Janus Emulsions for the Detection of Bacteria.

Janus emulsion assays that rely on carbohydrate-lectin binding for the detection of Escherichia coli bacteria are described. Surfactants containing mannose are self-assembled at the surface of Janus droplets to produce particles with lectin binding sites. Janus droplets orient in a vertical direction as a result of the difference in densities between the hydrocarbon and fluorocarbon solvents. Binding of lectin to mannose(s) causes agglutination and a tilted geometry. The distinct optical difference between naturally aligned and agglutinated Janus droplets produces signals that can be detected quantitatively. The Janus emulsion assay sensitively and selectively binds to E. coli at 104 cfu/mL and can be easily prepared with long-time stability. It provides the basis for the development of inexpensive portable devices for fast, on-site pathogen detection.

Foodborne pathogens are a growing global public health concern. An estimated 73,000 illnesses and 60 deaths occur annually in the United States alone as a result of consuming pathogen contaminated food and water.[1]Escherichia coli, for example, can be easily spread in contaminated food and water to cause serious illness and even death. In a serious 1996 E. coli outbreak in Japan, more than 6,000 primary schoolchildren became sick and at least 12 died;[2] while in Canada, seven of the thousands of people that fell ill died in 2000.[3] Such tragedies could have been avoided if inexpensive and fast devices to test large amounts of food and water for pathogenic bacteria prior to consumption were available. The conventional method for bacterial detection requires cell culturing and a multiday enrichment step.[4] Modern methods based on surface plasmon resonance (SPR),[5] the polymerase chain reaction (PCR),[6,7] and immunoassays[8] are much more rapid but require expensive equipment that has to be operated by trained technicians. These drawbacks of the current methods surrender the possibility of food testing before consumption. As a result, an on-site detection method that is rapid, inexpensive, and user-friendly is urgently needed.

We report an emulsion based agglutination assay for the selective and sensitive detection of bacteria. Fluid Janus droplets are powerful liquid phase sensing particles when the different hemispheres are functionalized to have orthogonal physical and biochemical properties. Janus particles with covalently modified surfaces have been used for sensing applications.[9,10] We produce liquid Janus emulsions with intrinsic functionalization by using surfactant-based recognition groups. Liquid Janus emulsions provide dynamic and compliant surfaces that mimic properties of live cells. We have targeted carbohydrate–lectin interactions that are critical to cellular recognition,[11] and utilize many weak interactions in a multivalent binding process.[12] Although a commercial agglutination assay (latex fixation assay) has been used for identifying bacteria, it involves the functionalization of latex beads with expensive antigen or antibody and counting agglutination sites under a microscope.[13] Our emulsion assay uses the carbohydrate surfactant molecule, which self-assembles at the droplet surfaces during the emulsification process so that no further functionalization is required for bacteria recognition. Additionally, the intrinsic optical lensing behavior of the Janus droplets also enables both qualitative and quantitative detection of protein and E. coli bacteria. Surfactants lower the interfacial tension between two immiscible liquids and stabilize emulsion droplets. Recently, we demonstrated that stimulus-responsive surfactants can produce dynamic complex emulsions that undergo morphological switching.[14] This mechanism depends on changes in concentration or effectiveness of the surfactants and hence requires many chemical reactions to change a single droplet. In this study, we report a more sensitive transduction mechanism that does not require changes in the interfacial tensions, but rather uses the changes in the alignment of the Janus droplets for the detection of analytes. Janus morphology was maintained during the binding process, and the analyte is directly visualized by the tilted Janus droplets.

Initially, we investigated the interactions between the Janus droplets and a mannose-binding lectin, concanavalin A (ConA), which serves as a functional substitute for E. coli bacteria.[15] A simple mannose carrying an anomeric C-14 alkyl chain (ManC14) was designed as the surfactant and was synthesized via a modified literature method.[16] Janus emulsions, composed of equal volumes of hexane and FC770 (a commercially available perfluoronated solvent from 3M) in aqueous continuous phase, were fabricated. Both monodispersed and polydispersed droplets were used in this study. The detailed fabrication procedure and the dynamic nature of these droplets are explained in the Supporting Information. ManC14 and Zonyl FS300, a commercially available fluorocarbon surfactant, were then used to stabilize the emulsion assay in the Janus morphology. The Janus emulsion assay can be prepared in large scale while maintaining the stability and sensing behavior over several months. The force of gravity aligned the denser FC-770 phase downward, leading to the spontaneous alignment of the Janus emulsions in an upright direction with the hydrocarbon phase and ManC14 on top (Figure a). Aligned Janus emulsions appeared as transparent simple droplets under the microscope, and the internal structure was not apparent (Figure b). However, upon the addition of a buffered solution of ConA and gentle agitation, bound Janus droplets realigned in a unique tilted configuration with the hexane faces joined together in an agglutinated configuration (Figure c) within seconds. The hydrocarbon surfactant ManC14 self-assembled at the hexane/water interface to lower the interfacial tension and created an affinity for ConA on the hydrocarbon hemisphere. ConA has four mannose binding subunits (Figure d) and cross-links the droplets via the hydrocarbon phase to generate the tilted (agglutinated) clusters (Figure e).

Figure 1

(a) Side view of a Janus droplet stabilized by ManC14 and Zonyl FS 300. (b, c) Optical micrographs of (b) transparent pristine monodispersed Janus emulsions and (c) agglutinated Janus emulsions scattering light after exposure to ConA. Scale bar 100 μm. (d, e) Schematic representation of Janus emulsion agglutination: (d) multivalent binding of ConA to ManC14; (e) agglutinated Janus emulsions with ConA and ManC14.

Janus emulsions can become H/F/W double emulsions when additional fluorocarbon surfactant is added. To confirm that the hexane phases of Janus droplets were connected via ConA, excess fluorocarbon surfactant Zonyl was added to the agglutinated emulsion assay to induce a morphology change from Janus to double emulsions. Under these conditions, nonagglutinated Janus emulsions transform symmetrically into double emulsions H/F/W (Figure a,c). However, with ConA-agglutinated Janus emulsions, the droplets maintained an asymmetric structure wherein the preorganized ConA:ManC14 groups behaved as a persistent connective anchor to the hydrocarbon phase (Figure b,d and see also a video in the Supporting Information). Bovin serum albumin (BSA) was used as a non-mannose binding protein for the control experiments. No agglutination or significant perturbation of the optical properties was observed with even high concentration of BSA (up to 1 mg/mL, see the Supporting Information).

Figure 2

Scheme and optical images showing directional morphology change with addition of excess Zonyl surfactant. The hexane phase has been dyed in pink for display purposes. (a, c) Janus emulsion change into H/F/W double emulsion. (b, d) Agglutinated Janus emulsion with addition of ConA. Scale bar equals 50 μm.

Janus emulsions with the chosen fluids have compensating refractive indices which enable detection by optical transmission. Vertically aligned droplets on a horizontal surface are transparent, whereas the agglutinated droplets are highly scattering. (Refractive indices of fluids: hexane, 1.37; FC770, 1.27; water, 1.33. Ratio of water/FC770 = 1.05 ≈ hexane/water = 1.03, thus resulting in no scattering when light is transmitted through a vertically aligned Janus droplet.) This significant change can be easily observed by visual detection without any instrumentation or energy. Beyond a qualitative scattering/nonscattering assay, quantitative detection schemes are possible when image processing algorithms are employed to analyze the optical micrographs.

In an effort to create a qualitative binary assay for analytes, Janus emulsions were placed in a transparent analysis chamber that was positioned over a quick response (QR) code printed on paper (Figure a). Upon the addition of ConA, the Janus droplets agglutinated and the chamber became opaque, rendering the QR code unreadable by a smartphone (Figure b). This change occurred within less than five seconds after the addition of ConA and gentle agitation, which enables the Janus emulsion assay for a detection with instant readout. The Janus droplets behave as lens, and the optical scattering is strongest at distances >5 mm. At shorter distances, the QR code can still be scanned and the distance (D) at which the code was readable varies with ConA concentration (Figure c). The greater the D, the lower the concentration of ConA required to disable the QR code. As a result, binary distance dependent measurements can provide some level of quantitation.

Figure 3

(a) Schematic view of qualitative detection of the agglutinated Janus emulsions. The Janus emulsions are placed on a transparent analysis chamber. The QR code enables the binary qualitative detection of agglutination. (b) Optical signal detected using a QR code before and after exposure to ConA. (c) The focusing distance D, with droplet monolayer as a lens and QR code as the object. (d) Correlation of the threshold ConA concentration for the binary signal with D.

To precisely quantify the degree of agglutination, we implemented an image processing program to calculate the percentage of area covered by agglutinated Janus emulsions by evaluating the differences in optical intensity of the images before and after exposure to ConA. The program uses the adaptive thresholding algorithm to distinguish areas with higher transparency (pristine Janus emulsions) from the opaque regions (agglutinated Janus emulsions) (see Supporting Information). Optical micrographs of Janus emulsions, Figure a–c, show that the opaque regions increase with higher concentration of ConA. The agglutination level was defined by the percentage of areas covered by agglutinated (scattering) Janus droplets (Figure d). Each point represents an average of multiple pictures (N ≥ 5) obtained at the given concentration of ConA. The background without addition of ConA (Figure a) was analyzed with the software and showed nearly zero agglutination level output. We observed a linear correlation between agglutination level and the concentration of ConA up to 150 μg mL–1 (Figure d). At higher concentrations of ConA, agglutinated droplets saturated the imaging area, and thus a plateau in the agglutination percentage was observed.

Figure 4

Correlation of ConA concentration and agglutination level: (a) Janus emulsion without ConA; (b) with 0.03 mg mL–1 ConA; (c) with 0.12 mg mL–1 ConA. (d) Correlation between ConA concentration and agglutination level. Scale bar equals 250 μm.

Having established a detection scheme with the help of ConA, bacterial detection of E. coli ORN 178 strains was explored. These bacteria express the mannose-specific lectin, FimH, for the recognition and binding to host cells. Agglutination of droplets was observed 48 h after incubation with live E. coli. Unexpectedly, a change in morphology from Janus to H/F/W double emulsions was observed in addition to agglutination (Figure a). Symmetric Janus droplets are produced when the ManC14 and Zonyl concentrations are adjusted such that hexane/water and FC770/water interfacial tensions are equal. When live E. coli binds to ManC14, the cell appears to either reduce the effectiveness of ManC14 as surfactant at the interface or, perhaps more likely, remove some ManC14 from the droplets. The active ManC14 that was present on the surface of droplets may have been significantly decreased due to the high concentration of bacteria (>109 cfu/mL) after 48 h of proliferation. In this case, the Zonyl stabilized FC770/water interface had a lower interfacial tension resulting in the equilibrium morphology of the double emulsion (H/F/W). This morphological change was not observed upon the addition of ConA since the lectin itself is small and inanimate, and neither decreases the effectiveness of ManC14 nor removes it from the droplet. We speculate that the slower rate of agglutination for the emulsions with live bacteria as compared to ConA resulted from the dynamic nature of the pili that contain the FimH recognition elements.[17]

Figure 5

Micrographs showing emulsion agglutination with E. coli bacteria. (a) Janus emulsions change into H/F/W double emulsion after 48 h incubation with live ORN 178 E. coli. Agglutination is also observed. (b) Janus emulsion agglutination, 2 h after 4% paraformaldehyde treated ORN 178 E. coli bacteria (104 cfu/mL) were added. (c) No agglutination was observed with ORN 208 strains under the same testing conditions. Scale bar equals 100 μm.

To accelerate agglutination, bacteria were fixed via 4% paraformaldehyde.[18] While maintaining the FimH binding activity, the fixed pili are static,[19] similar to ConA, and are more efficient in agglutinating droplets. Janus emulsion agglutination was observed after 2 h with paraformaldehyde treated ORN 178 strains. To determine the limit of detection, treated bacteria were diluted to various concentrations and agglutination was detected using a smartphone and QR code recognition for ORN 178 strains at 104 cfu/mL (see the Supporting Information for a movie on smartphone-based E. coli detection). It is important to note that this method is comparable in sensitivity to the existing methods for pathogen detection. The conventional plating technique can detect single bacteria, but the culturing process takes several days. Other immunological and bioluminescence methods as well as the nucleic acid based assays have a detection limit of 103–104 cfu/mL, but require special laboratory equipment and trained technicians.[20]

As a control, ORN 208 strains, carrying a mutation in the FimH gene that compromises the pili’s ability to bind mannose, were subjected to the same tests, and no agglutination was observed at the concentrations that suffice to detect ORN 178 (Figure b, Figure c). Similar to the agglutination assay with ConA, agglutination was observed and the Janus morphology was maintained. A transformation to a double emulsion at these lower concentrations of fixed bacteria was not observed. We expect that this system can be further improved by employing more elaborate carbohydrate surfactants. In a real-world application, customized protocols will be necessary for sample preparation, and there may be interfering effects. To address the latter we have conducted investigations with non-mannose binding protein and find that the binding is not affected by the generic protein (Figure S4).

In summary, we have developed a Janus emulsion agglutination assay based on carbohydrate–lectin binding. The mannose surfactant functionalized emulsion assay described in this work was designed specifically for E. coli as a model system. The assays can be expanded to arrays with multiple carbohydrate surfactants to differentiate various types of bacterial strains. The self-assembly of glycosylated surfactant molecules on the surface of droplets provided multivalent binding sites to target analytes. We demonstrated that this agglutination detection method can be analyzed qualitatively with a QR code for a binary readout and quantitatively with designed image processing software. Both methods give results within a minute. The Janus emulsion assay allows for the detection of E. coli bacteria at a concentration of 104 cfu/mL. Therefore, this method is comparable in sensitivity to the existing methods for pathogen detection. The Janus emulsion agglutination assay is a fast, inexpensive, and sensitive method that can be implemented with commercial smartphones for on-site detection of biomolecules and pathogens.