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The goal of this study was to understand the potential interaction between Pseudomonas aeruginosa and Fusobacterium nucleatum within the middle ear.
We examined the microbiota of ear fluid and tympanostomy tubes (TTs) obtained from patients with posttympanostomy tube otorrhea. We also examined biofilms formed by P. aeruginosa and F. nucleatum, singly or together, under aerobic or anaerobic conditions.
While the facultative anaerobe P. aeruginosa dominated the bacterial population within the ear fluid, strict anaerobes, including F. nucleatum, dominated bacterial populations within the TTs. F. nucleatum was able to grow under aerobic conditions only in the presence of P. aeruginosa, whose growth reduced the level of dissolved oxygen within the broth to nearly anoxic condition within 4h after inoculation. The presence of P. aeruginosa allowed F. nucleatum to maintain its growth for 72h within the dual-species biofilm but not within the planktonic growth. Visualization of the biofilms revealed coaggregation of P. aeruginosa and F. nucleatum.
Extrapolation of these results suggests that, within the middle ear fluid, the growth of P. aeruginosa produces the anaerobic conditions required for the growth of F. nucleatum, both within effusion and within biofilms.
Chronic otitis media with effusion (COME) is an inflammatory process in the middle ear accompanied by accumulation of fluid . In the long term, COME may result in hearing loss leading to problems in speech or language development . Surgical intervention for COME includes the insertion of tympanostomy tubes (TTs). However, placement of TTs may lead to complications including posttympanostomy tube otorrhea (PTTO) and TT occlusion . While many bacterial pathogens commonly associated with PTTO are facultative anaerobes, including Pseudomonas aeruginosa, Staphylococcus aureus, and Haemophilus influenzae , recent studies suggest the presence of anaerobic pathogens such as Fusobacterium, Porphyromonas, and Peptostreptococcus as well [5–7]. On the surface of TTs, otopathogens form biofilms within which the bacteria are surrounded by an exopolysaccharide matrix (EPS) that protects them from the effect of antibiotics and host immune responses . Bacterial cells within the biofilm vary in their metabolic activity as well as in their exposure to ambient oxygen. Bacteria within the exterior surface of the biofilm have access to oxygen and nutrients, while, within the biofilm interior, the conditions are anoxic or anaerobic .
P. aeruginosa, a Gram-negative opportunistic pathogen that produces numerous virulence factors, causes infections of many body sites, including the respiratory tract and the middle ear [10, 11]. Fusobacterium, a strict anaerobic Gram-negative bacillus, constitutes part of the normal flora of the oropharynx . Fusobacteria also produce virulence factors including lipopolysaccharide, leukocidins, neutrophil-cytotoxic factors, lipases, hemolysins, hemagglutinins, and beta-lactamase [12, 13]. Fusobacteria cause local as well as invasive infections that manifest as head and neck infections, upper respiratory tract infections, or local septic thrombophlebitis with or without bacteremia [12–15].
Metagenomic techniques, including 16S rRNA-based pyrosequencing, characterize all bacteria, fungi, and viruses, at an infection site. Using 16S rRNA-based pyrosequencing, Liu et al.  characterized microbiota in middle ear, adenoid, and tonsil specimens obtained from pediatric patients. Results revealed the presence of diverse bacterial communities. Pseudomonadaceae dominated the middle ear microbiota while Streptococcaceae dominated tonsil microbiota. The adenoid microbiota was dominated by multiple bacteria including Pseudomonadaceae, Streptococcaceae, Fusobacteriaceae, and Pasteurellaceae .
It has been postulated that, during acute otitis media (AOM), the growth of anaerobic bacteria in the nasopharynx becomes possible due to changes in normal flora and the environment . Könönen et al.  detected many anaerobes within nasopharyngeal aspirates from children with AOM, with F. nucleatum and Prevotella melaninogenica predominating. Survival time of strict anaerobic bacteria was very short when grown under aerated conditions in the absence of aerobic and/or facultative anaerobic bacteria . In a previous study of the survival of four strict anaerobic species in aerated cultures, Bradshaw et al.  showed that the survival time for F. nucleatum and Veillonella dispar was about five min while that of Porphyromonas gingivalis and Prevotella nigrescens was less than four min. These organisms did not produce biofilms when grown alone aerobically; however, in the presence of aerobic/facultative anaerobic bacteria, these strict anaerobic species survived and grew in both planktonic and biofilm forms .
In this study, we investigated whether the growth of the facultative anaerobe P. aeruginosa would influence the survival and growth of F. nucleatum under aerobic conditions, either planktonically, in a mixed biofilm, or both.
The patient was initially examined by an otolaryngologist using otoscopy to confirm diagnosis of retained tube with or without contamination. Informed consent was obtained from the parents under guidelines of this study, which was reviewed and approved by the Texas Tech University Health Sciences Center Institutional Review Board. While the study patient was undergoing standard of care treatment for chronic PTTO, ear fluid was obtained by aspiration through the tympanostomy tubes. Mucopurulent otorrhea aspirated from the external auditory canal of each ear was placed into separate sterile specimen cups. The TTs were then carefully removed using alligator forceps and placed into separate sterile specimen cups. All samples were transported to the research laboratory within 1-2h of collection. Upon receipt in the laboratory, samples were refrigerated at 4°C for no longer than 24h prior to DNA isolation.
Each TT or the mucopurulent aspirate was suspended in 500μL RLT buffer (Qiagen, Valencia, CA) in the presence of β-mercaptoethanol. For complete bacterial lysis, a sterile 5mm steel bead (Qiagen) and 500μL sterile 0.1mm glass beads (Scientific Industries, Inc., NY) were added. The samples were briefly centrifuged, the supernatant fraction was isolated, and 200μL of 100% ethanol was added to a 350-μL aliquot of the supernatant. This mixture was then added to a DNA spin column and the DNA was recovered using QIAamp DNA Mini Kit (Qiagen) according to the manufacturer's recommendation. The DNA was eluted from the column with 30μL water and quantified using a NanoDrop spectrophotometer (Nyxor Biotech, Paris).
To amplify approximately 500bp of the 16S rRNA genes, we used the 16S universal Eubacterial primers 28F (5′-GAGTTTGATCNTGGCTCAG-3′) and 519R (5′-GTNTTACNGCGGCKGCTG-3′) . PCR was conducted using HotStarTaq Plus Master Mix Kit (Qiagen) under the following conditions: 95°C for 5min followed by 35 cycles of 95°C for 30s, 54°C for 40s, and 72°C for 1min, with a final elongation step at 72°C for 10min. Diffinity Rapid Tip (Diffinity Genomics, West Henrietta, NY) was used to clean the PCR products. PCR products were pooled and small fragments were removed by using Agencourt Ampure Beads (Beckman Coulter, CA).
Bacterial tag-encoded FLX-Titanium amplicon pyrosequencing was done at the Research and Testing Laboratories, Lubbock, TX, as previously described (Roche, Nutley, NJ) . DNA fragment sizes and concentration were accurately measured using DNA chips under a Bio-Rad Experion Automated Electrophoresis Station (Bio-Rad Laboratories, CA) and a GloMax-Multi Jr Detection System (Promega, Madison, WI). In a sample of double-stranded DNA, 7.2 million molecules, with an average size of 550bp, were combined with 7.2 million DNA capture beads and then amplified by emulsion PCR using the same primer set with added linker A and 8-bp barcode sequences at the 5′-end of 28F (primer 28F-A 5′-CCATCTCATCCCTGCGTGTCTCCGACTCAG-barcode-GAGTTTGATCNTGGCTCAG-3′) and biotin and the linker B sequence added to the 5′-end of 519R (primer 519R-B 5′-Biotin-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-GTNTTACNGCGGCKGCTG-3′) . Following bead recovery and enrichment, the bead-attached DNAs were denatured with NaOH and annealed with sequencing primers (Roche, Indianapolis, IN). Using the Genome Sequencer FLX System (Roche), a four-region 454 sequencing run was performed on a GS PicoTiterPlate. Forty tags were used on each quarter region of the plate.
The study was conducted using the prototrophic P. aeruginosa strain PAO1 that was originally isolated from an infected wound and the F. nucleatum strain VPI 4355 isolated from a cervicofacial lesion. The VPI 4355 strain was purchased from the American Type Culture Collection (Manassas, VA). For general growth, the strains were grown aerobically (18.6% ambient oxygen) or anaerobically (0% oxygen) at 37°C for up to 96h in 37°C in brain heart infusion (BHI) broth or on BHI agar plates (CRITERION; Hardy Diagnostics, Santa Maria, CA). Biofilms were developed on 6-mm cellulose disks (Becton Dickinson and Company, Sparks, MD) in 15-mL culture tubes containing 5mL of BHI broth. Previous studies suggested that the facultative bacteria initially grow in the middle ear and provide support for the growth of anaerobic bacteria, which arrive later as the oxygen level is reduced . Therefore, to mimic in vivo conditions, strains were inoculated individually or together (coculture) at 106 colony forming units (CFU) for PAO1 and 102CFU for VPI 4355.
At specific intervals depending on the experiment, the medium (planktonic culture) was removed from the tubes and serial 10-fold dilutions of the planktonic cultures were prepared. Ten μL aliquots of each dilution were spotted on BHI agar plates and the plates were incubated at 37°C for 14–16h and the CFU were counted.
The disks were removed from the culture tubes, rinsed with 1x phosphate buffered saline (PBS) to remove any planktonic cells, and transferred to 1.5mL microcentrifuge tubes containing 1mL of PBS. After vigorous vortexing (three times for 2-3min each time) to mechanically disrupt the biofilms and detach the bacteria from the disks, the cell suspension was serially diluted 10-fold in PBS.
The CFU/mL (planktonic cultures) or CFU/disk (biofilms) were determined using the following formula: CFU counted × dilution factor × 100.
Culture tubes containing 5mL of BHI broth and a cellulose disk were inoculated with ~106CFU of P. aeruginosa and 102CFU of F. nucleatum and incubated aerobically at 37°C for 8, 24, 48, or 72h. The disks were then removed, and the biofilms were analyzed by determining the CFU/disk as described above. The CFU/mL of P. aeruginosa and/or F. nucleatum planktonic growth was also determined.
Tubes containing BHI broth and a cellulose disk were inoculated with P. aeruginosa and F. nucleatum as described above and incubated aerobically at 37°C for 96h. The disks were then transferred into fresh BHI broth and the incubation continued for an additional 72h under the same conditions. Cellulose disks were then removed and the biofilms were analyzed as described above.
The P. aeruginosa/F. nucleatum biofilms were developed as described above. After 24h of incubation at 37°C, the disks were then divided into two sets. In one set, the disks were placed on the top of BHI agar plates and the plates were incubated aerobically for 48h at 37°C. In the other set, the disks were transferred to a fresh tube of BHI broth and incubated aerobically for 48h at 37°C. The disks were then removed from either the agar plate or the tube and the biofilms were analyzed.
Cultures of P. aeruginosa, F. nucleatum, or both were prepared in 50-mL conical tubes containing 15mL of BHI broth as described above. The tubes were incubated aerobically at 37°C and the level of DO2 (mg/L) was measured at 1, 2, 4, 8, and 24h using a Heavy Duty Dissolved Oxygen Meter (Extech Instruments, Nashua, NH).
Single- or dual-species biofilms were developed as described above and the disks were stained using FISH as previously described with slight modifications . Briefly, the disks were placed in a hybridization buffer (5M NaCl [18% v/v]/1M Tris/HCl, pH 7.2 [2% v/v]/10% SDS [0.1%]/formamide [20% v/v] in distilled H2O). Fluorescent labeled oligonucleotide probes were then added at a concentration of 50ng/μL. Hybridization was conducted in microcentrifuge tubes at 46°C for 5h. Following hybridization, disks were incubated twice for 15min at 46°C in wash buffer (5M NaCl [18% v/v]/1M Tris/HCl, pH 7.2 [2% v/v]/10% SDS [0.1%]). After washing, the disks were examined by confocal laser scanning microscopy (CLSM) as previously described . Oligonucleotide probes (P. aeruginosa, 5′-/5Cy3/GCTGGCCTAGCCTCCC-3′; F. nucleatum, 5′-/5Cy5/CGCAATACAGAGTTGAGCCCTGC-3′) used in this study were synthesized commercially (Integrated DNA Technologies; Coralville, IA). Excitation was carried out at 546nm for Cy3 and 633nm for Cy5. Fluorescence emission of the probes was measured at 493–538nm (Cy3) and 550–592nm (Cy5).
Pyrosequencing analysis revealed that the predominant genus present in the right and left ear fluid samples was the facultative anaerobe P. aeruginosa (62% and 67%, resp.) (Figure 1). However, the second most predominate genera were strict anaerobes; in the right ear fluid, genus Fusobacterium constituted 20% and genus Peptostreptococcus constituted 10% of the flora (Figure 1(a)), while, in the left ear fluid, genus Peptostreptococcus constituted 27% of the flora and genus Parvimonas constituted approximately 3% (Figure 1(b)). Similar facultatively anaerobic bacterial species were isolated from concomitant microbiology cultures of the ear fluid samples, while the anaerobic species found by pyrosequencing were not isolated (Table 1). Cultures were done using the four-quadrant semiquantitative method.
Genera identified from biofilms removed from the TT were similar but found in different proportions. On the TT from the right ear, genus Fusobacterium was dominant (86%) followed by the genera Pseudomonas and Streptococcus at 3% each (Figure 2(a)). Peptostreptococcus, at 42%, was the dominant genus found on the TT from the left ear followed by the genera Streptococcus (30%), Pseudomonas (11%), and Eikenella (11%) (Figure 2(b)). Additional genera were present in each specimen at less than 2.5% each. The relative percentages of the species discovered by pyrosequencing, which vary from sample to sample, are listed in Table 2.
Previous studies showed that, under aerobic conditions, the growth of aerobic or facultatively anaerobic bacteria within a biofilm reduces the level of oxygen present thereby facilitating the growth of strictly anaerobic bacteria . In patients with PTTO or TT occlusion, pathogenic bacteria within the middle ear may be found in planktonic form within the ear fluid and in biofilms on the mucosal surfaces of the middle ear or on the TT . Our recent pyrosequencing analysis revealed that, within either the left or right ear of the same patient, the ratio of aerobic to anaerobic bacteria within the ear fluid was similar (2.3:1 and 2:1, resp.) but varied considerably from that on the TT (1.1:1 and 1:13.6, resp.) (Figures (Figures11 and and2).2). Additionally, genetic signatures of P. aeruginosa and F. nucleatum were found in several different patients. Therefore, we examined the potential influence of the facultative bacterium P. aeruginosa on the strict anaerobe F. nucleatum within this unique environment. We inoculated culture tubes containing BHI broth with the P. aeruginosa strain PAO1 and the F. nucleatum strain VPI 4355 individually or together (coculture) and incubated the tubes aerobically or anaerobically at 37°C for 24h. Whether incubated individually or in coculture, PAO1 grew in both environments, although its growth was somewhat less robust when grown anaerobically (Figure 3). As expected, we recovered viable VPI 4355 only from the culture incubated anaerobically when the strain was inoculated individually (Figure 3). However, after 24h of incubation, the initial inoculum of VPI 4355 in the aerobically incubated coculture had increased by 5 logs and by 6 logs in the anaerobic coculture (Figure 3).
We then cocultured PAO1 and VPI 4355 aerobically for 72h and examined for the presence of the bacteria within biofilms formed on cellulose disks and within the planktonic cultures. Over the course of 72h, PAO1 achieved stationary phase growth within the biofilm (Figure 4(a)). The presence of PAO1 also allowed VPI 4355 to achieve sustained stationary phase growth within the biofilm (Figure 4(a)). Similar to its growth in biofilm, PAO1 achieved stationary phase growth in the planktonic coculture (Figure 4(b)). However, while the CFU of VPI 4355 increased at 24h, the numbers of CFU declined over the rest of the time course, with a significant drop in CFU between 48 and 72h (Figure 4(b)). These results suggest that, in an aerobically incubated coculture, P. aeruginosa supports the growth of F. nucleatum in both the planktonic and biofilm settings, although the biofilm setting appears to support F. nucleatum survival and growth better than planktonic culture (Figure 4).
P. aeruginosa may support the growth of F. nucleatum by severely restricting the amount of dissolved oxygen (DO2) within the medium. To examine this possibility, we inoculated BHI broth with PAO1, VPI 4355, or both, incubated the tubes at 37°C aerobically, and measured the level of DO2 at 24h after inoculation. As a control, we included uninoculated BHI broth. As expected, the level of DO2 in the control culture was essentially the same after 24h of incubation (Figure 5). Similarly, the level of DO2 in the individual VPI 4355 culture was comparable to that of the control culture (Figure 5). However, in cultures inoculated with PAO1 alone or in coculture with VPI 4355 the level of DO2 was significantly reduced (Figure 5).
To determine the time at which the level of DO2 in P. aeruginosa inoculated cultures falls, we compared the level of DO2 in uninoculated BHI broth with the level of DO2 in BHI broth inoculated with PAO1. The level of DO2 dropped precipitously and significantly by 4h after inoculation, and by 8h the level of DO2 was essentially zero or anaerobic, an effect which lasted through 24h (Figure 6). These results suggest that at early stages of growth P. aeruginosa reduces the level of DO2 sufficiently to sustain the growth of F. nucleatum.
The above results showed that when the environment surrounding the biofilms is anaerobic, F. nucleatum survives and grows within a dual-species biofilm. However, it is not known if F. nucleatum would survive upon the exposure of the established dual-species biofilm to aerobic conditions, that is, removal from the anoxic conditions within the culture tube. Unlike dental plaque, biofilms that develop on TTs may not be as dense and fluctuation in the oxygen level of the surrounding environment may influence the survival of F. nucleatum within the biofilm. To examine these possibilities, we developed two sets of PAO1/VPI 4355 biofilms on cellulose disks in BHI broth as described in Materials and Methods. After 24h of aerobic incubation (long enough for the broth to become anaerobic), we removed the disks and placed one set on the surface of BHI agar plates and the other set into fresh tubes of BHI broth. Plates and tubes were then incubated aerobically at 37°C for up to 48h.
F. nucleatum within the biofilm transferred to the BHI plate maintained their growth for 8h after transfer, increasing by ~1 log; but, by 24h after transfer, the CFU/disk of F. nucleatum had declined sharply, and, by 48h after transfer, no F. nucleatum was recovered (Figure 7(a)). P. aeruginosa, however, continued to grow throughout the 48h after transfer (Figure 7(a)). These results suggest that the growth of P. aeruginosa within the dual-species biofilm provided F. nucleatum with sufficient protection from ambient oxygen to maintain its growth for a short time, but P. aeruginosa could not protect against continued exposure to oxygen. The presence of P. aeruginosa within the biofilm is essential for the survival of F. nucleatum. When we developed a single F. nucleatum biofilm in BHI broth anaerobically and transferred the disk to BHI agar that was incubated aerobically, we recovered no CFU as soon as 2h after placement (data not shown).
In contrast, CFU of both P. aeruginosa and F. nucleatum within the biofilm transferred to BHI broth decreased by ~1 log in the first 8h (Figure 7(b)). While the CFU of PAO1 remained stable throughout the next 48h, the CFU of VPI 4355 remained stable for 24h and then declined again, dropping to ~104CFU/disk (Figure 7(b)). These results suggest that the presence of P. aeruginosa in the biofilm provided some protection from DO2 in the broth. However, it is possible that the limited amount of P. aeruginosa released from the biofilm was not sufficient to reduce the DO2 within the broth in time to maintain stable growth of F. nucleatum. These results suggest that planktonic growth of Pseudomonas aeruginosa around a dual-species biofilm is necessary to support the growth of Fusobacterium nucleatum within that biofilm.
In mixed-species biofilms, the spatial organization of the different species generally occurs in one of three forms: single-species microcolonies, coaggregates, or layered structures . In the single-species microcolonies, each species forms separate microcolonies while, in the coaggregates, cells of both species intermix . In the layered structure, the species build up in layers, often in a specific order . We examined the organization of the PAO1/VPI 4355 biofilm that was aerobically developed in BHI broth by FISH experiments using a specifically labeled fluorescent probe for each bacterium (Materials and Methods). PAO1 and VPI 4355 developed single-species biofilms under aerobic and anaerobic conditions, respectively (Figure 8). Under aerobic conditions, PAO1/VPI 4355 produced a coaggregated mixed-species biofilm (Figure 8).
As shown in Figure 1 and Table 1, the main microbial pathogen within the ear fluid, P. aeruginosa, was identified by both pyrosequencing and the standard laboratory culture. However, in addition to P. aeruginosa, pyrosequencing identified other microorganisms including the strict anaerobes, Peptostreptococcus, and Fusobacterium. Peptostreptococcus constituted 27% of the identified genera within the right ear fluid while Peptostreptococcus and Fusobacterium constituted 10% and 20% of the identified genera within the left ear fluid (Figure 1). The high percentage of these anaerobes suggests that they contribute to the PTTO. Thus, it is possible, as has been demonstrated by their presence affecting the healing process of chronic wounds, that the presence of these anaerobes prevents resolution of PTTO. Pyrosequencing may guide clinicians in facilitating healing of PTTO by defining the mixed populations of microorganisms frequently present in these infections so that appropriate antimicrobial therapy can be instituted. The other intriguing point that pyrosequencing analysis showed is the difference in the composition of the planktonic bacteria within each ear fluid and the bacteria within the biofilms on the TT.
Within a biofilm, the bacterial community is surrounded by an EPS matrix. In a mixed-species biofilm, some pathogens within the biofilm, such as P. aeruginosa, may primarily contribute to the EPS, which protects all bacteria within the biofilm, while others, such as F. nucleatum, may produce beta-lactamase, protecting all the bacteria within the biofilm from beta-lactam antibiotics [8, 12]. Additionally, certain species within the biofilm may provide the environmental conditions necessary for the survival and growth of other bacterial species. For example, even though the oral cavity is fully aerated, dental plaque (a biofilm) consists of both aerobic and anaerobic bacteria . Studies have shown that F. nucleatum serves as a bridge between noncoaggregating early (often aerobes) and late (often anaerobes) colonizers because it is capable of coaggregating with all species of oral bacteria [25, 26]. Perhaps, in this aspect, F. nucleatum serves the same role in biofilm formation by otopathogens on TT or on membranes of the middle ear. P. aeruginosa and F. nucleatum were coaggregated within the PAO1/VPI 4355 biofilm (Figure 8). While we used only two species, our pyrosequencing analysis suggested the presence of many more microbes, both aerobes and anaerobes (data not shown). Similar to the protection from ambient oxygen provided to F. nucleatum by the underlying Streptococcus species within dental plaque, P. aeruginosa provided such protection within our coculture model (Figures (Figures33 and and4).4). We showed that this protection specifically occurs by the reduction of dissolved oxygen with the fluid culture (Figure 5).
Within an infected site, bacteria interact with each other differently. Some bacteria may support each other's growth by supplying nutritional needs, as has been shown for the oral microflora within the dental plaque . In the present study, the interaction between P. aeruginosa and F. nucleatum is characterized by P. aeruginosa provision of growth support to F. nucleatum through reduction of the dissolved oxygen content of the broth medium (Figures (Figures55 and and6).6). This growth support occurs during planktonic growth but is more evident within the biofilm (Figure 4). Despite the presence of a constant amount of P. aeruginosa within the broth, the CFU of planktonic F. nucleatum had dropped significantly at 72h (Figure 4(b)). At this time we do not know the mechanism that led to the reduction of planktonic F. nucleatum. The phenomenon is not likely to be caused by the exhaustion of nutrients as P. aeruginosa maintained stationary phase growth over the same time period (Figure 4(b)).
In contrast, competitive interactions among bacteria within biofilms also occurs . One species may outcompete others because it can better utilize a given energy source . Other bacteria compete with each other over the limited nutrients by surface blanketing (occupying all the available adhesion sites) or by secreting compounds that actively eliminate other species . Not only does P. aeruginosa engage in surface blanketing, it produces extracellular proteins, such as pyocins, that target other competing Gram-negative bacteria including P. aeruginosa strains that are sensitive to that specific pyocin [29, 30]. At this time, we cannot exclude the possibility that P. aeruginosa produces potential extracellular factors that interfere with the growth of F. nucleatum. Using synthetic mucus medium, we have previously shown that P. aeruginosa eliminates S. aureus from biofilm-like structures within 56h . These factors may include pyocin, potential quinolone molecules, and other factors. We plan to examine this possibility by aerobically incubating dual BHI cultures of F. nucleatum and a P. aeruginosa mutant defective in the production of specific factors (e.g., pyocin, quorum sensing molecules) for 72h and determining if the growth of F. nucleatum is maintained.
In the oropharyngeal cavity, anaerobic bacteria outnumber aerobic bacteria 10–100:1 [32, 33]. Environmental and/or ecological changes within the nasopharynx of young children have been reported to favor anaerobic growth . It has been hypothesized that anaerobic bacteria from the oral cavity can travel retrograde up the Eustachian tube into the middle ear cavity, especially when chronic inflammation is present . Chronic suppurative otitis media involves perforation of the tympanic membrane, while the treatment for chronic serous otitis media often involves myringotomy and insertion of TT [7, 12, 15]. Based on our findings, we suggest the following model for the possible interaction between P. aeruginosa and F. nucleatum and the influence of the environment on their interaction within the middle ear (Figure 9). In the normal ear, the tympanic membrane allows diffusion of oxygen into the middle ear and acts as a barrier to entrance by P. aeruginosa, while the noninflamed Eustachian tube prevents entry of oropharyngeal bacteria such as F. nucleatum (Figure 9(a)). In the case of a child who suffers a perforated tympanic membrane or has had TT inserted to treat chronic serous otitis media, P. aeruginosa gains access to the middle ear (Figure 7(b)). As P. aeruginosa grows within the fluid, it significantly reduces the level of the dissolved oxygen and converts the conditions within the fluid into anaerobic conditions (Figure 9(a)). F. nucleatum migrates from the oral cavity up the inflamed Eustachian tube into the middle ear cavity where it also becomes established (Figure 9(c)). The two bacterial species live together within the middle ear fluid and coaggregate to form biofilms on the TT or on the mucosal surfaces.
The authors would like to thank Moamen El-Masry for his help in the data analysis and Joanna E. Swickard for critical reading of the manuscript. This study was supported in part by the Department of Surgery at Texas Tech University Health Sciences Center, Lubbock, TX.
The authors declare that there are no conflicts of interest regarding the publication of this article.