Maggot Excretions Inhibit Biofilm Formation on Biomaterials
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- Cazander, G., van de Veerdonk, M.C., Vandenbroucke-Grauls, C.M.J.E. et al. Clin Orthop Relat Res (2010) 468: 2789. doi:10.1007/s11999-010-1309-5
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Biofilm-associated infections in trauma surgery are difficult to treat with conventional therapies. Therefore, it is important to develop new treatment modalities. Maggots in captured bags, which are permeable for larval excretions/secretions, aid in healing severe, infected wounds, suspect for biofilm formation. Therefore we presumed maggot excretions/secretions would reduce biofilm formation.
We studied biofilm formation of Staphylococcus aureus, Staphylococcus epidermidis, Klebsiella oxytoca, Enterococcus faecalis, and Enterobacter cloacae on polyethylene, titanium, and stainless steel. We compared the quantities of biofilm formation between the bacterial species on the various biomaterials and the quantity of biofilm formation after various incubation times. Maggot excretions/secretions were added to existing biofilms to examine their effect.
Comb-like models of the biomaterials, made to fit in a 96-well microtiter plate, were incubated with bacterial suspension. The formed biofilms were stained in crystal violet, which was eluted in ethanol. The optical density (at 595 nm) of the eluate was determined to quantify biofilm formation. Maggot excretions/secretions were pipetted in different concentrations to (nonstained) 7-day-old biofilms, incubated 24 hours, and finally measured.
The strongest biofilms were formed by S. aureus and S. epidermidis on polyethylene and the weakest on titanium. The highest quantity of biofilm formation was reached within 7 days for both bacteria. The presence of excretions/secretions reduced biofilm formation on all biomaterials. A maximum of 92% of biofilm reduction was measured.
Our observations suggest maggot excretions/secretions decrease biofilm formation and could provide a new treatment for biofilm formation on infected biomaterials.
Infections of medical prosthetic devices in trauma and orthopaedic surgery are difficult to treat with conventional therapies like antibiotics and surgery , and can lead to severe consequences, such as removal of the implant with functional loss of the affected limb [18, 26]. The most frequently isolated bacteria causing these implant- and patient-related infections are S. aureus and the coagulase-negative S. epidermidis [1, 11]. Less common are Pseudomonas aeruginosa, Klebsiella oxytoca, Enterococcus faecalis, and Enterobacter cloacae. In prosthesis-associated infections, the causative bacteria form biofilms composed mainly of a polysaccharide matrix . The most important difference between bacteria in biofilms and planktonic microorganisms that can explain the alteration in antibiotic resistance is the metabolic state of biofilm bacteria . The genotype and phenotype of bacteria in biofilms and the protein expression are altered and the oxygen concentration in biofilms is limited . These changes result in metabolic quiescence, which could be overcome by providing alternative electron acceptors of fermentable substrates [3, 24]. Current antimicrobial therapies frequently cannot adequately treat biofilm-associated infections [8, 9, 24, 26] and therefore it is important to develop new treatment approaches to reduce biofilm formation (BF) on biomaterials.
The most important development in the treatment of infectious diseases during the last century was the discovery of penicillin by Fleming in 1928 . At approximately the same time, maggot debridement therapy (MDT) was introduced by William S. Baer, an orthopaedic surgeon who worked at Johns Hopkins Hospital in Baltimore, Maryland . Baer used MDT to treat children with, at that time, incurable osteomyelitis. Although Baer showed the beneficial effects of maggots of the Lucilia sericata, MDT essentially disappeared after the discovery of penicillin, which could control numerous types of severe infections . Because of increasing antibiotic resistance , larval therapy was reintroduced in the 1980s as a treatment for severely infected wounds . Maggots now are used successfully in various patient clinics [13, 25]. In 2004, MDT was approved by the US Food and Drug Administration (510[k] #33391) .
In our clinical practice, we use maggots captured in small nylon bags, consisting of a 2-mm thin foam layer of polyvinyl alcohol (Biobag®; BioMonde GmbH, Barsbüttel, Germany) . These bags are able to permeate maggot excretions and secretions (ES). We have observed healing of wound infections suspect for BF using maggots in such bags. In an earlier pilot study, we found ES reduced the quantity of immature biofilms of P. aeruginosa . However, the current research investigated, for the first time, the influence of a range of concentrations of ES on mature 7-day-old biofilms formed by new, commonly isolated bacterial species on different biomaterials. If maggot ES reduce BF of bacteria that frequently are isolated from biofilm-associated infections, ES could provide us with a new treatment possibility.
Therefore, we asked (1) whether five bacterial species (S. aureus, S. epidermidis, K. oxytoca, E. faecalis, and E. cloacae), were able to form biofilms on polyethylene (PE), titanium (TI), and/or surgical stainless steel (SSS), and if so, whether (2) the quantity of BF differed among the bacterial species, (3) the quantity of BF depended on the biomaterial surface, and (4) the quantity of biofilms of the biofilm-forming bacteria differed among 3, 5, 7, or 9 days of incubation time. Finally, we hypothesized (5) sterile maggot ES could decrease the growth of the bacterial biofilms on the commonly used biomaterials SSS, TI, and PE.
Materials and Methods
The custom-made, sterile comb-like models of regularly available orthopaedic implant materials, consisting of eight prongs were produced according to our design. These models of SSS, TI, and PE (Litos GmbH, Hamburg, Germany) were made to fit in a 96-well microtiter plate . Each prong was considered one test and experiments were performed at least 12 times.
S. aureus, S. epidermidis, K. oxytoca, E. faecalis, and E. cloacae all were isolated from infected prosthetic devices of patients in our clinic. BF was tested using a previously described model . Briefly, S. aureus and S. epidermidis were grown overnight in tryptic soy broth (TSB) medium (Becton, Dickinson & Co, Franklin Lakes, NJ) and K. oxytoca, E. faecalis, and E. cloacae in brain heart infusion (BHI) medium (Becton, Dickinson & Co) at 37°C. A stationary phase culture was made in either TSB or BHI to a density of McFarland 0.5 corresponding with 1.5 × 108 colony-forming units (CFUs) per μL. The inoculum was controlled by inoculating nutrient agar plates (Biotrading Benelux BV, Mijdrecht, The Netherlands) with 10-μL volumes of serial 1:10 dilutions of the bacterial suspension and counting the formed CFUs after incubation overnight at 37°C.
The bacterial suspension was diluted to a final inoculum of 2.5 × 105 bacteria per mL and a volume of 100 μL of this suspension was pipetted into 24 wells of a sterile 96-well flat-bottomed microtiter plate (Greiner Bio-one BV, Monroe, NC). One comb of each biomaterial was placed in eight of the wells and four of these microtiter plates with combs were incubated for 3, 5, 7, or 9 days at 37°C to form biofilms on the devices. Control combs were suspended in nutrient medium.
After the incubation time, each comb was washed under slow-running distilled water at room temperature for 30 seconds to remove planktonic cells. All comb models were stained for 15 minutes with 1% crystal violet , based on the methods of Pitts et al.  and Stepanovic et al. . Each comb was suspended in eight wells of a new microtiter plate filled with 270 μL ethanol absolute to absorb the crystal violet . The plates were left for 48 hours at room temperature to allow the stained biofilm bacteria to elute with ethanol. All stained biofilm bacteria are soluble in ethanol, however the biofilm on PE could not be eluted entirely in ethanol (maximum time tested was 96 hours), but we standardized the time of elution to 48 hours to guarantee reliable interpretation of the results. After gentle shaking of the microtiter plate, a volume of 150 μL of the ethanol and crystal violet solution was pipetted into a new plate and the optical density (OD) of this solution was measured at a wavelength of 595 nm and is representative for the quantity of biofilm formation . Biofilms of each bacterial species were formed at least in octuplicate, so that one comb was tested with each of the eight prongs suspended in a separate well with nutrient medium and bacterial suspension.
Sterile maggot ES of Instar-3 larvae (BioMonde GmbH) were collected as described previously . Briefly, the maggots were incubated in sterile tubes for 1 hour at 35°C in darkness. Then, ES were removed by pipette, divided in aliquots, and stored at −80°C. One ES pool was collected from at least 1000 maggots, which resulted in approximately 1200 μL ES per hour. The protein concentration was determined using the Pierce Bicinchoninic Acid Protein Assay kit (Pierce Biotechnology, Rockford, IL).
Biofilms were allowed to form on 13 combs of each of the materials for 7 days, two other combs were suspended in nutrient medium without bacteria as negative controls and represented the material-specific background absorbance. BF on two of the 13 combs was measured on Day 7. Two other combs were suspended in a new microtiter plate with medium and incubated another 24 hours to allow additional growth of the biofilm (the 8-day-old biofilms); nine combs were suspended in a logarithmic range of concentrations of ES, diluted in nutrient medium: 0.31, 0.93, 2.78, 8.33, 25, and 75 μg ES per well. All wells were incubated another 24 hours at 37°C and then we quantified the biofilm as described previously. This experiment investigated possible biofilm inhibition and breakdown by ES. Biofilm inhibition (or prevention) by ES was defined as BF that was lower than 8-day-old biofilms which grew further after Day 7. BF that was lower than 7-day-old BF after incubation in ES was defined as biofilm breakdown. Biofilm reduction is any effect of ES that results in less BF.
The first research question was not analyzed statistically because the results were obtained by observation only. For the second and the last research questions, Student’s t test for independent groups was used. The means of the 7-day-old biofilms of the biofilm-forming bacterial species were compared to analyze whether BF depended on the bacterial species. Furthermore, the mean BF with ES (per concentration) and the mean of the 8-day-old biofilm without ES were compared. For the third research question, one-way ANOVA was used and followed by the least significance difference post hoc test. All analyses met the assumption of homogeneity of variances (Levene’s statistic: p > 0.05). To analyze whether the BF depended on the material surface, the mean quantity of a 7-day-old biofilm was compared among the materials for each bacterium. The mean quantities of biofilms formed on Days 5, 7, and 9 for each bacterium were analyzed using repeated-measures ANOVA followed by the Bonferroni correction to investigate whether the BF changed among these 3 days. All analyses met the assumption of sphericity (Mauchly’s test: p > 0.05). All statistical analyses were performed using SPSS® for Windows®, Version 14.0 (SPSS Inc, Chicago, IL).
All tested bacterial species were able to form visible biofilms on PE, SSS, and TI, however biofilms of K. oxytoca, E. faecalis, and E. cloacae could barely be observed, in contrast to the clearly visible biofilms of S. aureus and S. epidermidis. Quantities of biofilm formed by K. oxytoca, E. faecalis, and E. cloacae were insufficient to be measured. Therefore, we focused on BF by S. aureus and S. epidermidis and continued the experiments with these two bacterial species.
Optical density (595 nm) for a 7-day-old biofilm by S. aureus
Surgical stainless steel
Optical density (595 nm) for a 7-day-old biofilm by S. epidermidis
Surgical stainless steel
Biofilm-associated infections related to implants cannot be treated easily and frequently the implanted device must be removed with severe consequences for the patient. Therefore, new approaches for these kinds of infections are needed. Cazander et al. previously reported maggot ES reduced BF of P. aeruginosa . In the current study, we investigated whether other bacterial species, namely, S. aureus, S. epidermidis, K. oxytoca, E. faecalis, and E. cloacae, were able to form biofilms on PE, TI, and SSS, and if so, whether the quantity of BF differed between the bacterial species, whether the quantity of BF depended on the biomaterial surface, and whether the largest amount of BF was formed after 3, 5, 7, or 9 days. Finally, we hypothesized sterile maggot ES could reduce BF on the biomaterials.
Several limitations of the study must be noted. First, we performed only a crystal violet assay as a standard method to measure biofilms, but other methods could be used in vitro  and in vivo . We modified the crystal violet assay to our design with the combs of PE, TI, and SSS, however the assay was based on the commonly used methods of Pitts et al.  and Stepanovic et al. . Second, every experiment was performed with one pool maggot ES, but we did not compare the effectiveness between the various pools. The use of different pools will not likely influence the conclusions of this research, because in an earlier study, the effectiveness of ES was compared and similar results of biofilm reduction occurred using various pools of ES . Our study conditions were adapted as much as possible to those in clinical practice. For example, ES were collected under standard conditions in darkness, had an acidity of pH 8, and were incubated at 35°C. Furthermore, the protein concentration from each collected ES was measured to standardize the various pools. The biomaterials were produced according to specifications for common implants for patients and all bacterial species were isolated from implant infections of patients in our clinic. Therefore, we believe these results were representative and sterile maggot ES reduce not only biofilms of P. aeruginosa  but also existing and mature biofilms of S. aureus and S. epidermidis.
We observed biofilms were formed by all tested bacterial species. These bacterial species were expected to form biofilms, as they all were isolated from device-related infections. The possible biofilm-forming capacities of the five tested species on medical devices have been described by others [4, 10, 20]. BF by K. oxytoca, E. faecalis, and E. cloacae was insufficient to be quantified. Nutrient media other than BHI were used to test BF by these bacteria but did not show BF. The highest amount of biofilm was formed by S. aureus and S. epidermidis, which are the most frequently isolated pathogens from orthopaedic surgical wounds .
BF between S. aureus and S. epidermidis were similar. One study has compared the quantity among these two bacterial species. Hudetz et al.  described equal BF but a stronger adherence to material surfaces by S. epidermidis.
The quantity of BF depended on the biomaterial surface, however published studies show differing results. Hudetz et al.  found that the kind of metal, TI or SSS, plays a minor role in the quantity of BF, whereas MacKintosh et al.  reported biomaterial surface characteristics do influence BF. We found TI had the least amount of biofilm in vitro formed by S. aureus and S. epidermidis. In a previous study, less biofilm was formed by P. aeruginosa on SSS than on TI . Therefore, we conclude that the quantity of BF depends on the biomaterial and on the bacterial specie creating the biofilm.
After 7 days of BF, the highest amount of biofilm was formed. In the first 7 days, the nutrient medium in the microtiter plate was not changed, because the biofilm bacteria were still viable as the biofilm kept growing. New nutrient medium with or without ES was added after 7 days of incubation to maintain the viability of the bacteria. The average time for biofilm maturation is 6 to 8 days [10, 22]. Although the 7-day-old biofilms in this study were not examined by confocal microscopy, their maturation process was more advanced than that of the previously tested 24-hour-old PAO1-biofilms which were decreased by ES . Thus, this research shows more evidence for the therapeutic potential of ES for treatment against biofilm-associated infections which involve mature biofilms.
The biofilm-decreasing capacity of maggot ES seems optimal in low protein concentrations from 0.31 up to 8.33 μg ES per well (3.1 to 83.3 μg ES per mL). In previous studies, protein concentrations of as much as 20 μg ES per well were reported as the most effective concentrations for biofilm reduction [6, 28]. There are several possible explanations for the fact that the influence of ES at higher concentrations than 20 μg ES per well declined . We hypothesize a cofactor necessary to regulate the process was depleted  or there is a nonenzymatic interaction. In future studies concentration ranges less than 0.31 μg ES per well will be tested to examine the lower limit amount of ES causing biofilm reduction.
Previous research suggests maggot ES do not possess direct bactericidal or bacteriostatic activity against planktonic organisms . Therefore, ES are not expected to reduce biofilm by destroying the bacteria in the matrix. However, the influence of ES on biofilm bacteria will be investigated in future studies, by examination of total viable counts of bacteria.
Maggot ES broke down existing biofilms, because all measurements were lower than the control BF after 7 days. However, they also seem to inhibit additional growth of BF as ES reduced BF to less than 100% in the experiments with a greater amount of biofilm on Day 8 compared with Day 7 (Fig. 4A–B). Therefore, potential therapeutic use of ES could be prevention or inhibition of BF, eg, flushing surgical wounds before closing and treatment against existing biofilm-associated infections, especially on orthopaedic medical devices. Further research is necessary to clarify the mechanism(s) of biofilm reduction by maggot ES and identify the substance(s) in ES responsible for these reductions.
We thank Corry Dorresteijn, Janity Pawiroredjo, and Lennaert Renwarin for assistance in the laboratory and Ron Otsen for the photographs.
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