Luminescent immunochromatography based on Eu³⁺ coordination compounds for detection of pathogenic microorganisms and bacterial toxins

INTRODUCTION

Immunochromatographic assay (ICA) in its various schemes is widely used as a rapid clinical and laboratory diagnostic tool for detecting pathogenic microorganisms and toxins in the fields of, inter alia, food safety and environmental monitoring.

Luminescent immunochromatographic assay (LICA) is a versatile rapid diagnostic method (e.g., for detection of specific antibodies to the foot-and-mouth disease virus in blood serum [1]), in which luminescent particles are used to label antibodies. LICA quantifies the blood level of cardiac markers by analyzing the luminescence intensity of a test strip [2][3]. The advantages of this method include its high reproducibility, sensitivity, and noise immunity against the natural fluorescence of the test sample. LICA is widely used for ensuring food safety [4][5] and environmental monitoring [6].

In comparison with conventional immunochromatography labels — colloidal gold nanoparticles (AuNPs), LICA provides a two- or threefold increase in sensitivity [7][8]. A comparison of fluorescent markers with AuNPs-based labels and magnetic nanoparticles in ICA can be found in [9]. Among the luminescent markers used in LICA, polymer microspheres with a diameter of 0.1–0.3 µm stand out. Their surface contains carboxyl groups, which allows covalent bonding with receptor proteins, e.g., immunoglobulins of various classes. When obtaining microspheres during polymerization, organic complexes of trivalent europium are introduced into the reaction environment, such as Eu(DBM)₃Phen, (1,10-phenanthroline)-tri- (dibenzoylmethanate) europium; Eu(TTA)₃Phen, (2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline-tri-tenoyl triphluoroacetonate) europium in the amount of no greater than 10 wt % [10]. Preparations of such microspheres absorb light in the near ultraviolet band at λ_max = 365 nm and fluoresce in the red region at λ_max = 615 nm, while possessing a narrow emission peak of fluorescence. Semiconductor diodes, photoelectronic multipliers, and video cameras are used to register the luminescence of the analytical and control zones of immunochromatography (AZ, CZ). The digital video recording (DVR) method of ICA results with various labels has a number of advantages over other design solutions. Thus, the DVR of AuNPs-based tests makes it possible to obtain quantitative data on the content of toxins in dairy products [11].

MATERIALS AND METHODS

In order to obtain conjugates, we used monoclonal antibodies MAB to the B-subunit of the cholera toxin (CT), clone 3D11 (HyTest, Russia); MAB to capsular F1 antigen of the plague pathogen; MAB to anthrax spores, clone SA26; MAB to SEB (staphylococcal enterotoxin В) clone S222 (VNCMDL, Russia); mouse polyclonal immunoglobulins to CCHF (Gamaleya National Research Center for Epidemiology and Microbiology). The same batches of antibody preparations were used to create LICHT and AuNPs-based tests.

The certified CT and SEB preparations, inactivated Y. pestis microbial cells (strain EV), inactivated B. anthracis cells, strain 942 (State Research Center for Applied Microbiology and Biotechnology), certified sucrose-acetone antigens of the CCHF virus (strain 741), genotype Europe 1 (Gamaleya National Research Center for Epidemiology and Microbiology) were used as analyzed antigens.

The synthesis of antibody conjugates with luminescent microspheres was carried out by covalent binding [12]. 5 µL of suspension of luminescent microspheres (1%, weight/volume) were dispersed in 1.0 mL of MES buffer (0.05 M, pH 6.0) and supplemented with 10 µL EDC and NHS solutions (0.5 mg/mL) to activate the carboxyl groups contained on their surface. The resulting suspension was stirred and shaken on a Vortex-3000 laboratory vortex shaker (Viggens, China) for 20 min at room temperature in the dark followed by centrifugation on a Thermo Scientific SL 4R Plus centrifuge (Thermo Fisher Scientific, USA) at ×9600 g for 15 min; the supernatant was discarded. The precipitate was resuspended in 1.0 mL of phosphate buffer (0.01 M, pH 7.4). Then 100 µL of an antibody solution was added at a concentration of 0.2 mg/mL. The resulting mixture of antibodies and activated luminescent microspheres was continuously stirred for 2 h at room temperature in the dark. Subsequently, 100 µL of a blocking solution (20% bovine serum albumin BSA) was added to block non-specific binding sites on the surface of the luminescent microspheres; the mixture was kept at room temperature for 1 h. The resulting suspension was centrifuged at 8000 g for 15 min, the supernatant was discarded, and 200 µL of a dispersing solution was added to the precipitate to prevent agglutination of conjugates of luminescent microspheres with antibodies (0.02 M, TRIS-HCl) containing 0.5% (weight/volume) trehalose, 10% (weight/volume) sucrose, 0.5% polyvinylpyrrolidone, 0.1% Tetronic 1307 (S9), 0.05% ProClinTM 300, 1% BSA and 0.1% Tween-20). Prior to application, the solution was stored at 4 °C.

For the formation of the LICHT analytical zone, the following antibodies were used: rabbit polyclonal antibodies to the B-subunit of the cholera toxin; MAB to the capsular F1 antigen of the plague pathogen clone F41F8C9; MAB to anthrax spores clone 278H4A7 (branch of the 48th Central Research Institute of the Russian Ministry of Defense, Kirov); mouse immunoglobulins to CCHF antigens (Gamaleya National Research Center for Epidemiology and Microbiology); MAB to SEB S643 (VNCMDL, Russia) at a concentration of 2.0 mg/mL. The antibodies of the LICHT control zone were goat antibodies to mouse immunoglobulins and goat antibodies to rabbit immunoglobulins (HyTest) at a concentration of 0.1 mg/mL.

A GFCP001000 glass fiber membrane and CFSP203000 and CFSP173000 cellulose membranes (Millipore), cards with TYPE-CNPF-SN12-L2-P25, 10 µ (Mdi, India) nitrocellulose membrane were used to manufacture the LICHT multimembrane composite. The finished test strips were placed in TYPE-Device-1 plastic frames (Mdi, India), the top cover of which was coated with a matte black paint. Prior to application to the glass fiber membrane, the conjugate of microspheres with antibodies was treated with ultrasound on a Labsonic 2000 dispersant (B. Braun, Germany) for 10 s followed by stirring. Then, a storage buffer was added to a concentration of 0.01%. The resulting conjugate was manually applied onto a GFCP001000 (Millipore) fiberglass membrane and dried at room temperature.

The measuring unit contains a fluorescent light source consisting of two 4 W mercury discharge lamps. The lamp flasks are made of Wood glass, which creates a field of uniform ultraviolet irradiation of immunochromatograms with a maximum wavelength at 365 nm, as well as a lamp power source. A solid-state video camera with a resolution of 1200×1600 pixels and a video shooting speed of 15 frames per sec is also located in the housing of the measuring unit. A SV580 glass luminescence emission filter is installed in front of the camera lens, ensuring a 90% transmission of radiation in the wavelength range from 600 nm to 900 nm. The video camera is connected to a laptop via a USB 2.0 connector. Plastic frames containing LICHT membranes are placed inside the device using a holder. The device allows simultaneous registration of up to five immunochromatograms; however, the possibility of measurement and single tests is also provided.

The images obtained using the device video camera were processed by a fluorescent immunochromatogram analysis software application running in Windows 7, 10.

A linear regression for the dependence of the luminescence intensity of microspheres on the membrane on the microsphere concentration was constructed using the least squares method using the Origine 6.1 software (OriginLab Corp.). The correlation coefficient of the linear relationship is R = 0.99.

Luminescent tests for the immunochromatographic detection of pathogenic microorganisms and toxins were developed in a sandwich format. A detailed description of AuNPs-based immunochromatographic tests in the sandwich format and the analytical procedure for detecting bacterial toxins and spore forms of microorganisms can be found in [13][14].

During the study, a liquid sample potentially containing pathogenic microorganisms or toxins was applied onto a sample substrate. Under the action of capillary forces, liquid moves through the multimembrane composite. First, the conjugate of microspheres with specific immunoglobulins immobilized on the surface is solubilized. The conjugate of microspheres is luminesced in the red region of the spectrum. In the presence of a detectable antigen in the sample, an antigenic immune complex is formed. This complex moves along the analytical membrane with an excess of conjugate with the flow of liquid. Next, the immune complex is captured on the analytical membrane by specific antibodies in the AZ, forming a sandwich. The unbound conjugate antibodies are captured by antibodies in the CZ of the test strip, which leads to the formation of two luminescent lines. In the absence of an antigen in the sample, an antigenic immune complex is not formed; therefore, the only line visible in ultraviolet light is formed by binding conjugate antibodies and CZ antibodies (anti-specific with respect to conjugate antibodies) only in the CZ. The appearance of tests for detecting cells of the vaccine strain of the plague causative agent based on AuNPs and on the basis of luminescent microspheres under ultraviolet irradiation with a wavelength of 365 nm is shown in Fig. 3.

Table 2 shows the detection (LICHT and AuNPs-based immunochromatography) thresholds for various pathogenic microorganisms and bacterial toxins.

Using the example of microorganisms of various taxonomic groups (vegetative and spore forms of bacteria, viruses, and bacterial toxins), Table 2 shows that the use of immunochromatography with conjugates based on microspheres with luminescent labeling of europium compounds provides a much greater sensitivity than the use of tests with AuNPs conjugates. The correctness of the comparison is ensured by using the same batches of antibodies to produce tests based on luminescent antibodies and tests based on colloidal gold nanoparticles. When comparing the sensitivity level, identical antigenic drugs were used.

DISCUSSION

The use of digital video recording of immunochromatograms in combination with microspheres containing europium complexes provides a significant gain in ICA sensitivity. This is due to the significant volume of microspheres containing a large number of europium complexes per particle and the photophysical properties of the europium complexes themselves. These compounds are excited by UV light in the near range of 365–370 nm and emit luminescence in the red region.

According to the passport data of the drug, the surface of one microsphere contains up to 353,000 of carboxyl groups with a microsphere average diameter of 190 nm. This allows for effective conjugation of luminescent microspheres with antibody proteins due to the formation of covalent bonds between the amino groups of antibodies and the carboxyl groups of microspheres. The conjugate of microspheres with immunoglobulins has a significant number of antibody valences, which contributes to the effective formation of immune complexes with antigens of bacteria, toxins, and viruses [16].

The use of video cameras as a radiation receiver is also a significant advantage in DVR [17], since the latter have high sensitivity and the ability to change the brightness, contrast, and gamut of the image. These properties of video cameras make it possible to improve the image of immunochromatograms in a wide range of luminescence intensity. In addition, the DVR does not require mechanical drives (actuators) to move immunochromatograms under the beam of exciting light.

We have obtained data on significant differences in the sensitivity of LICHT and AuNPs-based immunochromatographic tests in the detection of toxins and pathogenic microorganisms. The increased sensitivity of detection of microorganisms and toxins in the use of fluorescent tags compared to tests based on AuNPs is primarily due to the higher sensitivity of detection of fluorescent tags compared to the sensitivity of detection of colorimetric tags (AuNPs). An important factor in increasing sensitivity is the greater number of capture antibodies in the immunochromatographic conjugates of luminescent microspheres compared with similar conjugates of AuNPs. This is due to the geometric dimensions of the microparticles: the AuNPs average diameter is 30 nm, compared to the luminescent microspheres average diameter of 190 nm. These factors lead to a more efficient process of immunochromatography and detection results. It should be noted that the preparation of samples for analysis, the procedure for the analysis, and the time of its implementation do not change. Technologically, the production of LICHT and ICA tests based on AuNPs are also similar, with the exception of the conjugate synthesis stage. Therefore, no changes in the technological line of production equipment are required.

The high sensitivity of LICHT is important for the sanitary and hygienic aspect of the use of immunochromatography in general, making it possible to detect lower concentrations of pathogenic microorganisms and toxins in environmental objects, food products, and body fluids. LICHT can be useful for the immunochemical verification of microbial crops using the conventional microbiological method by reducing the cultivation time, allowing the identification of cells and bacterial toxins across a shorter period of time.

CONCLUSIONS