MEM INST OSWALDO CRUZ, RIO DE JANEIRO, 101(8) December 2006
PAGES: 875-880 DOI: S0074-02762006000800009 Full paper
Production, characterization, and application of antibodies against heat-labile type-I toxin for detection of enterotoxigenic Escherichia coli

Caroline A MenezesI; Sergio Y ImamuraI; Luiz R Trabulsi; Antônio Fernandes-FilhoII; Marina B MartinezII; Beatriz EC GuthIII; Dennys M GirãoIV; Roxane MF PiazzaI,1

ILaboratório de Bacteriologia, Instituto Butantan, Av. Vital Brazil 1500, 05503-900 São Paulo, SP, Brasil
IIDepartamento de Análises Clínicas e Toxicológicas, Faculdade de Ciências Farmacêuticas, Universidade de São Paulo, São Paulo, SP, Brasil
IIIDepartamento de Microbiologia, Imunologia e Parasitologia, Universidade Federal de São Paulo, São Paulo, SP, Brasil
IVDepartamento de Microbiologia Médica, Instituto Prof. Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brasil

Abstract

Strains of enterotoxigenic Escherichia coli (ETEC) are responsible for significant rates of morbidity and mortality among children, particularly in developing countries. The majority of clinical and public health laboratories are capable of isolating and identifying Salmonella, Shigella, Campylobacter, and Escherichia coli O157:H7 from stool samples, but ETEC cannot be identified by routine methods. The method most often used to identify ETEC is polymerase chain reaction for heat-stable and heat-labile enterotoxin genes, and subsequent serotyping, but most clinical and public health laboratories do not have the capacity or resources to perform these tests. In this study, polyclonal rabbit and monoclonal mouse IgG2b antibodies against ETEC heat-labile toxin-I (LT) were characterized and the potential applicability of a capture assay was analyzed. IgG-enriched fractions from rabbit polyclonal and the IgG2b monoclonal antibodies recognized LT in a conformational shape and they were excellent tools for detection of LT-producing strains. These findings indicate that the capture immunoassay could be used as a diagnostic assay of ETEC LT-producing strains in routine diagnosis and in epidemiological studies of diarrhea in developing countries as enzyme linked immunosorbent assay techniques remain as effective and economical choice for the detection of specific pathogen antigens in cultures.

Diarrhea caused approximately two million deaths per year worldwide in the last decade (WHO-UNICEF 2002), and was responsible for an estimated 16-32% (median 21%) of mortality in children aged 0-4 years in developing countries (Kosek et al. 2003). One of the major etiologic agents is enterotoxigenic Escherichia coli(ETEC), known to be endemic in essentially all developing countries. Besides ETEC strains are also usually responsible for the acute diarrhea that affects visitors to the tropics (Ericsson 2003). In Brazil, these pathogens are responsible for up to 20% of cases of infantile diarrhea, region and season dependent (Reis et al. 1982, Trabulsi et al. 1985, Gomes et al. 1991, Almeida et al. 1998, Souza et al. 2002, Fernandes-Filho et al. 2003, Franzolin et al. 2005, Barreto et al. 2006).

Specific virulence factors such as enterotoxins and colonization factors differentiate ETEC from other categories of diarrheagenic E. coli. ETEC belongs to a heterogeneous family of lactose-fermenting E. coli, belonging to a wide variety of O antigenic types. These strains produce enterotoxins (heat labile and/or heat stable), and colonization factors, which allow the organisms to readily colonize the small intestine and in this way cause diarrhea (Sack 1980, Wolf 1997, Nataro & Kaper 1998).

Since ETEC can be recognized by the enterotoxins it produces, diagnosis must depend upon identifying either heat-labile toxins (LT) and/or heat-stable toxin (ST). One or both toxins may be expressed by ETEC. LT belongs to a structurally and functionally related AB5 enterotoxin family, in which the A subunit has the toxic activity and B subunit is responsible for toxin binding to cell receptor.

Enzyme-linked immunosorbent assay (ELISA) techniques employing a 96-well microtiter plate format are simple to operate and remain an effective and economical choice for the detection of specific pathogens in cultures. Then, several immunological assays have been described, mainly the protocol that LT is captured by ganglioside GM1, its receptor in the host cell (Gustafsson & Molby 1982, Ristaino et al. 1983, Sven-nerholm & Wiklund 1983, Sen et al. 1984, Bongaerts et al. 1985). Additionally, agglutination assays were developed for LT detection (Speirs et al. 1991). Unfortunately, in spite of all these available techniques, there are still no simple, readily available methods that can be used to identify these organisms in minimally equipped laboratories. For that reason, many laboratories conducting studies on diarrhea in developing countries do not include ETEC in their routine diagnosis (Qadri et al. 2005).

We have previously described the development of a capture immunoassay for detection of ETEC producing LT-I (Menezes et al. 2003). The estimated accuracy of this assay was 78% of sensitivity, 94% of specificity, and 92% of efficiency. In this analysis, we have employed an IgG enriched fraction of a polyclonal rabbit and monoclonal mouse IgG2b anti-LT antibodies. In the present study, these antibodies were characterized immunochemically, besides we better describe the capture assay and check its applicability to detec LT-I in supernatants of bacterial isolates.

 

MATERIALS AND METHODS

Polymyxin B sulphate, Freund complete adjuvant, orthophenylenediamine (OPD), 3,3-Diaminobenzidine tetrahydrochloride (DAB), Coomassie blue R-250, polyethylene glycol 4000 (PEG), HAT medium, HT medium, anti mouse IgG1, IgG2a, IgG2b, IgG3, IgA, and IgM, were obtained from (Sigma Aldrich Co, St Louis, MA, US). RPMI media and foetal calf serum from Cultilab (Campinas, SP, Brazil). Horseradish peroxidase-conjugated anti-rabbit IgG, anti-mouse IgG, and anti-mouse IgG/A/M from Zymed Laboratories Inc (San Francisco, CA, US). Protein G and protein A Sepharose affinity chromatography column was purchased from GE Healthcare.

Bacterial strains - The bacterial isolates used in this study consisted in 44 strains previously defined as ETEC by genes presence: LT-I (30 isolates) and LT-I/ST-Ih (14 isolates) isolated from different geographic areas of Brazil (Nishimura et al. 1996, Girão et al. 2001, Souza et al. 2002, Fernandes-Filho et al. 2003). In addition, 298 E. coli strains isolated from stools of children, with and without diarrhea, from sporadic cases in Brazil previously determined by molecular methods as LT/ST negative (Fernandes-Filho et al. 2003) was used, as well as 25 enteric Gram-negative strains, other than E. coli, including Vibrio cholerae, Salmonella spp., Shigella spp., Klebsilella spp., Edwardsiella, Citrobacter spp., Morganella morgani, Proteus spp., Enterobacter spp.,and Providencia spp. isolates as part of our laboratory collection. E. coli H10407 (Evans et al. 1977) and 258909 (Qadri et al. 2000) were included as ETEC prototype strains.

Culture conditions- The strains were cultivated in 2% casamino acids, 0.15% yeast extract, and salts medium (CYE) (Evans et al. 1973) at 37ºC, 200 rpm for 18 h. Then each culture was incubated for 30 min at 37ºC, 200 rpm with polymyxin (1 mg/ml, final concentration) (Cerny & Tauber 1971, Strockbine et al. 1985) and centrifuged at 1600 x g for 20 min. The supernatants were kept at -20ºC until use.

Purified LT toxin- LT toxin was purified as described by Bowman and Clements (2001) and was kindly donated by Dr John D Clements from Department of Microbiology and Immunology, Tulane University Health Sciences Center, New Orleans, Louisiana, US.

Anti-LT-I polyclonal antibodies - New Zealand rabbits were immunized subcutaneously with 100 µg of purified LT in complete Freund's adjuvant. Serum samples were obtained just before immunization by auricular-venom method to be used as negative control in specific antibody evaluation. Serum samples were also obtained 30 days after antigen injection and subsequently analyzed by ELISA. The IgG-enriched fractions were obtained from rabbit antisera (Menezes et al. 2003) after being submitted to caprylic acid and ammonium sulphate precipitation as described by McKinney and Parkinson (1987), and its purity was observed by SDS/PAGE 15% (Laemmli 1970, Studier 1973) after Coomassie blue R-250 staining.

Monoclonal antibody (Mab) production - Four to six week-old female Balb/c mice were immunized with 2 µg of purified LT in complete Freund's adjuvant. The immunization protocol consisted of three injections of 20-µl of the toxin in PBS at four-weeks interval. Serum samples were obtained just before the first immunization by retro-orbital sinus method, to be used as negative control in specific antibody evaluation. Serum samples were also obtained ten days after the last antigen injection and subsequently analyzed by ELISA.The mouse with the highest antibody titer was boosted with 10 µg of purified LT without adjuvant four days prior to cell fusion, and then sacrificed by cervical dislocation. Popliteal lymphnodes were removed aseptically and single cell suspensions were prepared by mechanically disrupting the tissues through a sterile nylon cloth sieve (100 µm pore size) into RPMI media containing penicillin/streptomycin. The popliteal lymphnode cells were fused with SP2/O-Ag14 mouse myeloma cells (2:1) using polyethylene glycol 4000. The fused cells were suspended and selected in HAT-RPMI 1640 medium containing 10% FCS into 96-well microplates (Techno Plastic Products AG, TPP, Switzerland). The microplates were incubated at 37°C in the presence of 5% CO2 for 12 days. In order to screen cultures for antibodies production, 100 µl of culture supernatant were added to wells of 96-well (Nunc-Immuno PolySorp) plate previously coated with purified LT. The ELISA test was completed as described above. Hybridoms from cultures showing significant antibody production were selected and cloned by limiting dilution culture.

Isotyping of monoclonal antibody - Nunc-Immuno PolySorp plate was coated overnight at 4°C with a solution (100 µl/well) containing anti mouse IgG1 (10 µg/ml), IgG2a (10 µg/ml), IgG2b (10 µg/ml), IgG3 (10 µg/ml), IgA (100 µg/ml), and IgM (100 µg/ml) in 0.05 M sodium carbonate-bicarbonate buffer (pH 9.6). The reaction was followed by incubating supernatants of hybridoms and followed by a horseradish peroxidase-conjugated anti-mouse IgG/A/M antibody. The absence of non-specific IgM antibodies was assured by incubating the antibodies in wells coated with 0.05 M sodium carbonate-bicarbonate buffer (pH 9.6).

Purification of Mab- The supernatants from the selected clones were filtered (0.45 µm) and purified by affinity chromatography. The antibodies were eluted using 0.1 M citric acid solution (pH 3.0) and harvested in 1 M Tris-solution (pH 9.8). The antibody solution was concentrated by lyophilization and its purity was observed by SDS/PAGE 15% (Laemmli 1970, Studier 1973) after Coomassie blue R-250 staining.

Affinity of LT-antibodies - The dissociation constant (KD) of LT-antibodies was determined by their affinity to LT toxin as described by Friguet et al. (1985). Antibodies were incubated in solution with different antigen concentration until the equilibrium was reached, then a classical indirect ELISA measured the proportion of antibody that remained unsaturated at equilibrium. The dissociation constant was deduced by linear regression by Scatchard method.

LT-antibodies characterization by immunoblotting - To further access the reactivity of antibodies to purified LT toxin, an immunoblotting analysis was performed using polyclonal and monoclonal LT-antibodies. Briefly, 10 µg per slot of purified LT toxin were applied to a 15% SDS-polyacrilamide gel (Laemmli 1970, Studier 1973). After electrophoresis, the separated proteins were transferred to nitrocellulose membrane (Hybond C-Extra, Amersham Life Science) at 100 V for 18 h at 4ºC. The membrane was blocked with 3% BSA for 2 h and reacted with IgG-enriched fraction of polyclonal anti-LT antibody (5 µg/ml) and monoclonal LT-antibodies (18 µg/ml IgG1 or IgG2b) for 18 h at 4ºC. The membrane was then washed and incubated for 2 h with horseradish peroxidase-conjugated anti-mouse IgG diluted 1:10,000 or anti-rabbit IgG diluted 1/10,000. After washing, the substrate 3,3-Diaminobenzidine tetrahydrochloride plus hydrogen peroxide was added and the reaction was stopped by distilled water addition.

Sensitivity and specificity of capture assay in detecting LT-I - The sensitivity and specificity of the capture assay was determined as described by Menezes et al. (2003) in the standardization of the capture ELISA immunoassay. Here we tested different concentrations of purified LT (from 100 µg to 0.7 ng) or supernatants of bacterial isolates. ELISA optical densities (A492nm) data were analyzed by mean and standard error using GraphPad Prism 3.00®. Differences between ODs of LT producing- and non-producing strains were considered significant when the probability of equality was less than 0.05 (p < 0.05).

GM1 ELISA assay- Microtiter plates (Nunc Im-munoplate, Maxisorp) were incubated at 37ºC for 16 h with 1.25 µg/ml ganglioside GM1 (Sigma Aldrich Co.) in phosphate-buffered saline, pH 7.2 (PBS). And the reaction was developed according to Svennerholm and Wiklund (1983). Toxin bound to GM1 was then detected with 10 µg/ml of IgG2b monoclonal antibody, followed by anti-mouse IgG peroxidase diluted 1:10,000. The reaction was developed by adding freshly prepared solution of OPD plus H2O2 recording of the A492 on a Multiskan EX ELISA reader.

 

RESULTS

Polyclonal and Mab characterization - The immunization protocols used in both New Zealand rabbits and Balb/c mice generated high antibody titers against LT-I toxin. The mean of optical densities at 492 nm reached to 1.2 until 51,200 of serum dilutions in both rabbits and mice immunized with LT-I. In order to avoid cross-reaction of sera proteins other than IgG, polyclonal sera were submitted to caprylic acid and ammonium sulfate precipitations. The SDS/PAGE profile demonstrated that, despite the presence of minor proteins, the major polypeptide of apparent molecular weight of 150 kDa under non-reducing conditions (Fig. 1, lane 1), and two components of molecular weigh of approximately 50 kDa and 25 kDa, under reducing conditions, were observed in the IgG-enriched fraction (Fig. 1, lane 2). In addition, this fraction recognized both A and B subunits of LT-I by immunoblotting, with apparent molecular weights of 28 kDa and 12 kDa, respectively (Fig. 2, line 1), and presented a dissociation constant of 0.97 ' 10-7 M.

 

 

 

 

After the fusion with popliteal lymphnode and mouse myeloma cells and several sub cloning by limiting dilutions, two Mab were obtained, one IgG1 and one IgG2b, both of them specific for LT toxin. The monoclonal antibodies were purified by affinity chromatography and a component of apparent molecular weight of 146 kDa was observed in SDS-PAGE under non-reducing conditions (Fig. 1, lane 3), and in a reducing condition two components of apparent molecular weight of 50 kDa and 25 kDa were observed (Fig. 1, lane 4). They recognized by immunoblotting the A and B subunits of LT-I (Fig. 2, line 2). The IgG2b showed a constant dissociation of 2.2 ' 10-8 M. On the other hand, IgG1 Mab showed dissociation constant of 1.3 ' 10-7 M.

Sensitivity and specificity of capture assay in detecting purified LT and LT-I in supernatant of bacterial isolates - Twenty-five µg/ml of anti-rabbit LT IgG enriched fraction and 10 µg/ml of IgG2b Mab allowed the capture of less then 10 ng of purified toxin (Fig. 3). In the same antibody concentrations, the reaction cut off was 0.173, defined by mean and standard error of optical densities from supernatants of the 298 non-producing LT-I E. coli strains and the 25 enteric Gram-negative strains. The 46 LT-I producing strains presented a range of OD from 0.759 to 1.191 (median of 0.943), which allows a clear distinction between producing- and non-producing LT E. coli isolates (Fig. 4). Statistical analysis showed that the difference between LT producing- and non-producing strains by mean and standard deviation were considered significant (p < 0.0001) in the capture assay.

 

 

 

 

 

DISCUSSION

Evidence has accumulated showing that both LT A- and B-subunits have distinct immunomodulatory activities, which act synergistically, promoting a potent antitoxin response (Pizza et al. 2001, Fraser et al. 2003). Thus, as expected, both New Zealand rabbits and Balb/c mice immunized with low concentration of LT-I toxin elicited high antibody titers. However, despite of LT high immunogenicity, seven fusions with popliteal lymphnode cells and mouse myeloma cells were necessary to get two stable and positives clones, classified as IgG1 and IgG2b, both of them specific for LT. In contrast, Lindholm et al. (1983) obtained 70 secreting Mab against cholera toxin, in which 14 clones showed full cross-reactivity with LT, and they presented different IgG isotypes after immunizing mice intraperitoneally or intravenously and fusing the spleen cells. In this way, the selection of few IgG-secreting clones is probably related to the fact that we used popliteal lymphnode cells of immunized mice for the hybridization experiments, which was responsible for isotype selection and number of positive clones.

IgG-enriched fractions from rabbit polyclonal, and the IgG2b Mab recognized LT in a conformational shape (A and B subunit). Using these tools for detection of LT-producing strains the sensitivity and specificity of the capture immunoassay were 100 and 99%, respectively. The high sensitivity of the assay can be related to the use of CYE medium (Evans et al. 1973, Beutin et al. 1988) instead of Luria-Bertani (LB) broth medium, and also to the use of polymyxin (Cerny & Tauber 1971, Strockbine et al. 1985, Beutin et al. 1989, Bowman & Clements 2001). As LT is known to be peri-plasmatic in ETEC and not secreted into the medium, both conditions stimulate LT production.

Microtiter GM1 ganglioside methods are widely employed for the detection of LT toxin (Gustafsson & Molby 1982, Ristaino et al. 1983, Svennerholm & Wiklund 1983, Sen et al. 1984, Bongaerts et al. 1985). Thus, the sensitivity and specificity of the capture immunoassay standardized by Menezes et al. (2003) was compared with GM1 ELISA. Despite the fact that GM1 is commercially available, the specificity of the assay is antibody dependent. The IgG2b Mab recognized with more intensity the A subunit. This fact might explain the low sensitivity (69%) of GM1-ELISA in detecting LT-I producing strains in supernatants. The efficiency of the capture immunoassay was due to IgG-enriched fraction of rabbit LT antisera and IgG2b Mab, since both of them recognized LT in a conformational shape (A and B subunit) thus allowing the capture of even low expressing-LT-I ETEC isolates.

It is important to mention that the results presented here are part of a project in which polyclonal and Mab against virulence factors of diarrheagenic E. coli patho-types have been raised. The development of immunoassays for detecting these pathogens is the goal of our group (Menezes et al. 2003, Koga et al. 2003, Vilhena-Costa et al. 2006). These findings indicate that the capture immunoassay could be used as a diagnostic assay of ETEC LT-producing strains in routine diagnosis and in epidemiological studies of diarrhea in Brazil and other developing countries.

 

ACKNOWLEDGMENTS

To Dr John D Clements, Department of Microbiology and Immunology, Tulane University Health Sciences Center, New Orleans, US for kindly providing purified LT toxin; Vanessa Bueris, Dr Waldir P Elias, and Dr Martha H Sonobe for helpful suggestions and discussions.

 

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Received 6 June 2006
Accepted 19 September 2006
Financial support: Fapesp (grant 99/09458-0 to RMFP and fellowship to CAM), CNPq fellowship to SYI

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