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Novel Chlamydiae and Amoebophilus endosymbionts are prevalent in wild isolates of the model social amoeba Dictyostelium discoideum
Amoebae interact with bacteria in multifaceted ways. Amoeba predation can serve as a selective pressure for the development of bacterial virulence traits. Bacteria may also adapt to life inside amoebae, resulting in symbiotic relationships. Indeed, particular lineages of obligate bacterial endosymbi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518690/ https://www.ncbi.nlm.nih.gov/pubmed/34159734 http://dx.doi.org/10.1111/1758-2229.12985 |
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author | Haselkorn, Tamara S. Jimenez, Daniela Bashir, Usman Sallinger, Eleni Queller, David C. Strassmann, Joan E. DiSalvo, Susanne |
author_facet | Haselkorn, Tamara S. Jimenez, Daniela Bashir, Usman Sallinger, Eleni Queller, David C. Strassmann, Joan E. DiSalvo, Susanne |
author_sort | Haselkorn, Tamara S. |
collection | PubMed |
description | Amoebae interact with bacteria in multifaceted ways. Amoeba predation can serve as a selective pressure for the development of bacterial virulence traits. Bacteria may also adapt to life inside amoebae, resulting in symbiotic relationships. Indeed, particular lineages of obligate bacterial endosymbionts have been found in different amoebae. Here, we screened an extensive collection of Dictyostelium discoideum wild isolates for the presence of these bacterial symbionts using endosymbiont specific PCR primers. We find that these symbionts are surprisingly common, identified in 42% of screened isolates (N = 730). Members of the Chlamydiae phylum are particularly prevalent, occurring in 27% of the amoeba isolated. They are novel and phylogenetically distinct from other Chlamydiae. We also found Amoebophilus symbionts in 8% of screened isolates (N = 730). Antibiotic‐cured amoebae behave similarly to their Chlamydiae or Amoebophilus‐infected counterparts, suggesting that these endosymbionts do not significantly impact host fitness, at least in the laboratory. We found several natural isolates were co‐infected with multiple endosymbionts, with no obvious fitness effect of co‐infection under laboratory conditions. The high prevalence and novelty of amoeba endosymbiont clades in the model organism D. discoideum opens the door to future research on the significance and mechanisms of amoeba–symbiont interactions. |
format | Online Article Text |
id | pubmed-8518690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85186902021-10-21 Novel Chlamydiae and Amoebophilus endosymbionts are prevalent in wild isolates of the model social amoeba Dictyostelium discoideum Haselkorn, Tamara S. Jimenez, Daniela Bashir, Usman Sallinger, Eleni Queller, David C. Strassmann, Joan E. DiSalvo, Susanne Environ Microbiol Rep Brief Reports Amoebae interact with bacteria in multifaceted ways. Amoeba predation can serve as a selective pressure for the development of bacterial virulence traits. Bacteria may also adapt to life inside amoebae, resulting in symbiotic relationships. Indeed, particular lineages of obligate bacterial endosymbionts have been found in different amoebae. Here, we screened an extensive collection of Dictyostelium discoideum wild isolates for the presence of these bacterial symbionts using endosymbiont specific PCR primers. We find that these symbionts are surprisingly common, identified in 42% of screened isolates (N = 730). Members of the Chlamydiae phylum are particularly prevalent, occurring in 27% of the amoeba isolated. They are novel and phylogenetically distinct from other Chlamydiae. We also found Amoebophilus symbionts in 8% of screened isolates (N = 730). Antibiotic‐cured amoebae behave similarly to their Chlamydiae or Amoebophilus‐infected counterparts, suggesting that these endosymbionts do not significantly impact host fitness, at least in the laboratory. We found several natural isolates were co‐infected with multiple endosymbionts, with no obvious fitness effect of co‐infection under laboratory conditions. The high prevalence and novelty of amoeba endosymbiont clades in the model organism D. discoideum opens the door to future research on the significance and mechanisms of amoeba–symbiont interactions. John Wiley & Sons, Inc. 2021-06-22 2021-10 /pmc/articles/PMC8518690/ /pubmed/34159734 http://dx.doi.org/10.1111/1758-2229.12985 Text en © 2021 The Authors. Environmental Microbiology Reports published by Society for Applied Microbiology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Brief Reports Haselkorn, Tamara S. Jimenez, Daniela Bashir, Usman Sallinger, Eleni Queller, David C. Strassmann, Joan E. DiSalvo, Susanne Novel Chlamydiae and Amoebophilus endosymbionts are prevalent in wild isolates of the model social amoeba Dictyostelium discoideum |
title | Novel Chlamydiae and Amoebophilus endosymbionts are prevalent in wild isolates of the model social amoeba Dictyostelium discoideum
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title_full | Novel Chlamydiae and Amoebophilus endosymbionts are prevalent in wild isolates of the model social amoeba Dictyostelium discoideum
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title_fullStr | Novel Chlamydiae and Amoebophilus endosymbionts are prevalent in wild isolates of the model social amoeba Dictyostelium discoideum
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title_full_unstemmed | Novel Chlamydiae and Amoebophilus endosymbionts are prevalent in wild isolates of the model social amoeba Dictyostelium discoideum
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title_short | Novel Chlamydiae and Amoebophilus endosymbionts are prevalent in wild isolates of the model social amoeba Dictyostelium discoideum
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title_sort | novel chlamydiae and amoebophilus endosymbionts are prevalent in wild isolates of the model social amoeba dictyostelium discoideum |
topic | Brief Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518690/ https://www.ncbi.nlm.nih.gov/pubmed/34159734 http://dx.doi.org/10.1111/1758-2229.12985 |
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