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Experimental Listeria–Tetrahymena–Amoeba food chain functioning depends on bacterial virulence traits

BACKGROUND: Some pathogenic bacteria have been developing as a part of terrestrial and aquatic microbial ecosystems. Bacteria are consumed by bacteriovorous protists which are readily consumed by larger organisms. Being natural predators, protozoa are also an instrument for selection of virulence tr...

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Autores principales: Pushkareva, Valentina I., Podlipaeva, Julia I., Goodkov, Andrew V., Ermolaeva, Svetlana A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6874821/
https://www.ncbi.nlm.nih.gov/pubmed/31757213
http://dx.doi.org/10.1186/s12898-019-0265-5
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author Pushkareva, Valentina I.
Podlipaeva, Julia I.
Goodkov, Andrew V.
Ermolaeva, Svetlana A.
author_facet Pushkareva, Valentina I.
Podlipaeva, Julia I.
Goodkov, Andrew V.
Ermolaeva, Svetlana A.
author_sort Pushkareva, Valentina I.
collection PubMed
description BACKGROUND: Some pathogenic bacteria have been developing as a part of terrestrial and aquatic microbial ecosystems. Bacteria are consumed by bacteriovorous protists which are readily consumed by larger organisms. Being natural predators, protozoa are also an instrument for selection of virulence traits in bacteria. Moreover, protozoa serve as a “Trojan horse” that deliver pathogens to the human body. Here, we suggested that carnivorous amoebas feeding on smaller bacteriovorous protists might serve as “Troy” themselves when pathogens are delivered to them with their preys. A dual role might be suggested for protozoa in the development of traits required for bacterial passage along the food chain. RESULTS: A model food chain was developed. Pathogenic bacteria L. monocytogenes or related saprophytic bacteria L. innocua constituted the base of the food chain, bacteriovorous ciliate Tetrahymena pyriformis was an intermediate consumer, and carnivorous amoeba Amoeba proteus was a consumer of the highest order. The population of A. proteus demonstrated variations in behaviour depending on whether saprophytic or virulent Listeria was used to feed the intermediate consumer, T. pyriformis. Feeding of A. proteus with T. pyriformis that grazed on saprophytic bacteria caused prevalence of pseudopodia-possessing hungry amoebas. Statistically significant prevalence of amoebas with spherical morphology typical for fed amoebas was observed when pathogenic L. monocytogenes were included in the food chain. Moreover, consumption of tetrahymenas fed with saprophytic L. innocua improved growth of A. proteus population while L. monocytogenes-filled tetrahymenas provided negative effect. Both pathogenic and saprophytic bacteria were delivered to A. proteus alive but only L. monocytogenes multiplied within amoebas. Observed differences in A. proteus population behaviour suggested that virulent L. monocytogenes might slow down restoration of A. proteus ability to hunt again and thus restrict the size of A. proteus population. Comparison of isogenic bacterial pairs that did or did not produce the haemolysin listeriolysin O (LLO) suggested a role for LLO in passing L. monocytogenes along the food chain. CONCLUSIONS: Our results support the idea of protozoa as a means of pathogen delivery to consumers of a higher order and demonstrated a dual role of protozoa as both a “Trojan horse” and “Troy.”
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spelling pubmed-68748212019-11-25 Experimental Listeria–Tetrahymena–Amoeba food chain functioning depends on bacterial virulence traits Pushkareva, Valentina I. Podlipaeva, Julia I. Goodkov, Andrew V. Ermolaeva, Svetlana A. BMC Ecol Research Article BACKGROUND: Some pathogenic bacteria have been developing as a part of terrestrial and aquatic microbial ecosystems. Bacteria are consumed by bacteriovorous protists which are readily consumed by larger organisms. Being natural predators, protozoa are also an instrument for selection of virulence traits in bacteria. Moreover, protozoa serve as a “Trojan horse” that deliver pathogens to the human body. Here, we suggested that carnivorous amoebas feeding on smaller bacteriovorous protists might serve as “Troy” themselves when pathogens are delivered to them with their preys. A dual role might be suggested for protozoa in the development of traits required for bacterial passage along the food chain. RESULTS: A model food chain was developed. Pathogenic bacteria L. monocytogenes or related saprophytic bacteria L. innocua constituted the base of the food chain, bacteriovorous ciliate Tetrahymena pyriformis was an intermediate consumer, and carnivorous amoeba Amoeba proteus was a consumer of the highest order. The population of A. proteus demonstrated variations in behaviour depending on whether saprophytic or virulent Listeria was used to feed the intermediate consumer, T. pyriformis. Feeding of A. proteus with T. pyriformis that grazed on saprophytic bacteria caused prevalence of pseudopodia-possessing hungry amoebas. Statistically significant prevalence of amoebas with spherical morphology typical for fed amoebas was observed when pathogenic L. monocytogenes were included in the food chain. Moreover, consumption of tetrahymenas fed with saprophytic L. innocua improved growth of A. proteus population while L. monocytogenes-filled tetrahymenas provided negative effect. Both pathogenic and saprophytic bacteria were delivered to A. proteus alive but only L. monocytogenes multiplied within amoebas. Observed differences in A. proteus population behaviour suggested that virulent L. monocytogenes might slow down restoration of A. proteus ability to hunt again and thus restrict the size of A. proteus population. Comparison of isogenic bacterial pairs that did or did not produce the haemolysin listeriolysin O (LLO) suggested a role for LLO in passing L. monocytogenes along the food chain. CONCLUSIONS: Our results support the idea of protozoa as a means of pathogen delivery to consumers of a higher order and demonstrated a dual role of protozoa as both a “Trojan horse” and “Troy.” BioMed Central 2019-11-22 /pmc/articles/PMC6874821/ /pubmed/31757213 http://dx.doi.org/10.1186/s12898-019-0265-5 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Pushkareva, Valentina I.
Podlipaeva, Julia I.
Goodkov, Andrew V.
Ermolaeva, Svetlana A.
Experimental Listeria–Tetrahymena–Amoeba food chain functioning depends on bacterial virulence traits
title Experimental Listeria–Tetrahymena–Amoeba food chain functioning depends on bacterial virulence traits
title_full Experimental Listeria–Tetrahymena–Amoeba food chain functioning depends on bacterial virulence traits
title_fullStr Experimental Listeria–Tetrahymena–Amoeba food chain functioning depends on bacterial virulence traits
title_full_unstemmed Experimental Listeria–Tetrahymena–Amoeba food chain functioning depends on bacterial virulence traits
title_short Experimental Listeria–Tetrahymena–Amoeba food chain functioning depends on bacterial virulence traits
title_sort experimental listeria–tetrahymena–amoeba food chain functioning depends on bacterial virulence traits
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6874821/
https://www.ncbi.nlm.nih.gov/pubmed/31757213
http://dx.doi.org/10.1186/s12898-019-0265-5
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