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Black Queen Evolution and Trophic Interactions Determine Plasmid Survival after the Disruption of the Conjugation Network

Mobile genetic elements such as conjugative plasmids are responsible for antibiotic resistance phenotypes in many bacterial pathogens. The ability to conjugate, the presence of antibiotics, and ecological interactions all have a notable role in the persistence of plasmids in bacterial populations. H...

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Autores principales: Cairns, Johannes, Koskinen, Katariina, Penttinen, Reetta, Patinen, Tommi, Hartikainen, Anna, Jokela, Roosa, Ruusulehto, Liisa, Viitamäki, Sirja, Mattila, Sari, Hiltunen, Teppo, Jalasvuori, Matti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6172774/
https://www.ncbi.nlm.nih.gov/pubmed/30320219
http://dx.doi.org/10.1128/mSystems.00104-18
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author Cairns, Johannes
Koskinen, Katariina
Penttinen, Reetta
Patinen, Tommi
Hartikainen, Anna
Jokela, Roosa
Ruusulehto, Liisa
Viitamäki, Sirja
Mattila, Sari
Hiltunen, Teppo
Jalasvuori, Matti
author_facet Cairns, Johannes
Koskinen, Katariina
Penttinen, Reetta
Patinen, Tommi
Hartikainen, Anna
Jokela, Roosa
Ruusulehto, Liisa
Viitamäki, Sirja
Mattila, Sari
Hiltunen, Teppo
Jalasvuori, Matti
author_sort Cairns, Johannes
collection PubMed
description Mobile genetic elements such as conjugative plasmids are responsible for antibiotic resistance phenotypes in many bacterial pathogens. The ability to conjugate, the presence of antibiotics, and ecological interactions all have a notable role in the persistence of plasmids in bacterial populations. Here, we set out to investigate the contribution of these factors when the conjugation network was disturbed by a plasmid-dependent bacteriophage. Phage alone effectively caused the population to lose plasmids, thus rendering them susceptible to antibiotics. Leakiness of the antibiotic resistance mechanism allowing Black Queen evolution (i.e. a “race to the bottom”) was a more significant factor than the antibiotic concentration (lethal vs sublethal) in determining plasmid prevalence. Interestingly, plasmid loss was also prevented by protozoan predation. These results show that outcomes of attempts to resensitize bacterial communities by disrupting the conjugation network are highly dependent on ecological factors and resistance mechanisms. IMPORTANCE Bacterial antibiotic resistance is often a part of mobile genetic elements that move from one bacterium to another. By interfering with the horizontal movement and the maintenance of these elements, it is possible to remove the resistance from the population. Here, we show that a so-called plasmid-dependent bacteriophage causes the initially resistant bacterial population to become susceptible to antibiotics. However, this effect is efficiently countered when the system also contains a predator that feeds on bacteria. Moreover, when the environment contains antibiotics, the survival of resistance is dependent on the resistance mechanism. When bacteria can help their contemporaries to degrade antibiotics, resistance is maintained by only a fraction of the community. On the other hand, when bacteria cannot help others, then all bacteria remain resistant. The concentration of the antibiotic played a less notable role than the antibiotic used. This report shows that the survival of antibiotic resistance in bacterial communities represents a complex process where many factors present in real-life systems define whether or not resistance is actually lost.
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spelling pubmed-61727742018-10-12 Black Queen Evolution and Trophic Interactions Determine Plasmid Survival after the Disruption of the Conjugation Network Cairns, Johannes Koskinen, Katariina Penttinen, Reetta Patinen, Tommi Hartikainen, Anna Jokela, Roosa Ruusulehto, Liisa Viitamäki, Sirja Mattila, Sari Hiltunen, Teppo Jalasvuori, Matti mSystems Research Article Mobile genetic elements such as conjugative plasmids are responsible for antibiotic resistance phenotypes in many bacterial pathogens. The ability to conjugate, the presence of antibiotics, and ecological interactions all have a notable role in the persistence of plasmids in bacterial populations. Here, we set out to investigate the contribution of these factors when the conjugation network was disturbed by a plasmid-dependent bacteriophage. Phage alone effectively caused the population to lose plasmids, thus rendering them susceptible to antibiotics. Leakiness of the antibiotic resistance mechanism allowing Black Queen evolution (i.e. a “race to the bottom”) was a more significant factor than the antibiotic concentration (lethal vs sublethal) in determining plasmid prevalence. Interestingly, plasmid loss was also prevented by protozoan predation. These results show that outcomes of attempts to resensitize bacterial communities by disrupting the conjugation network are highly dependent on ecological factors and resistance mechanisms. IMPORTANCE Bacterial antibiotic resistance is often a part of mobile genetic elements that move from one bacterium to another. By interfering with the horizontal movement and the maintenance of these elements, it is possible to remove the resistance from the population. Here, we show that a so-called plasmid-dependent bacteriophage causes the initially resistant bacterial population to become susceptible to antibiotics. However, this effect is efficiently countered when the system also contains a predator that feeds on bacteria. Moreover, when the environment contains antibiotics, the survival of resistance is dependent on the resistance mechanism. When bacteria can help their contemporaries to degrade antibiotics, resistance is maintained by only a fraction of the community. On the other hand, when bacteria cannot help others, then all bacteria remain resistant. The concentration of the antibiotic played a less notable role than the antibiotic used. This report shows that the survival of antibiotic resistance in bacterial communities represents a complex process where many factors present in real-life systems define whether or not resistance is actually lost. American Society for Microbiology 2018-10-02 /pmc/articles/PMC6172774/ /pubmed/30320219 http://dx.doi.org/10.1128/mSystems.00104-18 Text en Copyright © 2018 Cairns et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Cairns, Johannes
Koskinen, Katariina
Penttinen, Reetta
Patinen, Tommi
Hartikainen, Anna
Jokela, Roosa
Ruusulehto, Liisa
Viitamäki, Sirja
Mattila, Sari
Hiltunen, Teppo
Jalasvuori, Matti
Black Queen Evolution and Trophic Interactions Determine Plasmid Survival after the Disruption of the Conjugation Network
title Black Queen Evolution and Trophic Interactions Determine Plasmid Survival after the Disruption of the Conjugation Network
title_full Black Queen Evolution and Trophic Interactions Determine Plasmid Survival after the Disruption of the Conjugation Network
title_fullStr Black Queen Evolution and Trophic Interactions Determine Plasmid Survival after the Disruption of the Conjugation Network
title_full_unstemmed Black Queen Evolution and Trophic Interactions Determine Plasmid Survival after the Disruption of the Conjugation Network
title_short Black Queen Evolution and Trophic Interactions Determine Plasmid Survival after the Disruption of the Conjugation Network
title_sort black queen evolution and trophic interactions determine plasmid survival after the disruption of the conjugation network
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6172774/
https://www.ncbi.nlm.nih.gov/pubmed/30320219
http://dx.doi.org/10.1128/mSystems.00104-18
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