Cargando…
Paraburkholderia Symbionts Display Variable Infection Patterns That Are Not Predictive of Amoeba Host Outcomes
Symbiotic interactions exist within a parasitism to mutualism continuum that is influenced, among others, by genes and context. Dynamics of intracellular invasion, replication, and prevalence may underscore both host survivability and symbiont stability. More infectious symbionts might exert higher...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349545/ https://www.ncbi.nlm.nih.gov/pubmed/32575747 http://dx.doi.org/10.3390/genes11060674 |
_version_ | 1783557079591550976 |
---|---|
author | Miller, Jacob W. Bocke, Colleen R. Tresslar, Andrew R. Schniepp, Emily M. DiSalvo, Susanne |
author_facet | Miller, Jacob W. Bocke, Colleen R. Tresslar, Andrew R. Schniepp, Emily M. DiSalvo, Susanne |
author_sort | Miller, Jacob W. |
collection | PubMed |
description | Symbiotic interactions exist within a parasitism to mutualism continuum that is influenced, among others, by genes and context. Dynamics of intracellular invasion, replication, and prevalence may underscore both host survivability and symbiont stability. More infectious symbionts might exert higher corresponding costs to hosts, which could ultimately disadvantage both partners. Here, we quantify infection patterns of diverse Paraburkholderia symbiont genotypes in their amoeba host Dictyostelium discoideum and probe the relationship between these patterns and host outcomes. We exposed D. discoideum to thirteen strains of Paraburkholderia each belonging to one of the three symbiont species found to naturally infect D. discoideum: Paraburkholderia agricolaris, Paraburkholderia hayleyella, and Paraburkholderia bonniea. We quantified the infection prevalence and intracellular density of fluorescently labeled symbionts along with the final host population size using flow cytometry and confocal microscopy. We find that infection phenotypes vary across symbiont strains. Symbionts belonging to the same species generally display similar infection patterns but are interestingly distinct when it comes to host outcomes. This results in final infection loads that do not strongly correlate to final host outcomes, suggesting other genetic factors that are not a direct cause or consequence of symbiont abundance impact host fitness. |
format | Online Article Text |
id | pubmed-7349545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73495452020-07-14 Paraburkholderia Symbionts Display Variable Infection Patterns That Are Not Predictive of Amoeba Host Outcomes Miller, Jacob W. Bocke, Colleen R. Tresslar, Andrew R. Schniepp, Emily M. DiSalvo, Susanne Genes (Basel) Article Symbiotic interactions exist within a parasitism to mutualism continuum that is influenced, among others, by genes and context. Dynamics of intracellular invasion, replication, and prevalence may underscore both host survivability and symbiont stability. More infectious symbionts might exert higher corresponding costs to hosts, which could ultimately disadvantage both partners. Here, we quantify infection patterns of diverse Paraburkholderia symbiont genotypes in their amoeba host Dictyostelium discoideum and probe the relationship between these patterns and host outcomes. We exposed D. discoideum to thirteen strains of Paraburkholderia each belonging to one of the three symbiont species found to naturally infect D. discoideum: Paraburkholderia agricolaris, Paraburkholderia hayleyella, and Paraburkholderia bonniea. We quantified the infection prevalence and intracellular density of fluorescently labeled symbionts along with the final host population size using flow cytometry and confocal microscopy. We find that infection phenotypes vary across symbiont strains. Symbionts belonging to the same species generally display similar infection patterns but are interestingly distinct when it comes to host outcomes. This results in final infection loads that do not strongly correlate to final host outcomes, suggesting other genetic factors that are not a direct cause or consequence of symbiont abundance impact host fitness. MDPI 2020-06-20 /pmc/articles/PMC7349545/ /pubmed/32575747 http://dx.doi.org/10.3390/genes11060674 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Miller, Jacob W. Bocke, Colleen R. Tresslar, Andrew R. Schniepp, Emily M. DiSalvo, Susanne Paraburkholderia Symbionts Display Variable Infection Patterns That Are Not Predictive of Amoeba Host Outcomes |
title | Paraburkholderia Symbionts Display Variable Infection Patterns That Are Not Predictive of Amoeba Host Outcomes |
title_full | Paraburkholderia Symbionts Display Variable Infection Patterns That Are Not Predictive of Amoeba Host Outcomes |
title_fullStr | Paraburkholderia Symbionts Display Variable Infection Patterns That Are Not Predictive of Amoeba Host Outcomes |
title_full_unstemmed | Paraburkholderia Symbionts Display Variable Infection Patterns That Are Not Predictive of Amoeba Host Outcomes |
title_short | Paraburkholderia Symbionts Display Variable Infection Patterns That Are Not Predictive of Amoeba Host Outcomes |
title_sort | paraburkholderia symbionts display variable infection patterns that are not predictive of amoeba host outcomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349545/ https://www.ncbi.nlm.nih.gov/pubmed/32575747 http://dx.doi.org/10.3390/genes11060674 |
work_keys_str_mv | AT millerjacobw paraburkholderiasymbiontsdisplayvariableinfectionpatternsthatarenotpredictiveofamoebahostoutcomes AT bockecolleenr paraburkholderiasymbiontsdisplayvariableinfectionpatternsthatarenotpredictiveofamoebahostoutcomes AT tresslarandrewr paraburkholderiasymbiontsdisplayvariableinfectionpatternsthatarenotpredictiveofamoebahostoutcomes AT schnieppemilym paraburkholderiasymbiontsdisplayvariableinfectionpatternsthatarenotpredictiveofamoebahostoutcomes AT disalvosusanne paraburkholderiasymbiontsdisplayvariableinfectionpatternsthatarenotpredictiveofamoebahostoutcomes |