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Effects of a Ciliate Protozoa Predator on Microbial Communities in Pitcher Plant (Sarracenia purpurea) Leaves

  • Taylor K. Paisie,

    Affiliation Department of Earth, Ocean and Atmospheric Science, Florida State University, Tallahassee, Florida, United States of America

  • Thomas E. Miller,

    Affiliation Department of Biological Science, Florida State University, Tallahassee, Florida, United States of America

  • Olivia U. Mason

    Affiliation Department of Earth, Ocean and Atmospheric Science, Florida State University, Tallahassee, Florida, United States of America

Effects of a Ciliate Protozoa Predator on Microbial Communities in Pitcher Plant (Sarracenia purpurea) Leaves

  • Taylor K. Paisie, 
  • Thomas E. Miller, 
  • Olivia U. Mason


The aquatic communities found within the water filled leaves of the pitcher plant, Sarracenia purpurea, have a simple trophic structure providing an ideal system to study microscale interactions between protozoan predators and their bacterial prey. In this study, replicate communities were maintained with and without the presence of the bactivorous protozoan, Colpoda steinii, to determine the effects of grazing on microbial communities. Changes in microbial (Archaea and Bacteria) community structure were assessed using iTag sequencing of 16S rRNA genes. The microbial communities were similar with and without the protozoan predator, with>1000 species. Of these species, Archaea were negligible, with Bacteria comprising 99.99% of the microbial community. The Proteobacteria and Bacteroidetes were the most dominant phyla. The addition of a protozoan predator did not have a significant effect on microbial evenness nor richness. However, the presence of the protozoan did cause a significant shift in the relative abundances of a number of bacterial species. This suggested that bactivorous protozoan may target specific bacterial species and/or that certain bacterial species have innate mechanisms by which they evade predators. These findings help to elucidate the effect that trophic structure perturbations have on predator prey interactions in microbial systems.


The effect of predators on the prey community is a well-studied area of ecology (e.g., [1]). Predators generally reduce the abundance of prey, which can, in turn, affect the abundance of predators and result in oscillations between predator and prey. Predators can cause prey extinction or prevent prey from colonizing new habitats. Predators can also control biodiversity through either selective feeding by the predators, differential responses of the prey, or indirect interactions through prey species (e.g., keystone predation and trophic cascades).

However, little is known about the effects of predators on microbial communities [2],[3]. Predation by bactivores is difficult to observe in situ; therefore, it is not often studied. Further, the rich diversity of microorganisms creates methodological challenges, rendering it difficult to predict overall effects of predation on microbial community structure. It is unknown if standard ecological predictions of predator-prey dynamics and effects of predators on prey community composition will apply in highly speciose microbial communities [4].

There is significant potential for predators to affect microbial community structure. Prior studies have shown that predation by protists can be a dominant factor controlling total bacterial abundances [5],[6]. Bacteria consumed by predators such as protozoans and rotifers are primarily captured through filter feeding and grazing on particles [7]. This predation can be size-selective [5], with possible escape from predation by both smaller [8] and larger size classes of Bacteria. Other bacterial traits, such as motility and shape, may also generate differences in predation of Bacteria by protozoa [5],[8],[9].

Simek et al. [10] used size fractionation and denaturing gradient gel electrophoresis (DGGE) to demonstrate that the protozoa community did affect the bacterial community composition. Using similar methods, Weinbauer et al. [11] also found that protozoa can significantly reduce species diversity (number of DGGE bands). Predators can also affect the relative abundances of Bacteria and, thus, bacterial community composition through selective feeding [6],[12]. For example, prior studies have shown that filamentous Bacteria can evade predation, allowing them to dominate bacterial communities when predators are present [13]. The advent of high-throughput sequencing technologies, such as iTag sequencing of 16S rRNA genes, provides important new tools for more highly resolved characterization of microbial community structure in the context of predator-prey interaction.

To examine microscale predator-prey interactions, we used the microcosms [14] found in water-filled leaves of the carnivorous pitcher plant, Sarracenia purpurea. These inquiline communities have a simple trophic structure [15], making them ideal for evaluating the influence protozoa predation has on a natural microbial community. During the growing season, S. purpurea makes new leaves ∼ every 4 weeks; prior to opening, the leaves are sterile [16]. The leaves fill with rainwater and produce nectar on the lip, attracting insects, primarily ants, that fall in the water and drown [17]. The water in the leaf is rapidly colonized by a number of other specialist species [18], including a high diversity of Bacteria [19],[20]. Prey that are trapped in the leaves of the pitcher plant are broken down by detritivores, which are consumed by bactivorous protozoans and rotifers (see review in [17]). These bacterivores are consumed by the mosquito larva, Wyeomyia smithii [20]. Interactions between the invertebrate and microbial community were previously documented, including “cascading” effects of mosquito larvae on bacterial diversity [16].

The microbial communities in the pitcher plant, S. purpurea, have been described in several previous studies. In S. purpurea pitcher fluids, Krieger and Kourtev [20] analyzed 16S rRNA genes using DGGE and sequencing, while Gray et al. [19] used cloning and sequencing; both reported that Alphaproteobacteria, Betaproteobacteria and Bacteroidetes were dominant. Peterson et al. [16] used terminal restriction fragment length polymorphism (TRFLP) to analyze the microbial diversity in S. purpurea's pitcher fluids and suggested that the microbial community is influenced by, among other factors, the presence or absence of bacterial predators.

Here we used iTag sequencing of archaeal and bacterial16S rRNA genes from the fluid of pitcher plants maintained with and without the protozoan, Colpoda steinii. A total of 1.3 million 16S rRNA gene sequences were generated and analyzed. This method provides a highly resolved platform to examine microscale effects of predators on prey community structure. Further, the high-sequence coverage allows for analysis of a large number of sample replicates. In this paper, we provide a preliminary description of the Archaea and Bacteria found in pitcher plants. Further, we describe the effect of a single protozoan predator on patterns of relative abundance of species within the microbial community.

Materials and Methods

Sample Collection and Processing

The microbial samples of pitcher plant fluids were obtained from the Apalachicola National Forest, which is maintained by the National Forest Service, US Department of the Interior. No permissions were required to remove microbial water samples from the pitcher plant leaves and none of the microbial species used in this study are listed as endangered or threatened. Approximately 50 plants were chosen haphazardly from across Crystal Bog (30°11′N, 84°54′W). Fluid (10–15 ml) was extracted asceptically from a randomly chosen single leaf per plant, avoiding leaves that had red or pink tainted fluid, indicating anoxia, and brown and dying leaves to prevent anomalies associated with older leaves [18]. The fluid was immediately cooled and transported to the lab, where it was combined into one flask and sequentially filtered through 200, 50, and 4 µM filters using aseptic techniques. After filtration, the broth was inspected for protozoa or anything other than Bacteria and Archaea by censusing three samples of 0.01 ml using a phase-contrast microscope at 100×.

The study was conducted in greenhouses at Florida State University using plants obtained from the Apalachicola National Forest under Forest Products Free Use Permit No. 5713 to T. E. Miller. Newly opened leaves capable of holding 15–20 ml of fluid were identified on separate plants. Aliquots of the filtered microbial broth (10 mL) were then placed in 20 of these newly opened leaves, along with two dead ants (Solonopsis invicta), a common prey found in pitcher plants in the wild [18]. The leaves of half the plants were inoculated with 0.05 ml (approximately 50 cells) of Colpoda steinii, a medium-sized (∼50 µM) ciliate that we have used in a variety of other experiments [21],[22]. Those samples with C. steinii are referred to as +CS and those without as –CS. The C. steinii stock was originally derived from pitcher plants in the same area of the Apalachicola National Forest. The leaves were left uncovered and maintained at temperatures similar to those found in the field. Each leaf was resampled 5 days later by removing all water; the samples were immediately processed as described below. Two leaves had holes and did not contain sufficient fluid, while one sample was contaminated during processing, leaving 9 samples maintained with no protozoa and 8 with C. steinii.

DNA Extraction and purification

The microbial communities in the pitcher plant fluids were concentrated by centrifugation. DNA was extracted from the pellet by suspension in a modified CTAB extraction buffer ((10% CTAB (hexadecyltrimethylammonium bromide), 1M NaCl and 0.5M phosphate buffer, pH 8) with 0.1M ammonium aluminum sulfate, 25∶24∶1 phenol∶chloroform∶isoamyl alcohol) and subjecting it to bead beating using a FastPrep-24 (MP Biomedicals, Solon, OH) at 5.5 meters per second for 45 seconds. DNA was purified using the QIAGEN AllPrep DNA/RNA Kit (QIAGEN, Germantown, MD) following the manufacturer's protocol.

16S rRNA Gene Sequencing and Analysis

16S rRNA genes were amplified from the purified DNA extracts in duplicate using archaeal and bacterial primers 515F and 806R, which targets the V4 region of E. coli in accordance with the protocol described by Caporaso et al. [23],[24] and used by the Earth Microbiome Project (, with a slight modification: specifically, the annealing temperature was modified to 60°C. Multiplexed sample amplicons were sequenced with Ilumina's MiSeq in accordance with Caporaso et al. [24] Sequences were analyzed using the QIIME version 1.7.0 [25] pipeline. Raw sequences were demultiplexed and then quality filtered using the default parameters in QIIME. Sequences are in NCBI's sequence read archive under accession number SRP048740. Sequences were then clustered into operational taxonomic units (OTUs), which was defined as ≥97% 16S rRNA gene sequence similarity, using UCLUST [26] with the open reference clustering protocol ( The resulting representative sequences set were aligned using PyNAST [27] and given a taxonomic classification using RDP [28], retrained with the Greengenes version 13.5 [29]. The resulting OTU table was filtered to keep only OTUs that had at least 10 sequences, and then converted to relative abundance. The differences in relativized OTU abundances in communities with and without the C. steinii predator were analyzed using nonparametric statistics (Mann-Whitney) to test for statistically significant differences using METAGENassist [30] and the application of a False Discovery Rate (FDR) to account for multiple comparisons. A heatmap of statistically significantly different species with and without the protozoan was generated in R with the Vegan package. Alpha diversity metrics were determined using QIIME. Specifically, Chao1, Shannon index, observed species, dominance (defined as the sum of the squares of the frequencies of each species) were determined. Statistical differences in these metrics were assessed by Student's t-test. The QIIME generated, rarefied, OTU abundances in the 17 different samples were then analyzed using non-metric multidimensional (NMDS) scaling in R using metaMDS in Vegan package, with three axes specified. P-values were derived from 999 permutations of the data.

Results and Discussion

Protozoa growth in S. purpurea leaves in the greenhouse

C. steinii populations were established in all the leaves where it was introduced; mean densities after 5 days were 454.4 cells/mL (standard deviation = 288.6). No C. steinii were found in any of the control pitchers. Although not observed in the microbial broth prior to inoculation, a protozoan contaminant, the small flagellate Bodo menges, was found in all of the pitchers at a density of 377.2 cells/mL (standard deviation = 229.1) at the end of our five-day study. This species is common in pitcher plants [18] and the contamination probably occurred through insufficient filtering of the field-collected samples. Bodo menges is known to be a competitive subordinate to C. steinii [22], however we found no significant difference in B. menges abundance between leaves with and without C. steinii (t = 0.47, P = 0.64).

Community structure in S. purpurea inquiline Bacteria

Analyses of the 16S rRNA gene iTag data revealed that the microbial community in S. purpurea leaves, regardless of the presence or absence of a predator, was dominated by the Proteobacteria phylum, and in particular, by the sub-phyla Betaproteobacteria, Alphaproteobacteria and Gammaproteobacteria (Fig. 1). Of these three sub-phyla, Betaproteobacteria were the most prevalent (Fig. 1). Proteobacteria have been reported as the most abundant phylum in several studies of the pitcher plant microbial community, including S. purpurea [16],[19],[20], S. minor [20],[31], and in S. alata [20],[32]. The second most abundant phylum was Bacteroidetes (Fig. 1); both Gray et al. [19] and Krieger & Kourtev [20] also reported finding an abundance of Bacteroidetes in S. purpurea.

Figure 1. Bar graph of normalized 16S rRNA iTag sequence data.

The most abundant classes are shown. Less abundant classes are summed under “Other.” Samples with C. steinii are referred to as +CS and those without as –CS.

Our iTag sequence data revealed 186 different genera, compared to a maximum of 19 genera using cloning and sequencing [19] in S. purpurea and 29 genera using a tag sequencing approach (454 pyrotag in a different host, S. alata; [32]). At a finer scale of taxonomic resolution, 1043 different OTUs were identified in our samples. However, rarefaction analysis (Fig. 2) revealed that even with the sequencing depth achieved here, no sample was nearing an asymptote, suggesting that greater sequencing coverage is required to capture the total breadth of microbial diversity in S. purpurea pitchers. Koopman et al. [32] similarly reported that they did not achieve an asymptote in their pyrotag data in S. alata.

Figure 2. Rarefaction curve of the number of observed OTUs from 16S rRNA iTag sequence data.

Variation in microbial community structure with and without C. steinii

The rarefied OTU data were further analyzed to quantify differences in the microbial communities with and without C. steinii (Fig. 2). No statistically significant differences in OTU richness (observed species; Table 1) with and without this predator were found. Alpha diversity was further explored to compare the microbial community in treatments with and without C. steinii. Chao1 [33] and Shannon diversity indices (Table 1) were not statistically different in leaves with and without the predator. Additionally, dominance values were determined for both sample types and found to be very low, nearly identical and not statistically significant for both sample types (0.08 with and without the C. steinii predator; dominance is on a scale of 0–1; Table 1).

Table 1. Alpha diversity statistics of microbial 16S rRNA gene sequence data in S. purpurea samples, with (+CS) and without C. steinii (−CS).

To determine which of the 1043 OTUs were significantly different in samples with and without the C. steinii predator, we conducted non-parametric Wilcoxon tests, corrected for a FDR, on each OTU after sample normalization (relative abundance). This analysis revealed that 42 OTUs were statistically different between communities with and without the C. steinii predator, with those changing the most shown in Figure 3. These 42 OTUs are from a broad variety of taxonomic groups, including Proteobacteria, Verrucomicrobia, Bacteroidetes, and Acidobacteria.

Figure 3. Heatmap of OTUs that were statistically significantly more abundant in samples with or without the protozoan predator (only the top ten OTUs that changed the most with protozoa and without protozoa are shown).

Those OTUs that were statistically significantly correlated with an NMDS axis are indicated by an *.

Very few previous studies have quantified the effects of predators on bacterial communities (however, see [6],[12]). We found no statistical difference in species richness, dominance or overall diversity between communities with and without the protozoan predator, C. steinii. Previous work in S. purpurea revealed that protozoa may decrease bacterial diversity, but the experiments have only indirectly manipulated bacterivores through their predator, larvae of the mosquito Wyeomyia smithii [16],[34].

While alpha diversity metrics were not significantly different with and without the C. steinii predator, beta diversity analysis revealed differences in the microbial community composition (Fig. 4), with a significant difference in scores for the third NMDS axis (ANOVA, P<0.001). Because the first two axes were not affected by the presence of the protozoan predator C. steinii, predation may not be the major factor determining among-leaf variation in microbial community structure, although predation clearly had a significant effect (Fig. 4a). NMDS analysis revealed that of the 42 OTUs discussed above, seven had statistically significant correlations with an NMDS axis 1 or 3 (r-value cutoff ≤0.03) (Fig. 4b). These seven OTUs are discussed in greater detail below.

Figure 4. Non-metric multidimensional scaling (NMDS) ordination of normalized 16S rRNA iTag sequence data.

(A) NMDS ordination of the first and third axes showing sample grouping based on the presence or absence of the protozoan predator. (B) NMDS ordination with those OTUs that were statistically significantly correlated with an axis and had a p-value < 0.03 shown by vectors.

Bacterial species influenced by the presence of C. steinii

Seven OTUs were significantly more abundant when C. steinii was absent. Many of these OTUs were highly similar to species found in aquatic environments, or were closely related to plankton, both of which may indicate a planktonic lifestyle of the species in question. A planktonic lifestyle may explain why the relative species abundance was higher when no C. steinii was present - because it is unable to seek refuge by attaching to a surface, such as a soil particle, to escape protozoan predation. A more detailed discussion regarding this hypothesis follows below. We acknowledge, however, investigating this hypothesis requires additional experiments beyond those described herein. Further, we recognize that close phylogenetic relationships (16S rRNA genes) between uncultured and cultured species is not indicative that the species in question is endowed with a particular attribute.

A Comamonadaceae species (OTU 1116384), a member of the Betaproteobacteria, was more abundant in leaves without predators than those with predators (Figs. 3 & 4b). This Comamonadaceae species was 99% similar to sequences retrieved from a wide variety of habitats, ranging from marine (Acc. KC872921) and freshwater (Acc. KF827131), to acidic water from a copper mine (Acc. KF287732) and to intestinal microbiota in migrating shorebirds in the Delaware Bay [35]. Roseateles depolymerans, a motile, rod shaped, bacteriochlorophyll containing microorganism isolated from freshwater [36], was closely related (99%) to the Comamonadaceae species. Given that the abundance of the Comamonadaceae species discussed here was statistically significantly higher without the predator, suggested it may be subject to protozoa grazing in the pitcher fluids. Its high similarity to species found in aquatic environments may indicate a planktonic lifestyle, which, as discussed above may preclude predator avoidance by particle attachment.

The Alphaproteobacteria, Caulobacteraceae species (OTU 673010) was more abundant in leaves without C. steinii than in those with it (Figs. 3 & 4b). This species was highly similar to microorganisms from several disparate environments. For example, it was 100% similar to microorganisms associated with insects (Acc. JQ894899 and [37]), forest soil [38], marine (Acc. KC001312) and freshwater [39] environments. Caulobacteraceae (OTU 673010) was 97% similar to several cultured representatives including Phenylobacterium lituiforme. P. lituiforme is a motile, facultative anaerobe isolated from a subsurface aquifer [40], thus may have a planktonic lifestyle. The close relationship of the Caulobacteraceae (OTU 673010) species with P. lituiforme and to microorganisms from other aquatic environments may indicate that it has a planktonic lifestyle, which could make it more susceptible to predation.

Similarly, the Alphaproteobacteria, Caulobacter (OTU 811257) was more abundant when no Colpoda steinii was present (Figs. 3 & 4b). This species was 100% similar to those from a wide variety of habitats, including coral (Acc. KJ601398), seawater (Acc. KF786782) and root nodules (Acc. KF596691). It was 100% similar to the cultured representative, Caulobacter crescentus, which is a motile species typically found in aquatic environments with low nutrient concentrations [41] - an environment found within the S. purpurea pitcher.

Terriglobus (OTU 250794) a species in the phylum Acidobacteria, was more abundant in leaves without Colpoda steinii (Figs. 3 & 4b). Sequences that were 100% similar to Terriglobus (OTU 250794) included microorganisms from sugarcane stem (Acc. KF241163), Nepenthes pitcher plants (Acc. JX532061), Eisenia fetida egg capsules [42] and acidic Sphagnum peat [43]. Terriglobus saanensis strain SP1PR4 [44] was highly similar (98%) to the Terriglobus (OTU 250794). Terriglobus saanensis, isolated from Artic tundra soil, is a non-motile, rod-shaped, aerobic bacterium [44]. The fact that our Terriglobus (OTU 250794) species is possibly soil associated, is not in agreement with the hypothesis we proposed above. The high sequence similarity of this species with Bacteria from other pitcher plants, suggested that it is a ubiquitous member of pitcher plants, and warrants more direct attention in future research, particularly in regards to its lifestyle - planktonic or particle associated.

Finally, the Alphaproteobacteria, Phenylobacterium (OTU 216823) had a higher relative abundance in leaves without C. steinii than those with it (Figs. 3 & 4b). This species was 100% similar to microorganisms associated with plant roots (e.g. Acc. FM956526) and a wetland [45]. Further, it was 98% similar to Phenylobacterium falsum, which was isolated from alkaline groundwater [46]. P. falsum is a small rod-shaped, aerobic, heterotrophic non-motile bacterium [46]. The close relationship of Phenylobacterium (OTU 216823) species to P. falsum may indicate that it is planktonic, but non-motile, which could render it difficult to escape predation-even more so than the potentially planktonic, motile species discussed above.

Bacterial species that may be capable of escaping C. steinii predation

The Alphaproteobacteria, Rhizobiales (OTU 831178), was more abundant in the leaves with C. steinii than in those without (Figs. 3 & 4b). This species was 100% similar to microorganisms found in a wide variety of environments including, solanaceous crops [47], alluvial aquifers of the Makyeong River [48] and bacterial communities associated with spores of Gigaspora margarita (Acc. EU589423). The cultured species Bosea thiooxidans was 99% similar to the Rhizobiales species (OTU 831178) [49]. B. thiooxidans is a rod-shaped, motile bacterium isolated from soil [50]. This contrasts with the species discussed previously, in that the closest cultured representative is soil-associated, not planktonic. Our hypothesis that the protozoa predator may target planktonic Bacteria, rather than particle, or soil-associated species is supported. Alternatively its abundance may have been shaped by an interaction with other Bacteria that decreased in abundance when a predator was present. However, these hypotheses were not directly tested here, and require additional future analyses.

Emticicia (OTU 1126475), a Cytophagia in the Bacteroidetes phylum, was more abundant in samples with C. steinii than those without (Figs. 3 & 4b). The most similar (100%) sequences to this Emticicia species were retrieved from pasture soil (Acc. JN976780) and from the isolate Emticicia ginsengisoli strain Gsoil 085 [51]. The aerobic, non-motile, rod-shaped bacterium, E. ginsengisoli strain Gsoil 085, was isolated from soil samples in a ginseng field [51]. As discussed previously, Bacteroidetes is a major part of the microbial community of S. purpurea pitcher fluid [19],[20]. Gray et al. [19] reported that Bacteroidetes was a significant member of the microbial community in S. purpurea fluids, including those pitchers sampled at the Apalachicola National Forest, from where we obtained pitcher fluids for our greenhouse experiments. These authors suggested, however, that the variability in the abundance of Bacteroidetes from leaf-to-leaf may not result from the grazing pressure, but rather other environmental factors [19]. Our results suggest that predation does influence the abundance of a particular Bacteroidetes species. This finding further supports our hypothesis, in that the Emticicia (OTU 1126475) species, closely related to the soil isolate E. ginsengisoli, may not have a planktonic lifestyle, and may be able to attach to surfaces such as soil particles, thereby avoiding predation. Further, Gray et al. [19] highlighted the role Bacteroidetes play in degrading organic matter and in producing extracellular enzymes, which may be important mechanisms by which nutrients are made available to S. purpurea. Thus the ability of a Bacteroidetes to avoid predation may directly influence the fitness of S. purpurea.


The goal of this study was to determine the predator-prey effects of the protozoan, C. steinii, on the microbial community in S. purpurea pitcher fluids. Our results revealed that, while grazing by this protozoan in S. purpurea pitcher fluids resulted in statistically significant shifts in the relative abundance of 42 bacterial species, there was no change in overall microbial community richness or diversity. Of these 42 species, those that had a statistically higher relative abundance without C. steinii present were generally closely related to motile, planktonic species, leading us to hypothesize that, in our experiments, protozoa targeted microorganisms residing in the pitcher fluids, rather than those associated with particles, such as soil. This hypothesis is in agreement with our findings: that those microbial species that were more abundant in the samples with C. steinii described herein, were closely related to particle associated cultured representatives. Our findings help to resolve, at a microscale level, the effects perturbations have on trophic structures by the addition or removal of the protozoan predator. Although, it is likely that there are many factors that influence prey selection and predator avoidance, testing our hypothesis in future experiments is feasible. For example, differentiating between the microbial communities associated with particles and those associated with the pitcher fluids may reveal that protozoa do indeed target the plankton.

Author Contributions

Conceived and designed the experiments: TEM OUM. Performed the experiments: TKP TEM. Analyzed the data: TKP TEM OUM. Contributed reagents/materials/analysis tools: TEM OUM. Wrote the paper: TKP TEM OUM.


  1. 1. Kerfoot CW, Sih A (1987) Predation: Direct and Indirect Impacts on Aquatic Communities. Hanover and London: University Press of New England.
  2. 2. Sherr E, Sherr B (2002) Significance of predation by protists in aquatic microbial food webs. Antonie Van Leeuwenhoek 81:293–308.
  3. 3. Pernthaler J (2005) Predation on prokaryotes in the water column and its ecological implications. Nat Rev Microbiol 3: 537–546. Available:
  4. 4. Hill TCJ, Walsh KA, Harris JA, Moffet BF (2003) Using ecological diversity measures with bacterial communities. FEMS Microbiol Ecol 43:1–11.
  5. 5. Hahn MW, Höfle MG (2001) Grazing of protozoa and its effect on populations of aquatic bacteria. FEMS Microbiol Ecol 35:113–121.
  6. 6. Miki T, Jacquet S (2008) Complex interactions in the microbial world: underexplored key links between viruses, bacteria and protozoan grazers in aquatic environments. Aquat Microb Ecol 51:195–208.
  7. 7. Salcher M, Pernthaler J, Psenner R, Posch T (2005) Succession of bacterial grazing defense mechanisms against protistan predators in an experimental microbial community. Aquat Microb Ecol 38:215–229.
  8. 8. Jürgens K, Güde H (1994) The potential importance of grazing-resistant bacteria in planktonic systems. Mar Ecol Prog Ser Oldend 112:169–188.
  9. 9. Matz C, Jürgens K (2003) Interaction of nutrient limitation and protozoan grazing determines the phenotypic structure of a bacterial community. Microb Ecol 45:384–398.
  10. 10. Simek K, Pernthaler J, Weinbauer MG, Dolan JR, Nedoma J, et al. (2001) Changes in Bacterial Community Composition and Dynamics and Viral Mortality Rates Associated with Enhanced Flagellate Grazing in a Mesoeutrophic Reservoir. Appl Environ Microbiol 67:2723–2733.
  11. 11. Weinbauer MG, Hornák K, Jezbera J, Nedoma J, Dolan JR, et al. (2007) Synergistic and antagonistic effects of viral lysis and protistan grazing on bacterial biomass, production and diversity. Environ Microbiol 9:777–788.
  12. 12. Simek K, Vrba J, Pernthaler J, Posch T, Hartman P, et al. (1997) Morphological and compositional shifts in an experimental bacterial community influenced by protists with contrasting feeding modes. Appl Environ Microbiol 63:587–595.
  13. 13. Jürgens K, Stolpe G (1995) Seasonal dynamics of crustacean zooplankton, heterotrophic nanoflagellates and bacteria in a shallow, eutrophic lake. Freshw Biol 33:27–38.
  14. 14. Srivastava DS, Kolasa J, Bengtsson J, Gonzalez A, Lawler SP, et al. (2004) Are natural microcosms useful model systems for ecology? Trends Ecol Evol 19:379–384.
  15. 15. Bradshaw WE, Creelman RA (1984) Mutualism between the Carnivorous Purple Pitcher Plant and Its Inhabitants. Am Midl Nat 112:294–304.
  16. 16. Peterson CN, Day S, Wolfe BE, Ellison AM, Kolter R, et al. (2008) A keystone predator controls bacterial diversity in the pitcher-plant (Sarracenia purpurea) microecosystem. Environ Microbiol 10:2257–2266.
  17. 17. Miller TE, Kneitel JM (2005) Inquiline Communities in Pitcher Plants as a Prototypical Metacommunity. Pp. 122–145 in Holyoak, M., M. A. Leibold, and R. D. Holt (eds.), Metacommunities: Spatial Dynamics and Ecological Communities. University of Chicago Press, Chicago.
  18. 18. Miller TE, terHorst CP (2012) Testing successional hypotheses of stability, heterogeneity, and diversity in pitcher-plant inquiline communities. Oecologia 170:243–251.
  19. 19. Gray SM, Akob DM, Green SJ, Kostka JE (2012) The bacterial composition within the Sarracenia purpurea model system: local scale differences and the relationship with the other members of the food web. PLoS One 7:e50969.
  20. 20. Krieger JR, Kourtev PS (2012) Bacterial diversity in three distinct sub-habitats within the pitchers of the northern pitcher plant, Sarracenia purpurea. FEMS Microbiol Ecol 79:555–567.
  21. 21. terHorst C, Miller TE, Levitan D (2010) Evolution of prey in ecological time reduces the effect size of predators in experimental microcosms. Ecology 91:629–636.
  22. 22. Miller TE, Moran ER, terHorst CP (2014) Rethinking Niche Evolution: Experiments with Natural Communities of Protozoa in Pitcher Plants. Am Nat 184:277–83.
  23. 23. Caporaso JG, Lauber CL, Walters WA, Berg-Lyons D, Lozupone CA, et al. (2011) Global patterns of 16S rRNA diversity at a depth of millions of sequences per sample. Proc Natl Acad Sci U S A 108 Suppl: 4516–4522.
  24. 24. Caporaso JG, Lauber CL, Walters WA, Berg-Lyons D, Huntley J, et al. (2012) Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms. ISME J 6:1621–1624.
  25. 25. Caporaso JG, Kuczynski J, Stombaugh J, Bittinger K, Bushman F, et al. (2010) QIIME allows analysis of high-throughput community sequencing data. Nat Methods 7:335–336.
  26. 26. Edgar RC (2010) Search and clustering orders of magnitude faster than BLAST. Bioinformatics 26:2460–2461.
  27. 27. Caporaso JG, Bittinger K, Bushman FD, DeSantis TZ, Andersen GL, et al. (2010) PyNAST: a flexible tool for aligning sequences to a template alignment. Bioinformatics 26:266–267.
  28. 28. Wang Q, Garrity GM, Tiedje JM, Cole JR (2007) Naive Bayesian classifier for rapid assignment of rRNA sequences into the new bacterial taxonomy. Appl Environ Microbiol 73:5261–5267.
  29. 29. McDonald D, Price MN, Goodrich J, Nawrocki EP, DeSantis TZ, et al. (2012) An improved Greengenes taxonomy with explicit ranks for ecological and evolutionary analyses of bacteria and archaea. ISME J 6:610–618.
  30. 30. Arndt D, Xia J, Liu Y, Zhou Y, Guo AC, et al. (2012) METAGENassist: a comprehensive web server for comparative metagenomics. Nucleic Acids Res 40:W88–95.
  31. 31. Siragusa AJ, Swenson JE, Casamatta DA (2007) Culturable bacteria present in the fluid of the hooded-pitcher plant Sarracenia minor based on 16S rDNA gene sequence data. Microb Ecol 54:324–331.
  32. 32. Koopman MM, Fuselier DM, Hird S, Carstens BC (2010) The carnivorous pale pitcher plant harbors diverse, distinct, and time-dependent bacterial communities. Appl Environ Microbiol 76:1851–1860.
  33. 33. Chao A (1984) Nonparametric Estimation of the Number of Classes in a Population. Scand J Stat 11:265–270.
  34. 34. Kneitel JM, Miller TE (2002) Resource and top-predator regulation in the pitcher plant (Sarracenia purpurea) inquiline community. Ecology 83:680–688.
  35. 35. Ryu H, Grond K, Verheijen B, Elk M, Buehler DM, et al. (2014) Intestinal microbiota and species diversity of Campylobacter and Helicobacter spp. in migrating shorebirds in Delaware Bay. Appl Environ Microbiol 80:1838–1847.
  36. 36. Suyama T, Shigematsu T, Takaichit S (1999) Roseateles depolymerans gen. nov., sp. nov., a new bacteriochlorophyll a-containing obligate aerobe belonging to the beta-subclass of the Proteobacteria. Int J Syst Bacteriol: 449–457.
  37. 37. Colman DR, Toolson EC, Takacs-Vesbach CD (2012) Do diet and taxonomy influence insect gut bacterial communities? Mol Ecol 21:5124–5137.
  38. 38. Lin Y-T, Huang Y-J, Tang S-L, Whitman WB, Coleman DC, et al. (2010) Bacterial community diversity in undisturbed perhumid montane forest soils in Taiwan. Microb Ecol 59:369–378.
  39. 39. Michalsen MM, Peacock AD, Smithgal AN, White DC, Spain AM, et al. (2009) Treatment of nitric acid-, U(VI)-, and Tc(VII)-contaminated groundwater in intermediate-scale physical models of an in situ biobarrier. Environ Sci Technol 43:1952–1961.
  40. 40. Kanso S, Patel BKC (2004) Phenylobacterium lituiforme sp. nov., a moderately thermophilic bacterium from a subsurface aquifer, and emended description of the genus Phenylobacterium. Int J Syst Evol Microbiol 54:2141–2146.
  41. 41. Nierman WC, Feldblyum TV, Laub MT, Paulsen IT, Nelson KE, et al. (2001) Complete genome sequence of Caulobacter crescentus. Proc Natl Acad Sci U S A 98:4136–4141.
  42. 42. Davidson SK, Powell RJ, Stahl DA (2010) Transmission of a bacterial consortium in Eisenia fetida egg capsules. Environ Microbiol 12:2277–2288.
  43. 43. Pankratov TA, Serkebaeva YM, Kulichevskaya IS, Liesack W, Dedysh SN (2008) Substrate-induced growth and isolation of Acidobacteria from acidic Sphagnum peat. ISME J 2:551–560.
  44. 44. Rawat SR, Männistö MK, Starovoytov V, Goodwin L, Nolan M, et al. (2012) Complete genome sequence of Terriglobus saanensis type strain SP1PR4(T), an Acidobacteria from tundra soil. Stand Genomic Sci 7:59–69.
  45. 45. Bouali M, Zrafi I, Bakhrouf A, Chaussonnerie S, Sghir A (2014) Bacterial structure and spatiotemporal distribution in a horizontal subsurface flow constructed wetland. Appl Microbiol Biotechnol 98:3191–3203.
  46. 46. Tiago I, Mendes V, Pires C, Morais PV, Veríssimo A (2005) Phenylobacterium falsum sp. nov., an Alphaproteobacterium isolated from a nonsaline alkaline groundwater, and emended description of the genus Phenylobacterium. Syst Appl Microbiol 28:295–302.
  47. 47. Achari GA, Ramesh R (2014) Diversity, biocontrol, and plant growth promoting abilities of xylem residing bacteria from solanaceous crops. Int J Microbiol 2014:296521.
  48. 48. Kim S-J, Koh D-C, Park S-J, Cha I-T, Park J-W, et al. (2012) Molecular analysis of spatial variation of iron-reducing bacteria in riverine alluvial aquifers of the Mankyeong River. J Microbiol 50:207–217.
  49. 49. La Scola B, Barrassi L, Raoult D (2000) Isolation of new fastidious alpha Proteobacteria and Afipia felis from hospital water supplies by direct plating and amoebal co-culture procedures. FEMS Microbiol Ecol 34:129–137.
  50. 50. Das SK, Mishra AK, Tindall BJ, Rainey FA, Stackebrandt E (1996) Oxidation of thiosulfate by a new bacterium, Bosea thiooxidans (strain BI-42) gen. nov., sp. nov.: analysis of phylogeny based on chemotaxonomy and 16S ribosomal DNA sequencing. Int J Syst Bacteriol 46:981–987.
  51. 51. Liu Q-M, Ten LN, Yu H-S, Jin F-X, Im W-T, et al. (2008) Emticicia ginsengisoli sp. nov., a species of the family “Flexibacteraceae” isolated from soil of a ginseng field. Int J Syst Evol Microbiol 58:1100–1105.