Infection is an important source of mortality for avian embryos but parental behaviors and eggs themselves can provide a network of antimicrobial defenses. Mound builders (Aves: Megapodiidae) are unique among birds in that they produce heat for developing embryos not by sitting on eggs but by burying them in carefully tended mounds of soil and microbially decomposing vegetation. The low infection rate of eggs of one species in particular, the Australian brush-turkey (Alectura lathami), suggests that they possess strong defensive mechanisms. To identify some of these mechanisms, we first quantified antimicrobial albumen proteins and characterized eggshell structure, finding that albumen was not unusually antimicrobial, but that eggshell cuticle was composed of nanometer-sized calcite spheres. Experimental tests revealed that these modified eggshells were significantly more hydrophobic and better at preventing bacterial attachment and penetration into the egg contents than chicken eggs. Our results suggest that these mechanisms may contribute to the antimicrobial defense system of these eggs, and may provide inspiration for new biomimetic anti-fouling surfaces.
Eggs of all organisms are at risk of infection by microbes, which are ubiquitous and colonize any surface that has nutrients, heat and water available for growth (Singleton and Harper, 1998). Eggs contact microbes through the substrate on which they are laid, through materials in the nest (Mennerat et al., 2009) or directly from the parents' integument (Bruce and Drysdale, 1994). Bird parents typically maintain their eggs at a stable temperature and humidity during incubation, as these conditions are essential for normal embryonic development (Deeming, 2002). However, most microbes grow optimally under similar conditions (Madigan and Martinko, 2005); thus, avian nests during incubation provide an ideal environment for bacterial proliferation.
Diverse sets of pathogenic and non-pathogenic microorganisms have been identified on feathers and nests (Shawkey et al., 2005; Shawkey et al., 2006; Shawkey et al., 2009), including some of biomedical importance like Staphylococcus, Bacillus, Salmonella, Klebsiella, Enterococcus and Enterobacter (Literák et al., 1995; Singleton and Harper, 1998; Mills et al., 1999; Berger et al., 2003; Peralta-Sánchez et al., 2012). Pathogens pose a threat to egg integrity, as infection decreases embryonic viability (Cook et al., 2005a; Cook et al., 2005b), and are considered one of the main causes of embryonic death (Davies and Baggott, 1989; Pinowski et al., 1994; Deeming, 1995; D'Alba et al., 2011).
Because they impose severe costs and decrease their host fitness, microbes have selected for a diverse set of parental defense mechanisms. Two primary components constitute typical eggs' natural defenses against microbes: the eggshell, a physical barrier, and a system of chemicals that includes endogenous antibacterial proteins in the egg white and eggshell membranes (Board and Tranter, 1995; Hincke et al., 2008). Critically, incubation itself also strongly decreases bacterial growth on eggs (Cook et al., 2003; Cook et al., 2005b; Shawkey et al., 2009), either through activation of antimicrobial peptides in the shell (Wellman-Labadie et al., 2008) or through active drying of the eggshells during incubation (D'Alba et al., 2010a).
Although the eggshell presents a considerable barrier to microbial passage, it is permeated by thousands of microscopic pores that allow gas and water exchange (Balkan et al., 2006), in turn providing a pathway for bacterial contamination of egg contents (Board and Tranter, 1995). Thus, infections can occur through changes in the incubation environment (Cook et al., 2003). For example, increases in nest humidity and/or sudden fluctuations in temperature can enhance the risk of contamination through an increase in total bacterial load (Messens et al., 2005; De Reu et al., 2006).
Eggs of the family Megapodiidae potentially face one of the highest risks of egg infection among birds, because their eggs are not parentally incubated (Booth and Jones, 2002) and instead are laid in large mounds where the heat for incubation is produced by microbial decomposition of organic matter (Jones, 1988a). Despite incubating their eggs in these conditions, only about 9% of Australian brush-turkey (Alectura lathami, Gray) eggs become infected (Jones, 1988b). This remarkably low infection rate suggests either that the majority of bacteria in these mounds are non-pathogenic or that these eggs have a potent antimicrobial defense that is, to our knowledge, unstudied.
The proportions of pathogenic and non-pathogenic bacteria in megapode mounds have not yet been investigated, but known egg pathogens like Pseudomonas, Enterobacter, Klebsiella and Serratia are generally abundant in compost and soil (Beffa et al., 1996; Boulter et al., 2002; Santamaría and Toranzos, 2003). Evidence of defense mechanisms has been found previously (Board et al., 1982), where the presence of an unusual outer layer of calcium phosphate spheres outlining the cuticle in eggs of the megapode species Malleefowl (Leipoa ocellata) was briefly noted. The authors speculated that this layer was an adaptation to avoid microbial colonization of the eggs, but this hypothesis has never been tested and no other attempt has been made to elucidate the antimicrobial defense system in megapodes.
Here, we describe the structure of brush-turkey eggshells and test the hypothesis that their topography is responsible for decreasing bacterial attachment and/or penetration. Additionally, we test whether these eggs have high concentrations of antimicrobial proteins in their albumen as additional protection against infection.
Physical and chemical properties of the eggs
Brush-turkey eggshells are 1.5 times thinner than chicken eggshells (t=39.2, d.f.=18, P<0.001; Fig. 1A,B). Moreover, they show a distinctive morphology and arrangement of nanospheres on the cuticle. The spheres are on average 340±11.24 nm in diameter and form a layer 16.7±0.73 μm thick (Fig. 1C,D). The spheres often plug the shell pores (Fig. 1E). Energy-dispersive X-ray spectroscopy (EDX) analysis detected a peak concentration of phosphorus in the spheres layer (Fig. 1F).
We recorded a pH of 9.4 and 9.2, respectively, in chicken and brush-turkey albumen. Lysozyme concentration in brush-turkey eggs (2.15±0.17 mg ml−1) did not differ from that in chicken eggs (2.58±0.31 mg ml−1) (t=1.23, P=0.23).
Brush-turkey eggs approached superhydrophobicity, with a contact angle nearly twice that of chicken eggs (135.28±2.65 versus 66.55±3.20 deg, t=16.51, P<0.001; Fig. 2A). Hysteresis of brush-turkey shells was on average 27.49 deg and did not differ from hysteresis of chicken shells (t=0.38, P=0.73; Fig. 2B).
A significantly larger number of Pseudomonas aeruginosa and Escherichia coli cells were attached to chicken shells than to brush-turkey shells (Table 1; Fig. 3). The total count and density of Staphylococcus aureus cells on chicken and brush-turkey shells (Table 1; Fig. 3) did not significantly differ.
Bacteria penetrated the eggshell of chickens after only 2 days, and the peak of penetration occurred between days 4 and 6 of the 12 day assay. Overall, chicken eggs had higher penetration rates than brush-turkey eggs (P. aeruginosa, χ2=22.03, d.f.=1, P<0.01; E. coli, χ2=5.38, d.f.=1, P=0.02; Fig. 4). The risk of penetration increased with time and was 88% and 68% higher (P. aeruginosa and E. coli, respectively) for chicken eggs than for brush-turkey eggs (P. aeruginosa, Wald=10.57, P=0.01: E.coli, Wald=3.98, P=0.04; Fig. 4.). There was no effect of trial number on penetration rate by the two bacterial strains (P>0.05).
No eggshells were penetrated by S. aureus in any of the two trials.
Australian brush-turkeys incubate their eggs through microbial decomposition of organic material, leading to extremely high bacterial abundance near their eggs. Here we showed that the surface topography of brush-turkey eggs, determined by the presence of nanoscale spheres composed of calcium phosphate, renders the eggs hydrophobic, decreases bacterial attachment and is most likely the major component preventing trans-shell penetration.
Elemental analysis showed high concentrations of phosphorus on the layer of spheres of the brush-turkey cuticle, which likely corresponds to the presence of calcium phosphate (Board, 1982). A cuticle composed of calcium phosphate is rare compared with the more common calcium carbonate (vaterite) or the most ubiquitous organic cuticle (glycoprotein), and has only been found in eggshell cuticles of greater flamingos and guinea fowl (Tullett et al., 1976), grebes (Board et al., 1984) and Mallee fowl (Board et al., 1982). Unlike glycoproteins and vaterite, calcium phosphate does not dissolve in water and thus would not be easily destroyed by exposure to rain or mud in the nest. More importantly, unlike organic cuticles, an inorganic composition could resist digestion by bacteria or fungi, which are common under conditions of high humidity (Board et al., 1979) and likely prevalent in megapode mounds.
The surface of brush-turkey eggs approaches superhydrophobicity, similar to that which imparts self-cleaning properties in lotus-leaves, on which water forms droplets and rolls off the surface (Feng et al., 2002). However, unlike lotus leaves, brush-turkey eggs have high hysteresis, meaning that the water droplets remain pinned to the surface and thus do not roll off. Similar effects have recently been found in rose petals [the ‘petal effect’ (Feng et al., 2008)] and other plants (Chang et al., 2009), which the authors attribute to trapping of the water droplet (‘Cassie impregnating wetting state’) by micropapillae on the surface or hydrophobic chemicals (Chang et al., 2009). The petal effect on brush-turkey shells may trap condensed water at discrete points, preventing it from spreading uniformly over the surface and thereby inhibiting biofilm formation (Shawkey et al., 2009). Additionally, the geometry of a droplet ensures that little water is in direct contact with the shell surface, effectively isolating bacteria above it. Chicken eggshells showed high hysteresis in addition to hydrophilicity, meaning that water droplets spread to larger extents and remain adhered to the surface. Thus, bacterial mobility and associated opportunity to encounter pores for penetration into the eggshell is more limited in brush-turkey than in chicken eggshells.
This modified surface also appears to limit bacterial adhesion, as Gram-negative bacteria P. aeruginosa and E. coli attached with greater frequency to chicken shells than to brush-turkey shells. As with hydrophobicity, both eggshell topography and eggshell chemistry could contribute to this effect. Several studies have shown that the hydrophobicity and topography of a surface, e.g. an increased roughness (Arnold and Bailey, 2000) or nanostructural arrangements (Schumacher et al., 2007), decrease bacterial attachment in man-made and natural materials (Busscher and Weerkamp, 1987; Margel et al., 1993; Prime and Whitesides, 1993; Taylor et al., 1997; Wiencek and Fletcher, 1997). Thus, the eggshell topography of brush-turkeys may represent a way to prevent bacterial growth and potentially microbial infection without the use of chemicals, providing a new method for prevention of fouling on surfaces. Future work will determine the exact mechanism of attachment restriction by the spheres in megapode eggs through both characterization and biomimicry.
By contrast, S. aureus showed very low attachment to both kinds of eggshells. Staphylococci are known for their preferential ability to attach to certain surfaces like plastic and human tissues where proteins such as fibrinogen or fibronectin are found (Otto, 2008). Differences in bacterial attaching capabilities depend on several factors, including the presence of filamentous pili on the surface of the cell that are directly involved in the initial attachment to abiotic surfaces. Pili are present in P. aeruginosa and E.coli but not in S. aureus (Proft and Baker, 2009), potentially limiting their adhesive ability.
Finally, and most importantly, in all cases P. aeruginosa and E. coli (highly mobile infectious strains) penetrate chicken eggs more frequently and rapidly than brush-turkey eggs. Although gram-positive bacteria are the dominant flora of eggshells (Board, 1995), gram-negative bacteria are the most common contaminants of egg contents (Clay and Board, 1991; Board, 1995). Thus, the defense system of brush-turkey eggs, largely based on a modified eggshell surface, may help to prevent what would otherwise be a common cause of embryo mortality.
By contrast, lysozyme concentrations did not differ from those found in chicken eggs, suggesting that the brush-turkey albumen might have a similar or at least not more potent bactericidal capacity. A few studies have quantified antimicrobial proteins in eggs of birds in the wild and have reported a wide range of lysozyme concentrations, e.g. 0.65±0.76 μg ml−1 in blue tits (D'Alba et al., 2010b) compared with 5.91 mg ml−1 in the green-rumped parrotlet (Forpus passerinus) (Shawkey et al., 2008). It has been hypothesized that concentration of antimicrobial proteins in the eggs should increase with the risk of egg infection (Shawkey et al., 2008; D'Alba et al., 2010b). However, only one study so far has identified a pattern consistent with this hypothesis, i.e. the presence of more potent antimicrobial proteins in the eggshells of cavity-nesting versus open cup-nesting Anseriform species (Wellman-Labadie et al., 2008). Deposition of antimicrobial proteins in eggs is not a costly investment for mothers (Shawkey et al., 2008); however, it is possible that an increase in their content conflicts with the existence of different developmental demands of the embryos, including optimal water uptake, gas exchange, mobilization of nutrients within the egg and structural support to growing embryos (Board and Fuller, 1974). Inhibiting growth of pathogenic bacteria on the outer surface of the egg might be a more efficient way to prevent infection without compromising the properties of albumen.
Eggshell cuticles containing vaterite nanospheres have been noted (but not studied) on eggshells of six species including the double-crested cormorant (Phalacrocorax auritus), emperor penguin (Aptenodytes forsteri), great frigatebird (Fregata minor), hamerkop (Scopus umbreta) and smooth-billed ani (Crotophaga ani) (Mikhailov, 1997). The majority of these species incubate eggs in wet environments, where microbial abundance is likely high, suggesting that they may perform a similar function. Comparative work on eggs of other species in high-risk nesting habitats and biomimicry of this potentially useful structure will be a fertile ground for research.
MATERIALS AND METHODS
We collected 10 eggs from different Australian brush-turkey mounds located at suburban sites in Brisbane, Australia, during September 2011. Mound excavation and egg collection were performed under license by the Queensland Department of Environment and Heritage. We candled eggs at mounds to ensure that they were at early stages of development. We transported the eggs to the laboratory at Griffith University and kept them at 4°C. We used domestic chicken eggs (obtained directly from nests at Brunty Farms, Akron, OH, USA) as controls in all tests because (a) their cuticles lack nanospheres, (b) their microbiology is well understood (e.g. Board and Fuller, 1994) and (c) mechanical and chemical removal of the cuticle from brush-turkey shells compromised the integrity of the remaining shell.
We opened the eggs under sterile conditions within 24 h of collection. Egg contents were separated and a 4 ml sample of the albumen was poured into glass vials for use in antimicrobial tests. Only one egg showed any sign of embryonic development and, based on its ~0.5 cm size, was estimated to be 10 days of age (Wong, 1998). We cleaned the empty eggshells by rinsing them 5 times with water and once with 70% alcohol, then allowed them to dry for at least 24 h. We then cut 10 squares (1 cm2) from the equatorial region of each of the empty shells using a diamond-tipped circular saw (Turbo carver, LLC, WA, USA) to ensure that the structural integrity of the shell was retained. These shell pieces were used to test the bacterial attachment and eggshell penetration (see below).
Physical and chemical properties of the eggs
We used scanning electron microscopy (SEM) to measure eggshell thickness and the dimensions of the cuticle and spheres on the surface of the eggs. We mounted a small piece of shell from each egg on an aluminium stub, sputter-coated it with silver and viewed it on an SEM (JSM7401F, JEOL, Japan) fitted with an energy-dispersive analyzer (EDX). Five measurements of shell thickness and at least 10 of sphere diameter were taken per sample and averaged using ImageJ software (available for download at http://rsb.info.nih.gov/nih-image/index.html). We analyzed the elemental composition of the brush-turkey shell cuticle using EDX. This standard method uses X-rays emitted from the sample during bombardment by an electron beam to characterize the elemental composition of materials.
For lysozyme concentrations we used a modified version of the lyso-plate method (Osserman and Lawlor, 1966). Briefly, we added 25 mg dried Micrococcus lysodeikticus (Sigma, St Louis, MO, USA) to 50 ml 1% agar (Difco, Detroit, MI, USA) and kept the suspension at a temperature of 50–60°C. Then 150 μl of this suspension was added to each 10 μl albumen sample in a 96-well plate. We obtained a standard curve by adding the bacterial suspension to serial dilutions of a standard lysozyme solution. Plates were incubated overnight at room temperature and absorbance was measured with a Versamax microplate reader at 850 nm. The concentration of lysozyme in each sample was calculated by comparison of absorbance values to those in the standard curve. A detailed description of this method is given elsewhere (Shawkey et al., 2008).
Because water is required by most microbes and is essential for biofilm formation (Costerton et al., 1999; Hall-Stoodley et al., 2004), non-wetting surfaces could limit microbial growth. Wettability describes the behavior of a liquid on a solid substrate and depends on the substrate's hydrophobicity. We quantified hydrophobicity of each shell using contact angle goniometry. We measured the contact angle (θc) of 10 μl droplets of deionized water placed on each eggshell surface. Contact angles were measured by the sessile drop method, using a microscope with a commercial contact angle goniometer. A surface is considered hydrophilic if θc<90 deg, hydrophobic if θc>90 deg and superhydrophobic if θc>150 deg (Zhang et al., 2008). A second component of wettability is the tendency of water droplets to slide off a surface or stick to it. To quantify the level of attachment of drops to eggshells, we measured contact angle hysteresis using the tilting base method (Eral et al., 2013). We placed a droplet on each shell piece while attached to the goniometer. We then tilted the eggshell from 0 deg to 90 deg and measured the receding (separating from surface) and advancing (approaching to the surface) angles of the drop. The difference between these two angles is the contact angle hysteresis. Thus, poorly wetted surfaces are considered to be hydrophobic (liquid does not spread out) and have low contact angle hysteresis (the liquid shows low adhesion to the surface).
To test whether the sphere layer prevents bacterial attachment, we performed cell-attachment assays. We immersed small squares (1 cm2) of brush-turkey and chicken eggshells into suspensions of a known concentration [determined by serial decimal dilution, plating out on tryptic soy agar (TSA) and incubation overnight at 37°C] of Pseudomonas aeruginosa, Staphylococcus aureus or Escherichia coli. These strains were chosen so that both gram-positive (S. aureus) and gram-negative (E. coli, P. aeruginosa) bacteria were tested. After 3 h, we rinsed the shells with deionized water and counted the number of bacteria attached to the shell surface using SEM. We performed bacterial cell counts on five random locations across each shell piece. To control for variation in sampling area, we also calculated bacterial density per μm2 of shell surface.
We then used a modified version of a technique developed previously (Board and Board, 1967) to test the effectiveness of the eggshell at preventing microbial trans-shell penetration. We filled 4 ml sterile VIS macro cuvettes (Spectrecology, GA, USA) with molten TSA containing 1 g l−1 2,3,5-triphenyl tetrazolium chloride (TTC; Sigma-Aldrich, Bornem, Belgium). Once the agar set, we covered the cuvettes with the square eggshell pieces and sealed all four edges with silicone. Where penetration occurred, TTC was reduced to red formazan, making quantification of bacterial penetration possible. We inoculated eggshells with 10 μl of bacterial solution and incubated them for 12 days at 33°C and 90% relative humidity to mimic conditions in the mound (Jones and Goth, 2008). For each brush-turkey and chicken shell sample, we recorded the time (days) it took to first observe bacterial penetration. This assay was repeated twice.
Continuous data on eggshell thickness and lysozyme concentration met the assumptions of normality (visual inspection of Q–Q plots) and hence were analyzed using t-tests. Data from the bacterial attachment assays were not normal, so we used non-parametric comparisons (Mann–Whitney) of cell count and bacterial density. We used Cox regression to describe how the risk of penetration changes over time in chicken and brush-turkey eggs. All parametric statistical tests were two-tailed.
We thank members of the Shawkey Lab for and two anonymous reviewers for their comments on earlier versions of the manuscript.
L.D. and M.D.S. conceived, designed and carried out experiments. D.N.J., C.E. and H.T.B. performed data collection and logistic support. All authors performed manuscript writing and revision.
The authors declare no competing financial interests.
This work was supported by Human Frontier Science Program Young Investigator's grant RGY-0083 and AFOSR FA9550-13-1-0222, both to M.D.S.
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