Low metabolic activity of biofilm formed by Enterococcus faecalis isolated from healthy humans and wild mallards (Anas platyrhynchos)
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It is widely known that Enterococcus faecalis virulence is related to its biofilm formation. Although Enterococci are common commensal organisms of the gastrointestinal tract, the difference between commensal and pathogen strains remain unclear. In this study, we compare the biochemical profile of the biofilms formed by two groups of medical and two groups of commensal strains. The medical strains were isolated as pathogens from infections of urinary tract and other infections (wounds, pus and bedsores), and the commensal strains were taken from faeces of healthy volunteers and faeces of wild mallards (Anas platyrhynchos) living in an urban environment. The properties of biofilms formed by medical and commensal strains differed significantly. Commensal strains showed lower metabolic activity and glucose uptake and higher biofilm biomass than the medical ones. Consistent with glucose uptake experiments, we found that the glucose dehydrogenase gene was more expressed in medical strains. These results indicate that higher metabolic activity and lower protein concentration of E. faecalis cells within biofilms are formed during infections.
KeywordsEnterococcus faecalis strains Biofilm Metabolic activity Protein concentration
Enterococci are common commensal organisms of the gastrointestinal tract (Mohamed et al. 2004). On the other hand, Enterococcus faecalis is one of the most common causes of serious nosocomial and urinary tract infections (Sood et al. 2008). Despite many studies and recognition of virulence factors (e.g. Eaton and Gasson 2001; Furumura et al. 2006; Gülhan et al. 2006; Jarzembowski et al. 2009), processes that determine host–Enterococcus relationships remain poorly understood. Enterococci virulence could be related to biofilm formation (Parsek and Singh 2003; Sood et al. 2008). In the biofilm, cells are organised into structured communities enclosed within a matrix, and such a structure is phenotypically different from that formed by planktonic cells. Biofilm cells are more resistant to host defences and display a significant decrease in susceptibility to antibiotics (Costerton et al. 1999). The formation of cells occurs in response to a variety of cues, including high cell density, nutrient deprivation and physical environmental stress (O’Toole et al. 2000). Bacterial biofilm causes significant problems in many areas, both in the treatment and prevention of infections (e.g. persistent and recurrent infections as well as device-related infections) (Donlan and Costerton 2002). Enterococcus faecalis is capable of colonizing a wide range of hosts and environments showing great genome plasticity and diversity (Aakra et al. 2007). However, differences between an enterococcal pathogens and an apparently safe commensal strains is unclear and little is known about differences in biochemical properties between commensal and pathogenic strains (Eaton and Gasson 2001; Shiloach et al. 2010).
Our study aims to compare metabolic activity and biofilm composition of pathogenic and commensal E. faecalis strains with special emphasis on those isolated from wild birds.
Materials and methods
A total of 65 strains of E. faecalis were examined, including 32 commensal and 33 medical strains. Seventeen strains from the second group were isolated from urinary tract infections (UTI) (urine and swabs of urinary tract) and 16 strains from other infections (wounds, pus and bedsores), and were all taken only from humans. These samples were collected in the Kościerzyna Medical Centre. The commensal strains were isolated both from humans (faecal samples from 16 volunteers) and from wild birds living in urban environments (faecal swabs taken from the cloaca of 16 mallards Anas platyrhynchos caught in Gdańsk). Isolates were identified and recognized as a different E. faecalis strains by ID 32 STREP (bioMérieux).
For determination of biofilm dry weight, protein concentration and biofilm metabolic activity as well as cell enumeration of all four groups of strains were taken into account. For detection of glucose dehydrogenase gene expression, commensal strains from human and mallard faeces and strains from urinary tract infections were chosen. Additionally, two strains from urinary tract infections, two from human faeces and two from mallard faeces were randomly chosen for analysis of growth curves.
Determination of biofilm dry weight
Biofilms formed in a sterile well plate after 72 h were scraped from the bottom of the well, suspended in 1 ml of 0.9 % NaCl and sonicated for 2 min on ice. Whole volume of biofilm solution was carefully inoculated into previously weighed cellulose membrane with pore size 0.2 μm (Whatman, Kent, UK). The membrane was placed at 56 °C for 2 h and weighed again. Biofilm dry weights were obtained as the differences between these two measurements. As a negative control, a membrane inoculated with sterile 0.9 % NaCl and dried as a sample was weighed. The result was presented as a biomass of the biofilm per 1 cm2 of its surface.
Biofilms formed in a sterile well plate after 72 h were scraped from the bottom of the well, suspended in 1 ml of 0.9 % NaCl and sonicated for 2 min on ice. Then, 1 μl of the sonicated biofilm sample was diluted in 103 and 106 μl of sterile 0.9 % NaCl. Next, 10 μl of diluted sample was plated onto agar plates and incubated overnight (18–20 h) at 37 °C. Inoculum of viable cells in the biofilm was determined by the enumeration of colonies on the agar as colony-forming units per 1 mg of biofilm (CFU/mg) and per 1 cm2 of biofilm surface (CFU/cm2).
Determination of protein concentration
Protein concentration in the biofilm was determined using the BCA Protein Assay Kit (Pierce, USA). Biofilms formed in a sterile well plate after 72 h were scraped from the bottom of the well, suspended in 1 ml of 0.9 % NaCl and sonicated for 2 min on ice. Then, 20 μl of sonicated biofilm was sampled and the microplate procedure was used according to the manufacturer’s instructions. The result was presented per 1 cm2 of biofilm-forming surface and 1 mg of the biofilm.
Determination of biofilm metabolic activity
Metabolic activity was measured by glucose uptake, reduction of the XTT and glucose dehydrogenase gene expression. Measuring glucose uptake was performed as described earlier by Cerca et al. (2005) with a minor modification. Briefly, cells in sterile 6-well plates (TRP, Switzerland) were filled with 3 ml of Brain Heart Infusion (BHI) and inoculated with 10 μl of an 18-h culture normalised to an optical density of 0.5. As a control, additional wells were filled with sterile BHI. After 24 h, 2 ml of medium was replaced with fresh broth. The culture was terminated after 72 h, the medium was aspirated and wells were washed with sterile 0.9 % NaCl. Next, 1 ml of 0.1 % solution of glucose was added to each well and the plate was incubated for another hour at 37 °C. After incubation, 10 μl was aspirated to measure glucose concentration. Glucose uptake was determined with Glucose TR kit (Spinreact, Spain), measured at 505 nm with an ELISA reader and calculated as the difference between initial (0.1 %) and final glucose concentration.
XTT assay was performed using flat bottom polystyrene plates (TRP). Bacterial strains were grown at 37 °C for 72 h in BHI. After incubation, the medium was aspirated and the wells were washed with 0.9 % NaCl. The metabolic activity of the cells was determined with the Cell Proliferation Kit (XTT-based) (Biological Industries) according to the manufacturer’s manual. This technique is focused on the metabolic activity of viable cells and involves the use of tetrazolium salts, including 5-cyano-2,3-ditolyl tetrazolium chloride (CTC) and 2,3-bis (2-methoxy-4-nitro-5-sulfophenyl)-5-[(phenylamino)carbonyl]-2H-tetrazolium hydroxide (XTT). The XTT assay is based on the reduction of the XTT dye to water-soluble formazan (Roehm et al. 1991). The absorbance of the cell supernatant is proportional to the metabolic activity of the cells. In this study, the absorbance was measured at 490 nm with an ELISA reader.
For FLOW-FISH detection of glucose dehydrogenase gene expression, Molecular Beacon (MB) probes (CGCGATCCACCAGTCACGAATGATGCGATCGCG) were designed with the software package (Beacon Designer; Biosoft). The FLOW-FISH method allows the analysis of single/particular cells in the sample and thus the evaluation of heterogeneity in the bacterial population. FITC-labelled oligonucleotides were synthesized commercially (Metabion) and tested for specificity against the set of reference organisms. Molecular beacon probes were additionally labelled with Dabcyl’5 as a quencher. Enfl84 probe (Waar et al. 2005) targeting E. faecalis 16S RNA and nonsense sequence probe was used respectively as a positive and negative reference.
For hybridisation, the procedure described by Waar et al. (2005) was adopted and modified according to the previous pilot study (Jarzembowski et al. 2009). Briefly, the cell membrane was permeabilizated by incubation for 30 min at 37 °C in permeabilisation buffer (TE) consisting of 1 mg lysozyme/ml (DNA Gdańsk). Then, the cells were suspended in 1 ml of 0.9 % NaCl and sonicated for 2 min on ice. Finally, the cells were centrifuged for 5 min at 2,500 rpm, washed and suspended in 200 μl PBS buffer. Subsequently, 200 μl hybridisation buffer containing a FITC-labelled probe (1 ng) was added. The probes were hybridised for 45 min at Tm temperature.
Fluorescence of particles was determined by a FACS Scan flow cytometer (Becton Dickinson, San Jose, CA, USA). Percentage unstained particles (no. FL1 < 10/no. FL1 > 10) and mean fluorescence per particle (FL1/FSC) were analysed.
Growth curves determination
The isolates were grown on a Brain Heart Infusion Agar (BHIA) plate at 37 °C for 48 h, after which they were inoculated in Brain Heart Infusion (BHI) at 37 °C with constant agitation (120 rpm). In order to evaluate the kinetics growth, 200 μl of the suspension was removed every hour and its optical density determined using a plate reader with a wavelength of 640 nm.
Since a zero value was obtained in some cases, 0.001 was added to all data in order to enable log-transformation of 0 values. All data were log-transformed (log10) to normalise variables and a constant value of 3 was added to bring minimum values after transformation to above zero. Thus, the transformation followed the equation: x’ = log10(x + 0.001) + 3, where x is the original value and x’ the value after transformation. Nested ANOVA were used in all analyses with the four group of strains (isolated as a pathogen from urine in urinary tract infections, isolated as a pathogen from other infections, isolated as a commensal from faeces of healthy volunteers and isolated as a commensal from faeces of birds living in urban environments) nested in two strain types (medical and commensal strains). Data obtained in percent scale was transformed using arcsin√x function after dividing the percentage by 100. Statistical methods followed Zar (1996).
Mean values and ranges of biochemical parameters for medical and commensal strains measured in this study
Difference between means
Biomass of biofilm (mg/cm2)
Glucose uptake (μg/cm2)
Glucose uptake (μg/mg of biofilm)
Amount of protein (μg/cm2)
Amount of protein (μg/mg of biofilm)
XTT result (AU/mg of biofilm)
XTT result (AU/cell x105)
Mean values of CFU/mg, CFU/cm2, amount of protein per mg and XTT value per cell did not differ among the four strain types (nested ANOVA: among strains within strain type, p > 0.05 in all cases).
We showed that medical strains of E. faecalis display higher metabolic activity and lower biomass in biofims than commensal strains. Our results suggest that metabolic activity of enterococci does not correlate with higher cell concentrations in biofilms. It is possible that increases in EPS production might account for lower biomass in some biofilm-forming strains. However, we have not investigated this point, as we have focused our attention on the cellular component of enterococcal biofilms.
We revealed that the medical strains of E. faecalis had higher metabolic activity and lower biomass of biofilm than the commensal strains. These results indicate that higher metabolic activity of enterococci was not related to higher concentration of cells in biofilm. Low biomass of biofilm can be the result of spread adaptation of the medical strain (Ahimou et al. 2007).
Glucose uptake was significantly higher in strains isolated from patients with urinal infections in comparison with those from healthy people. The same differences were observed at the transcription level (FLOW-FISH results) and when we compare growth curves. It is obvious that frequent cell division demands higher metabolic activity. On the other hand, the correlation of the results obtained by three different approaches means the difference between the studied strains is evident.
Some studies have shown that among E. faecalis, glucose supplementation enhances biofilm formation (Baldassarri et al. 2001), whereas other researchers have demonstrated glucose-mediated inhibition of biofilm production (Kristich et al. 2004). This divergence might be a result of a bimodal fashion of glucose-mediated biofilm formation, where greater biomass of biofilm would be created at the extremes of the environmental conditions, which could potentially provide the organism with a survival benefit in suboptimal growth conditions (Pillai et al. 2004). However, glucose uptake might result from cell density and correlate with the density of CFU in the biofilms (Cerca et al. 2005).
Although we showed statistically significant differences in biochemical properties between the medical and the commensal strains, it should be noted that environmental and clinical biofilms rarely, if ever, consist only of cells from a single species. Therefore, further studies are needed to analyse the influence of other species on E. faecalis biofilm. Moreover, when comparing results obtained from bird and human strains, differences in ammonia metabolism should be considered. Birds excrete urate instead of the toxic urea as do mammals. Urea in mammals is flushed out from the body with a great amount of water, while urate in birds is largely insoluble and uses very little water to be excreted (Goldstein and Skadhauge 1999). Thus, differences between strains collected from birds and from humans might be caused by biochemical adaptations to different media.
Not only glucose uptake but also lower amounts of protein found in the medical strains suggests slower growth of biofilm in these strain types in comparison with the commensal ones. This comes from the assumption that the concentration of proteins increases during biofilm development (Toledo-Arana et al. 2001; Tendolkar et al. 2004) and surface proteins can mediate biofilm formation (Geoghegan et al. 2010).
We have found marked differences in the biochemical properties of biofilms formed by strains of different origins. The medical strains formed thinner biofilm (lower amount of cells on the same area) with higher metabolic activity than the commensal strains. However, because of high divergence of features within groups of strains, it is still impossible to “forecast” bacteria–host relationships based on the biochemical properties of their biofilms.
This work was supported by the Medical University of Gdańsk research grant (GUMed W-65) and was financed partly by University of Gdańsk research grant (BW 1440-5-0099-7). We are grateful to Katarzyna Żółkoś for her help in catching mallards and Magdalena Remisiewicz for correcting the English. Catarina Seabra helped in preparing assays.
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