible, infected, and recovered. Each of these three states is partitioned into two compartments representing young, potentially reproductive, and old, post-reproductive, hosts, yielding 6 compartments in total. In order to describe competition and collaboration between old and young compartments, we model the reproductive success to depend on the fraction of young individuals in the population. Collaborative populations with relatively greater numbers of post-reproductive hosts enjoy greater reproductive success whereas in purely competitive populations, increasing the post-reproductive subpopulation reduces reproductive success. CONCLUSIONS: We demonstrate that, in collaborative host populations, pathogens strictly impacting older, post-reproductive individuals can reduce population fitness even more than pathogens that directly impact younger, potentially reproductive individuals. In purely competitive populations, the reverse is observed, and we demonstrate that endemic, virulent pathogens can oxymoronically form a mutualistic relationship with the host, increasing the fitness of the host population. Applications to endangered species conservation and invasive species containment are discussed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13062-022-00343-9. |
format | Online Article Text |
id | pubmed-9652831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96528312022-11-15 Host age structure reshapes parasite symbiosis: collaboration begets pathogens, competition begets virulent mutualists Portner, Carsten O. S. Rong, Edward G. Ramirez, Jared A. Wolf, Yuri I. Bosse, Angelique P. Koonin, Eugene V. Rochman, Nash D. Biol Direct Research BACKGROUND: Symbiotic relationships are ubiquitous in the biosphere. Inter-species symbiosis is impacted by intra-specific distinctions, in particular, those defined by the age structure of a population. Older individuals compete with younger individuals for resources despite being less likely to reproduce, diminishing the fitness of the population. Conversely, however, older individuals can support the reproduction of younger individuals, increasing the population fitness. Parasitic relationships are commonly age structured, typically, more adversely affecting older hosts. RESULTS: We employ mathematical modeling to explore the differential effects of collaborative or competitive host age structures on host-parasite relationships. A classical epidemiological compartment model is constructed with three disease states: susceptible, infected, and recovered. Each of these three states is partitioned into two compartments representing young, potentially reproductive, and old, post-reproductive, hosts, yielding 6 compartments in total. In order to describe competition and collaboration between old and young compartments, we model the reproductive success to depend on the fraction of young individuals in the population. Collaborative populations with relatively greater numbers of post-reproductive hosts enjoy greater reproductive success whereas in purely competitive populations, increasing the post-reproductive subpopulation reduces reproductive success. CONCLUSIONS: We demonstrate that, in collaborative host populations, pathogens strictly impacting older, post-reproductive individuals can reduce population fitness even more than pathogens that directly impact younger, potentially reproductive individuals. In purely competitive populations, the reverse is observed, and we demonstrate that endemic, virulent pathogens can oxymoronically form a mutualistic relationship with the host, increasing the fitness of the host population. Applications to endangered species conservation and invasive species containment are discussed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13062-022-00343-9. BioMed Central 2022-11-12 /pmc/articles/PMC9652831/ /pubmed/36371206 http://dx.doi.org/10.1186/s13062-022-00343-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Portner, Carsten O. S. Rong, Edward G. Ramirez, Jared A. Wolf, Yuri I. Bosse, Angelique P. Koonin, Eugene V. Rochman, Nash D. Host age structure reshapes parasite symbiosis: collaboration begets pathogens, competition begets virulent mutualists |
title | Host age structure reshapes parasite symbiosis: collaboration begets pathogens, competition begets virulent mutualists |
title_full | Host age structure reshapes parasite symbiosis: collaboration begets pathogens, competition begets virulent mutualists |
title_fullStr | Host age structure reshapes parasite symbiosis: collaboration begets pathogens, competition begets virulent mutualists |
title_full_unstemmed | Host age structure reshapes parasite symbiosis: collaboration begets pathogens, competition begets virulent mutualists |
title_short | Host age structure reshapes parasite symbiosis: collaboration begets pathogens, competition begets virulent mutualists |
title_sort | host age structure reshapes parasite symbiosis: collaboration begets pathogens, competition begets virulent mutualists |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652831/ https://www.ncbi.nlm.nih.gov/pubmed/36371206 http://dx.doi.org/10.1186/s13062-022-00343-9 |
work_keys_str_mv | AT portnercarstenos hostagestructurereshapesparasitesymbiosiscollaborationbegetspathogenscompetitionbegetsvirulentmutualists AT rongedwardg hostagestructurereshapesparasitesymbiosiscollaborationbegetspathogenscompetitionbegetsvirulentmutualists AT ramirezjareda hostagestructurereshapesparasitesymbiosiscollaborationbegetspathogenscompetitionbegetsvirulentmutualists AT wolfyurii hostagestructurereshapesparasitesymbiosiscollaborationbegetspathogenscompetitionbegetsvirulentmutualists AT bosseangeliquep hostagestructurereshapesparasitesymbiosiscollaborationbegetspathogenscompetitionbegetsvirulentmutualists AT koonineugenev hostagestructurereshapesparasitesymbiosiscollaborationbegetspathogenscompetitionbegetsvirulentmutualists AT rochmannashd hostagestructurereshapesparasitesymbiosiscollaborationbegetspathogenscompetitionbegetsvirulentmutualists |