- Research article
- Open Access
Experimental Listeria–Tetrahymena–Amoeba food chain functioning depends on bacterial virulence traits
BMC Ecology volume 19, Article number: 47 (2019)
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.
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.
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.”
Terrestrial and aquatic ecosystems include multiple populations of prokaryotic and eukaryotic organisms that function as a whole, united by the complicated food web. Zooplankton including bacterivorous ciliates, flagellates, and amoebas control the bacterial populations in an ecosystem [1, 2]. By consuming bacteria, and then being consumed by predators of higher orders such as metazooplankton, nematodes etc., protozoa represent an important link between aquatic and terrestrial microbial food chains . Unicellular predators consume bacteria both directly and indirectly, supporting bacterial migration from lower to higher orders along the food chains [2, 4, 5].
In recent years, it has become clear that a number of bacteria have developed specific mechanisms of defence against unicellular predators [6,7,8]. These might be surface modifications or the production of toxic products [8, 9]. Pathogenic bacteria, which are members of terrestrial and aquatic ecosystems, often use virulence factors as a mechanism of defence against microbial predators [10,11,12,13]. Incomplete digestion in protozoan phagosomes is also particularly typical for pathogenic bacteria [13,14,15,16,17,18,19].
The Gram-positive pathogenic bacterium Listeria monocytogenes is widely spread in nature. It has been isolated from multiple natural habitats including soil, sewage, plant debris, plants, and animals such as sheep and cattle, wild deer, boars, small rodents, birds, and fish [20,21,22,23,24,25,26,27]. Soil seems to be an initial point from where L. monocytogenes contaminates plants to spread further to herbivorous animals, and soil is a final stop where bacteria come to with animal faeces . Multiple cases of L. monocytogenes isolation from fish and molluscs suggested that it is common in aquatic habitats. Interaction of L. monocytogenes with other members of terrestrial and aquatic ecosystems should be essential for its prolonged survival in the environment [27,28,29].
Listeria monocytogenes is a facultative intracellular pathogen. The thiol dependent haemolysin listeriolysin O (LLO) is a key virulence factor required for its intracellular survival . Bacteria lacking the LLO-encoding gene hly are avirulent in animal models . LLO is a multifunctional protein . Its pore-forming activity facilitates phagosomal membrane disruption and entrance of the pathogen into the cytosol, as well as active invasion of mammalian cells [33, 34]. When L. monocytogenes was co-cultivated with the common ciliate Tetrahymena pyriformis, LLO-producing bacteria were shown to be toxic for protozoa, caused protozoan encystment, and were more successful than isogenic LLO-lacking bacteria suggesting a leading role of LLO in bacterial survival in the presence of T. pyriformis . L. innocua is the closest saprophytic species to L. monocytogenes that lacks major virulence determinants including LLO .
Tetrahymena pyriformis and Amoeba proteus are two widely spread protozoa that live in fresh water over a wide range of conditions. In the wild, Tetrahymena feed on bacteria. In laboratory conditions, axenic T. piriformis culture is used as a standard model for studies of interactions between bacteria and unicellular predators . A. proteus is among the largest free-living phagotrophic protists with a cell size of up to 800 μm . This is a carnivorous amoeba that preferably grazes on smaller protists such as some ciliates, flagellates, unicellular algae, yeasts, etc. .
It was hypothesized that some small soil and freshwater amoebas may act as “Trojan horses” and deliver amoeba-resistant bacteria into the human body [15, 38,39,40]. However, large free-living amoebas, like representatives of the genus Amoeba, might serve as “Troy” themselves when they consume smaller species of protists filled with resistant bacteria. To get evidences on this dual role of protozoa we developed an experimental food chain that included either the pathogenic L. monocytogenes or the saprophytic L. innocua, the bacteriovorous ciliate T. pyriformis and the carnivorous amoeba A. proteus. We were interested in a role of pathogenic bacteria in microbial food chain, and particularly, in a difference in microbial food chain dynamics in dependence on whether saprophytic or virulent bacteria comprise the base of the food web.
Characterization of A. proteus grazing on virulent and saprophytic Listeria
Listeria monocytogenes and the saprophytic species L. innocua were used to feed A. proteus. The starving A. proteus population was stable under experimental conditions used and maintained its size constant in the absence of addition of bacteria. There was a gradual increase in the A. proteus population grazing on L. innocua within 24 h. In contrast, the population of A. proteus grazing on L. monocytogenes decreased. Rates of changes in A. proteus population measured as percentage change per hour were 1.316 ± 0.31% and − 0.798 ± 0.42% in the presence of L. innocua and L. monocytogenes, respectively (Fig. 1, p < 0.005).
Addition of both pathogenic and non-pathogenic bacteria caused changes in amoebal morphology (Fig. 2a–c). These changes, including dragging of pseudopodia and the assumption of a spherical, round-shaped form typical for fed amoebas, were correlated with the appearance of digestive phagosomes within amoebas and appeared to be associated with grazing. Amoebas with altered morphology (spherical) were observed as early as 1 h and up to 24 h (the end of the experiment) post bacterial addition. Another portion of the A. proteus population retained the morphology typical for hungry cells with characteristic pseudopodia. Enumeration of amoebas with spherical and pseudopodia-possessing (hungry) morphology revealed a statistically significant difference between populations that grazed on virulent and saprophytic bacteria (Fig. 2d, e). In the presence of L. monocytogenes, the mean value of morphologically spherical amoebas was 4 times higher than that of hungry amoebas (Fig. 3d, 50th percentile 4.5 vs 1.5 of spherical and hungry cells per viewing field, respectively, after 1 h of co-incubation with bacteria p < 0.05). The ratio of spherical to hungry amoebas changed slowly with time (4.50 vs 1.5 and 4.5 vs 0.6, at 3 and 24 h, respectively; p < 0.05). In the presence of L. innocua, the mean number of spherical amoebas was less (1.6–2.5 times) than that of amoebas with hungry morphology since the 1st up to 24 h of co-incubation (50th percentile 1.5 vs 3.5 and 2.0 vs 5.0 for amoebas with spherical and hungry morphology in 1 h and 24 h, respectively, p = 0.09; 0.29).
Establishing a Listeria–Tetrahymena–Amoeba food chain model
We compared pathogenic and saprophytic bacteria in the model food chain Listeria–T. pyriformis–A. proteus. T. pyriformis grazed on pathogenic L. monocytogenes or saprophytic L. innocua were used to feed starved A. proteus, and uninfected tetrahymenas were used as a control.
The total number of amoebas slowly changed over the course of the 24 h experiment. Dynamics of amoebas population fed with L. monocytogenes-filled tetrahymenas was negative. In contrast, consumption of tetrahymenas fed with saprophytic L. innocua improved growth of A. proteus population as well as consumption of intact ciliates. Percentage change per hour was − 0.418 ± 0.19%, 0.62 ± 0.26% and 0.78 ± 0.18% in the presence of L. innocua-fed, L. monocytogenes-fed and control intact T. pyriformis, respectively (Fig. 3a, p < 0.005).
Enumeration of intracellular bacteria passed to A. proteus by T. pyriformis revealed that both pathogenic and saprophytic bacteria might be delivered alive to amoebas (zero time point in Fig. 3b). Meanwhile, other behaviours of pathogenic and saprophytic bacteria were different. A noticeable drop in the number of L. innocua was observed within first the 2 h, which was followed by a slight decline. In contrast, the number of intracellular L. monocytogenes remained stable over the first 2 h. The decrease in the number of L. monocytogenes observed between the 2nd and 6th h changed to resurgence by 24 h (Fig. 3b, Additional file 1: Table S1).
Statistically significant prevalence of amoebas with spherical morphology over pseudopodia-possessing hungry amoebas was observed when pathogenic L. monocytogenes were included in the food chain (Fig. 3e, 50th percentile 4.5, 5.5, 4.5 vs 1.25, 0.7, 0.6 for spherical and hungry amoebas at 1, 3, and 24 h, respectively; p < 0.05). Feeding of A. proteus with T. pyriformis that grazed on saprophytic bacteria caused a slow growth of the amoebal population and prevalence of hungry amoebas with unchanged morphology (Fig. 3f, 1.0, 1.0, 0.45 vs 3.55, 3.6, 3.2, for spherical and hungry amoebas at 1, 3, and 24 h, respectively; p < 0.05).
LLO is involved in interactions of L. monocytogenes with A. proteus
To address the role of LLO in interactions of L. monocytogenes and A. proteus and to evaluate its role in the passage of L. monocytogenes along the food chain, we compared two isogenic pairs, each including LLO expressing and non-expressing strains. The first pair was the wild-type L. monocytogenes strain EGDe and its deviation with the deletion of the LLO-encoding gene hly (EGDeΔhly). The second pair included the L. innocua NCTC11288 and its derivative that carried a plasmid pHly/PrfA*. The plasmid pHly/PrfA* carried the LLO-encoding hly gene and the prfA* gene, which encodes a constantly active transcriptional regulator PrfA* to provide a constant high-level expression of LLO.
Listeriolysin O expression by Listerias caused a decrease in the A. proteus population with negative percentage rates independently of whether bacteria were engulfed by amoebas themselves or delivered with T. pyriformis (Fig. 4). However, when LLO non-expressing bacteria were compared, a difference between L. monocytogenes EGDeΔhly and L. innocua was observed that was dependent on whether bacteria were delivered directly or via T. pyriformis. Even lacking LLO, L. monocytogenes EGDeΔhly bacteria stimulated some decrease in A. proteus population. However, no toxic effects were observed when T. pyriformis was used as an intermediate link between L. monocytogenes EGDeΔhly and A. proteus.
Electron microscopic studies of interactions in the Listeria–Tetrahymena–Amoeba chain
To further address interactions between microorganisms along the food chain, transmission electron microscopy (TEM) was used. Vacuoles that contained the ciliate were observed within A. proteus at 3 h post addition of native T. pyriformis (Fig. 5a). At the same time point, in accordance with the data of bacterial plating (see Fig. 3a), live bacteria were observed within T. pyriformis vacuoles in the L. monocytogenes–T. pyriformis–A. proteus food chain, i.e. when A. proteus grazed on T. pyriformis which in turn had been fed with L. monocytogenes (Fig. 5b, c). Disruption of T. pyriformis internal structures might allow for bacteria to occupy the total volume of the phagosome. Further samples revealed vacuoles filled with bacteria and remnants of T. pyriformis that supported this idea (Fig. 5d). Bacteria seemed to be still viable and some of them appeared to be dividing. Investigation of A. proteus in the L. innocua–T. pyriformis–A. proteus food chain was performed at the same 3 h time interval post addition of T. pyriformis to A. proteus. It demonstrated phagosomes that contained T. pyriformis. Vacuoles filled with live or partly digested bacteria were observed within ciliates (Fig. 5e).
Listeriolysin O is known to be a key factor that contributes to phagosomal disruption in mammalian cells . The multiple bacteria concentrated in phagosomes of A. proteus seemed to be associated with perforation of the phagosomal membrane of the protozoa. Bacteria concentrated near the membrane, which lost its integrity (Fig. 6). Perforations were observed when phagosomes contained wild type L. monocytogenes (Fig. 6a) and LLO-producing L. innocua/pHly/PrfA* (Fig. 6b).
Here, we report the development of an experimental model of the microbial food chain that included virulent or saprophytic Listeria spp, the ciliate T. pyriformis, and the giant amoeba A. proteus. We demonstrated that: (i) the dynamics and physiology of the A. proteus population was dependent on whether virulent or saprophytic bacteria were used to feed T. pyriformis; (ii) live virulent L. monocytogenes might be delivered to A. proteus by T. pyriformis; and (iii) that passage along the food chain was dependent on L. monocytogenes virulence factor LLO.
Since the pioneering work of Ly and Mueller , Tetrahymena spp. and Acanthamoeba spp. have been used as models for the study of L. monocytogenes interactions with bacteriovorous protozoa [13, 16, 41,42,43,44,45,46].
In the present work, in contrast to the small obligatory bacterivorous protists, we used a giant amoeba A. proteus. A. proteus is a carnivorous protozoan organism though it is capable of digesting bacteria as well [47, 48]. A. proteus grazing on both L. monocytogenes and its saprophytic counterpart L. innocua changed its morphology to a spherical one that is characteristic of prey digesting amoebas. A statistically significant difference was observed in the relative number of amoebas with spherical and pseudopodia-possessing hungry morphology between amoebas that grazed on virulent or saprophytic bacteria. Spherical cells prevailed when amoebas were fed virulent bacteria. Cells with morphology characteristic of hungry amoebas were more numerous when amoebas hunted on saprophytic bacteria. This difference suggested that virulent L. monocytogenes slowed down restoration of A. proteus morphology from spherical to that possessing pseudopodia with the ability to hunt again. The inability to hunt could be a reason to restrict the size of A. proteus population. This suggestion might explain the previously described discrepancy between absence of a short-term cytotoxicity and a global negative effect of L. monocytogenes on the protozoan population in conditions of prolonged co-incubation of bacteria and protozoa [13, 16, 41,42,43,44, 46, 49].
The food web in terrestrial and aquatic ecosystems includes multiple levels of unicellular consumers. To understand circulation of human pathogens in natural habitats, it is important to study not only mechanisms of bacterial survival within protozoa but also the manner by which pathogenic bacteria are inserted into the microbial food web. From the point of view of matter and energy flow, T. pyriformis filled with virulent or saprophytic bacteria represented an equal portion of a meal for A. proteus. However, the changes in the A. proteus population were dependent on which bacteria was used to feed T. pyriformis. Our data are in line with general considerations demonstrating that introduction of parasites noticeably disturbs major parameters of food web functioning .
Protozoa are a natural reservoir of pathogenic facultative intracellular bacteria and protect these bacteria from unfavourable environmental factors. They are also an instrument for the selection of virulence traits and the Trojan horses that deliver pathogens to the human body . Our results support the idea of protozoa as a means of delivery of bacteria resistant to digestion to consumers of a higher order and demonstrated a dual role for protozoa as both a “Trojan horse” and “Troy.” The last observations supposed the role of protozoa in the development of traits required for bacterial passage along the food chain.
The developed model of the microbial food chain was used to study a role of the thiol-dependent haemolysin LLO, which is a L. monocytogenes key virulence factor. The LLO was chosen because it was shown to contribute to bacterial survival in the presence of T. pyriformis and Acanthamoeba castellanii [13, 43]. Obtained results suggested that LLO was important for the passage of L. monocytogenes along the microbial food chain to higher order consumers. This suggestion was supported by changes in the A. proteus population in dependence of whether LLO-producing or non-producing bacteria were used to feed T. pyriformis.
Taken together, our results suggested that pathogenic bacteria, when introduced into the food chain, behave differently from saprophytic bacteria and may possibly disturb the flow of nutrients and energy to consumers at higher orders. The demonstrated dual role of protozoa as “Trojan horse” as well as “Troy” underscores their importance in the evolution of bacterial pathogenic traits in microbial ecosystems.
Microbial strains and growth conditions
Bacterial strains included the wild type L. monocytogenes strain EGDe (serovar 1/2a, , its derivative EGDeΔhly lacking the LLO-encoding gene hly (the strain was kindly provided by Prof. Vazquez-Boland, Univ. Edinburgh), the wild type L. innocua strain NCTC 11288 (serovar 6a), and the derivative of the last strain L. innocua NCTC 11288::pHly/PrfA . The strain L. innocua NCTC 11288::pHly/PrfA* carried a high copy number plasmid pHly/PrfA* which expressed LLO under the positive control of the constitutively active transcriptional regulator PrfA* . Bacteria were kept frozen at − 80 °C. About a week before the experiment started, bacteria were plated onto Brain Heart Infusion (BHI, BD, Sparks, MD, USA) agar and grown at 28 °C. For plasmid-carrying strains, the medium was supplemented with erythromycin (10 μg ml−1). An isolated colony was used to inoculate BHI broth. The culture was grown at 28 °C with shaking for 18–20 h. The overnight culture was diluted (1:100) in fresh BHI broth and grown to an OD600 of 1.0. Then, the bacteria were harvested, washed with phosphate-buffered saline (PBS_, resuspended in PBS supplemented with 10% glycerol (1:100 of the initial culture volume), aliquoted, and frozen at − 80 °C. The bacterial concentration was determined by thawing an individual vial and plating serial dilutions on BHI agar. Immediately before the experiment, bacteria were thawed and serial dilutions prepared in PBS were added to the protist culture in the pointed concentration.
Axenic T. pyriformis from the Collection of the Gamaleya Institute was maintained on diluted BHI broth (dBHI, BD, 3 g of powder per 1 l of distilled water) supplemented with gentamycin 100 μg ml−1, Diflucan 100 μg ml−1, and Cyfran 100 μg ml−1 at 28 °C. The culture was propagated by a dilution of 1:10 into fresh medium weekly. Ten days before the experiment started, antibiotics were removed from the dBHI medium and the culture of T. pyriformis was amplified by a dilution 1:5 every 4 days. The culture was used in the experiment 3 days after the last seeding.
Strains “B” and “CCAP LB1503/4” of A. proteus, from the Collection of the Institute of Cytology RAS , were used in experiments. Amoebae were cultured on Prescott mineral medium  at room temperature according to a standard procedure, and fed with T. pyriformis GL ciliates every 48 h .
To evaluate an effect of pathogenic and saprophytic bacteria on A. proteus, amoebas were starved for 3 days, then the bacterial culture, prepared as described above, was added to A. proteus at a multiplicity of 1000:1 (bacteria:amoeba). The co-culture was maintained in the wet chamber at room temperature for 24 h.
Microbial food chain modelling
Three-day old T. pyriformis culture was diluted up to 105 cells ml−1 with fresh dBHI medium. Bacterial culture prepared as described above was introduced into protozoan culture at a multiplicity of 1000:1 (bacteria:protozoa). The co-culture was maintained at 28 °C without agitation for 1 h. Then, protozoa were pelleted by centrifuging at 700 rpm for 10 min, washed with sterile PBS, and resuspended in fresh dBHI medium containing 100 μg ml−1 gentamycin to remove extracellular bacteria. One hour later, tetrahymenas were washed with PBS, resuspended in Prescott mineral medium, and added to A. proteus at a concentration of 100:1 (tetrahymena:amoeba). The co-culture of Tetrahymena and Amoeba was maintained in a wet chamber at room temperature. Non-swallowed tetrahymenas were removed at 1 h.
To count T. pyriformis, ciliates were fixed with L buffer (30% acetic acid—70% ethanol) added at a ratio of 1:1. Then, ciliates were counted by microscopy. Amoebas were quantified without fixing using the AxioCam ERc5s (Carl Zeiss) microscope at 100× magnification. Twenty fields of vision were included in analysis from one experiment. Typical fields of vision for different experiments are shown at Figures. The word “hungry” designates pseudopodia-possessing cells with morphology typical for starved amoebas. The word “spherical” designates round-shaped cells that is characteristic of prey digesting amoebas. Rates of changes in amoebal population were calculated as a regression coefficient in the linear regression equation describing changes in amoebal population in each experiment. Then an arithmetic mean and standard error from all experiments were calculated.
Washed protozoa were lysed with 1% Triton X-100. Decimal serial dilutions were plated onto BHI agar in duplicates and incubated at 37 °C. Bacterial colonies were counted at 24 h.
Transmission electron microscopy
Transmission electron microscopic (TEM) investigations were performed in general as described in . In short, microorganisms were concentrated, fixed with phosphate-buffered osmium tetroxide, dehydrated in alcohols of increasing concentrations, and embedded in araldite M. Ultrathin sections were produced on an LKB-3 ultratome, and studied in a GEM 100B electron microscope. Up to six sections for one sample were studied.
All experiments were performed using duplicate samples and repeated 3 to 6 times. The data are presented as the mean ± standard deviation (SD) from independent experiments. The data on morphological changes are presented as boxplots from three independent experiments with 20 fields of view each. A two-tailed t-test was used for assessment of statistical significance.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
transmission electron microscopy
brain hear infusion
phosphate buffered saline
Jurgens K, Matz C. Predation as a shaping force for the phenotypic and genotypic composition of planktonic bacteria. Antonie van Leeuwenhoek Int J Gen Mol Microbiol. 2002;81:413–34.
Sherr EB, Sherr BF. Significance of predation by protists in aquatic microbial food webs. Antonie van Leeuwenhoek Int J Gen Mol Microbiol. 2002;81:293–308.
Coleman DC. The microbial loop concept as used in terrestrial soil ecology studies. Microb Ecol. 1994;28:245–50.
Frederiksen M, Edwards M, Richardson AJ, Halliday NC, Wanless S. From plankton to top predators: bottom-up control of a marine food web across four trophic levels. J Anim Ecol. 2006;75:1259–68.
Montagnes DJS, Dower JF, Figueiredo GM. The protozooplankton-ichthyoplankton trophic link: an overlooked aspect of aquatic food webs. J Eukaryot Microbiol. 2010;57:223–8.
Pernthaler J. Predation on prokaryotes in the water column and its ecological implications. Nat Rev Microbiol. 2005;3:537–46.
Matz C, Kjelleberg S. Off the hook—how bacteria survive protozoan grazing. Trends Microbiol. 2005;13:302–7.
Jousset A, Rochat L, Scheu S, Bonkowski M, Keel C. Predator-prey chemical warfare determines the expression of biocontrol genes by rhizosphere-associated pseudomonas fluorescens. Appl Environ Microbiol. 2010;76:5263–8.
Wildschutte H, Wolfe DM, Tamewitz A, Lawrence JG. Protozoan predation, diversifying selection, and the evolution of antigenic diversity in Salmonella. Proc Natl Acad Sci USA. 2004;101:10644–9.
Abd H, Wretlind B, Saeed A, Idsund E, Hultenby K, Sandström G. Pseudomonas aeruginosa utilises its type III secretion system to kill the free-living amoeba Acanthamoeba castellanii. J Eukaryot Microbiol. 2008;55:235–43.
Matz C, Moreno AM, Alhede M, Manefield M, Hauser AR, Givskov M, et al. Pseudomonas aeruginosa uses type III secretion system to kill biofilm-associated amoebae. ISME J. 2008;2:843–52.
Miyata ST, Kitaoka M, Brooks TM, McAuley SB, Pukatzki S. Vibrio cholerae requires the type VI secretion system virulence factor vasx to kill Dictyostelium discoideum. Infect Immun. 2011;79:2941–9.
Pushkareva VI, Ermolaeva SA. Listeria monocytogenes virulence factor listeriolysin O favors bacterial growth in co-culture with the ciliate Tetrahymena pyriformis, causes protozoan encystment and promotes bacterial survival inside cysts. BMC Microbiol. 2010;10:26.
Pushkareva VI. Experimental evaluation of interaction between Yersinia pestis and soil infusoria and possibility of prolonged preservation of bacteria in the protozoan oocysts. Zh Mikrobiol Epidemiol Immunobiol. 2003;(4):40–4.
Greub G, Raoult D. Microorganisms resistant to free-living amoebae. Clin Microbiol Rev. 2004;17:413–33.
Akya A, Pointon A, Thomas C. Viability of Listeria monocytogenes in co-culture with Acanthamoeba spp. FEMS Microbiol Ecol. 2009;70:20–9.
Akya A, Pointon A, Thomas C. Listeria monocytogenes does not survive ingestion by Acanthamoeba polyphaga. Microbiology. 2010;156:809–18.
Lambrecht E, Baré J, Van Damme I, Bert W, Sabbe K, Houf K. Behavior of Yersinia enterocolitica in the presence of the Bacterivorous Acanthamoeba castellanii. Appl Environ Microbiol. 2013;79:6407–13.
Gryseels S, Amissah D, Durnez L, Vandelannoote K, Leirs H, de Jonckheere J, et al. Amoebae as potential environmental hosts for Mycobacterium ulcerans and other mycobacteria, but Doubtful Actors in Buruli Ulcer Epidemiology. PLoS Negl Trop Dis. 2012;6:e1764.
Weis J, Seeliger HP. Incidence of Listeria monocytogenes in nature. Appl Microbiol. 1975;30:29–32.
Nightingale KK, Schukken YH, Nightingale CR, Fortes ED, Ho AJ, Her Z, et al. Ecology and transmission of Listeria monocytogenes infecting ruminants and in the farm environment. Appl Environ Microbiol. 2004;70:4458–67.
Zaytseva E, Ermolaeva S, Somov GP. Low genetic diversity and epidemiological significance of Listeria monocytogenes isolated from wild animals in the far east of Russia. Infect Genet Evol. 2007;7:736–42.
Wacheck S, Fredriksson-Ahomaa M, König M, Stolle A, Stephan R. Wild boars as an important reservoir for foodborne pathogens. Foodborne Pathog Dis. 2010;7:307–12.
Locatelli A, Spor A, Jolivet C, Piveteau P, Hartmann A. Biotic and abiotic soil properties influence survival of Listeria monocytogenes in soil. PLoS ONE. 2013;8:e75969.
Sasaki Y, Goshima T, Mori T, Murakami M, Haruna M, Ito K, et al. Prevalence and antimicrobial susceptibility of foodborne bacteria in wild boars (Sus scrofa) and wild deer (Cervus nippon) in Japan. Foodborne Pathog Dis. 2013;10:985–91.
Linke K, Rückerl I, Brugger K, Karpiskova R, Walland J, Muri-Klinger S, et al. Reservoirs of Listeria species in three environmental ecosystems. Appl Environ Microbiol. 2014;80:5583–92.
Voronina OL, Ryzhova NN, Kunda MS, Kurnaeva MA, Semenov AN, Aksenova EI, et al. Diversity and pathogenic potential of Listeria monocytogenes isolated from environmental sources in the Russian Federation. Int J Mod Eng Res. 2015;5:5–13.
Jeyasekaran G, Karunasagar I, Karunasagar I. Incidence of Listeria spp. in tropical fish. Int J Food Microbiol. 1996;31:333–40.
Rodas-Suárez OR, Flores-Pedroche JF, Betancourt-Rule JM, Quiñones-Ramírez EI, Vázquez-Salinas C. Occurrence and antibiotic sensitivity of Listeria monocytogenes strains isolated from oysters, fish, and estuarine water. Appl Environ Microbiol. 2006;72:7410–2.
Bielecki J, Youngman P, Connelly P, Portnoy DA. Bacillus subtilis expressing a haemolysin gene from Listeria monocytogenes can grow in mammalian cells. Nature. 1990;345:175–6.
Cossart P, Vicente MF, Mengaud J, Baquero F, Perez-Diaz JC, Berche P. Listeriolysin O is essential for virulence of Listeria monocytogenes: direct evidence obtained by gene complementation. Infect Immun. 1989;57:3629–36.
Seveau S. Multifaceted activity of listeriolysin O, the cholesterol-dependent cytolysin of Listeria monocytogenes. Subcell Biochem. 2014;80:161–95.
Vadia S, Arnett E, Haghighat AC, Wilson-Kubalek EM, Tweten RK, Seveau S. The pore-forming toxin listeriolysin o mediates a novel entry pathway of L. monocytogenes into human hepatocytes. PLoS Pathog. 2011;7:e1002356.
Kanayama Y, Kaneko M, Emoto Y, Emoto M. Listeriolysin O, but not Murine E-cadherin, is involved in invasion of Listeria monocytogenes into Murine Liver Parenchymal Cells. Open Microbiol J. 2015;9:81–3.
Glaser P, Frangeul L, Buchrieser C, Rusniok C, Amend A, Baquero F, et al. Comparative genomics of Listeria species. Science. 2001;294:849–52.
Ruehle MD, Orias E, Pearson CG. Tetrahymena as a unicellular model eukaryote: genetic and genomic tools. Genetics. 2016;203:649–65.
Yudin AL. Amoeba and other protozoa. In: Dettlaff TA, Vassetzky SG, editors. Animal species for developmental studies. Vol. 1. Invertebrates. New York: Consultants Bureau; 1990. p. 1–11.
Pogorelov VI, Pinigin AF, Maramovich AS, Pushkareva VI, Litvin VI, Lykova MV, et al. The interrelationships between Vibrio cholerae and the infusorian Tetrahymena pyriformis. Zh Mikrobiol Epidemiol Immunobiol. 1995;(2):22–6.
Amann R, Springer N, Schönhuber W, Ludwig W, Schmid EN, Müller KD, et al. Obligate intracellular bacterial parasites of acanthamoebae related to Chlamydia spp. Appl Environ Microbiol. 1997;63:115–21.
Harb OOS, Gao LL, Abu Kwaik Y, Abu Y. From protozoa to mammalian cells: a new paradigm in the life cycle of intracellular bacterial pathogens. Environ Microbiol. 2000;2:251–65.
Ly TMC, Muller HE. Ingested Listeria monocytogenes survive and multiply in protozoa. J Med Microbiol. 1990;33:51–4.
Brandl MT, Rosenthal BM, Haxo AF, Berk SG. Enhanced survival of Salmonella enterica in vesicles released by a soilborne Tetrahymena species. Appl Environ Microbiol. 2005;71:1562–9.
Zhou X, Elmose J, Call DR. Interactions between the environmental pathogen Listeria monocytogenes and a free-living protozoan (Acanthamoeba castellanii). Environ Microbiol. 2007;9:913–22.
Gourabathini P, Brandi MT, Redding KS, Gunderson JH, Berk SG. Interactions between food-borne pathogens and protozoa isolated from lettuce and spinach. Appl Environ Microbiol. 2008;74:2518–25.
Huws SA, Morley RJ, Jones MV, Brown MRW, Smith AW. Interactions of some common pathogenic bacteria with Acanthamoeba polyphaga. FEMS Microbiol Lett. 2008;282:258–65.
Doyscher D, Fieseler L, Dons L, Loessner MJ, Schuppler M. Acanthamoeba feature a unique backpacking strategy to trap and feed on Listeria monocytogenes and other motile bacteria. Environ Microbiol. 2013;15:433–46.
Salt GW. Feeding activity by Amoeba proteus. Exp Cell Res. 1961;24:618–20.
Jeon KW. The large, free-living Amoebae: wonderful cells for biological studies. J Eukaryot Microbiol. 1995;42:1–7.
Akya A, Pointon A, Thomas C. Mechanism involved in phagocytosis and killing of Listeria monocytogenes by Acanthamoeba polyphaga. Parasitol Res. 2009;105:1375–83.
Sukhdeo MV. Where are the parasites in food webs? Parasit Vectors. 2012;5:239.
Berdieva M, Bogolyubov D, Podlipaeva Y, Goodkov A. Nucleus-associated actin in Amoeba proteus. Eur J Protistol. 2016;56:191–9.
Prescott DM, Carrier RF. Chapter 5 Experimental procedures and cultural methods for Euplotes eurystomus and Amoeba proteus. In: Methods in cell biology. vol. 1. 1964. p. 85–95.
Authors thank Mr. P. Belyaev for the help with statistical data analysis.
Funding was provided by Ministry of Health of Russian Federation.
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Pushkareva, V.I., Podlipaeva, J.I., Goodkov, A.V. et al. Experimental Listeria–Tetrahymena–Amoeba food chain functioning depends on bacterial virulence traits. BMC Ecol 19, 47 (2019) doi:10.1186/s12898-019-0265-5
- Pathogenic bacteria
- Free-living protozoa
- Host–parasite interactions
- Food web