versión On-line ISSN 1414-431X
Braz J Med Biol Res v.33 n.7 Ribeirão Preto jul. 2000
Braz J Med Biol Res, July 2000, Volume 33(7) 823-827
The use of filter paper plasticized with polyvinyl alcohol-glutaraldehyde in ELISA
1Laboratório de Imunopatologia Keizo Asami, Departamentos de 2Medicina Tropical and 3Bioquímica, Universidade Federal de Pernambuco, 4Centro de Pesquisas Aggeu Magalhães, FIOCRUZ, and 5Fundação de Hematologia e Hemoterapia de Pernambuco, Recife, PE, Brasil
6Departamento de Química, Universidade Federal de São Carlos, São Carlos, SP, Brasil
Material and Methods
Results and Discussion
Correspondence and Footnotes
F1-antigen purified from Yersinia pestis was covalently linked to 5-mm diameter filter paper discs plasticized with polyvinyl alcohol-glutaraldehyde. These discs were used both for ELISA and dot-ELISA for the detection of anti-F1 IgG in rabbits. The best conditions were achieved using 1.25 µg of F1 antigen/disc, 3% w/v skim milk in PBS as blocking agent, anti-IgG peroxidase conjugate diluted 12,000 times, and serum from rabbits immunized or not against Y. pestis, diluted 6,400 times. The absorbance values obtained from the comparative study between this procedure and conventional ELISA were not significantly different but the low cost of the reagents employed in ELISA using the filter paper discs plasticized with polyvinyl alcohol-glutaraldehyde makes this method economically attractive.
Key words: filter paper, polyvinyl alcohol, glutaraldehyde, ELISA, dot-ELISA, plague
Plague, an acute tropical disease caused by Yersinia pestis, is still an important public health issue in developing countries (1). Human cases of plague, which had virtually disappeared in Madagascar after the 1930's, reappeared in 1990 with more than 200 confirmed or presumptive cases reported each year since then (2). From 1980 to 1993, 763 cases of plague were recorded in Brazil (3). This disease is unlikely to disappear due to the wide range of mammalian hosts and their attendant fleas (4). On the other hand, the presence of significant levels of specific anti-F1A antibodies among rodents and wild or domestic carnivores (dogs and cats) indicates that all Brazilian plague foci remain active in spite of the absence of human cases (5).
The Centro de Pesquisas Aggeu Magalhães/FIOCRUZ is responsible for monitoring the occurrence of new plague cases in Northeastern Brazil. The serologic diagnosis is made by the passive hemagglutination assay (PHA), as recommended by the World Health Organization Committee specialized in plague.
Almeida and Ferreira (6) evaluated the results obtained from PHA, ELISA and dot-ELISA for the detection of plague-infected patients from Northeastern Brazil and demonstrated that PHA is not a sensitive test due to the large number of false-negative results. Thus, the serologic diagnosis of plague is still an important subject for scientific investigation.
Detection of anti-F1 IgG by ELISA has also been used for sero-epidemiological studies in Madagascar (7). Modern approaches have been reported such as the use of a fiber optic biosensor (8,9) and a PCR-based procedure (10). In our laboratories, different methods for the serologic diagnosis of this pathology have been proposed (10-14). Dacron plates and polyvinyl alcohol-glutaraldehyde discs have been used in these procedures.
In the present study, filter paper plasticized with polyvinyl alcohol-glutaraldehyde was investigated as support for the serologic diagnosis of plague.
Synthesis of filter paper plasticized with polyvinyl alcohol-glutaraldehyde
Polyvinyl alcohol (0.5 g; Reagen, Rio de Janeiro, RJ, Brazil) was dissolved in 5 ml of deionized water by heating. After cooling at 25oC, glutaraldehyde (1.25 ml of 25% w/v solution; Sigma Chemical Co., St. Louis, MO, USA) and H2SO4 (1 ml of a 0.3 M solution) were successively added under stirring. This mixture (about 7.3 ml) was then poured onto a Petri dish (9 cm in diameter) and 1 sheet of filter paper (ADVANTEC Toyo Roshi International, Inc., Dublin, CA, USA), measuring 5.5 cm in diameter, grade 2, was immersed in the mixture on the Petri dish. The soaked filter paper was allowed to dry at 25oC lying on the top of a beaker for 2-3 h. The entire procedure was carried out under a hood.
Antigen and sera
F1 antigen (4 mg/ml) from Y. pestis was obtained by the method of Baker et al. (15). Sera from rabbits immunized or not against Y. pestis and 67 µM phosphate-buffered saline (PBS), pH 7.2, containing 1 M NaCl were used as control. Goat anti-rabbit IgG labeled with horseradish peroxidase was purchased from Sigma.
The plasticized filter paper was cut into small discs using a paper punch (5 mm in diameter). The discs were then introduced into microwells of tissue culture plates containing 100 µl of F1 antigen, diluted to 1:320 (1.25 µg) and incubated at 25oC for 1 h. These antigen/plasticized discs were then washed twice with PBS containing 0.05% w/v Tween 20 (Sigma), blocked with skim milk (3% w/v in PBS; Molico milk, Nestlé) at 4oC for 12 h and washed once with PBS/Tween.
The antigen/plasticized discs were incubated with 100 µl of serum diluted 1:6,400 in PBS at 37oC for 30 min. After washing five times with PBS/Tween, the antigen-antibody-disc complex was incubated with 100 µl of goat anti-rabbit IgG conjugated with horseradish peroxidase, diluted 12,000 times in PBS, at 37oC for 30 min. Five washings with PBS/Tween were then carried out. The substrate solution (100 µl), consisting of 0.325% (w/v) orthophenylenediamine dihydrochloride (OPD; Sigma) and 0.085% v/v H2O2, prepared in 0.3 M Tris-citrate buffer, pH 6.0, was added and incubated at room temperature (28oC) for 15 min in the dark. The reaction was stopped with 2.5 M H2SO4 (25 µl), the discs were removed and the plates read in an ELISA reader (Bio-rad) at 492 nm.
The procedure was standardized according to previous studies on the best antigen concentration, blocking conditions, conjugate titration, and sera.
Antigen concentration. Samples (100 µl) of F1 antigen solution at concentrations ranging from 0.08 to 10 µg were added to the plasticized discs in flat-bottomed microplates and left to stand overnight at 25oC for 1 h, for protein (F1 antigen) immobilization.
Blocking conditions. The conditions used were as described by Araujo et al. (13).
Conjugate titration. Goat anti-rabbit IgG conjugated with horseradish peroxidase was diluted from 1:1,500 to 1:24,000 in PBS.
Serum titration. Positive sera were diluted from 1:400 to 1:51,200 in PBS and ELISA was carried out using the best conditions for blocking, conjugate dilution and antigen concentration.
Several polymers have been investigated as an alternative solid phase to be used in immunoassays. Lehtonen and Viljanen (16), studying the concentration of antigen in ELISA for the detection of chicken anti-bovine serum albumin, used three polymers as solid phase and two immobilization procedures: polystyrene and nylon (adsorption) and cyanogen bromide-activated paper (covalent link). There was a noticeable release of the adsorbed antigen during the assay from both polystyrene (30%) and nylon (60%). Desorption of antigen from activated paper during the assay was lower than with polystyrene or nylon. Bode et al. (17), studying the detection of antigen of four adenoviruses and anti-adenoviruses, reported the sensitivity of the membrane discs (nitrocellulose) to be 9-10-fold higher than in a conventional ELISA using polystyrene solid phase supports.
De Saeger and Van Peteghem (18) proposed a dipstick enzyme immunoassay for rapid antigen detection on a membrane precoated with rabbit anti-mouse immunoglobulins and monoclonal anti-T-2 toxin antibodies for the detection of Fusarium T-2 toxin in wheat.
In the present study, ELISA was based on the covalent link of F1 antigen on discs of filter paper plasticized with polyvinyl alcohol-glutaraldehyde.
Figure 1 shows the relationship between the concentration of F1 antigen on the proposed matrix and the results obtained by ELISA. A typical hyperbolic Michaelis-Menten curve (19) obtained due to the saturation of antigen-antibody complex revealed that the minimum amount of fixed antigen to produce maximum absorbance is equal to 1.25 µg protein. Figure 2 shows the relationship between goat anti-rabbit IgG conjugate dilution and ELISA performance. The 1:12,000 dilution can be used as the best conjugate concentration. The titration of immunized and non-immunized serum against F1 antigen, illustrated in Figure 3, shows that a 1:6,200 dilution would be recommended since the highest F factor value was estimated at this concentration (F @ 12). A remarkable difference in absorbance was observed between immunized and non-immunized sera, while values close to zero were detected for the control (PBS).
The antigen/plasticized discs used for this serum titration were impregnated by the colored products released during ELISA development (OPD oxidation by peroxidase). The color intensity was directly proportional to absorbance and remained unaltered for about two days. Thus, one can set up a dot-ELISA based on this antigen/plasticized discs.
A comparative study between this method and conventional ELISA based on antigen adsorption on polyvinyl chloride plates is shown in Figure 4. In this experiment, sera were collected from immunized rabbits (N = 8) and non-immunized rabbits (N = 9). Firstly, regarding the sera from immunized rabbits, the mean values (± SD) of 0.667 ± 0.264 and 0.536 ± 0.326 were calculated for the ELISA absorbance values using plasticized filter paper and conventional procedures, respectively. The independent t-test applied to both mean values at the 0.05 level showed no significant difference (t = 0.875 and P = 0.396). Also, a linear correlation was observed when plasticized filter paper values were plotted against those obtained by the conventional procedure (r = 0.986 and P = 0.00037). For the sera collected from non-immunized rabbits (N = 9) mean values of 0.127 ± 0.103 and 0.065 ± 0.045 were estimated for the plasticized filter paper and conventional ELISA procedures, respectively. The independent t-test between these values was not significant (t = 1.652 and P = 0.118). A linear correlation was also observed between the two procedures (r = 0.952 and P = 0.00007). In summary, ELISA performed on this basis is comparable to that performed by the conventional procedure.
The present results indicate that filter paper plasticized with polyvinyl alcohol-glutaraldehyde can be an alternative support for immunoassays. It is easy to synthesize and the antigen is covalently linked, therefore avoiding false-negative results due to antigen leaching. The reagents are of low cost and easy acquisition; ELISA and dot-ELISA can be simultaneously performed either in the laboratory or in the field. Small amounts of antigen (1.25 µg) and conjugate (dilution 1:12,000) were employed in the present model (experimental plague). High sensitivity was also achieved (serum dilution up to 1:51,200 still revealed differences between immunized and non-immunized serum, with an F factor higher than 5).
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Address for correspondence: L.B. Carvalho Jr., Laboratório de Imunopatologia Keizo Asami, UFPE, 50670-420 Recife, PE, Brasil. Fax: +55-81-271-8485. E-mail: firstname.lastname@example.org
Publication supported by FAPESP. Received June 21, 1999. Accepted March 10, 2000.